STUDY_ACCESSION	STUDY	reason
GCST007684	Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST007685	Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST007686	Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST010563	Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits.	Missing MAPPED_TRAIT_URI
GCST010564	Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits.	Missing MAPPED_TRAIT_URI
GCST010565	Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits.	Missing MAPPED_TRAIT_URI
GCST011378	The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages.	Missing MAPPED_TRAIT_URI
GCST011401	A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST011402	A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST011998	Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012420	A Genome-Wide Association Study in Human Lymphoblastoid Cells Supports Safety of Mitochondrial Complex I Inhibitor.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012436	Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD.	Missing MAPPED_TRAIT_URI
GCST012437	Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD.	Missing MAPPED_TRAIT_URI
GCST012441	Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD.	Missing MAPPED_TRAIT_URI
GCST012479	First genome-wide association study on rocuronium dose requirements shows association with SLCO1A2.	Missing MAPPED_TRAIT_URI
GCST012493	An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training-induced muscle fiber hypertrophy in younger men.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012500	Genome-wide association study of cardiac troponin I in the general population.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012501	Identification of Three Loci Associated with Achilles Tendon Injury Risk from a Genome-wide Association Study.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012516	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012517	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012518	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012519	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012520	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012521	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012522	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90013686	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing MAPPED_TRAIT_URI
GCST90016666	Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.	Missing MAPPED_TRAIT_URI
GCST90016667	Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.	Missing MAPPED_TRAIT_URI
GCST90016668	Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.	Missing MAPPED_TRAIT_URI
GCST90016669	Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.	Missing MAPPED_TRAIT_URI
GCST90016670	Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.	Missing MAPPED_TRAIT_URI
GCST90016675	Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.	Missing MAPPED_TRAIT_URI
GCST90018716	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing MAPPED_TRAIT_URI
GCST90018936	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing MAPPED_TRAIT_URI
GCST90019043	Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90019044	Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90019045	Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90020216	Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHD.	Missing MAPPED_TRAIT_URI
GCST90025936	Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.	Missing MAPPED_TRAIT_URI
GCST90025937	Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90027882	Single nucleotide variations in ZBTB46 are associated with post-thrombolytic parenchymal haematoma.	Missing MAPPED_TRAIT_URI
GCST90032665	Human genomics of the humoral immune response against polyomaviruses.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90032670	Human genomics of the humoral immune response against polyomaviruses.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90032674	Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.	Missing MAPPED_TRAIT_URI
GCST90044847	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000002	High-resolution whole-genome association study of Parkinson disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000005	Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000010	Novel genes identified in a high-density genome wide association study for nicotine dependence.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000013	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000016	Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000020	Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000026	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000032	A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000041	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000044	Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000063	A whole genome association study of neuroticism using DNA pooling.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000064	Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000072	ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000077	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000079	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000080	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000084	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000086	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000087	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000089	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000090	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000092	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000093	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000095	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000097	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000098	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000099	Framingham Heart Study genome-wide association: results for pulmonary function measures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000100	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000101	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000102	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000104	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000105	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000106	Framingham Heart Study genome-wide association: results for pulmonary function measures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000107	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000108	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000109	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000110	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000111	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000126	A genome-wide association study of sporadic ALS in a homogenous Irish population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000129	Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000155	Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000163	A genome-wide association study in 574 schizophrenia trios using DNA pooling.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000164	Genomewide association for schizophrenia in the CATIE study: results of stage 1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000172	Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000186	Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000201	Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000202	Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000209	Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000211	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000212	Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000215	Identification of loci associated with schizophrenia by genome-wide association and follow-up.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000226	Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000229	Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000235	Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000236	Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000245	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000247	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000253	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000255	Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000260	Screening for replication of genome-wide SNP associations in sporadic ALS.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000261	Genomewide association study for susceptibility genes contributing to familial Parkinson disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000265	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000266	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000267	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000268	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000269	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000271	A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000272	Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000273	Genome-wide association scan for five major dimensions of personality.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000278	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000279	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000280	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000281	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000304	Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000306	From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000307	Sequence variants at 22q13 are associated with prostate cancer risk.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000309	Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000310	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000314	A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000315	Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000323	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000326	Genome-wide association study of acute post-surgical pain in humans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000327	Genome-wide association study of anthropometric traits in Korcula Island, Croatia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000330	Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000344	Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000349	Genome-wide and candidate gene association study of cigarette smoking behaviors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000356	Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000359	A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000361	Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000376	A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000387	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000407	Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000411	A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000412	Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000413	A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000417	Genome-wide association study of bipolar disorder in European American and African American individuals.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000447	A genome-wide association study of hypertension and blood pressure in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000461	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000468	Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000469	Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000473	Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000474	Genome-wide association study of exercise behavior in Dutch and American adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000477	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000487	Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000490	Genomewide association study for onset age in Parkinson disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000491	A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000496	A genome-wide linkage and association scan reveals novel loci for autism.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000509	A genomewide association study of citalopram response in major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000511	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000512	Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000515	IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000520	Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000540	A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000551	Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000556	A genome-wide association study of amygdala activation in youths with and without bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000558	A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000566	A genome-wide association study for age-related hearing impairment in the Saami.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000567	Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000575	Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000576	Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000577	MGAT5 alters the severity of multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000578	Genome-wide association study of recurrent early-onset major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000579	Common genetic variation and performance on standardized cognitive tests.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000596	Multistage genomewide association study identifies a locus at 1q41 associated with rate of HIV-1 disease progression to clinical AIDS.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000597	Voxelwise genome-wide association study (vGWAS).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000607	Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000614	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000615	Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000628	Chemerin, a novel adipokine in the regulation of angiogenesis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000630	A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000632	A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000633	Genetic variants and risk of lung cancer in never smokers: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000636	Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000642	Genome-wide association study of height and body mass index in Australian twin families.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000654	Genome-wide association study of bipolar I disorder in the Han Chinese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000655	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000656	Host determinants of HIV-1 control in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000658	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000659	Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000661	Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000676	Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000684	Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000689	Genome-wide association study of major recurrent depression in the U.K. population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000691	Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000714	Genome-wide association study of conduct disorder symptomatology.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000715	Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000720	Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000724	A genome-wide association study of neuroticism in a population-based sample.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000743	Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000744	Genetic variants that affect length/height in infancy/early childhood in Vietnamese-Korean families.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000745	Genome-wide association study of pancreatic cancer in Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000747	A genome-wide association study of self-rated health.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000748	Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000751	Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000754	A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000765	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000766	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000767	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000770	Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000778	Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000779	Genome-wide association scan of trait depression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000783	Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000785	Joint influence of small-effect genetic variants on human longevity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000789	Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000797	Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000798	The TCF7L2 diabetes risk variant is associated with HbA₁(C) levels: a genome-wide association meta-analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000800	Common variants at 19p13 are associated with susceptibility to ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000813	Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000816	Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000820	Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000822	Genome-wide association study of antipsychotic-induced QTc interval prolongation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000823	Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000825	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000837	Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000838	Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000839	Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000840	Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000852	Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000854	Genome-wide association study of suicide attempts in mood disorder patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000856	Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000857	Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000861	A genome-wide association study of DSM-IV cannabis dependence.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000862	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000869	Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000871	Genome-wide association study on overall survival of advanced non-small cell lung cancer patients treated with carboplatin and paclitaxel.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000873	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000878	Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000881	A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000883	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000884	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000885	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000890	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000891	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000892	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000894	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000895	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000896	Genome-wide interrogation identifies YAP1 variants associated with survival of small-cell lung cancer patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000898	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000899	Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000900	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000902	Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000903	Genome-wide association study of blood pressure response to methylphenidate treatment of attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000904	Variants in several genomic regions associated with asperger disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000905	Whole genome association scan for genetic polymorphisms influencing information processing speed.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000908	A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000909	A genome-wide association study for diabetic nephropathy genes in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000910	Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000918	Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000922	Meta-analysis of genome-wide association studies for personality.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000924	Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000932	Genome-wide association study of hoarding traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000938	Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000939	A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000956	The nuclear transcription factor PKNOX2 is a candidate gene for substance dependence in European-origin women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000962	Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000969	Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000972	Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000976	Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000977	Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000980	Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST000982	Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000983	A non-synonymous polymorphism in galactose mutarotase (GALM) is associated with serotonin transporter binding potential in the human thalamus: results of a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000990	Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001002	Cerivastatin, genetic variants, and the risk of rhabdomyolysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001012	Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001014	HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001016	Atopy history and the genomics of wheezing after influenza vaccination in children 6-59 months of age.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001017	Genome-wide meta-analysis for severe diabetic retinopathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001018	Common variation in GPC5 is associated with acquired nephrotic syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001019	Meta-analysis of genome-wide association for migraine in six population-based European cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001020	Genome-wide association study identifies genetic loci associated with iron deficiency.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001024	A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001030	Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001031	Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001034	Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001035	Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001045	Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001046	Replication of 13 obesity loci among Singaporean Chinese, Malay and Asian-Indian populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001048	Genetic and clinical correlates of early-outgrowth colony-forming units.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001052	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001053	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001054	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001055	A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001061	Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001065	Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001066	Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001081	Association study on long-living individuals from Southern Italy identifies rs10491334 in the CAMKIV gene that regulates survival proteins.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001083	Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001092	Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001095	Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001096	Genome-wide association study of severity in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001102	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001104	GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001108	Genome-wide association study of smoking behaviours in patients with COPD.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001110	A genome-wide association study for quantitative traits in schizophrenia in China.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001111	Genome-wide association study of smoking behaviours in patients with COPD.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001112	Genome-wide association study of smoking behaviours in patients with COPD.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001113	Genome-wide association study of smoking behaviours in patients with COPD.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001115	Genome-wide association analysis of age at onset in schizophrenia in a European-American sample.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001119	DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001121	A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001125	Genome-wide association of BMI in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001135	Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001136	Interstitial lung disease in gefitinib-treated Japanese patients with non-small-cell lung cancer: genome-wide analysis of genetic data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001154	Genome-wide association study of the child behavior checklist dysregulation profile.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001157	Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001164	Genome-wide association study on bipolar disorder in the Bulgarian population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001166	A genome-wide association study of aging.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001167	A genome-wide association study of aging.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001186	Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rash.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001188	Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001189	Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001196	DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001201	Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001204	Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001208	Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001210	The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001211	Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001214	A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001244	Genome-wide association scan for childhood caries implicates novel genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001245	Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001254	Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001271	The genetics of antipsychotic induced tremors: a genome-wide pathway analysis on the STEP-BD SCP sample.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001272	Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001282	Genome-wide association study of Alzheimer's disease with psychotic symptoms.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001284	Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001286	Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001287	Genome-wide association study in German patients with attention deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001291	Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001304	Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001308	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001313	Genome-wide association study of comorbid depressive syndrome and alcohol dependence.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001315	Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001325	Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001330	Genetic variants and environmental factors associated with hormonal markers of ovarian reserve in Caucasian and African American women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001342	A comprehensive genetic association study of Alzheimer disease in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001343	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001352	Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001353	Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001354	Heritability of submaximal exercise heart rate response to exercise training is accounted for by nine SNPs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001356	Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001365	A genome-wide association study of the Protein C anticoagulant pathway.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001366	Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001369	A genome-wide association search for type 2 diabetes genes in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001373	Novel genetic markers of breast cancer survival identified by a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001376	Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001380	Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001389	The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001390	A genome-wide association study identifies four genetic markers for hematological toxicities in cancer patients receiving gemcitabine therapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001402	Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001404	A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001417	Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001423	A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001428	Genome-wide association study of intelligence: additive effects of novel brain expressed genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001431	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001440	Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001442	Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001446	A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001448	A novel locus for body mass index on 5p15.2: a meta-analysis of two genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001453	Genome-wide association study of SSRI/SNRI-induced sexual dysfunction in a Japanese cohort with major depression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001458	Genome-wide association study of treatment refractory schizophrenia in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001460	A high-density genome-wide association screen of sporadic ALS in US veterans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001462	Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001469	A mega-analysis of genome-wide association studies for major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001470	SSBP2 variants are associated with survival in glioblastoma patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001477	A genome-wide association study of female sexual dysfunction.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001494	A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001495	Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001510	Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001511	The genetic architecture of economic and political preferences.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001512	The genetic architecture of economic and political preferences.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001513	The genetic architecture of economic and political preferences.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001514	The genetic architecture of economic and political preferences.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001515	The genetic architecture of economic and political preferences.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001518	Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001519	The genetic architecture of economic and political preferences.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001520	Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001521	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001523	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001528	Possible association of CUX1 gene polymorphisms with antidepressant response in major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001531	A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001540	Genome-wide association study identifies candidate genes for male fertility traits in humans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001542	Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001543	Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001545	Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001546	Genomic determinants of motor and cognitive outcomes in Parkinson's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001547	A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001549	PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001553	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001555	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001558	A genome-wide association study for irinotecan-related severe toxicities in patients with advanced non-small-cell lung cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001559	A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001567	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001569	Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001572	Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001583	A variant in the LRRFIP1 gene is associated with adiposity and inflammation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001584	Bivariate genome-wide association study suggests that the DARC gene influences lean body mass and age at menarche.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001586	A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001588	Genome-wide association study of periodontal pathogen colonization.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001590	Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001597	Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001598	Genome-wide linkage and association scans for pulse pressure in Chinese twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001599	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001601	Genome-wide association study of a quantitative disordered gambling trait.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001616	The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001619	Individual common variants exert weak effects on the risk for autism spectrum disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001626	Genome-wide association study identifies TNFSF13 as a susceptibility gene for IgA in a South Chinese population in smokers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001629	Genome-wide association study of prognosis in advanced non-small cell lung cancer patients receiving platinum-based chemotherapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001636	Genome-wide association study of obsessive-compulsive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001638	Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001644	Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001647	A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001648	A genome-wide association study of breast cancer in women of African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001656	Bivariate genome-wide association study suggests fatty acid desaturase genes and cadherin DCHS2 for variation of both compressive strength index and appendicular lean mass in males.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001657	Genome-wide association study of multiplex schizophrenia pedigrees.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001658	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001663	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001667	A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001668	Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001680	Genetic variants near PDGFRA are associated with corneal curvature in Australians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001689	A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001692	Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001694	Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001704	A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001715	Genome-wide association of mood-incongruent psychotic bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001721	Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001732	Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001734	Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001736	Novel susceptibility genes associated with diabetic cataract in a Taiwanese population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001739	A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001744	Impact of four loci on serum tamsulosin hydrochloride concentration.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001747	Genome-wide association study of aspirin-exacerbated respiratory disease in a Korean population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001749	Genome-wide association study of survival in patients with pancreatic adenocarcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001751	Genome-wide association study identifies a potent locus associated with human opioid sensitivity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001753	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001754	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001756	Genome-wide association study identified UQCC locus for spine bone size in humans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001757	Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001760	White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001764	White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001766	Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001771	TMPRSS9 and GRIN2B are associated with neuroticism: a genome-wide association study in a European sample.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001786	Genome-wide association scan of dental caries in the permanent dentition.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001802	A genome-wide association study of depressive symptoms.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001811	Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001816	Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001817	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001818	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001819	Identification of a candidate gene for astigmatism.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001820	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001822	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001823	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001824	Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001831	Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001832	A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001833	Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001835	Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001836	BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001837	Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001839	Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001843	Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001847	A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of urinary symptoms after radiotherapy for prostate cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001854	Genome-wide association study of retinopathy in individuals without diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001872	Genome-wide association study of antiphospholipid antibodies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001879	A genome-wide scan for breast cancer risk haplotypes among African American women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001888	Exploring the genetic basis of chronic periodontitis: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001890	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001895	Genetic determinants of dabigatran plasma levels and their relation to bleeding.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001896	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001897	Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001901	A genome-wide association study of survival in small-cell lung cancer patients treated with irinotecan plus cisplatin chemotherapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001909	Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001911	A genome-wide association study of bronchodilator response in asthmatics.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001918	Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001920	Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001921	Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001922	Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001925	Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001926	Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001927	Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001931	Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001934	Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001935	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001943	Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001944	Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001949	Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001952	The molecular genetic architecture of self-employment.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001958	Genetic variants associated with disordered eating.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001959	Genetic variants associated with disordered eating.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001960	Genetic variants associated with disordered eating.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001961	Genetic variants associated with disordered eating.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001966	Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001971	Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001972	Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001975	Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001977	Genome-wide association study in a Chinese population with diabetic retinopathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001983	Genome-wide scan of job-related exhaustion with three replication studies implicate a susceptibility variant at the UST gene locus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001990	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001991	Weight loss after gastric bypass is associated with a variant at 15q26.1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001993	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001994	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001995	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001996	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001997	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001998	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST001999	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002000	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002001	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002002	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002003	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002004	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002005	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002006	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002007	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002008	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002009	Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002013	Genome wide association study of age at menarche in the Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002017	Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002018	Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002028	Genome-wide association study of serum selenium concentrations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002029	Genome-wide association study of degenerative bony changes of the temporomandibular joint.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002037	Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002046	A genome-wide association study of a sustained pattern of antidepressant response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002049	A genome-wide association study of sleep habits and insomnia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002050	A genome-wide association study of sleep habits and insomnia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002052	A genome-wide association study of sleep habits and insomnia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002053	A genome-wide association study of sleep habits and insomnia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002054	A genome-wide association study of sleep habits and insomnia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002059	A genome-wide association study for reading and language abilities in two population cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002060	A genome-wide association study for reading and language abilities in two population cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002062	A genome-wide association study for reading and language abilities in two population cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002064	Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002067	Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002074	Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002077	Parkinson disease loci in the mid-western Amish.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002080	Genome-wide meta-analysis identifies new susceptibility loci for migraine.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002092	Genetics of callous-unemotional behavior in children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002095	Genome-wide association analysis accounting for environmental factors through propensity-score matching: application to stressful live events in major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002097	Genetics of coronary artery calcification among African Americans, a meta-analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002104	A genome-wide association study (GWAS) for bronchopulmonary dysplasia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002106	Identification of regions associated with variation in sensitivity to food-related odors in the human genome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002108	A genome-wide association study in Koreans identifies susceptibility loci for allergic nickel dermatitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002109	Genome wide association analysis of a founder population identified TAF3 as a gene for MCHC in humans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002111	Genome-wide association study of the five-factor model of personality in young Korean women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002114	Genome-wide association study (GWAS) for molar-incisor hypomineralization (MIH).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002120	Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002122	A genome-wide association study of total serum and mite-specific IgEs in asthma patients.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002123	A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab family.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002124	A genome-wide association study of total serum and mite-specific IgEs in asthma patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002125	A genome-wide association study of total serum and mite-specific IgEs in asthma patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002126	Genome-wide association study of chronic periodontitis in a general German population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002127	Genome-wide association study of chronic periodontitis in a general German population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002129	Genome-wide association study of chronic periodontitis in a general German population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002130	A genome-wide association study of behavioral disinhibition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002131	A genome-wide association study of behavioral disinhibition.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002132	A genome-wide association study of behavioral disinhibition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002134	A genome-wide association study of behavioral disinhibition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002135	A genome-wide association study of behavioral disinhibition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002136	Genome-wide association study of chronic periodontitis in a general German population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002141	A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002150	Genome-wide analyses of borderline personality features.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002151	Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002152	ITGB5 and AGFG1 variants are associated with severity of airway responsiveness.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002156	Genome-wide association study for biomarker identification of Rapamycin and Everolimus using a lymphoblastoid cell line system.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002157	Genome-wide association study for biomarker identification of Rapamycin and Everolimus using a lymphoblastoid cell line system.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002162	Gene network analysis in a pediatric cohort identifies novel lung function genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002163	Gene network analysis in a pediatric cohort identifies novel lung function genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002164	Gene network analysis in a pediatric cohort identifies novel lung function genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002165	Gene network analysis in a pediatric cohort identifies novel lung function genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002168	Genome-wide association study and meta-analysis of intraocular pressure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002176	A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002177	A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002178	A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002179	A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002180	A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002185	Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002187	Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002188	Genetic predictors of risk and resilience in psychiatric disorders: a cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002192	Genome-wide association studies and epistasis analyses of candidate genes related to age at menarche and age at natural menopause in a Korean population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002194	Common variation contributes to the genetic architecture of social communication traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002200	Genome-wide association study of co-occurring anxiety in major depression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002202	Genome-wide association study of co-occurring anxiety in major depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002203	Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naïve patients with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002205	Genome-wide association study of handedness excludes simple genetic models.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002206	Genome-wide association study of handedness excludes simple genetic models.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002207	Genome-wide association study of liver enzymes in korean children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002208	Genome-wide association study of liver enzymes in korean children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002209	Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002211	Genome-wide association study of atypical psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002218	Genome-wide association study of endometrial cancer in E2C2.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002228	Genome-wide association study of autistic-like traits in a general population study of young adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002230	A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002232	A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002256	A genome-wide association study of third molar agenesis in Japanese and Korean populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002258	A genome-wide association study of third molar agenesis in Japanese and Korean populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002263	Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002265	Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002266	Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002268	Common genetic variants on 1p13.2 associate with risk of autism.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002269	Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002274	No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002278	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002281	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002282	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002284	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002285	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002296	Is the gene-environment interaction paradigm relevant to genome-wide studies? The case of education and body mass index.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002298	RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002308	Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002310	Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002312	Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002325	BAIAP2 is related to emotional modulation of human memory strength.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002339	Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002341	A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002343	Discovery of genetic biomarkers contributing to variation in drug response of cytidine analogues using human lymphoblastoid cell lines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002345	Discovery of genetic biomarkers contributing to variation in drug response of cytidine analogues using human lymphoblastoid cell lines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002347	Genome-wide association study to characterize serum bilirubin elevations in patients with HCV treated with GS-9256, an HCV NS3 serine protease inhibitor.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002348	Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002349	Genome-wide association study to characterize serum bilirubin elevations in patients with HCV treated with GS-9256, an HCV NS3 serine protease inhibitor.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002354	A genome-wide association study of anorexia nervosa.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002356	A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002359	A genome-wide association meta-analysis of plasma Aβ peptides concentrations in the elderly.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002360	A genome-wide association meta-analysis of plasma Aβ peptides concentrations in the elderly.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002361	Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002362	A genome-wide association meta-analysis of preschool internalizing problems.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002366	Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002372	Genetic influences on political ideologies: twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002375	Genome-wide analysis of methotrexate pharmacogenomics in rheumatoid arthritis shows multiple novel risk variants and leads for TYMS regulation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002377	Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002379	Clinical, serologic, and genetic factors associated with pyoderma gangrenosum and erythema nodosum in inflammatory bowel disease patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002381	Common quantitative trait locus downstream of RETN gene identified by genome-wide association study is associated with risk of type 2 diabetes mellitus in Han Chinese: a Mendelian randomization effect.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002382	Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002386	Heritability and genetic association analysis of cognition in the Diabetes Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002392	A genome-wide gene-environment interaction analysis for tobacco smoke and lung cancer susceptibility.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002393	Genome-wide association study of smoking behaviours among Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002394	Genome-wide association study of smoking behaviours among Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002395	Genome-wide association study of smoking behaviours among Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002396	Genome-wide association study of smoking behaviours among Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002397	Genome-wide interaction study of smoking and bladder cancer risk.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002399	Genome-wide association study identifies new disease loci for isolated clubfoot.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002401	A genome-wide association study of clinical symptoms of dissociation in a trauma-exposed sample.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002405	Genome-wide association study of HPV-associated cervical cancer in Japanese women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002407	Susceptibility to chronic mucus hypersecretion, a genome wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002408	Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002412	Genetic variations associated with postoperative recurrence in stage I non-small cell lung cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002418	A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002419	Bipolar disorder with comorbid binge eating history: a genome-wide association study implicates APOB.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002420	Bipolar disorder with comorbid binge eating history: a genome-wide association study implicates APOB.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002427	Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002432	Genome-wide association study identifies ALLC polymorphisms correlated with FEV₁ change by corticosteroid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002435	Genome wide association study: searching for genes underlying body mass index in the Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002436	Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002438	Genome-wide association study of maternal and inherited loci for conotruncal heart defects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002440	Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002445	Genome-wide interaction studies reveal sex-specific asthma risk alleles.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002465	Genome-wide association study supports the role of the immunological system and of the neurodevelopmental processes in response to haloperidol treatment.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002470	A novel SNP associated with nighttime pulse pressure in young-onset hypertension patients could be a genetic prognostic factor for cardiovascular events in a general cohort in Taiwan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002472	TAOK3, a novel genome-wide association study locus associated with morphine requirement and postoperative pain in a retrospective pediatric day surgery population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002479	Lupus nephritis susceptibility loci in women with systemic lupus erythematosus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002482	Novel genetic variants modify the effect of smoking on carotid plaque burden in Hispanics.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002491	Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002495	Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002503	Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002504	The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002505	Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002507	A genome-wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic pain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002508	C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002510	C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002515	A genome-wide association study identifies susceptibility loci of silica-related pneumoconiosis in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002518	Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002519	Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002521	Genome-wide association and network analysis of lung function in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002524	Genome wide association scan for chronic periodontitis implicates novel locus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002536	The genetics of hemoglobin A2 regulation in sickle cell anemia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002540	Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002551	Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002552	Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002567	Genetic variant predicts bevacizumab-induced hypertension in ECOG-5103 and ECOG-2100.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002569	Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002570	Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002571	Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002573	Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002574	Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002577	Genome-wide association study of survival in early-stage non-small cell lung cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002579	A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002589	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002590	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002595	Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002596	No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002599	GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002604	A genetic locus in 7p12.2 associated with treatment resistant schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002608	Genome-wide interrogation of longitudinal FEV1 in children with asthma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002613	Dissecting the genetics of chronic mucus hypersecretion in smokers with and without COPD.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002615	Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002616	A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002618	Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002619	Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002621	Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002629	Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002632	Genome-wide analysis of hepatic lipid content in extreme obesity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002635	Genome-wide exploration identifies sex-specific genetic effects of alleles upstream NPY to increase the risk of severe periodontitis in men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002637	Genome-wide association study of medication adherence in chronic diseases in the korean population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002638	Epidemiological and genome-wide association study of gastritis or gastric ulcer in korean populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002639	A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002641	Gene by stress genome-wide interaction analysis and path analysis identify EBF1 as a cardiovascular and metabolic risk gene.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002642	Ancestry and other genetic associations with plasma PCSK9 response to simvastatin.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002653	Meta-analysis of genome-wide association studies for circulating phylloquinone concentrations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002654	Genetic variation in the HLA region is associated with susceptibility to herpes zoster.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002664	Genome-wide association study identifies three novel genetic markers associated with elite endurance performance.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002676	Genome wide association study identifies a novel putative mammographic density locus at 1q12-q21.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002682	Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002684	A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002691	A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci among Red Blood Cell Transfusion Recipients with Sickle Cell Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002692	The National Longitudinal Study of Adolescent to Adult Health (Add Health) sibling pairs genome-wide data.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002694	"Results of a ""GWAS plus:"" general cognitive ability is substantially heritable and massively polygenic."	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002696	Genome-wide and gene-based association studies of anxiety disorders in European and African American samples.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002699	A genome-wide association study of suicide severity scores in bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002704	A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002706	Heritability and molecular genetic basis of electrodermal activity: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002708	Heritability and molecular genetic basis of acoustic startle eye blink and affectively modulated startle response: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002709	Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002710	Heritability and molecular genetic basis of antisaccade eye tracking error rate: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002715	A twin study of breastfeeding with a preliminary genome-wide association scan.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002716	SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002717	Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002719	Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002723	Genetic contributions to urgency urinary incontinence in women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002724	Genome-Wide Association Study Identification of Novel Loci Associated with Airway Responsiveness in Chronic Obstructive Pulmonary Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002725	Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002727	A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002728	Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002732	Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002734	No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002735	A pilot genome-wide association study of breast cancer susceptibility loci in Indonesia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002744	Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002749	Identification of genetic variants or genes that are associated with Homoharringtonine (HHT) response through a genome-wide association study in human lymphoblastoid cell lines (LCLs).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002750	A genome-wide association study of chronic obstructive pulmonary disease in Hispanics.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002752	A genome-wide association study of early spontaneous preterm delivery.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002755	Identifying genetic loci associated with antidepressant drug response with drug-gene interaction models in a population-based study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002760	Investigating the genetics of hippocampal volume in older adults without dementia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002761	Investigating the genetics of hippocampal volume in older adults without dementia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002769	Genome-wide association study of virologic response with efavirenz-containing or abacavir-containing regimens in AIDS clinical trials group protocols.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002770	Genetics of hand grip strength in mid to late life.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002771	Genome-wide association study of virologic response with efavirenz-containing or abacavir-containing regimens in AIDS clinical trials group protocols.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002775	Genetic Determinants of Survival in Patientswith Alzheimer’s Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002781	A genome-wide association study of periodontitis in a Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002786	15q12 variants, sputum gene promoter hypermethylation, and lung cancer risk: a GWAS in smokers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002788	Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002789	Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002790	Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002793	Genetic variants associated with vein graft stenosis after coronary artery bypass grafting.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002799	Genome-wide association study of parity in Bangladeshi women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002800	Genome-wide association study of parity in Bangladeshi women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002801	Genome-wide association study of parity in Bangladeshi women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002803	Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002805	First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002806	First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002809	Characteristics of Bipolar I patients grouped by externalizing disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002812	Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002815	Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002818	Novel genetic locus implicated for HIV-1 acquisition with putative regulatory links to HIV replication and infectivity: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002820	A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002821	A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002822	A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002825	Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002826	Modulation of genetic associations with serum urate levels by body-mass-index in humans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002841	A common variant of ubiquinol-cytochrome c reductase complex is associated with DDH.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002847	Prediction of breast cancer survival using clinical and genetic markers by tumor subtypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002854	The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002856	Genetic variants in LEKR1 and GALNT10 modulate sex-difference in carotid intima-media thickness: a genome-wide interaction study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002857	Genome-wide association study of serum minerals levels in children of different ethnic background.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002860	Genome-wide association study of serum minerals levels in children of different ethnic background.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002862	Genome-wide association study of behavioural and psychiatric features in human prion disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002863	Genome-wide association study of behavioural and psychiatric features in human prion disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002864	Genome-wide association study of behavioural and psychiatric features in human prion disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002866	Genome-wide association study of behavioural and psychiatric features in human prion disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002867	Genome-wide association study of behavioural and psychiatric features in human prion disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002871	Genome-wide association study of behavioural and psychiatric features in human prion disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002885	Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002888	Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002891	Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002892	Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002895	Genome-wide association study of susceptibility loci for breast cancer in Sardinian population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002901	Polymorphism at 19q13.41 Predicts Breast Cancer Survival Specifically after Endocrine Therapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002904	Genetic and clinical factors associated with obesity among adult survivors of childhood cancer: A report from the St. Jude Lifetime Cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002913	Investigation of susceptibility genes triggering lachrymal/salivary gland lesion complications in Japanese patients with type 1 autoimmune pancreatitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002916	Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002917	Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002924	Pharmacoethnicity in Paclitaxel-Induced Sensory Peripheral Neuropathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002941	A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002948	Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002951	Genome-wide association study of leukotriene modifier response in asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002954	A genome-wide association study of late-onset Alzheimer's disease in a Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002960	A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002963	Genome-wide association study of posttraumatic stress disorder in a cohort of Iraq-Afghanistan era veterans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002969	A genome-wide association study of suicidal behavior.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002972	A genome-wide association study of suicidal behavior.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002973	A genome-wide association study of suicidal behavior.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002974	A genome-wide association study of suicidal behavior.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002975	Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002976	Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002982	Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST002984	A genome-wide approach to children's aggressive behavior: The EAGLE consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002985	A genome-wide approach to children's aggressive behavior: The EAGLE consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002989	Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003002	A genome-wide association study identifies multiple loci for variation in human ear morphology.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003005	A genome-wide association study identifies multiple loci for variation in human ear morphology.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003006	Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003008	Genome-wide association analysis identified splicing single nucleotide polymorphism in CFLAR predictive of triptolide chemo-sensitivity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003012	Associations of Sleep Apnea, NRG1 Polymorphisms, Alcohol Consumption, and Cerebral White Matter Hyperintensities: Analysis with Genome-Wide Association Data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003016	CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003025	New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003026	Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003030	Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003042	Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003050	Genome-wide association study of schizophrenia in Ashkenazi Jews.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003055	Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003056	Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003058	Genome Wide Association Study for Predictors of Progression Free Survival in Patients on Capecitabine, Oxaliplatin, Bevacizumab and Cetuximab in First-Line Therapy of Metastatic Colorectal Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003059	A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003062	A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003063	A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003064	Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003065	Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003066	Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003067	Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003068	Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003069	Genetic underpinnings of left superior temporal gyrus thickness in patients with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003070	Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003071	Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003078	Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003079	Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003081	Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003083	Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003084	Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003089	Genetics of long-term treatment outcome in bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003095	Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003096	Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003099	Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003100	Genome-wide association study of prostate cancer-specific survival.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003101	Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003104	Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003108	Genome-wide association study on antipsychotic-induced weight gain in the CATIE sample.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003109	Genome-wide association study on antipsychotic-induced weight gain in the CATIE sample.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003121	The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003126	No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003130	Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003131	A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003132	A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003133	A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003134	A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003135	A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003137	A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003138	Candidate Loci are Revealed by an Initial Genome-wide Association Study of Juvenile Osteochondritis Dissecans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003139	Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003140	Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003141	Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003142	Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003146	Genome-wide Association Study of Postburn Scarring Identifies a Novel Protective Variant.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003151	White Matter Lesion Progression: Genome-Wide Search for Genetic Influences.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003152	White Matter Lesion Progression: Genome-Wide Search for Genetic Influences.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003158	Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003160	Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003161	Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003171	Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003172	Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003173	Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003174	Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003175	A genome-wide association study on amyotrophic lateral sclerosis in the Taiwanese Han population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003176	Genome-wide association study in Spanish identifies ADAM metallopeptidase with thrombospondin type 1 motif, 9 (ADAMTS9), as a novel asthma susceptibility gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003178	Genome-Wide Association Study of Event-Free Survival in Diffuse Large B-Cell Lymphoma Treated With Immunochemotherapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003182	Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003186	Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003189	Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003190	Genome-wide association study with the risk of schizophrenia in a Korean population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003192	Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003193	Pharmacogenetic study of long-term response to interferon-β treatment in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003195	Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003200	Genome-wide association study identifies candidate loci associated with postoperative fentanyl requirements after laparoscopic-assisted colectomy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003205	Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003206	Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003207	Genomic and transcriptomic predictors of triglyceride response to regular exercise.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003209	Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003212	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003213	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003221	Genome-Wide Association Studies of the Human Gut Microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003225	Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003226	Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003229	Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003231	Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003233	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003234	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003235	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003240	A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003241	A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003243	A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003245	Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003248	Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003249	Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003250	Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003254	Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003263	A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003265	A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003341	Genome-wide association analysis to predict optimal antipsychotic dosage in schizophrenia: a pilot study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003361	Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003375	Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003379	Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003382	Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003394	Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003396	Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003397	Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003398	Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003420	Genome-wide association study of colorectal cancer in Hispanics.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003426	HLA-DRB1*16: 01-DQB1*05: 02 is a novel genetic risk factor for flupirtine-induced liver injury.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003431	Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003433	A Common Variant in the SETD7 Gene Predicts Serum Lycopene Concentrations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003437	A Genome-Wide Test of the Differential Susceptibility Hypothesis Reveals a Genetic Predictor of Differential Response to Psychological Treatments for Child Anxiety Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003439	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003440	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003441	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003443	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003444	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003446	Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003449	Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003451	A genome-wide association study of pulmonary tuberculosis in Morocco.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003457	Genetic analysis of advanced glycation end products in the DHS MIND study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003458	No Evidence of a Common DNA Variant Profile Specific to World Class Endurance Athletes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003461	Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003469	Genome-wide association study of response to cognitive-behavioural therapy in children with anxiety disorders.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003472	Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003473	Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003481	Genetic variants in RBFOX3 are associated with sleep latency.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003482	Novel genetic risk factors for asthma in African American children: Precision Medicine and the SAGE II Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003485	A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003487	A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003488	A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003495	Genome-wide Association Studies of Posttraumatic Stress Disorder in 2 Cohorts of US Army Soldiers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003541	A genome-wide association study of non-HPV-related head and neck squamous cell carcinoma identifies prognostic genetic sequence variants in the MAP-kinase and hormone pathways.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003564	Investigation of Genetic Variation Underlying Central Obesity amongst South Asians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003584	Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003591	A genome-wide association study in Caucasian women suggests the involvement of HLA genes in the severity of facial solar lentigines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003600	Genome-wide gene-environment interaction analysis of pesticide exposure and risk of Parkinson's disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003612	Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003615	Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003616	THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003623	A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003624	A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003630	Genome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003631	A meta-analysis of reflux genome-wide association studies in 6750 Northern Europeans from the general population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003640	Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003644	Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003645	Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003647	Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003648	Genome-wide association study of pathological gambling.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003649	Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003650	Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003656	A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003657	A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003663	Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003667	Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003671	International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003673	Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003684	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003685	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003686	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003687	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003688	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003689	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003742	A genome wide association study suggests the association of muskelin with early onset bipolar disorder: Implications for a GABAergic epileptogenic neurogenesis model.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003768	Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003771	Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003772	Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003773	Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003778	Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003779	Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003782	Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003783	A genome-wide association study in multiple system atrophy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003784	A genome-wide association study in multiple system atrophy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003791	Metformin pharmacogenomics: a genome-wide association study to identify genetic and epigenetic biomarkers involved in metformin anticancer response using human lymphoblastoid cell lines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003792	Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003800	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003801	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003802	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003803	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003804	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003805	Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003806	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003807	Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003808	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003809	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003810	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003811	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003812	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003813	Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003816	Genetic Polymorphisms in the Long Noncoding RNA MIR2052HG Offer a Pharmacogenomic Basis for the Response of Breast Cancer Patients to Aromatase Inhibitor Therapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003817	Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28Day Mortality.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003820	Genome-Wide Association Study of Radiographic Knee Osteoarthritis in North American Caucasians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003824	Genome-Wide Association Study Identifies ZNF354C Variants Associated with Depression from Interferon-Based Therapy for Chronic Hepatitis C.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003827	Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003829	Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003832	Identification of Four Novel Loci in Asthma in European American and African American Populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003840	Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003849	Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003861	The Genetic Landscape of Renal Complications in Type 1 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003862	The Genetic Landscape of Renal Complications in Type 1 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003863	The Genetic Landscape of Renal Complications in Type 1 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003865	The Genetic Landscape of Renal Complications in Type 1 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003866	The Genetic Landscape of Renal Complications in Type 1 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003867	The Genetic Landscape of Renal Complications in Type 1 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003878	Genome-Wide Association of Heroin Dependence in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003882	Genome-wide Association Study of Parental Life Span.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003900	A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003918	Genome-wide association scans for idiopathic osteonecrosis of the femoral head in a Korean population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003963	Genome-wide association scan of neuropathic pain symptoms post total joint replacement highlights a variant in the protein-kinase C gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST003964	Bortezomib-induced peripheral neuropathy: A genome-wide association study on multiple myeloma patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004012	Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004014	Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004052	Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004054	Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004055	Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004056	Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004057	Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004058	Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004060	6q12 and 11p14 variants are associated with postnatal exhaled nitric oxide levels and respiratory symptoms.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004062	Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004082	Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004084	Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004085	Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004087	Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004095	Genome-wide association study in takotsubo syndrome - Preliminary results and future directions.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004096	Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004097	Genome-wide association study identifies four SNPs associated with response to platinum-based neoadjuvant chemotherapy for cervical cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004102	Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004103	Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004104	Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004106	Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004108	Genome-wide interaction study of dust mite allergen on lung function in children with asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004110	The complex genetics of gait speed: genome-wide meta-analysis approach.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004114	Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004115	Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004118	Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004125	PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004134	Genome-Wide Association Studies of Multiple Keratinocyte Cancers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004143	Interaction between Single Nucleotide Polymorphism and Urinary Sodium, Potassium, and Sodium-Potassium Ratio on the Risk of Hypertension in Korean Adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004158	Genetic contributions to self-reported tiredness.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004163	Genome-wide study of resistant hypertension identified from electronic health records.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004178	A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004179	A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004182	A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004224	A genome-wide trans-ethnic interaction study links the PIGR-FCAMR locus to coronary atherosclerosis via interactions between genetic variants and residential exposure to traffic.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004230	Genome-wide association study of sepsis in extremely premature infants.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004240	Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004245	Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004251	LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohn's disease patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004253	Single-nucleotide polymorphisms are associated with cognitive decline at Alzheimer's disease conversion within mild cognitive impairment patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004261	Genome-Wide Association and Replication Study of Hepatotoxicity Induced by Antiretrovirals Alone or with Concomitant Anti-Tuberculosis Drugs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004262	Genome-Wide Association and Replication Study of Hepatotoxicity Induced by Antiretrovirals Alone or with Concomitant Anti-Tuberculosis Drugs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004263	Genome-wide association screens for Achilles tendon and ACL tears and tendinopathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004265	Genome-wide association screens for Achilles tendon and ACL tears and tendinopathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004268	Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004270	Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004271	Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004273	Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004274	Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004275	Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004283	Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004289	Genetic determinants of adiponectin regulation revealed by pregnancy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004291	Identification of genes associated with dissociation of cognitive performance and neuropathological burden: Multistep analysis of genetic, epigenetic, and transcriptional data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004303	A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004304	Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004305	Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004306	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004308	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004309	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004310	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004312	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004314	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004316	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004317	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004319	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004320	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004322	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004323	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004324	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004325	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004327	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004328	Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004353	Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004358	HLA-A 31:01 is not associated with the development of methotrexate pneumonitis in the UK population: results from a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004361	SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004362	SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004363	SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004368	Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004369	Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004379	Genome-wide association study of erythrocyte density in sickle cell disease patients.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004383	Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004400	Association of CD8+ T-cells with bone erosion in patients with rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004401	Genome-wide screening for DNA variants associated with reading and language traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004402	Genome-wide screening for DNA variants associated with reading and language traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004406	Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004407	Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004408	Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004409	Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004410	Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004411	Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004426	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004427	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004434	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004437	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004445	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004446	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004447	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004448	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004450	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004453	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004455	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004458	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004459	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004461	Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004488	A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004493	GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004494	GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004502	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004506	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004509	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004520	Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004523	A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004524	A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004569	A genome-wide association study of neuroticism in a population-based sample.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004577	Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004579	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004580	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004581	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004582	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004583	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004584	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004585	A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004586	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004587	Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004638	A genetic variant near GATA3 implicated in inherited susceptibility and etiology of benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004639	Genome-Wide Association Study of Dietary Pattern Scores.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004640	Genome-Wide Association Study of Dietary Pattern Scores.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004641	Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004644	Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004645	Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004646	Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004647	Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004648	Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004656	Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004679	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004680	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004681	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004682	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004683	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004684	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004685	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004686	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004689	A chromosome 5q31.1 locus associates with tuberculin skin test reactivity in HIV-positive individuals from tuberculosis hyper-endemic regions in east Africa.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004690	A chromosome 5q31.1 locus associates with tuberculin skin test reactivity in HIV-positive individuals from tuberculosis hyper-endemic regions in east Africa.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004703	Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004706	A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004707	A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004709	A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004715	Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004718	Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004720	Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004721	Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004722	Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004723	Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004725	A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004727	Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004728	Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004729	Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004730	Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004731	Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004736	Genome-wide association analysis identifies a GLUL haplotype for familial hepatitis B virus-related hepatocellular carcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004738	Genome-wide association studies of placebo and duloxetine response in major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004747	Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004757	Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004764	Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004768	Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004769	Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004770	Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004774	An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004778	The SNP-set based association study identifies ITGA1 as a susceptibility gene of attention-deficit/hyperactivity disorder in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004780	The low single nucleotide polymorphism heritability of plasma and saliva cortisol levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004790	Genome-wide association study of cardiotoxicity in the NCCTG N9831 (Alliance) adjuvant trastuzumab trial.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004791	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004792	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004793	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004794	Genome-wide association analysis identifies common variants influencing infant brain volumes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004796	Genome-wide association analysis identifies common variants influencing infant brain volumes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004800	Genes and pathways underlying susceptibility to impaired lung function in the context of environmental tobacco smoke exposure.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004808	Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004812	Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004823	A genome-wide association study of cognitive function in Chinese adult twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004828	Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004830	Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004831	Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004839	Japanese genome-wide association study identifies a significant colorectal cancer susceptibility locus at chromosome 10p14.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004859	Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004868	Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004879	Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004884	Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004888	Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004890	Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004896	Genome-wide association study evaluating single-nucleotide polymorphisms and outcomes in patients with advanced stage serous ovarian or primary peritoneal cancer: An NRG Oncology/Gynecologic Oncology Group study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004897	Genome-wide association study evaluating single-nucleotide polymorphisms and outcomes in patients with advanced stage serous ovarian or primary peritoneal cancer: An NRG Oncology/Gynecologic Oncology Group study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004921	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004922	Discovery of susceptibility loci associated with tuberculosis in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004938	Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004942	Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004943	Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004949	Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004953	A genome-wide association study of early gamma-band response in a schizophrenia case-control sample.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004958	Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004970	Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004977	Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004980	Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004987	A molecular pathway analysis informs the genetic risk for arrhythmias during antipsychotic treatment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004990	Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004991	The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004993	The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004994	The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST004997	The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004998	Biological function integrated prediction of severe radiographic progression in rheumatoid arthritis: a nested case control study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005016	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005017	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005018	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005019	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005020	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005021	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005025	Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005027	Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005039	Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005040	Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005041	Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005050	Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005051	Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005057	A genome-wide association study links small-vessel ischemic stroke to autophagy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005091	Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005092	Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005094	Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005095	Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005108	Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005110	Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005111	Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005115	No genetic association detected with mepolizumab efficacy in severe asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005128	Genome-wide association study identifies a novel locus for cannabis dependence.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005133	Genome-wide association study identifies a novel locus for cannabis dependence.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005148	Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005149	Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005151	Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005152	Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005153	Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005161	Genetic determinants of circulating GIP and GLP-1 concentrations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005162	Genetic determinants of circulating GIP and GLP-1 concentrations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005163	Genetic determinants of circulating GIP and GLP-1 concentrations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005164	Genetic determinants of circulating GIP and GLP-1 concentrations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005169	EPHA6 rs4857055 C > T polymorphism associates with hypertension through triglyceride and LDL particle size in the Korean population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005173	Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005174	Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005175	Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005178	Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005182	Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005183	Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005184	Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005214	Bone mineral density in children with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005218	A central role for GRB10 in regulation of islet function in man.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005221	A central role for GRB10 in regulation of islet function in man.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005223	A central role for GRB10 in regulation of islet function in man.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005230	Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005236	Problematic alcohol use associates with sodium channel and clathrin linker 1 (SCLT1) in trauma-exposed populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005240	Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005241	Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005242	Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005246	Hierarchical investigation of genetic influences on response inhibition in healthy young adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005247	Genome-Wide Association Study of Male Sexual Orientation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005268	A family-based genome-wide association study of chronic rhinosinusitis with nasal polyps implicates several genes in the disease pathogenesis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005270	Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005272	Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005286	Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005331	Cerebral tryptophan metabolism and outcome of tuberculous meningitis: an observational cohort study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005332	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005333	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005342	Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005343	Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005351	Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005352	Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005357	Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005368	Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005419	A Genome-wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005435	Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005514	Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005518	A High-risk Haplotype for Premature Menopause in Childhood Cancer Survivors Exposed to Gonadotoxic Therapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005521	Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to β-Blockers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005532	Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005535	Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005539	Immunochip-based analysis: high-density genotyping of immune-related loci sheds further light on the autoimmune genetic architecture of alopecia areata.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005550	Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005553	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005557	Heritability and Genome-Wide Association Analyses of Serum Uric Acid in Middle and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005559	Genome-wide association study (GWAS) of human host factors influencing viral severity of herpes simplex virus type 2 (HSV-2).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005574	A novel variant in GLIS3 is associated with osteoarthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005578	Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005652	A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005653	A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005654	A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005670	Untargeted metabolomics identifies trimethyllysine, a TMAO-producing nutrient precursor, as a predictor of incident cardiovascular disease risk.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005688	Genetic Survey of Adult-Onset Idiopathic Intracranial Hypertension.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005691	Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005713	Genome-wide association study identifies two loci influencing plasma neurofilament light levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005721	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005722	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005723	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005725	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005726	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005727	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005728	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005753	Genetic Variants in CPA6 and PRPF31 are Associated with Variation in Response to Metformin in Individuals with Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005766	Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005767	Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005769	Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005774	Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005777	Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005783	Clinical and genetic risk factors for decreased bone mineral density in Japanese patients with inflammatory bowel disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005784	Clinical and genetic risk factors for decreased bone mineral density in Japanese patients with inflammatory bowel disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005797	Genetic contribution to 'theory of mind' in adolescence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005801	ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005802	ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005804	Genome-wide meta-analyses identifies novel taxane-induced peripheral neuropathy-associated loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005811	Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005813	Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005815	Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005833	Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005834	Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005844	Genetic variations and risk of placental abruption: A genome-wide association study and meta-analysis of genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005855	Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005856	Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005859	Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005860	Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005861	Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005866	Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005869	Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005871	Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005872	Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005875	Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005876	Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005880	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005882	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005883	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005885	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005887	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005890	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005893	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005894	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005895	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005903	Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005912	Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005914	Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005915	Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005917	The genetics of smoking in individuals with chronic obstructive pulmonary disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005918	The genetics of smoking in individuals with chronic obstructive pulmonary disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005936	Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005937	Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005939	Mapping genetic variants for cranial vault shape in humans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005947	A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005948	A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005954	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005968	Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005970	Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST005971	Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006035	Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006039	Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006043	Genetic Variants Influencing Plasma Renin Activity in Hypertensive Patients From the PEAR Study (Pharmacogenomic Evaluation of Antihypertensive Responses).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006044	Genome-wide analysis identifies 12 loci influencing human reproductive behavior.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006047	Genome-wide analysis identifies 12 loci influencing human reproductive behavior.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006055	Genome-wide association study of the plasma triglyceride response to an n-3 polyunsaturated fatty acid supplementation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006059	Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006060	Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006069	Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006072	Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006087	Genome-Wide Association Study of Familial Lung Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006103	Genome-wide associated loci influencing interleukin (IL)-10, IL-1Ra, and IL-6 levels in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006104	Genome-wide associated loci influencing interleukin (IL)-10, IL-1Ra, and IL-6 levels in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006106	Identification of five novel genetic loci related to facial morphology by genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006120	Hidden heterogeneity in Alzheimer's disease: Insights from genetic association studies and other analyses.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006121	Hidden heterogeneity in Alzheimer's disease: Insights from genetic association studies and other analyses.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006132	Nuclear receptor and VEGF pathways for gene-blood lead interactions, on bone mineral density, in Korean smokers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006133	Nuclear receptor and VEGF pathways for gene-blood lead interactions, on bone mineral density, in Korean smokers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006139	17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006144	Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006146	Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006147	Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006149	Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006151	Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006152	Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006153	Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006196	Identification of non-HLA genes associated with development of islet autoimmunity and type 1 diabetes in the prospective TEDDY cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006197	Identification of non-HLA genes associated with development of islet autoimmunity and type 1 diabetes in the prospective TEDDY cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006202	NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006208	NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006210	NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006220	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006222	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006223	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006224	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006225	Pathway-Wide Genetic Risks in Chlamydial Infections Overlap between Tissue Tropisms: A Genome-Wide Association Scan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006226	Genome-Wide Association Study of Erosive Tooth Wear in a Finnish Cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006248	Identifying the genetic risk factors for treatment response to lurasidone by genome-wide association study: A meta-analysis of samples from three independent clinical trials.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006254	Multi-level genomic analyses suggest new genetic variants involved in human memory.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006256	Multi-level genomic analyses suggest new genetic variants involved in human memory.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006257	Type 2 Diabetes Mellitus: Integrative Analysis of Multiomics Data for Biomarker Discovery.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006266	A Deep Learning Approach for Predicting Antidepressant Response in Major Depression Using Clinical and Genetic Biomarkers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006267	A Deep Learning Approach for Predicting Antidepressant Response in Major Depression Using Clinical and Genetic Biomarkers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006273	Genome-wide association study of nocturnal blood pressure dipping in hypertensive patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006277	Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degeneration.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006282	Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006283	Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006293	Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006295	Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006296	Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006297	Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006298	Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006301	Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006302	Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006326	Meta-analysis of genome-wide association studies for personality.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006364	Identification of novel susceptibility loci associated with hepatitis B surface antigen seroclearance in chronic hepatitis B.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006401	A comprehensive evaluation of the genetic architecture of sudden cardiac arrest.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006406	Genome-wide association study of cognitive flexibility assessed by the Wisconsin Card Sorting Test.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006411	Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006413	Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006422	Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006427	GWAS and systems biology analysis of depressive symptoms among smokers from the COPDGene cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006428	A genome-wide association study of suicide attempts and suicidal ideation in U.S. military veterans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006429	A genome-wide association study of suicide attempts and suicidal ideation in U.S. military veterans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006430	Genetics of Obesity Traits: A Bivariate Genome-Wide Association Analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006435	Genome-Wide Association Study Links Receptor Tyrosine Kinase Inhibitor Sprouty 2 to Thrombocytopenia after Coronary Artery Bypass Surgery.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006440	Identification of novel loci associated with infant cognitive ability.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006443	Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006445	Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006447	Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006460	Ancestry and Genetic Associations with Bronchopulmonary Dysplasia in Preterm Infants.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006466	Identification of nine new susceptibility loci for endometrial cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006469	Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006470	Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006485	Genetic Determinants of Telomere Length in African American Youth.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006492	Single-nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006493	Analysis of the genetic component of systemic sclerosis in Iranian and Turkish populations through a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006494	Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006495	Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006496	Genome Wide Association Study Reveals Novel Genetic Loci Associated With Change in Renal Function in Heart Transplant Recipients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006515	Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006521	Investigation of the Predisposing Factor of Pemphigus and its clinical subtype through a Genome-wide association and next generation sequence analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006523	Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006528	Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006529	Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006530	Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006531	Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006532	Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006534	Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006535	A GWAS meta-analysis from 5 population-based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006541	A univariate perspective of multivariate genome-wide association analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006542	Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006547	Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006576	Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006582	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006607	Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006608	Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006610	Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006616	Transethnic and race-stratified genome-wide association study of fibroid characteristics in African American and European American women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006617	Transethnic and race-stratified genome-wide association study of fibroid characteristics in African American and European American women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006633	Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006639	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006640	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006641	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006642	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006643	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006644	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006645	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006646	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006647	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006648	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006649	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006650	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006651	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006652	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006653	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006654	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006657	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006658	Sex Differences in Genetic Associations With Longevity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006663	Genome-wide association study for multiple phenotype analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006664	Genome-wide association study for multiple phenotype analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006676	A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006680	Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006720	Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006813	Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006814	Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006815	Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006817	Association of Novel ALX4 Gene Polymorphisms with Antidepressant Treatment Response: Findings from the CO-MED Trial.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006858	Genome-wide Association Study of Leisure-Time Exercise Behavior in Japanese Adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006864	A univariate perspective of multivariate genome-wide association analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006909	Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006928	Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006930	Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006933	Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006934	Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006936	Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: a population-based exome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006957	Association of modifiers and other genetic factors explain Marfan syndrome clinical variability.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST006990	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006991	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006992	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006994	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006995	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006999	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007003	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007005	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007013	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007016	Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007041	A genome-wide association study identifies a 3'UTR genetic variant of RARB associated with carotid intima-media thickness in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007052	A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007058	A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007059	New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007060	New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007061	New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007088	A genome-wide association study identifies a 3'UTR genetic variant of RARB associated with carotid intima-media thickness in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007100	Genome-wide association study of inhaled corticosteroid response in admixed children with asthma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007102	Genome-wide association study of seasonal affective disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007105	Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007107	Genome-wide analysis of polymorphism × sodium interaction effect on blood pressure identifies a novel 3'-BCL11B gene desert locus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007123	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007126	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007127	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007135	Genome-wide association analysis of common genetic variants of resistant hypertension.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007138	Genome-wide association analysis suggests novel loci for Hashimoto's thyroiditis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007153	Genetic influences on delayed reward discounting: A genome-wide prioritized subset approach.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007187	Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007188	Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007189	Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007192	Identification of the TIFAB Gene as a Susceptibility Locus for Coronary Artery Aneurysm in Patients with Kawasaki Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007199	Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007202	Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007203	Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007204	Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007206	Genome-wide association study identifies RBFOX1 locus influencing brain glucose metabolism.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007207	Sex differences in the genetic architecture of obsessive-compulsive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007208	Sex differences in the genetic architecture of obsessive-compulsive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007231	A Sex-Stratified Genome-Wide Association Study of Tuberculosis Using a Multi-Ethnic Genotyping Array.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007235	Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007239	Genome-wide association study (GWAS) of ovarian cancer in Japanese predicted regulatory variants in 22q13.1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007242	Genetic architecture of human thinness compared to severe obesity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007251	Genetic influence on scar height and pliability after burn injury in individuals of European ancestry: A prospective cohort study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007252	Genetic influence on scar height and pliability after burn injury in individuals of European ancestry: A prospective cohort study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007258	Bactericidal/Permeability-Increasing Fold-Containing Family B Member 4 May Be Associated with NSAID-Induced Enteropathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007259	Genome wide association study to identify predictors for severe skin toxicity in colorectal cancer patients treated with cetuximab.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007261	The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007262	The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007265	The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007277	Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007279	A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007283	Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007287	Genome-Wide Gene-Environment Interaction Analysis Using Set-Based Association Tests.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007290	Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007292	Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007304	Variation in SIPA1L2 is Correlated with Phenotype Modification in CMT Type 1A.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007316	Exploratory genome-wide association analysis of response to ketamine and a polygenic analysis of response to scopolamine in depression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007317	Exploratory genome-wide association analysis of response to ketamine and a polygenic analysis of response to scopolamine in depression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007318	Genetic data and cognitively defined late-onset Alzheimer's disease subgroups.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007330	Genetic data and cognitively defined late-onset Alzheimer's disease subgroups.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007332	Genetic data and cognitively defined late-onset Alzheimer's disease subgroups.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007333	Genetic data and cognitively defined late-onset Alzheimer's disease subgroups.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007334	Genetic data and cognitively defined late-onset Alzheimer's disease subgroups.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007355	Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007356	Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007364	Identification and replication of six new loci associated with gallstone disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007376	Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007377	Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007379	Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007391	Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007392	A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007395	A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007397	A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007398	A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007399	A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007403	Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007404	Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007405	Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007412	Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007413	Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007415	Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007420	Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007424	Novel genes and insights in complete asthma remission.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007425	A genome-wide association study identifies a 3'UTR genetic variant of RARB associated with carotid intima-media thickness in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007426	Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007428	Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007449	Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007450	Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007465	Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007466	Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007467	Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007469	Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007471	Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007473	Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007475	Genome-wide association study of germline variants and breast cancer-specific mortality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007476	Genome-wide association study of germline variants and breast cancer-specific mortality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007477	Genome-wide association study of germline variants and breast cancer-specific mortality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007478	Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007493	Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007495	Genome-wide association study suggests impact of chromosome 10 rs139401390 on kidney function in patients with coronary artery disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007496	Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007497	The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007498	The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007499	The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007501	Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007503	Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007509	Genomic analyses in african populations identify novel risk loci for cleft palate.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007519	Longitudinal analysis to better characterize Asthma-COPD Overlap Syndrome (ACOS): Findings from an adult asthma cohort in Korea (COREA).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007521	Longitudinal analysis to better characterize Asthma-COPD Overlap Syndrome (ACOS): Findings from an adult asthma cohort in Korea (COREA).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007538	Genetic risk score combining six genetic variants associated with the cellular NRF2 expression levels correlates with Type 2 diabetes in the human population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007547	Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007549	The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA?	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007550	The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA?	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007555	Identification of common genetic risk variants for autism spectrum disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007558	Genomics and response to long-term oxygen therapy in chronic obstructive pulmonary disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007619	Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007622	Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007623	Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007624	Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007626	Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007627	Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007629	Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007639	Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007643	An initial genetic analysis of gemcitabine-induced high-grade neutropenia in pancreatic cancer patients CALGB 80303 (Alliance).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007644	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007645	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007646	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007647	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007648	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007649	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007658	Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007660	Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007665	Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007666	Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007667	Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007672	Genome-wide association meta-analysis of functional outcome after ischemic stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007673	Genome-wide association meta-analysis of functional outcome after ischemic stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007674	Genome-wide association meta-analysis of functional outcome after ischemic stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007675	Genome-wide association meta-analysis of functional outcome after ischemic stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007676	Genome-wide association meta-analysis of functional outcome after ischemic stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007677	Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007678	Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007679	Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007682	Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007690	The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007693	Genetic effects on information processing speed are moderated by age--converging results from three samples.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007694	Genetic effects on information processing speed are moderated by age--converging results from three samples.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007696	Genetic effects on information processing speed are moderated by age--converging results from three samples.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007700	A case-control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007726	Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007732	Eleven loci with new reproducible genetic associations with allergic disease risk.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007734	Genetic risk score raises the risk of incidence of chronic kidney disease in Korean general population-based cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007766	Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007796	Clinical and Genome-Wide Analysis of Cisplatin-Induced Tinnitus Implicates Novel Ototoxic Mechanisms.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007809	A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007810	A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007811	A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007812	A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007813	A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007814	A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007817	Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007819	Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007820	Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007821	Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007823	Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007824	Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007830	Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007831	Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007851	Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007860	Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007864	Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007880	Genome-wide analysis of emotional lability in adult attention deficit hyperactivity disorder (ADHD).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007921	Genome-wide association study of right-sided colonic diverticulosis in a Korean population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007947	Genome-wide analyses of psychological resilience in U.S. Army soldiers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007949	Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007951	Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007976	Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007977	Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007978	Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007980	Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST007981	Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008016	Exome-Wide Association Study Identified New Risk Loci for Hirschsprung's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008018	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008020	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008021	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008022	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008023	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008024	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008033	Genetic analyses of diverse populations improves discovery for complex traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008051	Genetic analyses of diverse populations improves discovery for complex traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008098	A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008106	A Genome-Wide Functional Genomics Approach Identifies Susceptibility Pathways to Fungal Bloodstream Infection in Humans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008116	Genome-wide association study identifies 30 loci associated with bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008117	Genome-wide association study identifies 30 loci associated with bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008119	GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008120	GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008122	GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008123	GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008138	A case-only genome-wide association study on gene-sex interaction in allergic rhinitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008140	Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008142	Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008143	Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008145	Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008146	Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008148	Genome-wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008150	Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008169	Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008173	Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008175	Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008176	Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008177	Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008178	Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008179	Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008180	Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008181	Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008223	A Genetic Locus on Chromosome 2q24 Predicting Peripheral Neuropathy Risk in Type 2 Diabetes: Results From the ACCORD and BARI 2D Studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008224	Sex specific associations in genome wide association analysis of renal cell carcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008230	Integrative approach identifies corticosteroid response variant in diverse populations with asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008236	Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008237	Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008238	Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008239	Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008240	Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008241	Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008246	Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008247	Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008270	Post-traumatic stress following military deployment: Genetic associations and cross-disorder genetic correlations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008272	Pathway analysis of a genome-wide gene by air pollution interaction study in asthmatic children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008273	Pathway analysis of a genome-wide gene by air pollution interaction study in asthmatic children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008274	Genome-Wide Association Study of Cerebral Microbleeds on MRI.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008275	Genome-Wide Association Study of Cerebral Microbleeds on MRI.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008294	Genetic effects on efficacy to fluticasone propionate/salmeterol treatment in COPD.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008308	Variants in Immune-related Genes and Genital HPV 16 Persistence in Men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008314	Identification of SAMD9L as a susceptibility locus for intravenous immunoglobulin resistance in Kawasaki disease by genome-wide association analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008315	Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008319	Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008320	Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008358	A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008359	A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008360	A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008361	A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008368	Genome-wide meta-analysis identifies novel gender specific loci associated with thyroid antibodies level in Croatians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008369	Genome-wide meta-analysis identifies novel gender specific loci associated with thyroid antibodies level in Croatians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008379	Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008384	Shared genetic risk factors across carbamazepine-induced hypersensitivity reactions.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008387	The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008388	Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008397	Association of TRAP1 with Infliximab-Induced Mucosal Healing in Crohn's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008399	Genome-wide association meta-analysis of cocaine dependence: Shared genetics with comorbid conditions.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008436	Genetic loci associated with nonobstructive coronary artery disease in Caucasian women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008444	Genome-wide association analysis of HDL-C in a Lebanese cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008446	Genome-wide association studies of the self-rating of effects of ethanol (SRE).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008448	A genome-wide association study of gestational diabetes mellitus in Chinese women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008462	A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008466	GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008476	DSP variants may be associated with longitudinal change in quantitative emphysema.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008477	DSP variants may be associated with longitudinal change in quantitative emphysema.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008490	Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008491	Spatial correlations exploitation based on nonlocal voxel-wise GWAS for biomarker detection of AD.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008498	Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008499	Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008502	A genome-wide association study in low susceptibility to hepatitis C virus infection (GEHEP012 Study).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008503	Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008504	Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008505	Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008506	Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008507	Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008508	Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008513	Genetic Contributions to Health Literacy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008514	Genetic variation in FCER1A predicts peginterferon alfa-2a-induced hepatitis B surface antigen clearance in East Asian patients with chronic hepatitis B.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008517	Impact of IFNL4 Genetic Variants on Sustained Virologic Response and Viremia in Hepatitis C Virus Genotype 3 Patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008520	Impact of IFNL4 Genetic Variants on Sustained Virologic Response and Viremia in Hepatitis C Virus Genotype 3 Patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008525	A genome-wide association study of bitter and sweet beverage consumption.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008528	A genome-wide association study of bitter and sweet beverage consumption.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008530	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008531	A genome-wide association study of bitter and sweet beverage consumption.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008532	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008533	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008534	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008536	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008537	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008539	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008540	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008541	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008543	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008545	A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008546	A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008551	Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008552	Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008554	Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008566	Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008571	Identification of sequence variants influencing immunoglobulin levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008609	Sequence variants associating with urinary biomarkers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008618	Sequence variants associating with urinary biomarkers.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008641	Genomewide association study of C-peptide surfaces key regulatory genes in Indians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008643	Genetic Variants Influencing Joint Damage in Mexican Americans and European Americans With Rheumatoid Arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008660	Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008661	Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008666	Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008680	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008681	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008692	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008693	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008697	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008699	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008700	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008718	Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008730	Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008731	Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008732	Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008736	Genome-Wide Meta-Analysis of Blood Pressure Response to β1-Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008739	Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008740	Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008749	A genome-wide association and replication study of blood pressure in Ugandan early adolescents.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008750	A genome-wide association and replication study of blood pressure in Ugandan early adolescents.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008753	Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008755	Dissecting genetic factors affecting phenylephrine infusion rates during anesthesia: a genome-wide association study employing EHR data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008760	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008761	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008762	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008763	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008764	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008765	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008766	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008767	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008768	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008769	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008772	Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008793	Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008824	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008826	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008827	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008828	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008837	Genetic risk score raises the risk of incidence of chronic kidney disease in Korean general population-based cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008863	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008864	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008865	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008867	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008868	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008873	Genome-wide association study of cerebral small vessel disease reveals established and novel loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008889	Social and non-social autism symptoms and trait domains are genetically dissociable.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008891	Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008892	Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008894	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008898	GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008900	A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008905	Transcriptome association studies of neuropsychiatric traits in African Americans implicate PRMT7 in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008906	Transcriptome association studies of neuropsychiatric traits in African Americans implicate PRMT7 in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008913	CORR® ORS Richard A. Brand Award: Disruption in Peroxisome Proliferator-Activated Receptor-γ (PPARG) Increases Osteonecrosis Risk Through Genetic Variance and Pharmacologic Modulation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008917	Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008924	Genetic architecture of human plasma lipidome and its link to cardiovascular disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008938	Genetic architecture of human plasma lipidome and its link to cardiovascular disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008939	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008940	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008941	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008942	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008943	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008944	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008946	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008947	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008948	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008949	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008950	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008951	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008952	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008953	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008954	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008955	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008956	Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008957	Very low-depth whole-genome sequencing in complex trait association studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008963	Very low-depth whole-genome sequencing in complex trait association studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008964	Very low-depth whole-genome sequencing in complex trait association studies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008968	Genome-wide association study of white-coat effect in hypertensive patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008969	Genome-wide association study of white-coat effect in hypertensive patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008978	Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008979	Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008982	Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST008993	Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009002	Genomic Prediction of Tendinopathy Risk in Elite Team Sports.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009006	The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009007	Identification of novel epithelial ovarian cancer loci in Women of African Ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009008	Identification of novel epithelial ovarian cancer loci in Women of African Ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009031	Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009071	Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009072	Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009073	Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009074	Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009075	Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009077	Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009078	Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009086	Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009090	HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009100	Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009103	Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009130	A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009134	Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009139	Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009172	Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009173	Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009174	Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009175	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009176	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009177	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009178	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009179	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009180	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009181	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009182	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009183	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009184	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009185	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009186	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009187	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009188	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009189	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009190	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009191	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009192	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009193	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009194	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009195	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009196	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009197	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009198	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009199	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009200	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009201	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009202	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009203	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009204	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009205	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009206	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009208	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009209	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009210	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009211	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009213	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009214	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009215	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009216	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009217	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009219	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009220	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009221	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009222	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009236	Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009237	Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009253	Smoking Modifies the Genetic Risk for Early-Onset Periodontitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009254	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009255	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009256	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009257	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009258	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009259	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009260	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009261	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009262	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009263	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009264	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009265	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009266	Pilot GWAS of caries in African-Americans shows genetic heterogeneity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009267	Pilot GWAS of caries in African-Americans shows genetic heterogeneity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009268	Pilot GWAS of caries in African-Americans shows genetic heterogeneity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009269	Pilot GWAS of caries in African-Americans shows genetic heterogeneity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009276	Pharmacogenomics and Placebo Response in a Randomized Clinical Trial in Asthma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009277	Pharmacogenomics and Placebo Response in a Randomized Clinical Trial in Asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009282	Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009297	Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009298	Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009300	Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009301	Genome-wide association study on antipsychotic-induced weight gain in Europeans and African-Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009302	Genome-wide association study on antipsychotic-induced weight gain in Europeans and African-Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009305	Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009307	Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009308	Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009311	Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009313	Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009319	Genetic factors associated with elevation of uric acid after treatment with thiazide-like diuretic in patients with essential hypertension.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009321	Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009322	Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009323	Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009359	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009360	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009361	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009362	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009370	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009376	Genome-wide Network-assisted Association and Enrichment Study of Amyloid Imaging Phenotype in Alzheimer's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009377	Genetic variants affecting bone mineral density and bone mineral content at multiple skeletal sites in Hispanic children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009381	A Genome-Wide Association Study Identifies Five Novel Genetic Markers for Trastuzumab-Induced Cardiotoxicity in Japanese Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009385	A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and gene–environment interaction	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009403	GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009417	Genome-Wide Analyses Reveal Gene Influence on HIV Disease Progression and HIV-1C Acquisition in Southern Africa.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009421	Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009423	Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009424	Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009425	Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009426	Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009430	Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009431	Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009433	Genetics of cognitive trajectory in Brazilians: 15 years of follow-up from the Bambuí-Epigen Cohort Study of Aging.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009438	Incorporating spatial-anatomical similarity into the VGWAS framework for AD biomarker detection.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009439	Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009441	Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009442	Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009443	Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009444	Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009446	A Prospective Analysis of Genetic Variants Associated with Human Lifespan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009468	Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009471	Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009503	Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009504	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009506	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009507	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009508	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009515	First genome-wide association study of non-severe malaria in two birth cohorts in Benin.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009516	Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009525	Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009526	Polygenic risk score for disability and insights into disability-related molecular mechanisms.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009532	Candidate Gene and Genome-Wide Association Studies for Circulating Leptin Levels Reveal Population and Sex-Specific Associations in High Cardiovascular Risk Mediterranean Subjects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009542	A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009543	A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009544	A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009545	Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009547	A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009548	A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009549	A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009603	Wnt receptor gene FZD1 was associated with schizophrenia in genome-wide SNP analysis of the Australian Schizophrenia Research Bank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009612	Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009614	Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009617	Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009641	"General regression model: A ""model-free"" association test for quantitative traits allowing to test for the underlying genetic model."	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009642	Prevention of Potential Adverse Metabolic Effects of a Supplementation with Omega-3 Fatty Acids Using a Genetic Score Approach.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009674	Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009678	Genome-wide association study of cognitive performance in U.S. veterans with schizophrenia or bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009680	A meta-analysis of genome-wide association studies of multiple myeloma among men and women of African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009701	A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009702	A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009704	A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009705	A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009706	A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009707	A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009727	Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009796	Genome-Wide Association Study of Opioid Cessation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009809	GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009817	Genetic associations with clozapine-induced myocarditis in patients with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009818	Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009819	Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009820	Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009827	GWAS of five gynecologic diseases and cross-trait analysis in Japanese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009828	GWAS of five gynecologic diseases and cross-trait analysis in Japanese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009831	GWAS of five gynecologic diseases and cross-trait analysis in Japanese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009832	GWAS of five gynecologic diseases and cross-trait analysis in Japanese.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009835	Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009839	The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009840	Lack of association of genetic variants for diabetic retinopathy in Taiwanese patients with diabetic nephropathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009844	Genome-wide Association Study of Creativity Reveals Genetic Overlap With Psychiatric Disorders, Risk Tolerance, and Risky Behaviors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009849	Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009872	The Rare Variant rs35356162 in UHRF1BP1 Increases Bladder Cancer Risk in Han Chinese Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009891	A trans-ethnic two-stage polygenetic scoring analysis detects genetic correlation between osteoporosis and schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009892	A trans-ethnic two-stage polygenetic scoring analysis detects genetic correlation between osteoporosis and schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009894	Analysis of the genetic variants associated with circulating levels of sgp130. Results from the IMPROVE study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009896	Evaluation of vitamin D biosynthesis and pathway target genes reveals UGT2A1/2 and EGFR polymorphisms associated with epithelial ovarian cancer in African American Women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009897	Genome-Wide Association Study of Word Reading: Overlap with Risk Genes for Neurodevelopmental Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009925	Genome-wide Association Study for Urinary and Fecal Incontinence in Women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009936	Novel exomic rare variants associated with venous thrombosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009957	Gene-based association analysis reveals involvement of LAMA5 and cell adhesion pathways in nicotine dependence in African- and European-American samples.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009961	Insights into the genetic basis of retinal detachment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009976	Polygenic prediction and GWAS of depression, PTSD, and suicidal ideation/self-harm in a Peruvian cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009977	Polygenic prediction and GWAS of depression, PTSD, and suicidal ideation/self-harm in a Peruvian cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009979	Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009980	Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009983	Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009984	Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009985	Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST009998	Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009999	Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010000	Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010041	Identification of Novel Genes Associated with Cortical Thickness in Alzheimer's Disease: Systems Biology Approach to Neuroimaging Endophenotype.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010052	Genome-Wide Association Study of Ocular Sarcoidosis Confirms HLA Associations and Implicates Barrier Function and Autoimmunity in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010056	Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010058	Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010059	Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010061	Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010063	Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010076	Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010079	A Functional Variant Near XCL1 Gene Improves Breast Cancer Survival via Promoting Cancer Immunity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010081	The Genetic Variations Associated With Time to Aseptic Loosening After Total Joint Arthroplasty.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010082	The Genetic Variations Associated With Time to Aseptic Loosening After Total Joint Arthroplasty.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010087	Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010093	Genome-wide association study of emotional empathy in children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010094	Genome-wide association study of emotional empathy in children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010095	Genome-wide association study of emotional empathy in children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010116	Genome-Wide Association Study Reveals a Novel Association Between MYBPC3 Gene Polymorphism, Endurance Athlete Status, Aerobic Capacity and Steroid Metabolism.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010119	Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010120	Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010153	Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010169	Genetic Contributions to Maternal and Neonatal Vitamin D Levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010170	Genetic Contributions to Maternal and Neonatal Vitamin D Levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010171	Genetic Contributions to Maternal and Neonatal Vitamin D Levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010197	Protein quantitative trait locus study in obesity during weight-loss identifies a leptin regulator.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010216	Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010217	Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010218	Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010220	Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010221	Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010222	Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010248	Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010249	PRDM15 Is Associated with Risk of Chronic Obstructive Pulmonary Disease in a Rural Population in Chile.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010250	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010251	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010252	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010253	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010255	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010256	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010257	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010261	A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010264	A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010278	Genetics of physiological dysregulation: findings from the long life family study using joint models.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010289	Shared genetic background between children and adults with attention deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010290	Shared genetic background between children and adults with attention deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010292	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010293	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010294	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010295	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010296	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010297	A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010312	Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010317	Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010319	Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010336	Genome-wide association study of semen volume, sperm concentration, testis size, and plasma inhibin B levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010347	A survey of microRNA single nucleotide polymorphisms identifies novel breast cancer susceptibility loci in a case-control, population-based study of African-American women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010456	Genome-Wide Association Study of Genetic Variants Related to Anthracycline-Induced Cardiotoxicity in Early Breast Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010460	Genome-Wide Association Study of Lean Nonalcoholic Fatty Liver Disease Suggests Human Leukocyte Antigen as a Novel Candidate Locus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010463	Genome-Wide Association Meta-Analysis of Single-Nucleotide Polymorphisms and Symptomatic Venous Thromboembolism during Therapy for Acute Lymphoblastic Leukemia and Lymphoma in Caucasian Children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010466	Genome-wide association study of aggression and violence in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010467	Genome-wide association study of aggression and violence in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010477	Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010481	Genomewide Association Study of Acute Anterior Uveitis Identifies New Susceptibility Loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010482	Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010483	Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010484	Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC).	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010505	Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010506	Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010511	Genome-wide association study identifies genetic susceptibility loci and pathways of radiation-induced acute oral mucositis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010514	Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010538	Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010539	Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010540	Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010541	Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010561	Association between herpes simplex virus 1 exposure and the risk of depression in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010566	Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010574	Genetic Associations of Chronotype in the Finnish General Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010575	Genetic Associations of Chronotype in the Finnish General Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010576	Genetic Associations of Chronotype in the Finnish General Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010578	Genome-wide association study identifies TPH2 variant as a novel locus for severe CV-A6-associated hand, foot, and mouth disease in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010580	Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010597	Genome-Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010604	Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010605	Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010606	Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010652	Exome Array Analysis of Early-Onset Ischemic Stroke.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010654	Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010656	Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010676	Genome-wide association study identifies CDH13 as a susceptibility gene for rhododendrol-induced leukoderma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010677	Integrative omics analysis identifies macrophage migration inhibitory factor signaling pathways underlying human hepatic fibrogenesis and fibrosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010678	Integrative omics analysis identifies macrophage migration inhibitory factor signaling pathways underlying human hepatic fibrogenesis and fibrosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010683	GWAS for time to failure of kidney transplants from African American deceased donors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010717	Genetic Variant Associated with Survival of Patients with Stage II-III Colon Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010732	Genome-Wide Meta-Analysis Validates a Roless for S1PR1 in Microtubule Targeting Agent-Induced Sensory Peripheral Neuropathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010759	Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010760	Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010762	LRRTM4 and PCSK5 Genetic Polymorphisms as Markers for Cognitive Impairment in A Hypotensive Aging Population: A Genome-Wide Association Study in Taiwan.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010816	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010817	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010818	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010819	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010837	Identification of nine genes as novel susceptibility loci for early-onset ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010923	Polygenic Score for Beta-Blocker Survival Benefit in European Ancestry Patients with Reduced Ejection Fraction Heart Failure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010986	Genome-Wide Association Analysis of Longitudinal Bone Mineral Content Data From the Iowa Bone Development Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010987	Genome-Wide Association Analysis of Longitudinal Bone Mineral Content Data From the Iowa Bone Development Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST010993	Clinicogenomic factors of biotherapy immunogenicity in autoimmune disease: A prospective multicohort study of the ABIRISK consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011038	Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011041	Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011042	Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011043	Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011044	Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011066	Genomic Analysis Identifies New Loci Associated With Motor Complications in Parkinson's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011067	Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011068	Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011069	Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011105	Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011106	Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011107	A Genomewide Pharmacogenetic Study of Growth Hormone Responsiveness.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011136	Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011137	Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011138	Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011139	Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011151	Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011152	Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011158	Interactions of Habitual Coffee Consumption by Genetic Polymorphisms with the Risk of Prediabetes and Type 2 Diabetes Combined.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011178	Genetic determinants of lung cancer prognosis in never smokers: A pooled analysis in the International Lung Cancer Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011197	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011199	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011200	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011201	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011204	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011213	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011301	Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011304	Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011356	Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011358	Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011362	Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011371	Genetic Risk Score Constructed from Common Genetic Variants is Associated with Cardiovascular Disease Risk in Type 2 Diabetes Mellitus.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011384	Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011385	Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011386	Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011387	Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011388	Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011396	Genome-wide association study and polygenic risk score analysis of esketamine treatment response.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011397	Genome-wide association study and polygenic risk score analysis of esketamine treatment response.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011404	Genetic variants and functional pathways associated with resilience to Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011405	Genetic variants and functional pathways associated with resilience to Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011406	Genetic variants and functional pathways associated with resilience to Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011418	Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011421	A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011422	A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011423	A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011424	A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011434	Donor genetic variants as risk factors for thrombosis after liver transplantation: A genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011435	Amerindian Ancestry Influences Genetic Susceptibility to Chronic Obstructive Pulmonary Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011436	Extreme Phenotype Approach Suggests Taste Transduction Pathway for Carotid Plaque in a Multi-Ethnic Cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011463	Sex-Specific Genetic Associations for Barrett's Esophagus and Esophageal Adenocarcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011464	Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011476	Associations between COVID-19 and skin conditions identified through epidemiology and genomic studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011492	Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011516	A genome-wide association study identifying the SNPs predictive of rapid joint destruction in patients with rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011528	Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011531	Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011540	Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011584	Genomic analysis of germline variation associated with survival of colorectal cancer patients treated with chemotherapy plus biologics in CALGB/SWOG 80405 (Alliance).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011589	Novel Genetic Variant Predicts Surgical Recurrence Risk in Crohn's Disease Patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011637	Clinical and Genome-Wide Analysis of Multiple Severe Cisplatin-Induced Neurotoxicities in Adult-Onset Cancer Survivors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011657	Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011662	Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011664	Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011678	Depression in multiple sclerosis patients associated with risk variant near NEGR1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011679	Depression in multiple sclerosis patients associated with risk variant near NEGR1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011680	Depression in multiple sclerosis patients associated with risk variant near NEGR1.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011681	Genome-Wide Association Study Identifies Novel Colony Stimulating Factor 1 Locus Conferring Susceptibility to Cryptococcosis in Human Immunodeficiency Virus-Infected South Africans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011682	Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011688	Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011689	Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011690	Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011691	Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011692	Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011694	Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011706	Association of common genetic variants with brain microbleeds: A Genome-wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011710	Association of genetic variants in migraineurs with and without restless legs syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011716	Association between non-Caucasian-specific ASCC1 gene polymorphism and osteoporosis and obesity in Korean postmenopausal women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011717	Association between non-Caucasian-specific ASCC1 gene polymorphism and osteoporosis and obesity in Korean postmenopausal women.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011739	A Genome-Wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1 and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis In Brazil.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011774	Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011775	Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011782	Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011793	A Genome-Wide Association Study in Early COPD: Identification of One Major Susceptibility Loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011794	A Genome-Wide Association Study in Early COPD: Identification of One Major Susceptibility Loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011817	A genetic variant conferred high expression of CAV2 promotes pancreatic cancer progression and associates with poor prognosis.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011818	Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011826	A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011830	Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011831	Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011832	Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011836	Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011837	Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011893	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011896	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011897	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011898	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011900	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011901	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011903	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011904	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011909	A Genome-Wide Association Study for Hypertensive Kidney Disease in Korean Men.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011920	Genome-wide association study identifies 7q11.22 and 7q36.3 associated with noise-induced hearing loss among Chinese population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011929	Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011955	The influence of regression models on genome-wide association studies of alcohol dependence: a comparison of binary and quantitative analyses.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011958	Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir- and Tenofovir-containing Regimens.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011959	Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir- and Tenofovir-containing Regimens.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011961	A genome-wide association study for highly sensitive cardiac troponin T levels identified a novel genetic variation near a RBAK-ZNF890P locus in the Japanese general population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011973	Genome-Wide Analysis of Sex Disparities in the Genetic Architecture of Lung and Colorectal Cancers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011974	Genome-Wide Analysis of Sex Disparities in the Genetic Architecture of Lung and Colorectal Cancers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011978	CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011983	Genome-wide association study identifying novel variant for fasting insulin and allelic heterogeneity in known glycemic loci in Chilean adolescents: The Santiago Longitudinal Study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011984	Congenital heart disease risk loci identified by genome-wide association study in European patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011986	Congenital heart disease risk loci identified by genome-wide association study in European patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST011996	Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011998	Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012015	Two-stage genome-wide association study of chronic rhinosinusitis and disease subphenotypes highlights mucosal immunity contributing to risk.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012024	Integration of genome-wide association study and expression quantitative trait locus mapping for identification of endometriosis-associated genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012028	Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012046	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012049	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012051	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012055	A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012064	Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012065	Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012067	Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012068	Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012070	Genome-Wide Association Study of Response to Selenium Supplementation and Circulating Selenium Concentrations in Adults of European Descent.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012071	Genome-Wide Association Study of Response to Selenium Supplementation and Circulating Selenium Concentrations in Adults of European Descent.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012083	Contribution of a European-Prevalent Variant near CD83 and an East Asian-Prevalent Variant near IL17RB to Herpes Zoster Risk in Tofacitinib Treatment: Results of Genome-Wide Association Study Meta-Analyses.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012084	Contribution of a European-Prevalent Variant near CD83 and an East Asian-Prevalent Variant near IL17RB to Herpes Zoster Risk in Tofacitinib Treatment: Results of Genome-Wide Association Study Meta-Analyses.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012094	Genome-wide association study of patients with a severe major depressive episode treated with electroconvulsive therapy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012102	Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012103	Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012112	Genetic underpinnings of sociability in the general population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012113	Genetic underpinnings of sociability in the general population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012115	Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012116	Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012117	Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012118	Genetic determinants of immune-related adverse events in patients with melanoma receiving immune checkpoint inhibitors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012119	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012120	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012121	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012122	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012123	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012124	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012125	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012136	Genome-wide and candidate gene association analyses identify a 14-SNPs combination for hypertension in patients with type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012137	Genome-Wide Association Study of Motor Coordination.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012146	Genetic determinants of ferritin, haemoglobin levels and haemoglobin trajectories: results from Donor InSight.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012147	Genetic determinants of ferritin, haemoglobin levels and haemoglobin trajectories: results from Donor InSight.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012153	Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012158	Genome-wide association studies of antidepressant class response and treatment-resistant depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012160	Genome-wide association studies of antidepressant class response and treatment-resistant depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012161	Genomic Association Study for Cognitive Impairment in Parkinson's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012162	Genomic Association Study for Cognitive Impairment in Parkinson's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012163	Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012165	Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012166	Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012167	Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012168	Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012170	Genome-wide association analysis of cognitive function in Danish long-lived individuals.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012176	Rare variants in the DNA repair pathway and the risk of colorectal cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012181	Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012184	Pharmacogenomic Profile and Adverse Drug Reactions in a Prospective Therapeutic Cohort of Chagas Disease Patients Treated with Benznidazole.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012187	Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012188	Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012190	Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012192	Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012195	Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012205	Genetic architectures of proximal and distal colorectal cancer are partly distinct.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012207	Host genome wide association study of infant susceptibility to <i>Shigella</i>-associated diarrhea.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012209	Latent trait modeling of tau neuropathology in progressive supranuclear palsy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012221	Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012222	Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012224	Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012244	Genome-wide association studies of exacerbations in children using long-acting beta2-agonists.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012245	Genome-wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012255	Confident identification of subgroups from SNP testing in RCTs with binary outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012277	Variants at the MHC Region Associate With Susceptibility to <i>Clostridioides difficile</i> Infection: A Genome-Wide Association Study Using Comprehensive Electronic Health Records.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012279	Genome-wide association study of suicidal behaviour severity in mood disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012280	Genome-wide association study of suicidal behaviour severity in mood disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012283	Identification of genetic loci affecting body mass index through interaction with multiple environmental factors using structured linear mixed model.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012284	Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012286	Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012287	Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012288	Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012291	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012292	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012294	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012295	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012297	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012298	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012300	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012301	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012302	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012303	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012305	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012306	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012307	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012310	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012311	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012317	Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012318	Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012320	Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012325	Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012326	Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012328	Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012342	Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012343	Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012346	The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012356	Aberrant MCM10 SUMOylation induces genomic instability mediated by a genetic variant associated with survival of esophageal squamous cell carcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012357	Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012358	Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012359	Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012362	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012363	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012364	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012365	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012366	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012367	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012399	Integrative Genomics Analysis Reveals a 21q22.11 Locus Contributing Risk to COVID-19.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012418	Integrative omics provide biological and clinical insights into acute respiratory distress syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012420	A Genome-Wide Association Study in Human Lymphoblastoid Cells Supports Safety of Mitochondrial Complex I Inhibitor.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012421	Genetic risk factors for colorectal cancer in multiethnic Indonesians.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012433	Novel loci and mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012444	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012445	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012447	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012449	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012450	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012456	FAT4 identified as a potential modifier of orofacial cleft laterality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012458	FAT4 identified as a potential modifier of orofacial cleft laterality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012462	Identification of OCA2 as a novel locus for the co-morbidity of asthma-plus-eczema.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012466	Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012471	Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012472	Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012473	Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012474	Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012484	Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012486	Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST012493	An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training-induced muscle fiber hypertrophy in younger men.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012498	Both rare and common genetic variants contribute to autism in the Faroe Islands.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012500	Genome-wide association study of cardiac troponin I in the general population.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90000014	Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90000015	Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90000030	Genetic Meta-Analysis of Twin Birth Weight Shows High Genetic Correlation with Singleton Birth Weight.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90000256	Genomewide Association Study of Severe Covid-19 with Respiratory Failure.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90000295	Genetic and functional insights into the fractal structure of the heart.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90002226	The trans-ancestral genomic architecture of glycemic traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90002237	The trans-ancestral genomic architecture of glycemic traits.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006791	Meta-analysis of 26,638 Individuals Identifies Two Genetic Loci Associated with Left Ventricular Ejection Fraction.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006987	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006988	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006989	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006990	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90006991	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006992	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006993	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006994	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006995	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006996	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006997	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006998	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90006999	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007000	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007001	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007002	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007003	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007004	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007005	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90007006	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007007	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007008	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007009	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007011	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007012	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007314	Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007318	Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007323	Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007326	Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90007329	Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90010430	Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90010431	Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90010432	Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90010720	Genome-wide association study for circulating fibroblast growth factor 21 and 23.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90011820	Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90011821	Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90012207	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90012798	Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90012829	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90012830	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90012831	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90013452	"""The Heidelberg Five"" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment."	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90013453	"""The Heidelberg Five"" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment."	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90013454	"""The Heidelberg Five"" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment."	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90013559	Urinary metabolite quantitative trait loci in children and their interaction with dietary factors.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90013658	Common and Rare Variants Genetic Association Analysis of Circulating Neutrophil Extracellular Traps.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90013665	Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90014124	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90014126	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90014128	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90016622	Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90016992	Large-scale association analyses identify host factors influencing human gut microbiome composition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017018	Large-scale association analyses identify host factors influencing human gut microbiome composition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017130	Large-scale association analyses identify host factors influencing human gut microbiome composition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017131	Large-scale association analyses identify host factors influencing human gut microbiome composition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017132	Large-scale association analyses identify host factors influencing human gut microbiome composition.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017134	Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017147	Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017148	Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017202	Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017208	Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90017221	Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90020037	Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90020038	Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90020039	Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90020040	Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90020063	A Genome-Wide Association Study and Polygenic Risk Score Analysis of Posttraumatic Stress Disorder and Metabolic Syndrome in a South African Population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90020240	Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90025851	Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90025852	Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90025853	Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90025854	Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90025871	An association between chronic widespread pain and the gut microbiome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90025872	An association between chronic widespread pain and the gut microbiome.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90025928	Genome Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary Incontinence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90025931	<i>CDH12</i> as a Candidate Gene for Kidney Injury in Posterior Urethral Valve Cases: A Genome-wide Association Study Among Patients with Obstructive Uropathies.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90025934	Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90026409	Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026410	Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026411	Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026452	A genome-wide association study identifies novel susceptibility loci in chronic Chagas cardiomyopathy.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90026458	Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026459	Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026460	Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026523	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90026548	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026551	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026580	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026591	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026609	Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90026610	Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026611	Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90027021	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027022	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027024	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027025	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027026	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027070	Genetic association study of childhood aggression across raters, instruments, and age.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90027075	Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027076	Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027077	Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027236	A genome-wide association study of nausea incidence in varenicline-treated cigarette smokers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027255	Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90027258	Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90027263	Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90027269	Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90027270	Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027271	Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027894	Genome-wide Association Study Identified Chromosome 8 Locus Associated with Medication-related Osteonecrosis of the Jaw.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90027903	A genome-wide association study of quantitative computed tomographic emphysema in Korean populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027904	Sex-specific genetic factors affect the risk of early-onset periodontitis in Europeans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90029040	Genome-wide association study and polygenic risk score analysis for hearing measures in children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90029041	Genome-wide association study and polygenic risk score analysis for hearing measures in children.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90029045	Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90029046	Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90029057	Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90029062	Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90029167	Genome-wide association study identifies new loci associated with noise-induced tinnitus in Chinese populations.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90032157	A Genome-Wide Association Study on Liver Stiffness Changes during Hepatitis C Virus Infection Cure.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90032165	Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90032166	Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90032167	Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90032168	Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90032169	Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90032170	Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90044764	Association between polygenetic risk scores related to sarcopenia risk and their interactions with regular exercise in a large cohort of Korean adults.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90044777	Analysis of genetic and clinical factors associated with buprenorphine response.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90044847	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044849	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044850	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044855	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044859	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044861	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044863	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044865	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044870	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044871	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044872	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044879	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044884	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044887	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044889	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044890	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044892	Genetic predisposition to tinnitus in the UK Biobank population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044906	Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90044907	Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90052889	Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90052890	Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90052891	Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90052893	Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90052895	Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.	P-value fails significance threshold (5e-08) (mlog=7.3)
GCST90053837	A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000004	A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.	Missing both OR and beta
GCST000008	A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.	Missing both OR and beta
GCST000013	Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000071	Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.	Missing both OR and beta
GCST000077	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000079	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000080	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000081	Genome-wide association of sleep and circadian phenotypes.	Missing both OR and beta
GCST000082	Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.	Missing both OR and beta
GCST000083	Genome-wide association with select biomarker traits in the Framingham Heart Study.	Missing both OR and beta
GCST000084	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000085	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	Missing both OR and beta
GCST000086	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000087	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000088	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	Missing both OR and beta
GCST000089	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000090	Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000091	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	Missing both OR and beta
GCST000092	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000093	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000094	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	Missing both OR and beta
GCST000095	A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000096	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Missing both OR and beta
GCST000097	Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000098	Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000099	Framingham Heart Study genome-wide association: results for pulmonary function measures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000100	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000101	Genome-wide association with bone mass and geometry in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000102	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000103	Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.	Missing both OR and beta
GCST000104	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000105	A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000106	Framingham Heart Study genome-wide association: results for pulmonary function measures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000107	Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000108	Genome-wide association with diabetes-related traits in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000109	Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000110	Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000111	Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000121	Sorl1 as an Alzheimer's disease predisposition gene?	Missing both OR and beta
GCST000124	Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.	Missing both OR and beta
GCST000135	Newly identified loci that influence lipid concentrations and risk of coronary artery disease.	Missing both OR and beta
GCST000146	Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.	Missing both OR and beta
GCST000163	A genome-wide association study in 574 schizophrenia trios using DNA pooling.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000189	A genome-wide association study identifies protein quantitative trait loci (pQTLs).	Missing both OR and beta
GCST000201	Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000202	Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000204	A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.	Missing both OR and beta
GCST000211	Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000217	Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility.	Missing both OR and beta
GCST000226	Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000227	Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.	Missing both OR and beta
GCST000235	Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000245	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000246	Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.	Missing both OR and beta
GCST000247	Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000253	Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000255	Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000265	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000266	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000267	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000268	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000271	A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000272	Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000274	Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.	Missing both OR and beta
GCST000278	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000279	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000280	Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000281	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000294	Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.	Missing both OR and beta
GCST000300	A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection.	Missing both OR and beta
GCST000310	Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000313	Examination of the current top candidate genes for AD in a genome-wide association study.	Missing both OR and beta
GCST000319	Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study.	Missing both OR and beta
GCST000320	Genome-wide association study of panic disorder in the Japanese population.	Missing both OR and beta
GCST000326	Genome-wide association study of acute post-surgical pain in humans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000349	Genome-wide and candidate gene association study of cigarette smoking behaviors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000356	Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000358	Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.	Missing both OR and beta
GCST000360	A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.	Missing both OR and beta
GCST000378	A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis.	Missing both OR and beta
GCST000381	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits.	Missing both OR and beta
GCST000393	Genome-wide association study of blood pressure and hypertension.	Missing both OR and beta
GCST000395	Genome-wide association study identifies eight loci associated with blood pressure.	Missing both OR and beta
GCST000397	Multiple loci associated with indices of renal function and chronic kidney disease.	Missing both OR and beta
GCST000403	Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.	Missing both OR and beta
GCST000406	Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.	Missing both OR and beta
GCST000412	Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000436	A genome-wide association study of acenocoumarol maintenance dosage.	Missing both OR and beta
GCST000461	Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000467	Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy.	Missing both OR and beta
GCST000469	Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000476	Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.	Missing both OR and beta
GCST000477	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000480	Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.	Missing both OR and beta
GCST000484	Genome-wide scan of copy number variation in late-onset Alzheimer's disease.	Missing both OR and beta
GCST000492	First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.	Missing both OR and beta
GCST000498	A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.	Missing both OR and beta
GCST000514	Genomewide association study of movement-related adverse antipsychotic effects.	Missing both OR and beta
GCST000520	Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000522	Identification of 15 loci influencing height in a Korean population.	Missing both OR and beta
GCST000533	Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.	Missing both OR and beta
GCST000538	A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.	Missing both OR and beta
GCST000542	Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.	Missing both OR and beta
GCST000555	A genome-wide association study of carotid atherosclerosis in HIV-infected men.	Missing both OR and beta
GCST000566	A genome-wide association study for age-related hearing impairment in the Saami.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000573	Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.	Missing both OR and beta
GCST000577	MGAT5 alters the severity of multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000579	Common genetic variation and performance on standardized cognitive tests.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000580	Genome-wide association study of hematological and biochemical traits in a Japanese population.	Missing both OR and beta
GCST000590	Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels.	Missing both OR and beta
GCST000591	A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels.	Missing both OR and beta
GCST000597	Voxelwise genome-wide association study (vGWAS).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000604	ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.	Missing both OR and beta
GCST000609	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Missing both OR and beta
GCST000610	Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.	Missing both OR and beta
GCST000618	Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs.	Missing both OR and beta
GCST000621	C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies.	Missing both OR and beta
GCST000625	Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium.	Missing both OR and beta
GCST000628	Chemerin, a novel adipokine in the regulation of angiogenesis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000635	Genome-wide association of lipid-lowering response to statins in combined study populations.	Missing both OR and beta
GCST000636	Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000641	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Missing both OR and beta
GCST000649	New loci associated with kidney function and chronic kidney disease.	Missing both OR and beta
GCST000651	Genetic loci influencing kidney function and chronic kidney disease.	Missing both OR and beta
GCST000656	Host determinants of HIV-1 control in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000666	Genome-wide meta-analyses identify multiple loci associated with smoking behavior.	Missing both OR and beta
GCST000676	Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000693	Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.	Missing both OR and beta
GCST000697	Common genetic determinants of vitamin D insufficiency: a genome-wide association study.	Missing both OR and beta
GCST000706	Web-based, participant-driven studies yield novel genetic associations for common traits.	Missing both OR and beta
GCST000707	Web-based, participant-driven studies yield novel genetic associations for common traits.	Missing both OR and beta
GCST000708	Web-based, participant-driven studies yield novel genetic associations for common traits.	Missing both OR and beta
GCST000710	Web-based, participant-driven studies yield novel genetic associations for common traits.	Missing both OR and beta
GCST000729	ITPA polymorphism affects ribavirin-induced anemia and outcomes of therapy--a genome-wide study of Japanese HCV virus patients.	Missing both OR and beta
GCST000741	A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9.	Missing both OR and beta
GCST000744	Genetic variants that affect length/height in infancy/early childhood in Vietnamese-Korean families.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000746	The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12.	Missing both OR and beta
GCST000751	Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000753	A genome-wide association study of the metabolic syndrome in Indian Asian men.	Missing both OR and beta
GCST000755	Biological, clinical and population relevance of 95 loci for blood lipids.	Missing both OR and beta
GCST000759	Biological, clinical and population relevance of 95 loci for blood lipids.	Missing both OR and beta
GCST000760	Biological, clinical and population relevance of 95 loci for blood lipids.	Missing both OR and beta
GCST000765	Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000774	Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression.	Missing both OR and beta
GCST000778	Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000783	Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000785	Joint influence of small-effect genetic variants on human longevity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000792	Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese.	Missing both OR and beta
GCST000814	A genome-wide association study of red blood cell traits using the electronic medical record.	Missing both OR and beta
GCST000822	Genome-wide association study of antipsychotic-induced QTc interval prolongation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000823	Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000825	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000826	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	Missing both OR and beta
GCST000827	Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.	Missing both OR and beta
GCST000845	Fine-scale recombination rate differences between sexes, populations and individuals.	Missing both OR and beta
GCST000847	Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.	Missing both OR and beta
GCST000848	Fine-scale recombination rate differences between sexes, populations and individuals.	Missing both OR and beta
GCST000850	Genome-wide association analysis of body mass in chronic obstructive pulmonary disease.	Missing both OR and beta
GCST000862	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000866	Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.	Missing both OR and beta
GCST000872	Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.	Missing both OR and beta
GCST000873	A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000881	A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000883	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000884	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000885	Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000900	Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000903	Genome-wide association study of blood pressure response to methylphenidate treatment of attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000904	Variants in several genomic regions associated with asperger disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000918	Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000924	Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000932	Genome-wide association study of hoarding traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000936	Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families.	Missing both OR and beta
GCST000937	A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.	Missing both OR and beta
GCST000954	Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men.	Missing both OR and beta
GCST000955	A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease.	Missing both OR and beta
GCST000960	Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.	Missing both OR and beta
GCST000961	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.	Missing both OR and beta
GCST000966	Genome-wide association study of diabetic retinopathy in a Taiwanese population.	Missing both OR and beta
GCST000977	Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000981	Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset.	Missing both OR and beta
GCST000982	Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000983	A non-synonymous polymorphism in galactose mutarotase (GALM) is associated with serotonin transporter binding potential in the human thalamus: results of a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000987	Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.	Missing both OR and beta
GCST000990	Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST000995	Genome-wide association study of personality traits in bipolar patients.	Missing both OR and beta
GCST001016	Atopy history and the genomics of wheezing after influenza vaccination in children 6-59 months of age.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001021	Genome-wide association study identifies genetic loci associated with iron deficiency.	Missing both OR and beta
GCST001030	Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001037	Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes.	Missing both OR and beta
GCST001049	Genetic predictors of fibrin D-dimer levels in healthy adults.	Missing both OR and beta
GCST001057	A genome-wide association study on obesity and obesity-related traits.	Missing both OR and beta
GCST001059	Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women.	Missing both OR and beta
GCST001061	Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001065	Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001069	Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.	Missing both OR and beta
GCST001072	Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.	Missing both OR and beta
GCST001073	A genome-wide association study of metabolic traits in human urine.	Missing both OR and beta
GCST001074	Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.	Missing both OR and beta
GCST001076	Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients.	Missing both OR and beta
GCST001077	Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.	Missing both OR and beta
GCST001082	Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate.	Missing both OR and beta
GCST001083	Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001092	Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001096	Genome-wide association study of severity in multiple sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001109	Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium.	Missing both OR and beta
GCST001110	A genome-wide association study for quantitative traits in schizophrenia in China.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001111	Genome-wide association study of smoking behaviours in patients with COPD.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001119	DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001121	A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001122	Novel locus FER is associated with serum HMW adiponectin levels.	Missing both OR and beta
GCST001131	A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals.	Missing both OR and beta
GCST001149	Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.	Missing both OR and beta
GCST001154	Genome-wide association study of the child behavior checklist dysregulation profile.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001155	Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.	Missing both OR and beta
GCST001163	Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.	Missing both OR and beta
GCST001168	The landscape of recombination in African Americans.	Missing both OR and beta
GCST001182	Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations.	Missing both OR and beta
GCST001185	A genome-wide association study in europeans and South asians identifies 5 new Loci for coronary artery disease.	Missing both OR and beta
GCST001186	Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rash.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001189	Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001194	Combinations of newly confirmed Glioma-Associated loci link regions on chromosomes 1 and 9 to increased disease risk.	Missing both OR and beta
GCST001201	Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001204	Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001211	Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001212	Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.	Missing both OR and beta
GCST001214	A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001218	Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.	Missing both OR and beta
GCST001227	Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.	Missing both OR and beta
GCST001231	Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.	Missing both OR and beta
GCST001233	Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.	Missing both OR and beta
GCST001240	Genome-wide population-based association study of extremely overweight young adults--the GOYA study.	Missing both OR and beta
GCST001254	Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001280	Genome-wide association analysis of age-at-onset in Alzheimer's disease.	Missing both OR and beta
GCST001286	Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001287	Genome-wide association study in German patients with attention deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001288	Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure.	Missing both OR and beta
GCST001302	Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.	Missing both OR and beta
GCST001308	Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001311	A genome-wide scan for common variants affecting the rate of age-related cognitive decline.	Missing both OR and beta
GCST001314	CDH13 gene coding T-cadherin influences variations in plasma adiponectin levels in the Japanese population.	Missing both OR and beta
GCST001315	Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001330	Genetic variants and environmental factors associated with hormonal markers of ovarian reserve in Caucasian and African American women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001338	New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort.	Missing both OR and beta
GCST001343	Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001352	Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001353	Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001354	Heritability of submaximal exercise heart rate response to exercise training is accounted for by nine SNPs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001356	Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001358	Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.	Missing both OR and beta
GCST001359	Genome-wide association study in bipolar patients stratified by co-morbidity.	Missing both OR and beta
GCST001367	A genome-wide association and gene-environment interaction study for serum triglycerides levels in a healthy Chinese male population.	Missing both OR and beta
GCST001368	Identification of novel germline polymorphisms governing capecitabine sensitivity.	Missing both OR and beta
GCST001371	A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.	Missing both OR and beta
GCST001378	Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.	Missing both OR and beta
GCST001385	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	Missing both OR and beta
GCST001389	The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001402	Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001411	Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.	Missing both OR and beta
GCST001414	Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.	Missing both OR and beta
GCST001418	Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response.	Missing both OR and beta
GCST001419	Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.	Missing both OR and beta
GCST001421	Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh.	Missing both OR and beta
GCST001423	A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001431	Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001440	Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001450	Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.	Missing both OR and beta
GCST001469	A mega-analysis of genome-wide association studies for major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001471	Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence.	Missing both OR and beta
GCST001476	Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.	Missing both OR and beta
GCST001489	Identification of a novel percent mammographic density locus at 12q24.	Missing both OR and beta
GCST001490	CHRNB3 is more strongly associated with Fagerström test for cigarette dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results.	Missing both OR and beta
GCST001491	Genome-wide association study of antibody response to smallpox vaccine.	Missing both OR and beta
GCST001495	Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001507	Melanesian blond hair is caused by an amino acid change in TYRP1.	Missing both OR and beta
GCST001517	Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain.	Missing both OR and beta
GCST001518	Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001520	Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001521	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001522	Genome-wide association of pericardial fat identifies a unique locus for ectopic fat.	Missing both OR and beta
GCST001523	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001524	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Missing both OR and beta
GCST001525	Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.	Missing both OR and beta
GCST001530	Multiple loci influencing hippocampal degeneration identified by genome scan.	Missing both OR and beta
GCST001532	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Missing both OR and beta
GCST001533	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Missing both OR and beta
GCST001534	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Missing both OR and beta
GCST001535	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Missing both OR and beta
GCST001536	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Missing both OR and beta
GCST001537	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Missing both OR and beta
GCST001538	Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.	Missing both OR and beta
GCST001540	Genome-wide association study identifies candidate genes for male fertility traits in humans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001542	Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001543	Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001554	Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.	Missing both OR and beta
GCST001560	Genome-wide association analysis of circulating vitamin D levels in children with asthma.	Missing both OR and beta
GCST001572	Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001574	Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.	Missing both OR and beta
GCST001580	A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.	Missing both OR and beta
GCST001584	Bivariate genome-wide association study suggests that the DARC gene influences lean body mass and age at menarche.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001585	Genetic variants associated with breast size also influence breast cancer risk.	Missing both OR and beta
GCST001591	Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.	Missing both OR and beta
GCST001597	Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001598	Genome-wide linkage and association scans for pulse pressure in Chinese twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001599	Linkage and association of successful aging to the 6q25 region in large Amish kindreds.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001600	Genome-wide association study identifies common variants at TNFRSF13B associated with IgG level in a healthy Chinese male population.	Missing both OR and beta
GCST001623	Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.	Missing both OR and beta
GCST001626	Genome-wide association study identifies TNFSF13 as a susceptibility gene for IgA in a South Chinese population in smokers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001632	Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.	Missing both OR and beta
GCST001639	Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.	Missing both OR and beta
GCST001651	Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13).	Missing both OR and beta
GCST001654	Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis.	Missing both OR and beta
GCST001656	Bivariate genome-wide association study suggests fatty acid desaturase genes and cadherin DCHS2 for variation of both compressive strength index and appendicular lean mass in males.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001658	Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001663	Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001675	Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.	Missing both OR and beta
GCST001677	Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk.	Missing both OR and beta
GCST001691	Genome-wide association replicates the association of Duffy antigen receptor for chemokines (DARC) polymorphisms with serum monocyte chemoattractant protein-1 (MCP-1) levels in Hispanic children.	Missing both OR and beta
GCST001692	Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001694	Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001696	Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population.	Missing both OR and beta
GCST001710	HbA2 levels in normal adults are influenced by two distinct genetic mechanisms.	Missing both OR and beta
GCST001713	GWAS of dental caries patterns in the permanent dentition.	Missing both OR and beta
GCST001721	Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001722	Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study.	Missing both OR and beta
GCST001724	Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population.	Missing both OR and beta
GCST001730	A genome-wide association analysis of temozolomide response using lymphoblastoid cell lines shows a clinically relevant association with MGMT.	Missing both OR and beta
GCST001732	Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001734	Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001736	Novel susceptibility genes associated with diabetic cataract in a Taiwanese population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001737	Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.	Missing both OR and beta
GCST001760	White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001763	HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults.	Missing both OR and beta
GCST001764	White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001767	A genome-wide association study in Caucasian women points out a putative role of the STXBP5L gene in facial photoaging.	Missing both OR and beta
GCST001771	TMPRSS9 and GRIN2B are associated with neuroticism: a genome-wide association study in a European sample.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001773	Genome-wide association study of patient-rated and clinician-rated global impression of severity during antipsychotic treatment.	Missing both OR and beta
GCST001776	Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.	Missing both OR and beta
GCST001780	GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.	Missing both OR and beta
GCST001781	GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.	Missing both OR and beta
GCST001786	Genome-wide association scan of dental caries in the permanent dentition.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001788	Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratio.	Missing both OR and beta
GCST001790	Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.	Missing both OR and beta
GCST001798	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	Missing both OR and beta
GCST001801	A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.	Missing both OR and beta
GCST001802	A genome-wide association study of depressive symptoms.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001819	Identification of a candidate gene for astigmatism.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001848	Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.	Missing both OR and beta
GCST001850	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.	Missing both OR and beta
GCST001853	Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.	Missing both OR and beta
GCST001860	A genome-wide association study of brain lesion distribution in multiple sclerosis.	Missing both OR and beta
GCST001868	APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.	Missing both OR and beta
GCST001873	Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.	Missing both OR and beta
GCST001882	A genome-wide assessment of variability in human serum metabolism.	Missing both OR and beta
GCST001890	Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001910	Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2).	Missing both OR and beta
GCST001911	A genome-wide association study of bronchodilator response in asthmatics.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001923	Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.	Missing both OR and beta
GCST001926	Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001929	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Missing both OR and beta
GCST001931	Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001933	Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.	Missing both OR and beta
GCST001935	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001943	Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001944	Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001945	Genome-wide association study of body mass index in 23 000 individuals with and without asthma.	Missing both OR and beta
GCST001946	Genome-wide association study identifies genetic determinants of urine PCA3 levels in men.	Missing both OR and beta
GCST001950	Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.	Missing both OR and beta
GCST001952	The molecular genetic architecture of self-employment.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST001964	The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.	Missing both OR and beta
GCST001976	Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study.	Missing both OR and beta
GCST001990	Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002027	Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study.	Missing both OR and beta
GCST002037	Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002038	Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder.	Missing both OR and beta
GCST002040	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Missing both OR and beta
GCST002041	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.	Missing both OR and beta
GCST002045	GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.	Missing both OR and beta
GCST002048	Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.	Missing both OR and beta
GCST002057	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	Missing both OR and beta
GCST002058	GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.	Missing both OR and beta
GCST002061	Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.	Missing both OR and beta
GCST002063	Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.	Missing both OR and beta
GCST002071	Genetic loci for retinal arteriolar microcirculation.	Missing both OR and beta
GCST002077	Parkinson disease loci in the mid-western Amish.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002088	Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.	Missing both OR and beta
GCST002090	Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy.	Missing both OR and beta
GCST002092	Genetics of callous-unemotional behavior in children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002097	Genetics of coronary artery calcification among African Americans, a meta-analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002100	A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.	Missing both OR and beta
GCST002112	A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.	Missing both OR and beta
GCST002113	Genome-wide association study of lung function phenotypes in a founder population.	Missing both OR and beta
GCST002115	Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.	Missing both OR and beta
GCST002122	A genome-wide association study of total serum and mite-specific IgEs in asthma patients.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002123	A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab family.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002131	A genome-wide association study of behavioral disinhibition.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002142	Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene.	Missing both OR and beta
GCST002143	Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.	Missing both OR and beta
GCST002162	Gene network analysis in a pediatric cohort identifies novel lung function genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002163	Gene network analysis in a pediatric cohort identifies novel lung function genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002164	Gene network analysis in a pediatric cohort identifies novel lung function genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002165	Gene network analysis in a pediatric cohort identifies novel lung function genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002167	Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci.	Missing both OR and beta
GCST002168	Genome-wide association study and meta-analysis of intraocular pressure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002173	THOC5: a novel gene involved in HDL-cholesterol metabolism.	Missing both OR and beta
GCST002188	Genetic predictors of risk and resilience in psychiatric disorders: a cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002192	Genome-wide association studies and epistasis analyses of candidate genes related to age at menarche and age at natural menopause in a Korean population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002197	Genome-wide association study of ancestry-specific TB risk in the South African Coloured population.	Missing both OR and beta
GCST002202	Genome-wide association study of co-occurring anxiety in major depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002205	Genome-wide association study of handedness excludes simple genetic models.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002206	Genome-wide association study of handedness excludes simple genetic models.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002209	Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002211	Genome-wide association study of atypical psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002218	Genome-wide association study of endometrial cancer in E2C2.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002219	Discovery and refinement of loci associated with lipid levels.	Missing both OR and beta
GCST002220	Discovery and refinement of loci associated with lipid levels.	Missing both OR and beta
GCST002235	Genome-wide association study of opioid dependence: multiple associations mapped to calcium and potassium pathways.	Missing both OR and beta
GCST002239	Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.	Missing both OR and beta
GCST002241	Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.	Missing both OR and beta
GCST002242	Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.	Missing both OR and beta
GCST002247	Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.	Missing both OR and beta
GCST002248	Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits.	Missing both OR and beta
GCST002251	Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits.	Missing both OR and beta
GCST002253	Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits.	Missing both OR and beta
GCST002254	GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus.	Missing both OR and beta
GCST002274	No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002278	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002279	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	Missing both OR and beta
GCST002280	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	Missing both OR and beta
GCST002281	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002282	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002284	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002285	Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002287	Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.	Missing both OR and beta
GCST002290	Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.	Missing both OR and beta
GCST002291	Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics.	Missing both OR and beta
GCST002292	"ALDH2 is associated to alcohol dependence and is the major genetic determinant of ""daily maximum drinks"" in a GWAS study of an isolated rural Chinese sample."	Missing both OR and beta
GCST002295	Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.	Missing both OR and beta
GCST002296	Is the gene-environment interaction paradigm relevant to genome-wide studies? The case of education and body mass index.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002306	Genome-wide association study of bipolar disorder accounting for effect of body mass index identifies a new risk allele in TCF7L2.	Missing both OR and beta
GCST002307	Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9.	Missing both OR and beta
GCST002308	Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002311	Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans.	Missing both OR and beta
GCST002315	A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential.	Missing both OR and beta
GCST002325	BAIAP2 is related to emotional modulation of human memory strength.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002336	Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study.	Missing both OR and beta
GCST002342	Genetic predictors associated with improvement of asthma symptoms in response to inhaled corticosteroids.	Missing both OR and beta
GCST002343	Discovery of genetic biomarkers contributing to variation in drug response of cytidine analogues using human lymphoblastoid cell lines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002345	Discovery of genetic biomarkers contributing to variation in drug response of cytidine analogues using human lymphoblastoid cell lines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002358	Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries.	Missing both OR and beta
GCST002361	Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002386	Heritability and genetic association analysis of cognition in the Diabetes Heart Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002393	Genome-wide association study of smoking behaviours among Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002394	Genome-wide association study of smoking behaviours among Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002395	Genome-wide association study of smoking behaviours among Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002396	Genome-wide association study of smoking behaviours among Bangladeshi adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002397	Genome-wide interaction study of smoking and bladder cancer risk.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002398	Insight into genetic determinants of resting heart rate.	Missing both OR and beta
GCST002401	A genome-wide association study of clinical symptoms of dissociation in a trauma-exposed sample.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002408	Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002409	Common genetic variants and gene expression associated with white matter microstructure in the human brain.	Missing both OR and beta
GCST002429	ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology.	Missing both OR and beta
GCST002431	A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity.	Missing both OR and beta
GCST002435	Genome wide association study: searching for genes underlying body mass index in the Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002441	Genome-wide SNP associations with rubella-specific cytokine responses in measles-mumps-rubella vaccine recipients.	Missing both OR and beta
GCST002446	Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium.	Missing both OR and beta
GCST002449	Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium.	Missing both OR and beta
GCST002457	Genetic determinants of P wave duration and PR segment.	Missing both OR and beta
GCST002465	Genome-wide association study supports the role of the immunological system and of the neurodevelopmental processes in response to haloperidol treatment.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002485	Genetic variations affecting serum carcinoembryonic antigen levels and status of regional lymph nodes in patients with sporadic colorectal cancer from Southern China.	Missing both OR and beta
GCST002497	Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.	Missing both OR and beta
GCST002500	Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.	Missing both OR and beta
GCST002524	Genome wide association scan for chronic periodontitis implicates novel locus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002533	Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians.	Missing both OR and beta
GCST002542	Genome-wide association study of electrocardiographic parameters identifies a new association for PR interval and confirms previously reported associations.	Missing both OR and beta
GCST002549	Citalopram and escitalopram plasma drug and metabolite concentrations: genome-wide associations.	Missing both OR and beta
GCST002552	Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002555	Trans-ethnic meta-analysis of white blood cell phenotypes.	Missing both OR and beta
GCST002579	A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002587	Gene-smoking interactions identify several novel blood pressure loci in the Framingham Heart Study.	Missing both OR and beta
GCST002588	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	Missing both OR and beta
GCST002589	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002590	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002591	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	Missing both OR and beta
GCST002592	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	Missing both OR and beta
GCST002593	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	Missing both OR and beta
GCST002594	Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.	Missing both OR and beta
GCST002602	Genome-wide association study of vitamin D levels in children: replication in the Western Australian Pregnancy Cohort (Raine) study.	Missing both OR and beta
GCST002615	Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002616	A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002617	Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.	Missing both OR and beta
GCST002618	Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002627	Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.	Missing both OR and beta
GCST002628	Genome-wide analysis of hepatic lipid content in extreme obesity.	Missing both OR and beta
GCST002630	Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.	Missing both OR and beta
GCST002632	Genome-wide analysis of hepatic lipid content in extreme obesity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002634	Genome-wide association study identifies ITPR2 as a susceptibility gene for Kashin-Beck disease in Han Chinese.	Missing both OR and beta
GCST002641	Gene by stress genome-wide interaction analysis and path analysis identify EBF1 as a cardiovascular and metabolic risk gene.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002664	Genome-wide association study identifies three novel genetic markers associated with elite endurance performance.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002665	Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation.	Missing both OR and beta
GCST002670	Genome-wide association study of selenium concentrations.	Missing both OR and beta
GCST002692	The National Longitudinal Study of Adolescent to Adult Health (Add Health) sibling pairs genome-wide data.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002694	"Results of a ""GWAS plus:"" general cognitive ability is substantially heritable and massively polygenic."	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002696	Genome-wide and gene-based association studies of anxiety disorders in European and African American samples.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002699	A genome-wide association study of suicide severity scores in bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002714	Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes.	Missing both OR and beta
GCST002715	A twin study of breastfeeding with a preliminary genome-wide association scan.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002719	Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002724	Genome-Wide Association Study Identification of Novel Loci Associated with Airway Responsiveness in Chronic Obstructive Pulmonary Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002726	Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium.	Missing both OR and beta
GCST002728	Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002732	Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002746	Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels.	Missing both OR and beta
GCST002749	Identification of genetic variants or genes that are associated with Homoharringtonine (HHT) response through a genome-wide association study in human lymphoblastoid cell lines (LCLs).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002754	Pharmacodynamic genome-wide association study identifies new responsive loci for glucocorticoid intervention in asthma.	Missing both OR and beta
GCST002755	Identifying genetic loci associated with antidepressant drug response with drug-gene interaction models in a population-based study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002760	Investigating the genetics of hippocampal volume in older adults without dementia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002777	Genome-wide association study of lymphoblast cell viability after clozapine exposure.	Missing both OR and beta
GCST002788	Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002789	Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002790	Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002793	Genetic variants associated with vein graft stenosis after coronary artery bypass grafting.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002799	Genome-wide association study of parity in Bangladeshi women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002801	Genome-wide association study of parity in Bangladeshi women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002804	Genome-wide genetic investigation of serological measures of common infections.	Missing both OR and beta
GCST002805	First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002812	Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002815	Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002816	Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.	Missing both OR and beta
GCST002825	Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002837	Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular Hypertension.	Missing both OR and beta
GCST002839	Genome-wide association study of plasma levels of polychlorinated biphenyls disclose an association with the CYP2B6 gene in a population-based sample.	Missing both OR and beta
GCST002858	VPS13D Gene Variant Is Associated with Altered IL-6 Production and Mortality in Septic Shock.	Missing both OR and beta
GCST002859	VPS13D Gene Variant Is Associated with Altered IL-6 Production and Mortality in Septic Shock.	Missing both OR and beta
GCST002868	The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response.	Missing both OR and beta
GCST002872	Genomics and metabolomics of muscular mass in a community-based sample of UK females.	Missing both OR and beta
GCST002893	A genome-wide association study of body mass index across early life and childhood.	Missing both OR and beta
GCST002918	Comprehensive genome-wide evaluation of lapatinib-induced liver injury yields a single genetic signal centered on known risk allele HLA-DRB1*07:01.	Missing both OR and beta
GCST002921	Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma.	Missing both OR and beta
GCST002922	Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma.	Missing both OR and beta
GCST002926	Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.	Missing both OR and beta
GCST002941	A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002945	A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.	Missing both OR and beta
GCST002951	Genome-wide association study of leukotriene modifier response in asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002956	Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer.	Missing both OR and beta
GCST002957	Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer.	Missing both OR and beta
GCST002976	Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002984	A genome-wide approach to children's aggressive behavior: The EAGLE consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002985	A genome-wide approach to children's aggressive behavior: The EAGLE consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST002987	Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.	Missing both OR and beta
GCST002988	Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.	Missing both OR and beta
GCST003001	A genome-wide association study identifies multiple loci for variation in human ear morphology.	Missing both OR and beta
GCST003002	A genome-wide association study identifies multiple loci for variation in human ear morphology.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003005	A genome-wide association study identifies multiple loci for variation in human ear morphology.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003013	Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.	Missing both OR and beta
GCST003025	New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003030	Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003055	Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003070	Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003075	Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.	Missing both OR and beta
GCST003079	Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003081	Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003083	Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003084	Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003087	A novel interaction between the FLJ33534 locus and smoking in obesity: a genome-wide study of 14 131 Pakistani adults.	Missing both OR and beta
GCST003088	Plasma Levels of Soluble Interleukin-2 Receptor α: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan.	Missing both OR and beta
GCST003095	Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003096	Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003097	Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases.	Missing both OR and beta
GCST003101	Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003102	Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche.	Missing both OR and beta
GCST003109	Genome-wide association study on antipsychotic-induced weight gain in the CATIE sample.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003113	Genetic Interactions Explain Variance in Cingulate Amyloid Burden: An AV-45 PET Genome-Wide Association and Interaction Study in the ADNI Cohort.	Missing both OR and beta
GCST003114	Genome-wide association study on progression of carotid artery intima media thickness over 10 years in a Chinese cohort.	Missing both OR and beta
GCST003115	Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms.	Missing both OR and beta
GCST003118	A genome-wide association study of antidepressant response in Koreans.	Missing both OR and beta
GCST003119	Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality.	Missing both OR and beta
GCST003122	Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.	Missing both OR and beta
GCST003133	A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003183	Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load.	Missing both OR and beta
GCST003211	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	Missing both OR and beta
GCST003212	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003213	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003215	Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations.	Missing both OR and beta
GCST003221	Genome-Wide Association Studies of the Human Gut Microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003223	Genome-Wide Association Studies of the Human Gut Microbiota.	Missing both OR and beta
GCST003233	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003234	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003235	Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003248	Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003249	Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003256	Genetic Factors for the Severity of ACPA-negative Rheumatoid Arthritis in 2 Cohorts of Early Disease: A Genome-wide Study.	Missing both OR and beta
GCST003262	A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.	Missing both OR and beta
GCST003263	A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003264	A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.	Missing both OR and beta
GCST003265	A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003272	Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.	Missing both OR and beta
GCST003278	Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies.	Missing both OR and beta
GCST003319	Genome-wide environment interaction between depressive state and stressful life events.	Missing both OR and beta
GCST003340	Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis.	Missing both OR and beta
GCST003365	A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction.	Missing both OR and beta
GCST003374	Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.	Missing both OR and beta
GCST003383	Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.	Missing both OR and beta
GCST003390	Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.	Missing both OR and beta
GCST003423	Shared genetic contribution to Ischaemic Stroke and Alzheimer's Disease.	Missing both OR and beta
GCST003432	The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis.	Missing both OR and beta
GCST003434	Obsessive-compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs.	Missing both OR and beta
GCST003439	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003440	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003441	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003443	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003444	Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003445	Response to Intravenous Cyclophosphamide Treatment for Lupus Nephritis Associated with Polymorphisms in the FCGR2B-FCRLA Locus.	Missing both OR and beta
GCST003455	Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.	Missing both OR and beta
GCST003461	Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003465	Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks.	Missing both OR and beta
GCST003469	Genome-wide association study of response to cognitive-behavioural therapy in children with anxiety disorders.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003472	Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003474	A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.	Missing both OR and beta
GCST003475	A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.	Missing both OR and beta
GCST003476	A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.	Missing both OR and beta
GCST003477	A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.	Missing both OR and beta
GCST003478	A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.	Missing both OR and beta
GCST003479	A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.	Missing both OR and beta
GCST003480	A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.	Missing both OR and beta
GCST003484	Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease.	Missing both OR and beta
GCST003489	A genome-wide investigation of food addiction.	Missing both OR and beta
GCST003498	Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151).	Missing both OR and beta
GCST003518	Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study.	Missing both OR and beta
GCST003542	Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study.	Missing both OR and beta
GCST003588	Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.	Missing both OR and beta
GCST003591	A genome-wide association study in Caucasian women suggests the involvement of HLA genes in the severity of facial solar lentigines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003598	Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.	Missing both OR and beta
GCST003600	Genome-wide gene-environment interaction analysis of pesticide exposure and risk of Parkinson's disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003606	A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients.	Missing both OR and beta
GCST003616	THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003631	A meta-analysis of reflux genome-wide association studies in 6750 Northern Europeans from the general population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003637	A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.	Missing both OR and beta
GCST003642	Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.	Missing both OR and beta
GCST003643	Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.	Missing both OR and beta
GCST003644	Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003645	Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003646	Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.	Missing both OR and beta
GCST003647	Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003657	A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003660	Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.	Missing both OR and beta
GCST003667	Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003678	Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.	Missing both OR and beta
GCST003679	Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.	Missing both OR and beta
GCST003680	Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.	Missing both OR and beta
GCST003681	Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.	Missing both OR and beta
GCST003684	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003685	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003686	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003687	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003688	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003689	Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003773	Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003779	Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003790	Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity.	Missing both OR and beta
GCST003791	Metformin pharmacogenomics: a genome-wide association study to identify genetic and epigenetic biomarkers involved in metformin anticancer response using human lymphoblastoid cell lines.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003805	Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003807	Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST003814	Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.	Missing both OR and beta
GCST003815	Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans.	Missing both OR and beta
GCST003818	Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality.	Missing both OR and beta
GCST003830	A genome-wide analysis of the response to inhaled β2-agonists in chronic obstructive pulmonary disease.	Missing both OR and beta
GCST003841	Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.	Missing both OR and beta
GCST003844	52 Genetic Loci Influencing Myocardial Mass.	Missing both OR and beta
GCST003860	The Interplay Between Risky Sexual Behaviors and Alcohol Dependence: Genome-Wide Association and Neuroimaging Support for LHPP as a Risk Gene.	Missing both OR and beta
GCST003875	Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota.	Missing both OR and beta
GCST003879	Genetic Variants Associated with Circulating Parathyroid Hormone.	Missing both OR and beta
GCST003919	Bivariate genome-wide association analyses identified genetic pleiotropic effects for bone mineral density and alcohol drinking in Caucasians.	Missing both OR and beta
GCST003941	Novel HLA-DP region susceptibility loci associated with severe acute GvHD.	Missing both OR and beta
GCST003942	Novel HLA-DP region susceptibility loci associated with severe acute GvHD.	Missing both OR and beta
GCST003943	Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin.	Missing both OR and beta
GCST003944	Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin.	Missing both OR and beta
GCST003980	Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits.	Missing both OR and beta
GCST003982	Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits.	Missing both OR and beta
GCST003998	Detection and interpretation of shared genetic influences on 42 human traits.	Missing both OR and beta
GCST004000	Genome-wide quantitative trait loci mapping of the human cerebrospinal fluid proteome.	Missing both OR and beta
GCST004040	Genome-wide association study of paliperidone efficacy.	Missing both OR and beta
GCST004041	Genome-wide association study of paliperidone efficacy.	Missing both OR and beta
GCST004042	Genome-wide association study of paliperidone efficacy.	Missing both OR and beta
GCST004043	Genome-wide association study of paliperidone efficacy.	Missing both OR and beta
GCST004044	Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases.	Missing both OR and beta
GCST004045	Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases.	Missing both OR and beta
GCST004046	Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases.	Missing both OR and beta
GCST004088	Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only.	Missing both OR and beta
GCST004099	Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci.	Missing both OR and beta
GCST004107	Genome-wide interaction study of dust mite allergen on lung function in children with asthma.	Missing both OR and beta
GCST004108	Genome-wide interaction study of dust mite allergen on lung function in children with asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004125	PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004158	Genetic contributions to self-reported tiredness.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004164	Heritability and GWAS Studies for Monocyte-Lymphocyte Ratio.	Missing both OR and beta
GCST004185	Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.	Missing both OR and beta
GCST004206	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Missing both OR and beta
GCST004207	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Missing both OR and beta
GCST004208	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Missing both OR and beta
GCST004210	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Missing both OR and beta
GCST004211	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Missing both OR and beta
GCST004213	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Missing both OR and beta
GCST004214	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Missing both OR and beta
GCST004216	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Missing both OR and beta
GCST004230	Genome-wide association study of sepsis in extremely premature infants.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004254	Genetic Determinants of 1,3-Butadiene Metabolism and Detoxification in Three Populations of Smokers with Different Risks of Lung Cancer.	Missing both OR and beta
GCST004267	NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality.	Missing both OR and beta
GCST004268	Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004269	Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine.	Missing both OR and beta
GCST004271	Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004278	Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.	Missing both OR and beta
GCST004279	Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.	Missing both OR and beta
GCST004286	Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.	Missing both OR and beta
GCST004329	Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.	Missing both OR and beta
GCST004330	Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.	Missing both OR and beta
GCST004334	Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.	Missing both OR and beta
GCST004335	Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.	Missing both OR and beta
GCST004346	Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants.	Missing both OR and beta
GCST004365	Connecting genetic risk to disease end points through the human blood plasma proteome.	Missing both OR and beta
GCST004366	Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania.	Missing both OR and beta
GCST004371	Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment.	Missing both OR and beta
GCST004376	Heritability and genome-wide associations studies of cerebral blood flow in the general population.	Missing both OR and beta
GCST004377	ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains.	Missing both OR and beta
GCST004379	Genome-wide association study of erythrocyte density in sickle cell disease patients.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004385	Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.	Missing both OR and beta
GCST004386	Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.	Missing both OR and beta
GCST004387	Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.	Missing both OR and beta
GCST004388	Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.	Missing both OR and beta
GCST004423	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	Missing both OR and beta
GCST004424	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	Missing both OR and beta
GCST004425	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	Missing both OR and beta
GCST004428	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	Missing both OR and beta
GCST004429	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	Missing both OR and beta
GCST004440	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	Missing both OR and beta
GCST004441	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	Missing both OR and beta
GCST004448	Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004484	Genome- and CD4+ T-cell methylome-wide association study of circulating trimethylamine-N-oxide in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN).	Missing both OR and beta
GCST004490	Genome-wide association and interaction studies of CSF T-tau/Aβ42 ratio in ADNI cohort.	Missing both OR and beta
GCST004491	Genome-wide association and interaction studies of CSF T-tau/Aβ42 ratio in ADNI cohort.	Missing both OR and beta
GCST004492	Genome-wide association and interaction studies of CSF T-tau/Aβ42 ratio in ADNI cohort.	Missing both OR and beta
GCST004496	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Missing both OR and beta
GCST004497	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Missing both OR and beta
GCST004501	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Missing both OR and beta
GCST004502	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004506	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004507	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Missing both OR and beta
GCST004537	Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.	Missing both OR and beta
GCST004550	Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.	Missing both OR and beta
GCST004553	Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.	Missing both OR and beta
GCST004558	Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	Missing both OR and beta
GCST004563	Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	Missing both OR and beta
GCST004567	Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	Missing both OR and beta
GCST004570	Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?	Missing both OR and beta
GCST004571	Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?	Missing both OR and beta
GCST004575	A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants.	Missing both OR and beta
GCST004602	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.	Missing both OR and beta
GCST004616	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.	Missing both OR and beta
GCST004630	The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.	Missing both OR and beta
GCST004639	Genome-Wide Association Study of Dietary Pattern Scores.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004640	Genome-Wide Association Study of Dietary Pattern Scores.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004644	Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004679	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004680	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004681	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004682	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004683	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004684	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004685	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004686	Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004691	Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.	Missing both OR and beta
GCST004708	A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain.	Missing both OR and beta
GCST004709	A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004715	Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004735	Genetic factors affecting EBV copy number in lymphoblastoid cell lines derived from the 1000 Genome Project samples.	Missing both OR and beta
GCST004738	Genome-wide association studies of placebo and duloxetine response in major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004751	Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response.	Missing both OR and beta
GCST004758	Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).	Missing both OR and beta
GCST004759	Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.	Missing both OR and beta
GCST004768	Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004769	Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004771	Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.	Missing both OR and beta
GCST004776	Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.	Missing both OR and beta
GCST004797	Genome-wide association analysis identifies common variants influencing infant brain volumes.	Missing both OR and beta
GCST004814	Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study.	Missing both OR and beta
GCST004823	A genome-wide association study of cognitive function in Chinese adult twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004826	Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.	Missing both OR and beta
GCST004827	Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort.	Missing both OR and beta
GCST004828	Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004829	Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort.	Missing both OR and beta
GCST004830	Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004833	Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study.	Missing both OR and beta
GCST004842	Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth.	Missing both OR and beta
GCST004862	GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.	Missing both OR and beta
GCST004863	GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.	Missing both OR and beta
GCST004864	GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.	Missing both OR and beta
GCST004865	GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.	Missing both OR and beta
GCST004868	Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004894	Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease.	Missing both OR and beta
GCST004895	Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci.	Missing both OR and beta
GCST004899	Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.	Missing both OR and beta
GCST004920	Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.	Missing both OR and beta
GCST004922	Discovery of susceptibility loci associated with tuberculosis in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004924	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004925	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004926	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004927	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004928	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004929	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004930	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004931	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004932	Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation.	Missing both OR and beta
GCST004938	Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004942	Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004943	Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004955	Ancestry-specific and sex-specific risk alleles identified in a genome-wide gene-by-alcohol dependence interaction study of risky sexual behaviors.	Missing both OR and beta
GCST004956	Ancestry-specific and sex-specific risk alleles identified in a genome-wide gene-by-alcohol dependence interaction study of risky sexual behaviors.	Missing both OR and beta
GCST004958	Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004970	Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004983	Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.	Missing both OR and beta
GCST004988	Association analysis identifies 65 new breast cancer risk loci.	Missing both OR and beta
GCST004997	The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST004999	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005000	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005001	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005002	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005003	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005004	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005005	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005006	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005008	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005009	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005010	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005013	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005014	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005015	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	Missing both OR and beta
GCST005016	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005017	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005018	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005020	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005021	Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005022	Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression.	Missing both OR and beta
GCST005023	Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.	Missing both OR and beta
GCST005024	Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.	Missing both OR and beta
GCST005025	Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005026	Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.	Missing both OR and beta
GCST005027	Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005028	Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.	Missing both OR and beta
GCST005081	Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study.	Missing both OR and beta
GCST005082	Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study.	Missing both OR and beta
GCST005115	No genetic association detected with mepolizumab efficacy in severe asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005168	EPHA6 rs4857055 C > T polymorphism associates with hypertension through triglyceride and LDL particle size in the Korean population.	Missing both OR and beta
GCST005169	EPHA6 rs4857055 C > T polymorphism associates with hypertension through triglyceride and LDL particle size in the Korean population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005174	Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005176	Polymorphisms in the Wilms Tumor Gene Are Associated With Interindividual Variations in Rubella Virus-Specific Cellular Immunity After Measles-Mumps-Rubella II Vaccination.	Missing both OR and beta
GCST005189	An Unexpectedly Complex Architecture for Skin Pigmentation in Africans.	Missing both OR and beta
GCST005208	Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population.	Missing both OR and beta
GCST005214	Bone mineral density in children with acute lymphoblastic leukemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005232	Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism.	Missing both OR and beta
GCST005242	Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005246	Hierarchical investigation of genetic influences on response inhibition in healthy young adults.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005268	A family-based genome-wide association study of chronic rhinosinusitis with nasal polyps implicates several genes in the disease pathogenesis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005286	Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005287	GWAS of epigenetic aging rates in blood reveals a critical role for TERT.	Missing both OR and beta
GCST005332	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005333	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005334	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	Missing both OR and beta
GCST005335	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	Missing both OR and beta
GCST005336	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	Missing both OR and beta
GCST005342	Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005343	Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005351	Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005356	Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania.	Missing both OR and beta
GCST005357	Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005366	Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels.	Missing both OR and beta
GCST005368	Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005406	Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma.	Missing both OR and beta
GCST005409	Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma.	Missing both OR and beta
GCST005436	Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes.	Missing both OR and beta
GCST005437	Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes.	Missing both OR and beta
GCST005439	Genomewide association study of alcohol dependence and related traits in a Thai population.	Missing both OR and beta
GCST005440	Genomewide association study of alcohol dependence and related traits in a Thai population.	Missing both OR and beta
GCST005444	Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.	Missing both OR and beta
GCST005447	Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.	Missing both OR and beta
GCST005483	Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.	Missing both OR and beta
GCST005491	Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.	Missing both OR and beta
GCST005499	Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.	Missing both OR and beta
GCST005503	Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.	Missing both OR and beta
GCST005513	Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.	Missing both OR and beta
GCST005514	Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005515	Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease.	Missing both OR and beta
GCST005516	Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease.	Missing both OR and beta
GCST005517	Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease.	Missing both OR and beta
GCST005537	Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.	Missing both OR and beta
GCST005547	The PHF21B gene is associated with major depression and modulates the stress response.	Missing both OR and beta
GCST005551	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	Missing both OR and beta
GCST005552	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	Missing both OR and beta
GCST005553	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005554	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	Missing both OR and beta
GCST005555	Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations.	Missing both OR and beta
GCST005557	Heritability and Genome-Wide Association Analyses of Serum Uric Acid in Middle and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005559	Genome-wide association study (GWAS) of human host factors influencing viral severity of herpes simplex virus type 2 (HSV-2).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005568	High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis.	Missing both OR and beta
GCST005581	Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.	Missing both OR and beta
GCST005586	Multiplex genomewide association analysis of breast milk fatty acid composition extends the phenotypic association and potential selection of FADS1 variants to arachidonic acid, a critical infant micronutrient.	Missing both OR and beta
GCST005587	Multiplex genomewide association analysis of breast milk fatty acid composition extends the phenotypic association and potential selection of FADS1 variants to arachidonic acid, a critical infant micronutrient.	Missing both OR and beta
GCST005655	The genetics of seborrheic dermatitis: a candidate gene approach and pilot genome-wide association study.	Missing both OR and beta
GCST005656	Genome-Wide Association Study on Immunoglobulin G Glycosylation Patterns.	Missing both OR and beta
GCST005668	A common variant in ARHGEF10 alters delta-6 desaturase activity and influence susceptibility to hypertriglyceridemia.	Missing both OR and beta
GCST005686	Host genetic susceptibility to Clostridium difficile infections in patients undergoing autologous stem cell transplantation: a genome-wide association study.	Missing both OR and beta
GCST005688	Genetic Survey of Adult-Onset Idiopathic Intracranial Hypertension.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005713	Genome-wide association study identifies two loci influencing plasma neurofilament light levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005714	Genome-wide association study identified ATP6V1H locus influencing cerebrospinal fluid BACE activity.	Missing both OR and beta
GCST005721	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005722	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005723	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005724	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	Missing both OR and beta
GCST005725	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005726	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005727	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005728	Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005751	Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa.	Missing both OR and beta
GCST005753	Genetic Variants in CPA6 and PRPF31 are Associated with Variation in Response to Metformin in Individuals with Type 2 Diabetes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005755	Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition.	Missing both OR and beta
GCST005769	Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005777	Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005781	Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.	Missing both OR and beta
GCST005788	Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system.	Missing both OR and beta
GCST005789	Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system.	Missing both OR and beta
GCST005790	Assessment of rosacea symptom severity by genome-wide association study and expression analysis highlights immuno-inflammatory and skin pigmentation genes.	Missing both OR and beta
GCST005797	Genetic contribution to 'theory of mind' in adolescence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005800	Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome eight.	Missing both OR and beta
GCST005806	Genomic atlas of the human plasma proteome.	Missing both OR and beta
GCST005826	Genotypic variability based association identifies novel non-additive loci DHCR7 and IRF4 in sero-negative rheumatoid arthritis.	Missing both OR and beta
GCST005833	Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005834	Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005835	Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.	Missing both OR and beta
GCST005836	Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.	Missing both OR and beta
GCST005844	Genetic variations and risk of placental abruption: A genome-wide association study and meta-analysis of genome-wide association studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005859	Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005860	Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005863	Elucidating the genetic architecture of reproductive ageing in the Japanese population.	Missing both OR and beta
GCST005878	New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population.	Missing both OR and beta
GCST005925	Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study.	Missing both OR and beta
GCST005926	Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study.	Missing both OR and beta
GCST005935	Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy.	Missing both OR and beta
GCST005938	Mapping genetic variants for cranial vault shape in humans.	Missing both OR and beta
GCST005939	Mapping genetic variants for cranial vault shape in humans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005940	Mapping genetic variants for cranial vault shape in humans.	Missing both OR and beta
GCST005950	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	Missing both OR and beta
GCST005954	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST005959	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	Missing both OR and beta
GCST005962	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	Missing both OR and beta
GCST005966	Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.	Missing both OR and beta
GCST005967	Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.	Missing both OR and beta
GCST005968	Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006020	Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.	Missing both OR and beta
GCST006021	Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.	Missing both OR and beta
GCST006022	Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.	Missing both OR and beta
GCST006038	Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy.	Missing both OR and beta
GCST006039	Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006054	Genetic signatures of high-altitude adaptation in Tibetans.	Missing both OR and beta
GCST006069	Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006072	Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006073	Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202.	Missing both OR and beta
GCST006074	Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202.	Missing both OR and beta
GCST006099	Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE.	Missing both OR and beta
GCST006105	Identification of five novel genetic loci related to facial morphology by genome-wide association studies.	Missing both OR and beta
GCST006108	Identification of five novel genetic loci related to facial morphology by genome-wide association studies.	Missing both OR and beta
GCST006111	Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study.	Missing both OR and beta
GCST006112	Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study.	Missing both OR and beta
GCST006113	Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study.	Missing both OR and beta
GCST006114	Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study.	Missing both OR and beta
GCST006132	Nuclear receptor and VEGF pathways for gene-blood lead interactions, on bone mineral density, in Korean smokers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006133	Nuclear receptor and VEGF pathways for gene-blood lead interactions, on bone mineral density, in Korean smokers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006137	Identification of three novel loci of ALDH2 Gene for Serum Folate levels in a Male Chinese Population by Genome-Wide Association Study.	Missing both OR and beta
GCST006138	Human brain arousal in the resting state: a genome-wide association study.	Missing both OR and beta
GCST006166	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	Missing both OR and beta
GCST006167	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	Missing both OR and beta
GCST006168	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	Missing both OR and beta
GCST006169	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	Missing both OR and beta
GCST006170	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	Missing both OR and beta
GCST006171	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	Missing both OR and beta
GCST006172	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	Missing both OR and beta
GCST006187	A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.	Missing both OR and beta
GCST006188	A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.	Missing both OR and beta
GCST006190	A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.	Missing both OR and beta
GCST006192	A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.	Missing both OR and beta
GCST006193	A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.	Missing both OR and beta
GCST006195	A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.	Missing both OR and beta
GCST006204	NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.	Missing both OR and beta
GCST006205	NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.	Missing both OR and beta
GCST006207	NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study.	Missing both OR and beta
GCST006220	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006221	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	Missing both OR and beta
GCST006222	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006223	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006224	Genetic associations with childhood brain growth, defined in two longitudinal cohorts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006226	Genome-Wide Association Study of Erosive Tooth Wear in a Finnish Cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006228	Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.	Missing both OR and beta
GCST006231	Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.	Missing both OR and beta
GCST006259	The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.	Missing both OR and beta
GCST006286	Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in Duchenne muscular dystrophy.	Missing both OR and beta
GCST006287	The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.	Missing both OR and beta
GCST006290	Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.	Missing both OR and beta
GCST006301	Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006303	Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway.	Missing both OR and beta
GCST006306	Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels.	Missing both OR and beta
GCST006404	Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits.	Missing both OR and beta
GCST006415	Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology.	Missing both OR and beta
GCST006427	GWAS and systems biology analysis of depressive symptoms among smokers from the COPDGene cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006434	Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.	Missing both OR and beta
GCST006440	Identification of novel loci associated with infant cognitive ability.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006442	Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.	Missing both OR and beta
GCST006443	Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006444	Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis.	Missing both OR and beta
GCST006445	Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006446	Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis.	Missing both OR and beta
GCST006447	Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006468	Genome-wide scans reveal variants at EDAR predominantly affecting hair straightness in Han Chinese and Uyghur populations.	Missing both OR and beta
GCST006469	Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006470	Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006472	Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels.	Missing both OR and beta
GCST006479	Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease.	Missing both OR and beta
GCST006494	Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006495	Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006534	Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006542	Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006547	Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006576	Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006582	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006585	Co-regulatory networks of human serum proteins link genetics to disease.	Missing both OR and beta
GCST006606	Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis.	Missing both OR and beta
GCST006621	Cross-genetic determination of maternal and neonatal immune mediators during pregnancy.	Missing both OR and beta
GCST006625	Cross-genetic determination of maternal and neonatal immune mediators during pregnancy.	Missing both OR and beta
GCST006631	Genome-wide association study identifies glutamate ionotropic receptor GRIA4 as a risk gene for comorbid nicotine dependence and major depression.	Missing both OR and beta
GCST006633	Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006638	Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.	Missing both OR and beta
GCST006659	High Genetic Risk Scores of ASIC2, MACROD2, CHRM3, and C2orf83 Genetic Variants Associated with Polycystic Ovary Syndrome Impair Insulin Sensitivity and Interact with Energy Intake in Korean Women.	Missing both OR and beta
GCST006663	Genome-wide association study for multiple phenotype analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006664	Genome-wide association study for multiple phenotype analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006665	Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits.	Missing both OR and beta
GCST006666	Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits.	Missing both OR and beta
GCST006667	Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits.	Missing both OR and beta
GCST006668	Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits.	Missing both OR and beta
GCST006669	Genome-wide association study for multiple phenotype analysis.	Missing both OR and beta
GCST006680	Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006682	Family-based genome-wide association of inflammation biomarkers and fenofibrate treatment response in the GOLDN study.	Missing both OR and beta
GCST006703	Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste.	Missing both OR and beta
GCST006706	Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans.	Missing both OR and beta
GCST006817	Association of Novel ALX4 Gene Polymorphisms with Antidepressant Treatment Response: Findings from the CO-MED Trial.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006862	Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.	Missing both OR and beta
GCST006864	A univariate perspective of multivariate genome-wide association analysis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006865	Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.	Missing both OR and beta
GCST006907	Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.	Missing both OR and beta
GCST006908	Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.	Missing both OR and beta
GCST006909	Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006910	Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.	Missing both OR and beta
GCST006930	Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006931	Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.	Missing both OR and beta
GCST006976	Genome-wide association analyses identify 139 loci associated with macular thickness in the UK Biobank cohort.	Missing both OR and beta
GCST006987	A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia.	Missing both OR and beta
GCST006990	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006991	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006992	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006993	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST006994	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006995	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST006996	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST006998	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007000	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007001	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007002	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007003	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007004	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007005	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007006	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007007	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007008	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007009	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007012	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	Missing both OR and beta
GCST007013	Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007016	Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007017	Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.	Missing both OR and beta
GCST007037	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007038	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007039	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007045	PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.	Missing both OR and beta
GCST007052	A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007063	Genomics of body fat percentage may contribute to sex bias in anorexia nervosa.	Missing both OR and beta
GCST007065	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007066	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007067	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007068	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007069	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007070	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007071	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007072	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007073	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007074	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007075	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007076	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007077	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007078	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007079	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007080	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007081	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007082	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007083	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007084	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007085	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007086	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007087	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007094	Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.	Missing both OR and beta
GCST007095	Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.	Missing both OR and beta
GCST007096	Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.	Missing both OR and beta
GCST007097	Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.	Missing both OR and beta
GCST007098	Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.	Missing both OR and beta
GCST007099	Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.	Missing both OR and beta
GCST007103	Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.	Missing both OR and beta
GCST007104	Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.	Missing both OR and beta
GCST007120	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	Missing both OR and beta
GCST007121	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	Missing both OR and beta
GCST007122	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	Missing both OR and beta
GCST007123	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007124	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	Missing both OR and beta
GCST007125	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	Missing both OR and beta
GCST007126	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007127	Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007128	Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease.	Missing both OR and beta
GCST007129	Genome-wide association study for variants that modulate relationships between cerebrospinal fluid amyloid-beta 42, tau, and p-tau levels.	Missing both OR and beta
GCST007130	Genome-wide association study for variants that modulate relationships between cerebrospinal fluid amyloid-beta 42, tau, and p-tau levels.	Missing both OR and beta
GCST007146	Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis.	Missing both OR and beta
GCST007148	NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia.	Missing both OR and beta
GCST007149	NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia.	Missing both OR and beta
GCST007150	NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia.	Missing both OR and beta
GCST007202	Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007203	Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007204	Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007206	Genome-wide association study identifies RBFOX1 locus influencing brain glucose metabolism.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007207	Sex differences in the genetic architecture of obsessive-compulsive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007208	Sex differences in the genetic architecture of obsessive-compulsive disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007225	Clinical and Genetic Determinants of Varicose Veins.	Missing both OR and beta
GCST007227	Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits.	Missing both OR and beta
GCST007232	A Sex-Stratified Genome-Wide Association Study of Tuberculosis Using a Multi-Ethnic Genotyping Array.	Missing both OR and beta
GCST007252	Genetic influence on scar height and pliability after burn injury in individuals of European ancestry: A prospective cohort study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007254	Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression.	Missing both OR and beta
GCST007255	Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression.	Missing both OR and beta
GCST007256	Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression.	Missing both OR and beta
GCST007257	Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression.	Missing both OR and beta
GCST007260	The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma.	Missing both OR and beta
GCST007267	Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.	Missing both OR and beta
GCST007268	Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.	Missing both OR and beta
GCST007269	Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.	Missing both OR and beta
GCST007270	Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.	Missing both OR and beta
GCST007271	Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.	Missing both OR and beta
GCST007272	Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.	Missing both OR and beta
GCST007279	A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007282	Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.	Missing both OR and beta
GCST007284	Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.	Missing both OR and beta
GCST007286	Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.	Missing both OR and beta
GCST007321	Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.	Missing both OR and beta
GCST007344	Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.	Missing both OR and beta
GCST007357	Association of a Schizophrenia-Risk Nonsynonymous Variant With Putamen Volume in Adolescents: A Voxelwise and Genome-Wide Association Study.	Missing both OR and beta
GCST007383	Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population.	Missing both OR and beta
GCST007426	Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007447	Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.	Missing both OR and beta
GCST007448	Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry.	Missing both OR and beta
GCST007449	Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007450	Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007451	A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.	Missing both OR and beta
GCST007452	A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.	Missing both OR and beta
GCST007453	A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.	Missing both OR and beta
GCST007454	A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.	Missing both OR and beta
GCST007455	A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.	Missing both OR and beta
GCST007456	A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.	Missing both OR and beta
GCST007457	A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia.	Missing both OR and beta
GCST007475	Genome-wide association study of germline variants and breast cancer-specific mortality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007476	Genome-wide association study of germline variants and breast cancer-specific mortality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007477	Genome-wide association study of germline variants and breast cancer-specific mortality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007479	Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.	Missing both OR and beta
GCST007486	Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.	Missing both OR and beta
GCST007488	Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.	Missing both OR and beta
GCST007489	Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.	Missing both OR and beta
GCST007490	Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.	Missing both OR and beta
GCST007497	The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007498	The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007499	The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007504	Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.	Missing both OR and beta
GCST007505	Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.	Missing both OR and beta
GCST007538	Genetic risk score combining six genetic variants associated with the cellular NRF2 expression levels correlates with Type 2 diabetes in the human population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007544	Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease.	Missing both OR and beta
GCST007545	Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease.	Missing both OR and beta
GCST007546	Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease.	Missing both OR and beta
GCST007547	Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007558	Genomics and response to long-term oxygen therapy in chronic obstructive pulmonary disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007561	Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates.	Missing both OR and beta
GCST007576	Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms.	Missing both OR and beta
GCST007592	The molecular genetics of hand preference revisited.	Missing both OR and beta
GCST007594	The molecular genetics of hand preference revisited.	Missing both OR and beta
GCST007611	Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis.	Missing both OR and beta
GCST007612	Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis.	Missing both OR and beta
GCST007635	Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity.	Missing both OR and beta
GCST007636	Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity.	Missing both OR and beta
GCST007644	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007645	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007646	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007647	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007648	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007649	The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007650	Genomewide association study for C-reactive protein in Indians replicates known associations of common variants.	Missing both OR and beta
GCST007656	Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis.	Missing both OR and beta
GCST007658	Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007660	Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007661	Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels.	Missing both OR and beta
GCST007664	Anastrozole Aromatase Inhibitor Plasma Drug Concentration Genome-Wide Association Study: Functional Epistatic Interaction between SLC38A7 and ALPPL2.	Missing both OR and beta
GCST007668	A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes.	Missing both OR and beta
GCST007684	Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST007685	Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST007686	Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST007690	The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007693	Genetic effects on information processing speed are moderated by age--converging results from three samples.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007694	Genetic effects on information processing speed are moderated by age--converging results from three samples.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007703	Interethnic analyses of blood pressure loci in populations of East Asian and European descent.	Missing both OR and beta
GCST007705	Interethnic analyses of blood pressure loci in populations of East Asian and European descent.	Missing both OR and beta
GCST007706	Interethnic analyses of blood pressure loci in populations of East Asian and European descent.	Missing both OR and beta
GCST007719	Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion.	Missing both OR and beta
GCST007731	Genome-Wide Association Study Identifies a Genetic Prediction Model for Postoperative Survival in Patients with Hepatocellular Carcinoma.	Missing both OR and beta
GCST007739	A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry.	Missing both OR and beta
GCST007740	A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry.	Missing both OR and beta
GCST007741	A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry.	Missing both OR and beta
GCST007742	A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry.	Missing both OR and beta
GCST007743	A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry.	Missing both OR and beta
GCST007762	Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women.	Missing both OR and beta
GCST007766	Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007819	Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007825	Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis.	Missing both OR and beta
GCST007826	Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis.	Missing both OR and beta
GCST007827	Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis.	Missing both OR and beta
GCST007841	Leveraging Polygenic Functional Enrichment to Improve GWAS Power.	Missing both OR and beta
GCST007843	Studying the effects of haplotype partitioning methods on the RA-associated genomic results from the North American Rheumatoid Arthritis Consortium (NARAC) dataset.	Missing both OR and beta
GCST007851	Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007859	Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.	Missing both OR and beta
GCST007863	Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.	Missing both OR and beta
GCST007864	Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007916	Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.	Missing both OR and beta
GCST007920	Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.	Missing both OR and beta
GCST007981	Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST007989	Genome-wide mapping of global-to-local genetic effects on human facial shape.	Missing both OR and beta
GCST007994	Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies.	Missing both OR and beta
GCST008016	Exome-Wide Association Study Identified New Risk Loci for Hirschsprung's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008017	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	Missing both OR and beta
GCST008018	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008019	Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes.	Missing both OR and beta
GCST008030	Genetic analyses of diverse populations improves discovery for complex traits.	Missing both OR and beta
GCST008035	Genetic analyses of diverse populations improves discovery for complex traits.	Missing both OR and beta
GCST008038	Genetic analyses of diverse populations improves discovery for complex traits.	Missing both OR and beta
GCST008044	Genetic analyses of diverse populations improves discovery for complex traits.	Missing both OR and beta
GCST008054	Genetic analyses of diverse populations improves discovery for complex traits.	Missing both OR and beta
GCST008074	Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.	Missing both OR and beta
GCST008075	Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.	Missing both OR and beta
GCST008077	Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.	Missing both OR and beta
GCST008078	Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.	Missing both OR and beta
GCST008079	Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.	Missing both OR and beta
GCST008083	Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.	Missing both OR and beta
GCST008084	Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.	Missing both OR and beta
GCST008086	Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.	Missing both OR and beta
GCST008099	Omega-3 Fatty Acids and Genome-wide Interaction Analyses Reveal DPP10-Pulmonary Function Association.	Missing both OR and beta
GCST008108	Defining the genetic control of human blood plasma N-glycome using genome-wide association study.	Missing both OR and beta
GCST008141	Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.	Missing both OR and beta
GCST008143	Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008151	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008152	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008153	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008154	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008155	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008156	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008157	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008158	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008159	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008160	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008161	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008162	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008163	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Missing both OR and beta
GCST008171	Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation.	Missing both OR and beta
GCST008173	Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008174	Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium.	Missing both OR and beta
GCST008175	Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008198	Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns.	Missing both OR and beta
GCST008210	Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns.	Missing both OR and beta
GCST008224	Sex specific associations in genome wide association analysis of renal cell carcinoma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008230	Integrative approach identifies corticosteroid response variant in diverse populations with asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008236	Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008237	Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008238	Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008239	Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008258	Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations.	Missing both OR and beta
GCST008260	Group IIA Secretory Phospholipase A2 and Incident Cardiovascular Disease.	Missing both OR and beta
GCST008273	Pathway analysis of a genome-wide gene by air pollution interaction study in asthmatic children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008283	Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria.	Missing both OR and beta
GCST008284	Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria.	Missing both OR and beta
GCST008285	Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria.	Missing both OR and beta
GCST008287	Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria.	Missing both OR and beta
GCST008288	Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria.	Missing both OR and beta
GCST008290	Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria.	Missing both OR and beta
GCST008292	Genetic effects on efficacy to fluticasone propionate/salmeterol treatment in COPD.	Missing both OR and beta
GCST008294	Genetic effects on efficacy to fluticasone propionate/salmeterol treatment in COPD.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008316	Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.	Missing both OR and beta
GCST008321	Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.	Missing both OR and beta
GCST008329	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008330	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008331	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008332	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008333	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008334	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008335	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008336	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008337	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008338	Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.	Missing both OR and beta
GCST008339	Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.	Missing both OR and beta
GCST008370	Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.	Missing both OR and beta
GCST008371	Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.	Missing both OR and beta
GCST008372	Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.	Missing both OR and beta
GCST008373	Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.	Missing both OR and beta
GCST008422	GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations.	Missing both OR and beta
GCST008457	Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes.	Missing both OR and beta
GCST008458	Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes.	Missing both OR and beta
GCST008469	GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.	Missing both OR and beta
GCST008471	GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.	Missing both OR and beta
GCST008478	Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936.	Missing both OR and beta
GCST008491	Spatial correlations exploitation based on nonlocal voxel-wise GWAS for biomarker detection of AD.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008516	Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations.	Missing both OR and beta
GCST008532	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008536	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008539	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008540	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008541	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008543	Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008550	Factors associated with sharing e-mail information and mental health survey participation in large population cohorts.	Missing both OR and beta
GCST008563	Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.	Missing both OR and beta
GCST008565	Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.	Missing both OR and beta
GCST008566	Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008567	Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.	Missing both OR and beta
GCST008572	Identification of sequence variants influencing immunoglobulin levels.	Missing both OR and beta
GCST008576	Identification of sequence variants influencing immunoglobulin levels.	Missing both OR and beta
GCST008644	Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis.	Missing both OR and beta
GCST008666	Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008674	Pleiotropy informed adaptive association test of multiple traits using GWAS summary data.	Missing both OR and beta
GCST008675	Genome-wide Association Study of Maximum Habitual Alcohol Intake in >140,000 U.S. European and African American Veterans Yields Novel Risk Loci.	Missing both OR and beta
GCST008676	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	Missing both OR and beta
GCST008691	Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.	Missing both OR and beta
GCST008734	Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors.	Missing both OR and beta
GCST008737	Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.	Missing both OR and beta
GCST008745	Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.	Missing both OR and beta
GCST008746	Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.	Missing both OR and beta
GCST008759	New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances.	Missing both OR and beta
GCST008793	Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008804	Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.	Missing both OR and beta
GCST008809	Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.	Missing both OR and beta
GCST008818	Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics.	Missing both OR and beta
GCST008821	Sex differences in the genetic predictors of Alzheimer's pathology.	Missing both OR and beta
GCST008822	Sex differences in the genetic predictors of Alzheimer's pathology.	Missing both OR and beta
GCST008823	rs11670527 Upstream of ZNF264 Associated with Body Mass Index in the Coriell Personalized Medicine Collaborative.	Missing both OR and beta
GCST008824	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008825	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	Missing both OR and beta
GCST008826	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008827	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008828	Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008829	Sex differences in the genetic predictors of Alzheimer's pathology.	Missing both OR and beta
GCST008830	Sex differences in the genetic predictors of Alzheimer's pathology.	Missing both OR and beta
GCST008862	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	Missing both OR and beta
GCST008865	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008866	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	Missing both OR and beta
GCST008867	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008869	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	Missing both OR and beta
GCST008879	Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease.	Missing both OR and beta
GCST008887	Social and non-social autism symptoms and trait domains are genetically dissociable.	Missing both OR and beta
GCST008889	Social and non-social autism symptoms and trait domains are genetically dissociable.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008894	Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008900	A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008905	Transcriptome association studies of neuropsychiatric traits in African Americans implicate PRMT7 in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008906	Transcriptome association studies of neuropsychiatric traits in African Americans implicate PRMT7 in schizophrenia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008919	Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis.	Missing both OR and beta
GCST008920	Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis.	Missing both OR and beta
GCST008921	Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis.	Missing both OR and beta
GCST008925	Genetic architecture of human plasma lipidome and its link to cardiovascular disease.	Missing both OR and beta
GCST008927	Genetic architecture of human plasma lipidome and its link to cardiovascular disease.	Missing both OR and beta
GCST008957	Very low-depth whole-genome sequencing in complex trait association studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008959	Very low-depth whole-genome sequencing in complex trait association studies.	Missing both OR and beta
GCST008962	Very low-depth whole-genome sequencing in complex trait association studies.	Missing both OR and beta
GCST008963	Very low-depth whole-genome sequencing in complex trait association studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST008970	Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.	Missing both OR and beta
GCST008972	Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.	Missing both OR and beta
GCST008992	Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases.	Missing both OR and beta
GCST008993	Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009085	Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis.	Missing both OR and beta
GCST009105	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009106	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009107	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009108	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009109	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009110	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009114	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009115	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009116	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009119	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009120	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009121	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009122	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009123	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009124	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009126	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009128	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009129	Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank.	Missing both OR and beta
GCST009134	Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009153	Genetic predictors of chemotherapy-related amenorrhea in women with breast cancer.	Missing both OR and beta
GCST009155	Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis.	Missing both OR and beta
GCST009158	Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.	Missing both OR and beta
GCST009159	Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.	Missing both OR and beta
GCST009160	Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.	Missing both OR and beta
GCST009163	Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.	Missing both OR and beta
GCST009165	Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.	Missing both OR and beta
GCST009167	Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.	Missing both OR and beta
GCST009171	Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.	Missing both OR and beta
GCST009172	Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009173	Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009174	Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009175	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009176	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009177	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009178	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009179	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009180	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009181	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009182	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009183	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009184	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009185	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009186	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009187	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009188	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009189	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009190	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009191	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009192	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009193	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009194	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009195	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009196	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009197	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009198	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009199	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009200	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009201	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009202	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009203	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009204	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009205	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009206	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009207	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	Missing both OR and beta
GCST009208	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009209	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009210	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009211	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009212	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	Missing both OR and beta
GCST009213	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009214	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009215	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009216	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009217	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009218	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	Missing both OR and beta
GCST009219	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009220	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009221	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009222	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009243	Multivariate Genome-Wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy.	Missing both OR and beta
GCST009244	Multivariate Genome-Wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy.	Missing both OR and beta
GCST009249	Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status.	Missing both OR and beta
GCST009253	Smoking Modifies the Genetic Risk for Early-Onset Periodontitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009254	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009255	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009256	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009257	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009258	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009259	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009260	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009261	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009262	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009263	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009264	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009265	NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009277	Pharmacogenomics and Placebo Response in a Randomized Clinical Trial in Asthma.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009302	Genome-wide association study on antipsychotic-induced weight gain in Europeans and African-Americans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009304	Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.	Missing both OR and beta
GCST009310	Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.	Missing both OR and beta
GCST009311	Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009319	Genetic factors associated with elevation of uric acid after treatment with thiazide-like diuretic in patients with essential hypertension.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009325	Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.	Missing both OR and beta
GCST009326	Multivariate genome-wide analysis of stress-related quantitative phenotypes.	Missing both OR and beta
GCST009365	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	Missing both OR and beta
GCST009366	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	Missing both OR and beta
GCST009376	Genome-wide Network-assisted Association and Enrichment Study of Amyloid Imaging Phenotype in Alzheimer's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009377	Genetic variants affecting bone mineral density and bone mineral content at multiple skeletal sites in Hispanic children.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009378	Genetic variants affecting bone mineral density and bone mineral content at multiple skeletal sites in Hispanic children.	Missing both OR and beta
GCST009382	A Trans-ancestral Meta-Analysis of Genome-Wide Association Studies Reveals Loci Associated with Childhood Obesity.	Missing both OR and beta
GCST009384	Retrospective Association Analysis of Longitudinal Binary Traits Identifies Important Loci and Pathways in Cocaine Use.	Missing both OR and beta
GCST009391	A genome-wide association study of the human metabolome in a community-based cohort.	Missing both OR and beta
GCST009415	Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.	Missing both OR and beta
GCST009416	Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.	Missing both OR and beta
GCST009417	Genome-Wide Analyses Reveal Gene Influence on HIV Disease Progression and HIV-1C Acquisition in Southern Africa.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009434	Using Bayes model averaging to leverage both gene main effects and G ×  E interactions to identify genomic regions in genome-wide association studies.	Missing both OR and beta
GCST009435	Using Bayes model averaging to leverage both gene main effects and G ×  E interactions to identify genomic regions in genome-wide association studies.	Missing both OR and beta
GCST009438	Incorporating spatial-anatomical similarity into the VGWAS framework for AD biomarker detection.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009444	Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009449	A Prospective Analysis of Genetic Variants Associated with Human Lifespan.	Missing both OR and beta
GCST009450	A Prospective Analysis of Genetic Variants Associated with Human Lifespan.	Missing both OR and beta
GCST009466	Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.	Missing both OR and beta
GCST009469	Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy.	Missing both OR and beta
GCST009470	Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy.	Missing both OR and beta
GCST009471	Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009504	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009506	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009507	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009508	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009509	Transethnic meta-analysis of metabolic syndrome in a multiethnic study.	Missing both OR and beta
GCST009512	The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.	Missing both OR and beta
GCST009518	Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits.	Missing both OR and beta
GCST009533	Candidate Gene and Genome-Wide Association Studies for Circulating Leptin Levels Reveal Population and Sex-Specific Associations in High Cardiovascular Risk Mediterranean Subjects.	Missing both OR and beta
GCST009536	Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706).	Missing both OR and beta
GCST009537	Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706).	Missing both OR and beta
GCST009538	Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706).	Missing both OR and beta
GCST009539	Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706).	Missing both OR and beta
GCST009540	Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706).	Missing both OR and beta
GCST009542	A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009543	A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009544	A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009547	A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009548	A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009560	Early complement genes are associated with visual system degeneration in multiple sclerosis.	Missing both OR and beta
GCST009568	Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.	Missing both OR and beta
GCST009600	Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.	Missing both OR and beta
GCST009601	A GENETIC VARIANT IN THE BCL2 GENE ASSOCIATES WITH ADALIMUMAB RESPONSE IN HIDRADENITIS SUPPURATIVA CLINICAL TRIALS AND REGULATES EXPRESSION OF BCL2.	Missing both OR and beta
GCST009604	A meta-analysis of genome-wide association studies of epigenetic age acceleration.	Missing both OR and beta
GCST009641	"General regression model: A ""model-free"" association test for quantitative traits allowing to test for the underlying genetic model."	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009652	Common and rare sequence variants influencing tumor biomarkers in blood.	Missing both OR and beta
GCST009678	Genome-wide association study of cognitive performance in U.S. veterans with schizophrenia or bipolar disorder.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009681	Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.	Missing both OR and beta
GCST009682	Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.	Missing both OR and beta
GCST009684	Ordered multinomial regression for genetic association analysis of ordinal phenotypes at Biobank scale.	Missing both OR and beta
GCST009696	The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases.	Missing both OR and beta
GCST009703	Association of Cardiometabolic Genes with Arsenic Metabolism Biomarkers in American Indian Communities: The Strong Heart Family Study (SHFS).	Missing both OR and beta
GCST009720	Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema.	Missing both OR and beta
GCST009725	Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.	Missing both OR and beta
GCST009729	Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease.	Missing both OR and beta
GCST009730	Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease.	Missing both OR and beta
GCST009733	Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans.	Missing both OR and beta
GCST009756	FADS3 is a delta14Z sphingoid base desaturase that contributes to gender differences to the human plasma sphingolipidome.	Missing both OR and beta
GCST009780	A variant near DHCR24 associates with microstructural properties of white matter and peripheral lipid metabolism in adolescents.	Missing both OR and beta
GCST009799	GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.	Missing both OR and beta
GCST009809	GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009822	GWAS of five gynecologic diseases and cross-trait analysis in Japanese.	Missing both OR and beta
GCST009823	GWAS of five gynecologic diseases and cross-trait analysis in Japanese.	Missing both OR and beta
GCST009824	GWAS of five gynecologic diseases and cross-trait analysis in Japanese.	Missing both OR and beta
GCST009837	Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program.	Missing both OR and beta
GCST009838	Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program.	Missing both OR and beta
GCST009841	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009842	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009843	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009845	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009848	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009850	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009857	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009858	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009859	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009862	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009863	JASS: command line and web interface for the joint analysis of GWAS results.	Missing both OR and beta
GCST009865	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009866	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009867	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009868	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009871	Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank.	Missing both OR and beta
GCST009873	Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations.	Missing both OR and beta
GCST009889	The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders.	Missing both OR and beta
GCST009890	Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances.	Missing both OR and beta
GCST009893	Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses.	Missing both OR and beta
GCST009922	A Genome-Wide Association Study of a Biomarker of Nicotine Metabolism.	Missing both OR and beta
GCST009925	Genome-wide Association Study for Urinary and Fecal Incontinence in Women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009927	Genome-wide Association Study for Urinary and Fecal Incontinence in Women.	Missing both OR and beta
GCST009936	Novel exomic rare variants associated with venous thrombosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST009964	Stratified analyses of genome wide association study data reveal haplotypes for a candidate gene on chromosome 2 (KIAA1211L) is associated with opioid use in patients of Arabian descent.	Missing both OR and beta
GCST009998	Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010000	Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010002	Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia.	Missing both OR and beta
GCST010007	A new genetic locus for antipsychotic-induced weight gain: A genome-wide study of first-episode psychosis patients using amisulpride (from the OPTiMiSE cohort).	Missing both OR and beta
GCST010017	Minimal phenotyping yields genome-wide association signals of low specificity for major depression.	Missing both OR and beta
GCST010043	Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma.	Missing both OR and beta
GCST010060	Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.	Missing both OR and beta
GCST010065	Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.	Missing both OR and beta
GCST010069	Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.	Missing both OR and beta
GCST010079	A Functional Variant Near XCL1 Gene Improves Breast Cancer Survival via Promoting Cancer Immunity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010083	Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.	Missing both OR and beta
GCST010096	Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease.	Missing both OR and beta
GCST010097	Genome-wide association analysis of insomnia using data from Partners Biobank.	Missing both OR and beta
GCST010099	Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.	Missing both OR and beta
GCST010104	Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD.	Missing both OR and beta
GCST010105	Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans.	Missing both OR and beta
GCST010124	A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn's disease.	Missing both OR and beta
GCST010125	Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.	Missing both OR and beta
GCST010130	Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.	Missing both OR and beta
GCST010131	Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.	Missing both OR and beta
GCST010147	Genome-wide association study of white matter hyperintensity volume in elderly persons without dementia.	Missing both OR and beta
GCST010149	Genetic control of variability in subcortical and intracranial volumes.	Missing both OR and beta
GCST010170	Genetic Contributions to Maternal and Neonatal Vitamin D Levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010178	Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity.	Missing both OR and beta
GCST010196	Protein quantitative trait locus study in obesity during weight-loss identifies a leptin regulator.	Missing both OR and beta
GCST010206	Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations.	Missing both OR and beta
GCST010218	Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010219	Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.	Missing both OR and beta
GCST010220	Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010221	Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010226	Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes.	Missing both OR and beta
GCST010250	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010252	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010254	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	Missing both OR and beta
GCST010256	Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010261	A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010264	A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010265	A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels.	Missing both OR and beta
GCST010266	Two novel pleiotropic loci associated with osteoporosis and abdominal obesity.	Missing both OR and beta
GCST010267	Two novel pleiotropic loci associated with osteoporosis and abdominal obesity.	Missing both OR and beta
GCST010268	Two novel pleiotropic loci associated with osteoporosis and abdominal obesity.	Missing both OR and beta
GCST010269	Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis.	Missing both OR and beta
GCST010270	Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis.	Missing both OR and beta
GCST010271	Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis.	Missing both OR and beta
GCST010272	Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis.	Missing both OR and beta
GCST010278	Genetics of physiological dysregulation: findings from the long life family study using joint models.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010279	Genetics of physiological dysregulation: findings from the long life family study using joint models.	Missing both OR and beta
GCST010292	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010293	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010294	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010295	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010296	Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010297	A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010299	Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis.	Missing both OR and beta
GCST010302	Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.	Missing both OR and beta
GCST010303	Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.	Missing both OR and beta
GCST010305	A genome-wide association study identifies key modulators of complement factor H binding to malondialdehyde-epitopes.	Missing both OR and beta
GCST010312	Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010313	Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.	Missing both OR and beta
GCST010315	Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.	Missing both OR and beta
GCST010317	Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010319	Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010320	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Missing both OR and beta
GCST010321	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Missing both OR and beta
GCST010340	Genome-wide interaction analysis of pathological hallmarks in Alzheimer's disease.	Missing both OR and beta
GCST010343	Genome-wide interaction analysis of pathological hallmarks in Alzheimer's disease.	Missing both OR and beta
GCST010380	Genetic Association Reveals Protection against Recurrence of Clostridium difficile Infection with Bezlotoxumab Treatment.	Missing both OR and beta
GCST010396	Genome-wide associations of human gut microbiome variation and implications for causal inference analyses.	Missing both OR and beta
GCST010397	Genome-wide associations of human gut microbiome variation and implications for causal inference analyses.	Missing both OR and beta
GCST010421	Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.	Missing both OR and beta
GCST010426	Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.	Missing both OR and beta
GCST010456	Genome-Wide Association Study of Genetic Variants Related to Anthracycline-Induced Cardiotoxicity in Early Breast Cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010464	A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior.	Missing both OR and beta
GCST010485	Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC).	Missing both OR and beta
GCST010506	Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010512	Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals.	Missing both OR and beta
GCST010516	A single genetic locus associated with pediatric fractures: A genome-wide association study on 3,230 patients.	Missing both OR and beta
GCST010547	Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.	Missing both OR and beta
GCST010548	Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.	Missing both OR and beta
GCST010549	Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.	Missing both OR and beta
GCST010550	Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.	Missing both OR and beta
GCST010551	Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.	Missing both OR and beta
GCST010552	Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.	Missing both OR and beta
GCST010561	Association between herpes simplex virus 1 exposure and the risk of depression in UK Biobank.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010562	Association between herpes simplex virus 1 exposure and the risk of depression in UK Biobank.	Missing both OR and beta
GCST010567	Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways.	Missing both OR and beta
GCST010578	Genome-wide association study identifies TPH2 variant as a novel locus for severe CV-A6-associated hand, foot, and mouth disease in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010640	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010641	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010642	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010643	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010644	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010645	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010646	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010647	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010648	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010649	Multi-trait analysis for genome-wide association study of five psychiatric disorders.	Missing both OR and beta
GCST010650	Association Between Common Variants in RBFOX1, an RNA-Binding Protein, and Brain Amyloidosis in Early and Preclinical Alzheimer Disease.	Missing both OR and beta
GCST010653	GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer.	Missing both OR and beta
GCST010687	A genome-wide association study of polycystic ovary syndrome identified from electronic health records.	Missing both OR and beta
GCST010696	Understanding the genetic determinants of the brain with MOSTest.	Missing both OR and beta
GCST010697	Understanding the genetic determinants of the brain with MOSTest.	Missing both OR and beta
GCST010698	Understanding the genetic determinants of the brain with MOSTest.	Missing both OR and beta
GCST010699	Understanding the genetic determinants of the brain with MOSTest.	Missing both OR and beta
GCST010700	Understanding the genetic determinants of the brain with MOSTest.	Missing both OR and beta
GCST010701	Understanding the genetic determinants of the brain with MOSTest.	Missing both OR and beta
GCST010702	Understanding the genetic determinants of the brain with MOSTest.	Missing both OR and beta
GCST010703	Understanding the genetic determinants of the brain with MOSTest.	Missing both OR and beta
GCST010725	Insights into malaria susceptibility using genome-wide data on 17,000 individuals from Africa, Asia and Oceania.	Missing both OR and beta
GCST010736	Genome-Wide Association of Kidney Traits in Hispanics/Latinos Using Dense Imputed Whole-Genome Sequencing Data: The Hispanic Community Health Study/Study of Latinos.	Missing both OR and beta
GCST010737	Genome-Wide Association of Kidney Traits in Hispanics/Latinos Using Dense Imputed Whole-Genome Sequencing Data: The Hispanic Community Health Study/Study of Latinos.	Missing both OR and beta
GCST010759	Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010760	Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010766	A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.	Missing both OR and beta
GCST010767	A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.	Missing both OR and beta
GCST010768	A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.	Missing both OR and beta
GCST010769	A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.	Missing both OR and beta
GCST010770	A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.	Missing both OR and beta
GCST010771	A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.	Missing both OR and beta
GCST010772	A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.	Missing both OR and beta
GCST010774	A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.	Missing both OR and beta
GCST010818	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010867	Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.	Missing both OR and beta
GCST010900	A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma.	Missing both OR and beta
GCST010901	A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma.	Missing both OR and beta
GCST010922	Pleiotropic genomic variants at 17q21.31 associated with bone mineral density and body fat mass: a bivariate genome-wide association analysis.	Missing both OR and beta
GCST010923	Polygenic Score for Beta-Blocker Survival Benefit in European Ancestry Patients with Reduced Ejection Fraction Heart Failure.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010979	Association of an IGHV3-66 gene variant with Kawasaki disease.	Missing both OR and beta
GCST010986	Genome-Wide Association Analysis of Longitudinal Bone Mineral Content Data From the Iowa Bone Development Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST010992	Association of body mass index with colorectal cancer risk by genome-wide variants.	Missing both OR and beta
GCST010993	Clinicogenomic factors of biotherapy immunogenicity in autoimmune disease: A prospective multicohort study of the ABIRISK consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011004	Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C.	Missing both OR and beta
GCST011007	Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study.	Missing both OR and beta
GCST011008	Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study.	Missing both OR and beta
GCST011010	Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.	Missing both OR and beta
GCST011011	Genome wide association study identifies genetic associations with perceived age.	Missing both OR and beta
GCST011046	Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.	Missing both OR and beta
GCST011049	Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.	Missing both OR and beta
GCST011053	Genome-Wide Association Study for the Identification of Novel Genetic Variants Associated with the Risk of Neuroblastoma in Korean Children.	Missing both OR and beta
GCST011055	Volumetric GWAS of medial temporal lobe structures identifies an ERC1 locus using ADNI high-resolution T2-weighted MRI data.	Missing both OR and beta
GCST011056	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011057	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011058	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011059	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011060	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011061	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011062	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011063	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011064	A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.	Missing both OR and beta
GCST011066	Genomic Analysis Identifies New Loci Associated With Motor Complications in Parkinson's Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011067	Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011068	Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011069	Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011096	Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups.	Missing both OR and beta
GCST011097	Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups.	Missing both OR and beta
GCST011100	Multivariate genomic scan implicates novel loci and haem metabolism in human ageing.	Missing both OR and beta
GCST011102	Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis.	Missing both OR and beta
GCST011108	A prospective study of the associations among fine particulate matter, genetic variants, and the risk of colorectal cancer.	Missing both OR and beta
GCST011116	Genome-wide association study on coronary artery disease in type 1 diabetes suggests beta-defensin 127 as a risk locus.	Missing both OR and beta
GCST011136	Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011139	Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011141	Identifying Interactions between Dietary Sodium, Potassium, Sodium-Potassium Ratios, and FGF5 rs16998073 Variants and Their Associated Risk for Hypertension in Korean Adults.	Missing both OR and beta
GCST011151	Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011152	Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011154	Heritability and genome-wide association analyses of fasting plasma glucose in Chinese adult twins.	Missing both OR and beta
GCST011161	Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia.	Missing both OR and beta
GCST011163	Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia.	Missing both OR and beta
GCST011176	Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke.	Missing both OR and beta
GCST011177	Genetic determinants of lung cancer prognosis in never smokers: A pooled analysis in the International Lung Cancer Consortium.	Missing both OR and beta
GCST011178	Genetic determinants of lung cancer prognosis in never smokers: A pooled analysis in the International Lung Cancer Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011179	A large-scale genome-wide association study meta-analysis of cannabis use disorder.	Missing both OR and beta
GCST011197	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011198	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	Missing both OR and beta
GCST011207	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	Missing both OR and beta
GCST011210	Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.	Missing both OR and beta
GCST011319	Association of the RPA3-UMAD1 locus with interstitial lung diseases complicated with rheumatoid arthritis in Japanese.	Missing both OR and beta
GCST011320	A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer.	Missing both OR and beta
GCST011321	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011322	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011323	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011324	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011325	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011326	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011327	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011328	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011329	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011330	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011331	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011332	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011333	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011334	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011335	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011336	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011337	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011338	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011340	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011341	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011342	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011343	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011344	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Missing both OR and beta
GCST011345	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011346	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011347	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011348	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011349	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011350	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011351	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011352	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011353	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Missing both OR and beta
GCST011354	A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy.	Missing both OR and beta
GCST011359	Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism.	Missing both OR and beta
GCST011363	Replication of HLA class II locus association with susceptibility to podoconiosis in three Ethiopian ethnic groups.	Missing both OR and beta
GCST011372	Identification of Glycochenodeoxycholate 3-O-Glucuronide and Glycodeoxycholate 3-O-Glucuronide as Highly Sensitive and Specific OATP1B1 Biomarkers.	Missing both OR and beta
GCST011373	Identification of Glycochenodeoxycholate 3-O-Glucuronide and Glycodeoxycholate 3-O-Glucuronide as Highly Sensitive and Specific OATP1B1 Biomarkers.	Missing both OR and beta
GCST011377	A Genome Wide Association Study For Shoulder Impingement and Rotator Cuff Disease.	Missing both OR and beta
GCST011379	Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups.	Missing both OR and beta
GCST011380	Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups.	Missing both OR and beta
GCST011381	Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups.	Missing both OR and beta
GCST011382	Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups.	Missing both OR and beta
GCST011383	Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups.	Missing both OR and beta
GCST011387	Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011389	Genome-wide association study in a Korean population identifies six novel susceptibility loci for rheumatoid arthritis.	Missing both OR and beta
GCST011390	Genome-wide association study of corneal biomechanical properties identifies over 200 loci providing insight into the genetic aetiology of ocular diseases.	Missing both OR and beta
GCST011394	Four pleiotropic loci associated with fat mass and lean mass.	Missing both OR and beta
GCST011396	Genome-wide association study and polygenic risk score analysis of esketamine treatment response.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011397	Genome-wide association study and polygenic risk score analysis of esketamine treatment response.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011401	A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST011402	A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST011420	Regulatory CDH4 genetic variants associate with risk to develop capecitabine-induced hand-foot syndrome.	Missing both OR and beta
GCST011425	Genome-wide Analyses Identify a Novel Risk Locus for Nonsyndromic Cleft Palate.	Missing both OR and beta
GCST011426	Meta-analysis of genome-wide association study identifies FBN2 as a novel locus associated with systemic lupus erythematosus in Thai population.	Missing both OR and beta
GCST011427	Genome-wide pQTL analysis of protein expression regulatory networks in the human liver.	Missing both OR and beta
GCST011428	Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels.	Missing both OR and beta
GCST011433	Supervariants identification for breast cancer.	Missing both OR and beta
GCST011434	Donor genetic variants as risk factors for thrombosis after liver transplantation: A genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011435	Amerindian Ancestry Influences Genetic Susceptibility to Chronic Obstructive Pulmonary Disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011436	Extreme Phenotype Approach Suggests Taste Transduction Pathway for Carotid Plaque in a Multi-Ethnic Cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011438	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Missing both OR and beta
GCST011439	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Missing both OR and beta
GCST011440	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Missing both OR and beta
GCST011441	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Missing both OR and beta
GCST011461	Sex-Specific Genetic Associations for Barrett's Esophagus and Esophageal Adenocarcinoma.	Missing both OR and beta
GCST011462	Sex-Specific Genetic Associations for Barrett's Esophagus and Esophageal Adenocarcinoma.	Missing both OR and beta
GCST011476	Associations between COVID-19 and skin conditions identified through epidemiology and genomic studies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011491	Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus.	Missing both OR and beta
GCST011492	Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011493	Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus.	Missing both OR and beta
GCST011497	The Genetics of Circulating Resistin Level, A Biomarker for Cardiovascular Diseases, Is Informed by Mendelian Randomization and the Unique Characteristics of African Genomes.	Missing both OR and beta
GCST011498	Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma.	Missing both OR and beta
GCST011500	GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression.	Missing both OR and beta
GCST011501	GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression.	Missing both OR and beta
GCST011502	GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression.	Missing both OR and beta
GCST011503	GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression.	Missing both OR and beta
GCST011504	GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression.	Missing both OR and beta
GCST011516	A genome-wide association study identifying the SNPs predictive of rapid joint destruction in patients with rheumatoid arthritis.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011517	A genome-wide association study identifying the SNPs predictive of rapid joint destruction in patients with rheumatoid arthritis.	Missing both OR and beta
GCST011531	Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011534	Looking for Sunshine: Genetic Predisposition to Sun-Seeking in 265,000 Individuals of European Ancestry.	Missing both OR and beta
GCST011535	An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer.	Missing both OR and beta
GCST011537	HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study.	Missing both OR and beta
GCST011561	Identification of pleiotropic loci underlying hip bone mineral density and trunk lean mass.	Missing both OR and beta
GCST011564	New susceptibility alleles associated with severe coronary artery stenosis in the Lebanese population.	Missing both OR and beta
GCST011565	New susceptibility alleles associated with severe coronary artery stenosis in the Lebanese population.	Missing both OR and beta
GCST011566	New susceptibility alleles associated with severe coronary artery stenosis in the Lebanese population.	Missing both OR and beta
GCST011567	A genome-wide association study reveals a substantial genetic basis underlying the Ebbinghaus illusion.	Missing both OR and beta
GCST011568	A genome-wide association study reveals a substantial genetic basis underlying the Ebbinghaus illusion.	Missing both OR and beta
GCST011570	A genome-wide association study of asthma hospitalizations in adults.	Missing both OR and beta
GCST011576	Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.	Missing both OR and beta
GCST011578	Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.	Missing both OR and beta
GCST011581	Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.	Missing both OR and beta
GCST011584	Genomic analysis of germline variation associated with survival of colorectal cancer patients treated with chemotherapy plus biologics in CALGB/SWOG 80405 (Alliance).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011586	Association of genetic variation with cirrhosis: a multi-trait genome-wide association and gene-environment interaction study.	Missing both OR and beta
GCST011616	Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.	Missing both OR and beta
GCST011617	Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.	Missing both OR and beta
GCST011618	Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.	Missing both OR and beta
GCST011621	Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia.	Missing both OR and beta
GCST011637	Clinical and Genome-Wide Analysis of Multiple Severe Cisplatin-Induced Neurotoxicities in Adult-Onset Cancer Survivors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011656	Genome-wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk.	Missing both OR and beta
GCST011662	Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011676	Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.	Missing both OR and beta
GCST011681	Genome-Wide Association Study Identifies Novel Colony Stimulating Factor 1 Locus Conferring Susceptibility to Cryptococcosis in Human Immunodeficiency Virus-Infected South Africans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011696	Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.	Missing both OR and beta
GCST011701	Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals.	Missing both OR and beta
GCST011702	Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals.	Missing both OR and beta
GCST011703	Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals.	Missing both OR and beta
GCST011704	Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals.	Missing both OR and beta
GCST011706	Association of common genetic variants with brain microbleeds: A Genome-wide Association Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011707	Association of common genetic variants with brain microbleeds: A Genome-wide Association Study.	Missing both OR and beta
GCST011716	Association between non-Caucasian-specific ASCC1 gene polymorphism and osteoporosis and obesity in Korean postmenopausal women.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011739	A Genome-Wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1 and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis In Brazil.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011741	Genetic architecture of cardiometabolic risks in people living with HIV.	Missing both OR and beta
GCST011742	Genetic architecture of cardiometabolic risks in people living with HIV.	Missing both OR and beta
GCST011743	Genetic architecture of cardiometabolic risks in people living with HIV.	Missing both OR and beta
GCST011772	Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.	Missing both OR and beta
GCST011774	Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011788	Three pleiotropic loci associated with bone mineral density and lean body mass.	Missing both OR and beta
GCST011793	A Genome-Wide Association Study in Early COPD: Identification of One Major Susceptibility Loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011826	A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011829	Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease.	Missing both OR and beta
GCST011830	Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011837	Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011879	Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data.	Missing both OR and beta
GCST011880	Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data.	Missing both OR and beta
GCST011881	Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data.	Missing both OR and beta
GCST011882	Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data.	Missing both OR and beta
GCST011883	Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data.	Missing both OR and beta
GCST011884	Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data.	Missing both OR and beta
GCST011885	Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data.	Missing both OR and beta
GCST011886	Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data.	Missing both OR and beta
GCST011891	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	Missing both OR and beta
GCST011892	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	Missing both OR and beta
GCST011893	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011894	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	Missing both OR and beta
GCST011895	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	Missing both OR and beta
GCST011899	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	Missing both OR and beta
GCST011900	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011902	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	Missing both OR and beta
GCST011903	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011905	Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.	Missing both OR and beta
GCST011924	Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci.	Missing both OR and beta
GCST011925	Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci.	Missing both OR and beta
GCST011926	Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci.	Missing both OR and beta
GCST011927	Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci.	Missing both OR and beta
GCST011928	Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci.	Missing both OR and beta
GCST011932	Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis.	Missing both OR and beta
GCST011933	Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis.	Missing both OR and beta
GCST011937	Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study.	Missing both OR and beta
GCST011938	Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study.	Missing both OR and beta
GCST011939	Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study.	Missing both OR and beta
GCST011940	Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans.	Missing both OR and beta
GCST011952	Cerebral small vessel disease genomics and its implications across the lifespan.	Missing both OR and beta
GCST011953	Cerebral small vessel disease genomics and its implications across the lifespan.	Missing both OR and beta
GCST011954	Cerebral small vessel disease genomics and its implications across the lifespan.	Missing both OR and beta
GCST011956	Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus.	Missing both OR and beta
GCST011958	Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir- and Tenofovir-containing Regimens.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011959	Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir- and Tenofovir-containing Regimens.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011960	Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir- and Tenofovir-containing Regimens.	Missing both OR and beta
GCST011973	Genome-Wide Analysis of Sex Disparities in the Genetic Architecture of Lung and Colorectal Cancers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011974	Genome-Wide Analysis of Sex Disparities in the Genetic Architecture of Lung and Colorectal Cancers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011975	FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses.	Missing both OR and beta
GCST011978	CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011979	CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption.	Missing both OR and beta
GCST011995	Large genome-wide association study identifies three novel risk variants for restless legs syndrome.	Missing both OR and beta
GCST011996	Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011997	Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells.	Missing both OR and beta
GCST011998	Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST011999	A multi-ancestry sex stratified genome-wide association study of spontaneous clearance of hepatitis C virus.	Missing both OR and beta
GCST012012	A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects.	Missing both OR and beta
GCST012013	A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects.	Missing both OR and beta
GCST012015	Two-stage genome-wide association study of chronic rhinosinusitis and disease subphenotypes highlights mucosal immunity contributing to risk.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012016	Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study.	Missing both OR and beta
GCST012017	Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis.	Missing both OR and beta
GCST012020	A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos.	Missing both OR and beta
GCST012021	A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos.	Missing both OR and beta
GCST012046	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012047	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	Missing both OR and beta
GCST012048	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	Missing both OR and beta
GCST012050	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	Missing both OR and beta
GCST012051	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012053	Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.	Missing both OR and beta
GCST012055	A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012060	A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese.	Missing both OR and beta
GCST012061	A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese.	Missing both OR and beta
GCST012062	A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese.	Missing both OR and beta
GCST012063	A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese.	Missing both OR and beta
GCST012066	Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins.	Missing both OR and beta
GCST012069	Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins.	Missing both OR and beta
GCST012073	Genetic association of a gain of function interferon gamma receptor 1 (IFNGR1) polymorphism and the intergenic region LNCAROD/DKK1 with Behçet's disease.	Missing both OR and beta
GCST012094	Genome-wide association study of patients with a severe major depressive episode treated with electroconvulsive therapy.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012095	Genome-wide association study of patients with a severe major depressive episode treated with electroconvulsive therapy.	Missing both OR and beta
GCST012099	Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.	Missing both OR and beta
GCST012100	Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.	Missing both OR and beta
GCST012110	Genetic underpinnings of sociability in the general population.	Missing both OR and beta
GCST012111	Genetic underpinnings of sociability in the general population.	Missing both OR and beta
GCST012112	Genetic underpinnings of sociability in the general population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012113	Genetic underpinnings of sociability in the general population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012115	Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012116	Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012117	Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012118	Genetic determinants of immune-related adverse events in patients with melanoma receiving immune checkpoint inhibitors.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012119	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012120	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012121	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012122	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012123	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012124	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012125	Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012126	Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.	Missing both OR and beta
GCST012127	Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.	Missing both OR and beta
GCST012129	Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.	Missing both OR and beta
GCST012135	Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.	Missing both OR and beta
GCST012137	Genome-Wide Association Study of Motor Coordination.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012139	Genome-wide association study of high-sensitivity C-reactive protein, D-dimer and Interleukin-6 levels in multi-ethnic HIV+ cohorts.	Missing both OR and beta
GCST012147	Genetic determinants of ferritin, haemoglobin levels and haemoglobin trajectories: results from Donor InSight.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012148	Understanding the genetic architecture of the metabolically unhealthy normal weight and metabolically healthy obese phenotypes in a Korean population.	Missing both OR and beta
GCST012149	Understanding the genetic architecture of the metabolically unhealthy normal weight and metabolically healthy obese phenotypes in a Korean population.	Missing both OR and beta
GCST012156	Function of multiple sclerosis-protective HLA class I alleles revealed by genome-wide protein-quantitative trait loci mapping of interferon signalling.	Missing both OR and beta
GCST012157	Genome-wide association studies of antidepressant class response and treatment-resistant depression.	Missing both OR and beta
GCST012158	Genome-wide association studies of antidepressant class response and treatment-resistant depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012159	Genome-wide association studies of antidepressant class response and treatment-resistant depression.	Missing both OR and beta
GCST012160	Genome-wide association studies of antidepressant class response and treatment-resistant depression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012163	Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012176	Rare variants in the DNA repair pathway and the risk of colorectal cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012178	Smoking modifies pancreatic cancer risk loci on 2q21.3.	Missing both OR and beta
GCST012180	Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium.	Missing both OR and beta
GCST012181	Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012182	Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.	Missing both OR and beta
GCST012183	Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.	Missing both OR and beta
GCST012184	Pharmacogenomic Profile and Adverse Drug Reactions in a Prospective Therapeutic Cohort of Chagas Disease Patients Treated with Benznidazole.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012187	Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012188	Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012189	Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins.	Missing both OR and beta
GCST012190	Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012191	Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins.	Missing both OR and beta
GCST012195	Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012197	Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium.	Missing both OR and beta
GCST012199	Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma.	Missing both OR and beta
GCST012200	Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma.	Missing both OR and beta
GCST012201	Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma.	Missing both OR and beta
GCST012213	Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers.	Missing both OR and beta
GCST012214	Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk.	Missing both OR and beta
GCST012219	Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color.	Missing both OR and beta
GCST012221	Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012222	Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012225	Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes.	Missing both OR and beta
GCST012232	Genome-Wide Association Study and Identification of a Protective Missense Variant on Lipoprotein(a) Concentration: Protective Missense Variant on Lipoprotein(a) Concentration.	Missing both OR and beta
GCST012244	Genome-wide association studies of exacerbations in children using long-acting beta2-agonists.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012245	Genome-wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012251	Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder.	Missing both OR and beta
GCST012252	Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder.	Missing both OR and beta
GCST012255	Confident identification of subgroups from SNP testing in RCTs with binary outcomes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012256	Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome.	Missing both OR and beta
GCST012276	Variants at the MHC Region Associate With Susceptibility to <i>Clostridioides difficile</i> Infection: A Genome-Wide Association Study Using Comprehensive Electronic Health Records.	Missing both OR and beta
GCST012277	Variants at the MHC Region Associate With Susceptibility to <i>Clostridioides difficile</i> Infection: A Genome-Wide Association Study Using Comprehensive Electronic Health Records.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012281	Genome-wide long non-coding RNA association study on Han Chinese women identifies lncHSAT164 as a novel susceptibility gene for breast cancer.	Missing both OR and beta
GCST012282	Identification of genetic loci affecting body mass index through interaction with multiple environmental factors using structured linear mixed model.	Missing both OR and beta
GCST012283	Identification of genetic loci affecting body mass index through interaction with multiple environmental factors using structured linear mixed model.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012284	Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012285	Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression.	Missing both OR and beta
GCST012290	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	Missing both OR and beta
GCST012293	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	Missing both OR and beta
GCST012296	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	Missing both OR and beta
GCST012299	Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.	Missing both OR and beta
GCST012322	Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.	Missing both OR and beta
GCST012324	Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.	Missing both OR and beta
GCST012332	Sex-stratified genome-wide association study of multisite chronic pain in UK Biobank.	Missing both OR and beta
GCST012338	Variants in urate transporters, ADH1B, GCKR and MEPE genes associate with transition from asymptomatic hyperuricaemia to gout: results of the first gout versus asymptomatic hyperuricaemia GWAS in Caucasians using data from the UK Biobank.	Missing both OR and beta
GCST012339	Variants in urate transporters, ADH1B, GCKR and MEPE genes associate with transition from asymptomatic hyperuricaemia to gout: results of the first gout versus asymptomatic hyperuricaemia GWAS in Caucasians using data from the UK Biobank.	Missing both OR and beta
GCST012340	Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity.	Missing both OR and beta
GCST012341	Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity.	Missing both OR and beta
GCST012342	Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012349	The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.	Missing both OR and beta
GCST012350	The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.	Missing both OR and beta
GCST012351	The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.	Missing both OR and beta
GCST012352	The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.	Missing both OR and beta
GCST012353	Genome-wide association study of serum metabolites in the African American Study of Kidney Disease and Hypertension.	Missing both OR and beta
GCST012361	Improving brain age estimates with deep learning leads to identification of novel genetic factors associated with brain aging.	Missing both OR and beta
GCST012362	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012363	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012364	Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012368	Genome wide association study identifies four loci for early onset schizophrenia.	Missing both OR and beta
GCST012370	Genome-wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24.	Missing both OR and beta
GCST012381	A genome-wide association meta-analysis identifies new Eosinophilic esophagitis loci.	Missing both OR and beta
GCST012400	Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia.	Missing both OR and beta
GCST012401	Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia.	Missing both OR and beta
GCST012403	Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia.	Missing both OR and beta
GCST012414	Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.	Missing both OR and beta
GCST012420	A Genome-Wide Association Study in Human Lymphoblastoid Cells Supports Safety of Mitochondrial Complex I Inhibitor.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012421	Genetic risk factors for colorectal cancer in multiethnic Indonesians.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012429	Genome-wide association study identifies TNFSF15associated with childhood asthma.	Missing both OR and beta
GCST012431	Imputation and Reanalysis of ExomeChip Data Identifies Novel, Conditional and Joint Genetic Effects on Parkinson's Disease Risk.	Missing both OR and beta
GCST012434	Novel loci and mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys.	Missing both OR and beta
GCST012442	The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.	Missing both OR and beta
GCST012443	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	Missing both OR and beta
GCST012444	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012445	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012447	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012448	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	Missing both OR and beta
GCST012449	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012450	Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012455	FAT4 identified as a potential modifier of orofacial cleft laterality.	Missing both OR and beta
GCST012456	FAT4 identified as a potential modifier of orofacial cleft laterality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012457	FAT4 identified as a potential modifier of orofacial cleft laterality.	Missing both OR and beta
GCST012458	FAT4 identified as a potential modifier of orofacial cleft laterality.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012464	Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.	Missing both OR and beta
GCST012465	Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.	Missing both OR and beta
GCST012466	Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012472	Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012474	Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012475	Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study.	Missing both OR and beta
GCST012484	Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012487	Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.	Missing both OR and beta
GCST012490	Evaluate the effects of serum urate level on bone mineral density: a genome-wide gene-environment interaction analysis in UK Biobank cohort.	Missing both OR and beta
GCST012493	An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training-induced muscle fiber hypertrophy in younger men.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012498	Both rare and common genetic variants contribute to autism in the Faroe Islands.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012500	Genome-wide association study of cardiac troponin I in the general population.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST012501	Identification of Three Loci Associated with Achilles Tendon Injury Risk from a Genome-wide Association Study.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012516	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012517	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012518	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012519	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012520	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012521	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012522	Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST012523	A large-scale exome array analysis of venous thromboembolism.	Missing both OR and beta
GCST90000014	Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90000020	Unsupervised Modeling and Genome-Wide Association Identify Novel Features of Allergic March Trajectories.	Missing both OR and beta
GCST90000021	Unsupervised Modeling and Genome-Wide Association Identify Novel Features of Allergic March Trajectories.	Missing both OR and beta
GCST90000030	Genetic Meta-Analysis of Twin Birth Weight Shows High Genetic Correlation with Singleton Birth Weight.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90000061	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Missing both OR and beta
GCST90000062	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Missing both OR and beta
GCST90000063	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Missing both OR and beta
GCST90000065	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Missing both OR and beta
GCST90000181	Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.	Missing both OR and beta
GCST90000513	A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor.	Missing both OR and beta
GCST90000582	Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.	Missing both OR and beta
GCST90002228	The trans-ancestral genomic architecture of glycemic traits.	Missing both OR and beta
GCST90002283	Genome-wide association analysis of 17,019 Korean women identifies variants associated with facial pigmented spots.	Missing both OR and beta
GCST90002284	Genome-wide association analysis of 17,019 Korean women identifies variants associated with facial pigmented spots.	Missing both OR and beta
GCST90002296	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002302	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002308	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002309	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002313	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002314	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002320	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002321	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002325	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002326	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002328	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002331	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002332	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002334	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002337	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002338	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002344	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002349	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002350	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002355	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002357	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002361	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002366	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002367	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002368	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002371	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002372	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002378	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Missing both OR and beta
GCST90002390	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Missing both OR and beta
GCST90002391	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Missing both OR and beta
GCST90002392	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Missing both OR and beta
GCST90002393	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Missing both OR and beta
GCST90002401	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Missing both OR and beta
GCST90002403	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Missing both OR and beta
GCST90002424	Multi-ethnic transcriptome-wide association study of prostate cancer.	Missing both OR and beta
GCST90006990	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90007005	Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90010361	Quantitative and qualitative role of antagonistic heterogeneity in genetics of blood lipids.	Missing both OR and beta
GCST90010423	Genome-Wide Association Analysis Identified ANXA1 Associated with Shoulder Impingement Syndrome in UK Biobank Samples.	Missing both OR and beta
GCST90010427	The genetic architecture of structural left-right asymmetry of the human brain.	Missing both OR and beta
GCST90011293	A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data.	Missing both OR and beta
GCST90011294	A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data.	Missing both OR and beta
GCST90011295	A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data.	Missing both OR and beta
GCST90011296	A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data.	Missing both OR and beta
GCST90011297	A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data.	Missing both OR and beta
GCST90011298	A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data.	Missing both OR and beta
GCST90011766	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Missing both OR and beta
GCST90011768	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Missing both OR and beta
GCST90011770	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Missing both OR and beta
GCST90011823	Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.	Missing both OR and beta
GCST90011866	Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups.	Missing both OR and beta
GCST90012012	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012034	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012041	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012046	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012050	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012063	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012067	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012075	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012078	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Missing both OR and beta
GCST90012203	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012204	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012205	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012214	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012215	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012217	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012221	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012222	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012223	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012225	Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.	Missing both OR and beta
GCST90012790	Genetic predictors of participation in optional components of UK Biobank.	Missing both OR and beta
GCST90012791	Genetic predictors of participation in optional components of UK Biobank.	Missing both OR and beta
GCST90012792	Genetic predictors of participation in optional components of UK Biobank.	Missing both OR and beta
GCST90012793	Genetic predictors of participation in optional components of UK Biobank.	Missing both OR and beta
GCST90012794	Genetic predictors of participation in optional components of UK Biobank.	Missing both OR and beta
GCST90012825	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	Missing both OR and beta
GCST90012827	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	Missing both OR and beta
GCST90012828	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	Missing both OR and beta
GCST90012829	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90012830	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90012831	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90012832	Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.	Missing both OR and beta
GCST90012877	Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer's disease risk genes.	Missing both OR and beta
GCST90013411	Genome-Wide Association Study Identifies LINC01184/SLC12A2 As Risk Locus for Skin and Soft Tissue Infections.	Missing both OR and beta
GCST90013420	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Missing both OR and beta
GCST90013421	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Missing both OR and beta
GCST90013445	Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes.	Missing both OR and beta
GCST90013534	Large-scale meta-analysis across East Asian and European populations updated genetic architecture and variant-driven biology of rheumatoid arthritis, identifying 11 novel susceptibility loci.	Missing both OR and beta
GCST90013537	Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease.	Missing both OR and beta
GCST90013538	Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease.	Missing both OR and beta
GCST90013662	GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms.	Missing both OR and beta
GCST90013663	GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms.	Missing both OR and beta
GCST90013668	Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset.	Missing both OR and beta
GCST90013679	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013680	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013683	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013684	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013685	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013687	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013688	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013693	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013695	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013697	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013700	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013706	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013707	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013709	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013710	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013713	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013715	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013719	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013720	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013735	Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.	Missing both OR and beta
GCST90013832	Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.	Missing both OR and beta
GCST90013835	Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.	Missing both OR and beta
GCST90013836	Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.	Missing both OR and beta
GCST90013837	Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.	Missing both OR and beta
GCST90013838	Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.	Missing both OR and beta
GCST90013842	Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.	Missing both OR and beta
GCST90014023	Interpreting type 1 diabetes risk with genetics and single-cell epigenomics.	Missing both OR and beta
GCST90014033	Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.	Missing both OR and beta
GCST90014045	A multi-omics study links TNS3 and SEPT7 to long-term former smoking NSCLC survival.	Missing both OR and beta
GCST90014124	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90014125	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	Missing both OR and beta
GCST90014126	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90014127	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	Missing both OR and beta
GCST90014128	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90014129	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	Missing both OR and beta
GCST90014130	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	Missing both OR and beta
GCST90014131	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	Missing both OR and beta
GCST90014132	Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia.	Missing both OR and beta
GCST90014266	Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.	Missing both OR and beta
GCST90014268	A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects.	Missing both OR and beta
GCST90014290	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014292	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014294	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014295	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014296	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014298	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014299	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014300	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014301	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014302	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014303	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014304	Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.	Missing both OR and beta
GCST90014325	Prioritization of candidate causal genes for asthma in susceptibility loci derived from UK Biobank.	Missing both OR and beta
GCST90016585	Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.	Missing both OR and beta
GCST90016586	Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.	Missing both OR and beta
GCST90016588	Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.	Missing both OR and beta
GCST90016589	Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.	Missing both OR and beta
GCST90016590	Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.	Missing both OR and beta
GCST90016591	Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.	Missing both OR and beta
GCST90016593	Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.	Missing both OR and beta
GCST90016594	Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.	Missing both OR and beta
GCST90018576	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018585	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018586	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018603	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018606	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018627	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018629	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018631	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018642	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018643	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018644	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018651	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018654	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018685	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018695	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018714	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018722	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018723	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018739	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018744	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018746	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018757	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018759	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018771	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018775	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018784	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018796	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018799	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018801	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018802	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018805	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018806	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018811	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018813	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018815	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018819	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018821	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018823	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018824	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018826	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018829	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018831	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018838	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018839	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018840	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018841	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018846	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018847	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018849	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018851	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018852	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018857	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018858	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018860	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018863	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018864	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018866	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018870	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018871	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018872	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018874	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018878	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018883	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018884	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018885	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018895	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018905	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018907	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018908	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018911	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018915	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018921	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018926	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018932	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018933	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018934	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018935	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018938	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018939	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018942	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018943	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018944	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018959	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018964	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018966	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018977	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018979	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018991	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90018995	A cross-population atlas of genetic associations for 220 human phenotypes.	Missing both OR and beta
GCST90019034	Sortilin as a Biomarker for Cardiovascular Disease Revisited.	Missing both OR and beta
GCST90019035	Sortilin as a Biomarker for Cardiovascular Disease Revisited.	Missing both OR and beta
GCST90019043	Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90019044	Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90019045	Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90019492	Genetics of 35 blood and urine biomarkers in the UK Biobank.	Missing both OR and beta
GCST90019494	Genetics of 35 blood and urine biomarkers in the UK Biobank.	Missing both OR and beta
GCST90019497	Genetics of 35 blood and urine biomarkers in the UK Biobank.	Missing both OR and beta
GCST90019498	Genetics of 35 blood and urine biomarkers in the UK Biobank.	Missing both OR and beta
GCST90019504	Genetics of 35 blood and urine biomarkers in the UK Biobank.	Missing both OR and beta
GCST90019513	Genetics of 35 blood and urine biomarkers in the UK Biobank.	Missing both OR and beta
GCST90019516	Genetics of 35 blood and urine biomarkers in the UK Biobank.	Missing both OR and beta
GCST90019518	Genetics of 35 blood and urine biomarkers in the UK Biobank.	Missing both OR and beta
GCST90020041	Shared genetic study gives insights into the shared and distinct pathogenic immunity components of IgA nephropathy and SLE.	Missing both OR and beta
GCST90020042	Shared genetic study gives insights into the shared and distinct pathogenic immunity components of IgA nephropathy and SLE.	Missing both OR and beta
GCST90020047	Genetic variants of CYP4F12 gene are associated with glioma susceptibility.	Missing both OR and beta
GCST90020050	Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease.	Missing both OR and beta
GCST90020054	Genome-wide association study identifies multiple genetic loci for skin color in Korean women.	Missing both OR and beta
GCST90020091	Genome-Wide Association Study of Estradiol Levels, and the Causal Effect of Estradiol on Bone Mineral Density.	Missing both OR and beta
GCST90020092	Genome-Wide Association Study of Estradiol Levels, and the Causal Effect of Estradiol on Bone Mineral Density.	Missing both OR and beta
GCST90020093	Novel loci and potential mechanisms of major depressive disorder, bipolar disorder, and schizophrenia.	Missing both OR and beta
GCST90020094	Novel loci and potential mechanisms of major depressive disorder, bipolar disorder, and schizophrenia.	Missing both OR and beta
GCST90020095	Novel loci and potential mechanisms of major depressive disorder, bipolar disorder, and schizophrenia.	Missing both OR and beta
GCST90020240	Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90020241	Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India.	Missing both OR and beta
GCST90020242	Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India.	Missing both OR and beta
GCST90025849	Genome-Wide Association Study of Korean Asthmatics: A Comparison With UK Asthmatics.	Missing both OR and beta
GCST90025853	Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90025855	Genome-wide association study identifies susceptibility loci of brain atrophy to NFIA and ST18 in Alzheimer's disease.	Missing both OR and beta
GCST90025856	Genome-wide association study identifies susceptibility loci of brain atrophy to NFIA and ST18 in Alzheimer's disease.	Missing both OR and beta
GCST90025873	Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans.	Missing both OR and beta
GCST90025928	Genome Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary Incontinence.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90025929	Genome Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary Incontinence.	Missing both OR and beta
GCST90025937	Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90025945	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025947	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025948	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025949	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025951	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025952	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025953	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025954	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025955	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025956	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025957	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025958	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025959	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025960	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025961	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025962	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025963	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025964	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025965	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025966	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025969	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025970	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025972	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025973	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025974	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025976	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025979	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025980	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025983	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025986	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025987	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025988	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025989	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025990	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025992	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025993	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90025995	Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.	Missing both OR and beta
GCST90026409	Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026410	Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026411	Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026454	A genome-wide association study identifies novel susceptibility loci in chronic Chagas cardiomyopathy.	Missing both OR and beta
GCST90026455	Genome wide association study of HTLV-1-associated myelopathy/tropical spastic paraparesis in the Japanese population.	Missing both OR and beta
GCST90026457	Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS).	Missing both OR and beta
GCST90026458	Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026459	Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026460	Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS).	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026484	Genome-wide association study of stimulant dependence.	Missing both OR and beta
GCST90026486	Genome-wide association study of stimulant dependence.	Missing both OR and beta
GCST90026516	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	Missing both OR and beta
GCST90026518	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	Missing both OR and beta
GCST90026524	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	Missing both OR and beta
GCST90026526	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	Missing both OR and beta
GCST90026537	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026541	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026542	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026545	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026546	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026548	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026549	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026551	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026552	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026553	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026554	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026556	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026560	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026562	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026563	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026564	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026568	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026570	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026571	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026572	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026574	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026575	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026578	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026579	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026580	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026581	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026584	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026587	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026590	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026591	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026593	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026595	A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation.	Missing both OR and beta
GCST90026601	Potential Novel Genes for Late-Onset Alzheimer's Disease in East-Asian Descent Identified by APOE-Stratified Genome-Wide Association Study.	Missing both OR and beta
GCST90026610	Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90026648	Associations between pancreatic expression quantitative traits and risk of pancreatic ductal adenocarcinoma.	Missing both OR and beta
GCST90026656	Insomnia affects the levels of plasma bilirubin and protein metabolism: an observational study and GWGEIS in UK Biobank cohort.	Missing both OR and beta
GCST90026657	Insomnia affects the levels of plasma bilirubin and protein metabolism: an observational study and GWGEIS in UK Biobank cohort.	Missing both OR and beta
GCST90026658	Insomnia affects the levels of plasma bilirubin and protein metabolism: an observational study and GWGEIS in UK Biobank cohort.	Missing both OR and beta
GCST90027021	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027022	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027023	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	Missing both OR and beta
GCST90027024	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027025	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027026	A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027051	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027052	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027053	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027054	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027056	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027057	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027058	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027059	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027060	Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.	Missing both OR and beta
GCST90027075	Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027076	Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027077	Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027161	Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis.	Missing both OR and beta
GCST90027203	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027204	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027205	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027206	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027207	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027208	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027209	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027210	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027211	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027212	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027213	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027222	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027223	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027224	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027225	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027226	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027227	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027228	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027229	Key genetic variants associated with variation of milk oligosaccharides from diverse human populations.	Missing both OR and beta
GCST90027236	A genome-wide association study of nausea incidence in varenicline-treated cigarette smokers.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027239	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90027240	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90027241	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90027242	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90027243	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90027244	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90027246	Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.	Missing both OR and beta
GCST90027247	Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.	Missing both OR and beta
GCST90027248	Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.	Missing both OR and beta
GCST90027251	Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.	Missing both OR and beta
GCST90027270	Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027271	Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027899	A genome-wide association meta-analysis identifies new Eosinophilic esophagitis loci.	Missing both OR and beta
GCST90027902	A genome-wide association study of quantitative computed tomographic emphysema in Korean populations.	Missing both OR and beta
GCST90027903	A genome-wide association study of quantitative computed tomographic emphysema in Korean populations.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90027904	Sex-specific genetic factors affect the risk of early-onset periodontitis in Europeans.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90029044	Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.	Missing both OR and beta
GCST90029059	Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.	Missing both OR and beta
GCST90029067	Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population.	Missing both OR and beta
GCST90029118	Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.	Missing both OR and beta
GCST90032159	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90032160	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90032161	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90032162	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90032163	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90032164	Multivariate genome-wide analysis of education, socioeconomic status and brain phenome.	Missing both OR and beta
GCST90032654	Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank.	Missing both OR and beta
GCST90032655	Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank.	Missing both OR and beta
GCST90032657	Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank.	Missing both OR and beta
GCST90032658	Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank.	Missing both OR and beta
GCST90032659	Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank.	Missing both OR and beta
GCST90032663	Human genomics of the humoral immune response against polyomaviruses.	Missing both OR and beta
GCST90032665	Human genomics of the humoral immune response against polyomaviruses.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90032666	Human genomics of the humoral immune response against polyomaviruses.	Missing both OR and beta
GCST90032667	Human genomics of the humoral immune response against polyomaviruses.	Missing both OR and beta
GCST90032668	Human genomics of the humoral immune response against polyomaviruses.	Missing both OR and beta
GCST90032669	Human genomics of the humoral immune response against polyomaviruses.	Missing both OR and beta
GCST90032670	Human genomics of the humoral immune response against polyomaviruses.	Missing MAPPED_TRAIT_URI ; Missing both OR and beta
GCST90034520	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90034521	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90034522	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90034523	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90034524	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90034525	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90034526	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90034527	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90034528	Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.	Missing both OR and beta
GCST90038451	Similar Genetic Architecture of Alzheimer's Disease and Differential <i>APOE</i> Effect Between Sexes.	Missing both OR and beta
GCST90038452	Similar Genetic Architecture of Alzheimer's Disease and Differential <i>APOE</i> Effect Between Sexes.	Missing both OR and beta
GCST90038468	Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort.	Missing both OR and beta
GCST90038594	Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease.	Missing both OR and beta
GCST90044699	A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.	Missing both OR and beta
GCST90044778	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044780	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044788	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044791	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044795	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044798	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044804	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044805	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044807	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044817	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044818	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044820	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044825	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044829	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044831	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044836	Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations.	Missing both OR and beta
GCST90044847	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	Missing MAPPED_TRAIT_URI ; P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044849	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044850	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044855	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044859	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044860	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	Missing both OR and beta
GCST90044861	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044863	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044865	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044868	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	Missing both OR and beta
GCST90044870	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044871	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044872	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044873	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	Missing both OR and beta
GCST90044879	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044880	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	Missing both OR and beta
GCST90044884	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044887	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044888	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	Missing both OR and beta
GCST90044889	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044890	High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044891	Genetic predisposition to tinnitus in the UK Biobank population.	Missing both OR and beta
GCST90044892	Genetic predisposition to tinnitus in the UK Biobank population.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90044907	Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90052899	Novel recessive locus for body mass index in childhood asthma.	Missing both OR and beta
GCST90053834	Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia.	Missing both OR and beta
GCST90053835	Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia.	Missing both OR and beta
GCST90053836	Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia.	Missing both OR and beta
GCST90053837	A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer.	P-value fails significance threshold (5e-08) (mlog=7.3) ; Missing both OR and beta
GCST90053855	Genome-wide Association Study Identified Chromosome 8 Locus Associated with Medication-related Osteonecrosis of the Jaw.	Missing both OR and beta
GCST90054786	A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.	Missing both OR and beta
GCST90054787	A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.	Missing both OR and beta
GCST90054788	A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.	Missing both OR and beta
GCST90054789	A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.	Missing both OR and beta
GCST90054790	A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.	Missing both OR and beta
GCST90054791	A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.	Missing both OR and beta
GCST90056174	Assessing the impact of alcohol consumption on the genetic contribution to mean corpuscular volume.	Missing both OR and beta
GCST90085695	Overlapping common genetic architecture between major depressive disorders and anxiety and stress-related disorders.	Missing both OR and beta
GCST90085696	Overlapping common genetic architecture between major depressive disorders and anxiety and stress-related disorders.	Missing both OR and beta
GCST90085697	Overlapping common genetic architecture between major depressive disorders and anxiety and stress-related disorders.	Missing both OR and beta