Complement factor H polymorphism in age-related macular degeneration.
HTRA1 promoter polymorphism in wet age-related macular degeneration.
A genome-wide association study identifies novel risk loci for type 2 diabetes.
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.
A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease.
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.
Genome-wide association study identifies novel breast cancer susceptibility loci.
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.
Variants conferring risk of atrial fibrillation on chromosome 4q25.
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.
Genomewide association analysis of coronary artery disease.
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.
A genetic risk factor for periodic limb movements in sleep.
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.
Risk alleles for multiple sclerosis identified by a genomewide study.
Systematic association mapping identifies NELL1 as a novel IBD disease gene.
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.
A common variant of HMGA2 is associated with adult and childhood height in the general population.
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk.
A genomewide association study of skin pigmentation in a South Asian population.
Genetic determinants of hair, eye and skin pigmentation in Europeans.
Genetic determinants of hair, eye and skin pigmentation in Europeans.
Genetic determinants of hair, eye and skin pigmentation in Europeans.
Genetic determinants of hair, eye and skin pigmentation in Europeans.
Genetic determinants of hair, eye and skin pigmentation in Europeans.
Genetic determinants of hair, eye and skin pigmentation in Europeans.
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts.
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.
Common variants in the GDF5-UQCC region are associated with variation in human height.
Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study.
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
Sequence variants in the RNF212 gene associate with genome-wide recombination rate.
Sequence variants in the RNF212 gene associate with genome-wide recombination rate.
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
LDL-cholesterol concentrations: a genome-wide association study.
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer.
Multiple loci identified in a genome-wide association study of prostate cancer.
Multiple newly identified loci associated with prostate cancer susceptibility.
Newly identified genetic risk variants for celiac disease related to the immune response.
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout.
SLC2A9 influences uric acid concentrations with pronounced sex-specific effects.
Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.
Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene.
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci.
Genome-wide association analysis identifies 20 loci that influence adult height.
Many sequence variants affecting diversity of adult human height.
Identification of ten loci associated with height highlights new biological pathways in human growth.
Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function.
Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.
Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.
Multiple genetic loci for bone mineral density and fractures.
Multiple genetic loci for bone mineral density and fractures.
Common variants near MC4R are associated with fat mass, weight and risk of obesity.
Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
Two newly identified genetic determinants of pigmentation in Europeans.
Two newly identified genetic determinants of pigmentation in Europeans.
Common sequence variants on 20q11.22 confer melanoma susceptibility.
Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.
A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels.
Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis.
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.
SLCO1B1 variants and statin-induced myopathy--a genomewide study.
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations.
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus.
A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.
Common variants of FUT2 are associated with plasma vitamin B12 levels.
Common variants at CD40 and other loci confer risk of rheumatoid arthritis.
Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.
Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13.
Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.
A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis.
Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.
Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.
Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.
Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.
Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.
Common 5p15.33 and 6p21.33 variants influence lung cancer risk.
Lung cancer susceptibility locus at 5p15.33.
Susceptibility loci for intracranial aneurysm in European and Japanese populations.
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.
Variants in MTNR1B influence fasting glucose levels.
Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.
Common variants at 30 loci contribute to polygenic dyslipidemia.
Common variants at 30 loci contribute to polygenic dyslipidemia.
Common variants at 30 loci contribute to polygenic dyslipidemia.
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
New sequence variants associated with bone mineral density.
New sequence variants associated with bone mineral density.
Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.
Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.
Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.
A genome-wide association study identifies three loci associated with mean platelet volume.
Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.
Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q.
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.
Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.
Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21.
Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.
Variant in the sequence of the LINGO1 gene confers risk of essential tremor.
Genome-wide association study of biochemical traits in Korcula Island, Croatia.
Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
New susceptibility locus for coronary artery disease on chromosome 3q22.3.
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.
A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function.
Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
Genome-wide association and replication studies identified TRHR as an important gene for lean body mass.
Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.
A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms.
Common variants at ten loci influence QT interval duration in the QTGEN Study.
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).
Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.
Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.
COL4A1 is associated with arterial stiffness by genome-wide association scan.
Genome-wide association study of tanning phenotype in a population of European ancestry.
Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.
A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.
A common variant on chromosome 11q13 is associated with atopic dermatitis.
Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study.
Genomewide association studies of stroke.
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits.
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population.
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
Narcolepsy is strongly associated with the T-cell receptor alpha locus.
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.
Genome-wide association meta-analysis for total serum bilirubin levels.
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene.
Genome-wide association study of blood pressure and hypertension.
Genome-wide association study of blood pressure and hypertension.
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.
Genome-wide association study identifies eight loci associated with blood pressure.
Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.
Loci at chromosomes 13, 19 and 20 influence age at natural menopause.
Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.
Genetic variation in LIN28B is associated with the timing of puberty.
Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.
Genome-wide and fine-resolution association analysis of malaria in West Africa.
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.
A genome-wide association study of testicular germ cell tumor.
Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer.
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.
REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.
Common body mass index-associated variants confer risk of extreme obesity.
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
Common variants conferring risk of schizophrenia.
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Common variants on chromosome 6p22.1 are associated with schizophrenia.
Genome-wide association study of alcohol dependence.
Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease.
Genome-wide association study identifies five susceptibility loci for glioma.
Genome-wide association study identifies three loci associated with melanoma risk.
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.
Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer.
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.
Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European Caucasians.
Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.
Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3.
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.
Germline genomic variants associated with childhood acute lymphoblastic leukemia.
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.
Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk.
Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs.
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.
Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.
Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C.
IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy.
Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.
Genetic determinants of circulating sphingolipid concentrations in European populations.
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.
Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus.
Sequence variants in three loci influence monocyte counts and erythrocyte volume.
Sequence variants in three loci influence monocyte counts and erythrocyte volume.
Sequence variants in three loci influence monocyte counts and erythrocyte volume.
A genome-wide association analysis of serum iron concentrations.
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus.
Common variants in the trichohyalin gene are associated with straight hair in Europeans.
A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis.
Germline genetic variation in an organic anion transporter polypeptide associated with methotrexate pharmacokinetics and clinical effects.
A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population.
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.
Genome-wide association study reveals genetic risk underlying Parkinson's disease.
Common variants at five new loci associated with early-onset inflammatory bowel disease.
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.
A genome-wide association identified the common genetic variants  influence disease severity in beta0-thalassemia/hemoglobin E.
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals.
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.
Genome-wide association study identifies five loci associated with lung function.
Genomewide association study of leprosy.
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.
Variants of DENND1B associated with asthma in children.
Common genetic variation and the control of HIV-1 in humans.
A genome-wide perspective of genetic variation in human metabolism.
Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.
Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.
Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study.
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis.
Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels.
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.
Genetic variation in SCN10A influences cardiac conduction.
Several common variants modulate heart rate, PR interval and QRS duration.
Genome-wide association study of PR interval.
A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor.
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.
Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.
A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.
Common variants near TERC are associated with mean telomere length.
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Genome-wide association study of hematological and biochemical traits in a Japanese population.
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus.
Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults.
Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count.
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.
A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.
Common variants in KCNN3 are associated with lone atrial fibrillation.
Variants in FAM13A are associated with chronic obstructive pulmonary disease.
Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes.
Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels.
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci.
Multiple common variants for celiac disease influencing immune gene expression.
Common variants at 5q22 associate with pediatric eosinophilic esophagitis.
Genome-wide association identifies multiple ulcerative colitis susceptibility loci.
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).
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.
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.
Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.
New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study.
A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.
Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.
Genome-wide association study of height and body mass index in Australian twin families.
Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.
Genome-wide association study of intracranial aneurysm identifies three new risk loci.
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).
Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.
Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.
Genome-wide association study of circulating vitamin D levels.
Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes.
Meta-analysis and imputation refines the association of 15q25 with smoking quantity.
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.
Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.
Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.
Genome-wide association study identifies five new breast cancer susceptibility loci.
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis.
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility.
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.
Genome-wide analysis of genetic loci associated with Alzheimer disease.
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.
Digital quantification of human eye color highlights genetic association of three new loci.
A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC.
Genetic regulation of serum phytosterol levels and risk of coronary artery disease.
Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.
A genome-wide association study of optic disc parameters.
A genome-wide association study of optic disc parameters.
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.
Common genetic variants associate with serum phosphorus concentration.
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.
Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium.
Genome-wide association study of conduct disorder symptomatology.
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.
Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.
HLA has strongest association with IgA nephropathy in genome-wide analysis.
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.
Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.
Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci.
Genome-wide association analysis identifies multiple loci related to resting heart rate.
Genome-wide association of serum bilirubin levels in Korean population.
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.
A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury.
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.
Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene.
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.
Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.
A genome-wide scan for common alleles affecting risk for autism.
Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.
Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers.
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population.
Biological, clinical and population relevance of 95 loci for blood lipids.
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.
The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia.
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.
Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease.
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.
Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy.
A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population.
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.
Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.
E2-2 protein and Fuchs's corneal dystrophy.
Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma.
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.
Identification of new genetic risk variants for type 2 diabetes.
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.
Common variants at 10 genomic loci influence hemoglobin Aâ(C) levels via glycemic and nonglycemic pathways.
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.
Genetic variants influencing circulating lipid levels and risk of coronary artery disease.
Genetic variants influencing circulating lipid levels and risk of coronary artery disease.
Genetic variants influencing circulating lipid levels and risk of coronary artery disease.
A large-scale, consortium-based genomewide association study of asthma.
Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations.
A combined analysis of genome-wide association studies in breast cancer.
Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ.
A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population.
Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.
Adiponectin concentrations: a genome-wide association study.
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis.
Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2.
Genome-wide association analysis identifies three psoriasis susceptibility loci.
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.
Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
Genetic predictors of medically refractory ulcerative colitis.
ELF1 is associated with systemic lupus erythematosus in Asian populations.
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.
PCSK6 is associated with handedness in individuals with dyslexia.
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.
Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone.
Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity.
Common variants in DGKK are strongly associated with risk of hypospadias.
Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.
Integrative genomics identifies LMO1 as a neuroblastoma oncogene.
Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.
Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.
Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci.
Genetic correction of PSA values using sequence variants associated with PSA levels.
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes.
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus.
Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.
Genome-wide association study of serious blistering skin rash caused by drugs.
Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study.
IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations.
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population.
Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.
Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.
Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.
Common variants in ZNF365 are associated with both mammographic density and breast cancer risk.
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
A genome-wide association study of serum uric acid in African Americans.
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.
Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area.
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.
Genome-wide association studies of the PR interval in African Americans.
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.
Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.
CUBN is a gene locus for albuminuria.
Association of intronic sequence variant in the gene encoding spleen tyrosine kinase with susceptibility to vascular dementia.
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.
Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population.
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits.
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
Genome-wide association study identifies susceptibility loci for IgA nephropathy.
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.
Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited.
A genome-wide association study of attempted suicide.
Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci.
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption.
Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.
Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.
Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles.
Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.
Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma.
Genome-wide association study identifies a common variant associated with risk of endometrial cancer.
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.
Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients.
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.
GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma.
Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci.
Chromosome 7p11.2 (EGFR) variation influences glioma risk.
Genome-wide association study implicates PARD3B-based AIDS restriction.
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.
A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia.
A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility.
Genome-wide association study of relative telomere length.
Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas.
Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese.
Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21.
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease.
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.
Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations.
Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels.
Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment.
Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C.
Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore.
Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.
GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population.
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease.
Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.
Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma.
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.
Genome wide association study identifies KCNMA1 contributing to human obesity.
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population.
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.
Multiple loci are associated with white blood cell phenotypes.
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese.
Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers.
Genome-wide association study identifies common variants associated with circulating vitamin E levels.
Wnt signaling and Dupuytren's disease.
Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.
Genome-wide association study identifies new prostate cancer susceptibility loci.
Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.
European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.
A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population.
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.
Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease.
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA region.
Meta-analysis of new genome-wide association studies of colorectal cancer risk.
A genome-wide association study reveals a quantitative trait locus of adiponectin on CDH13 that predicts cardiometabolic outcomes.
Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations.
A genome-wide association study confirms previously reported loci for type 2 diabetes in Han Chinese.
Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations.
Genome-wide association study of epirubicin-induced leukopenia in Japanese patients.
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.
Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population.
Common variation at 10p12.31 near MLLT10 influences meningioma risk.
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.
A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3.
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.
A genome-wide association study identifies two new risk loci for Graves' disease.
Common variants at the promoter region of the APOM confer a risk of rheumatoid arthritis.
GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors.
A variant in MCF2L is associated with osteoarthritis.
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.
Genome-wide association study of circulating retinol levels.
Human metabolic individuality in biomedical and pharmaceutical research.
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
Genome-wide association study identifies four loci associated with eruption of permanent teeth.
A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection.
Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium.
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.
Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population.
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.
A whole-genome association study of major determinants for allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients.
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.
Genome-wide association study identifies five new schizophrenia loci.
Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.
Genetics of venous thrombosis: insights from a new genome wide association study.
A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.
A genome-wide association study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that affects disease progression of chronic HBV infection.
Mutations in BRIP1 confer high risk of ovarian cancer.
Genome-wide association study of coronary artery disease in the Japanese.
Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry.
Genetic determinants of serum testosterone concentrations in men.
A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
Genome-wide association study identifies three new melanoma susceptibility loci.
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
Identification of low-frequency variants associated with gout and serum uric acid levels.
Identification of low-frequency variants associated with gout and serum uric acid levels.
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1.
A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.
Genome-wide association study of Alzheimer's disease with psychotic symptoms.
Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.
Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe).
A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.
Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy.
Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2.
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.
A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1.
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer.
Loci affecting gamma-glutamyl transferase in adults and adolescents show age Ã SNP interaction and cardiometabolic disease associations.
A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.
A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.
Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.
Clinical and genetic association of serum ceruloplasmin with cardiovascular risk.
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.
Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.
UGT1A1 is a major locus influencing bilirubin levels in African Americans.
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function.
New gene functions in megakaryopoiesis and platelet formation.
New gene functions in megakaryopoiesis and platelet formation.
Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.
Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism.
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis.
A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303.
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.
Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults.
Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL.
A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese.
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.
A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy.
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.
Genome-wide associated loci influencing interleukin (IL)-10, IL-1Ra, and IL-6 levels in African Americans.
Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.
A genome-wide association study of gestational diabetes mellitus in Korean women.
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.
Discovery of common variants associated with low TSH levels and thyroid cancer risk.
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese.
Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.
Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups.
Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
Association of glycosylated hemoglobin with the gene encoding CDKAL1 in the Korean Association Resource (KARE) study.
1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.
1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.
Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.
Common variants at 11p13 are associated with susceptibility to tuberculosis.
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.
Genetic association of short sleep duration with hypertension incidence--a 6-year follow-up in the Korean genome and epidemiology study.
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.
Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position.
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.
Meta-analysis identifies common variants associated with body mass index in east Asians.
Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer.
Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men.
Genome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a).
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1.
A genome-wide association study identifies two susceptibility loci for duodenal ulcer in the Japanese population.
A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels.
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.
Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese.
Genome-wide association study of lung function decline in adults with and without asthma.
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population.
A genome-wide association study identifies three new risk loci for Kawasaki disease.
Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.
A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.
A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations.
A genome-wide association study in progressive multiple sclerosis.
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
Genome-wide association and functional follow-up reveals new loci for kidney function.
C-reactive protein (CRP) promoter polymorphisms influence circulating CRP levels in a genome-wide association study of African Americans.
Novel associations for hypothyroidism include known autoimmune risk loci.
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.
A genome-wide association meta-analysis identifies new childhood  obesity loci.
A genome-wide association study identifies UGT1A1 as a regulator of serum cell-free DNA in young adults: The Cardiovascular Risk in Young Finns Study.
Common variants at 12q15 and 12q24 are associated with infant head circumference.
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
Identification of common variants associated with human hippocampal and intracranial volumes.
Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Common variants at 6q22 and 17q21 are associated with intracranial volume.
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.
Fasting glucose GWAS candidate region analysis across ethnic groups in the Multiethnic Study of Atherosclerosis (MESA).
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
A genome-wide association study identifies susceptibility loci for Wilms tumor.
Human genome-wide association and mouse knockout approaches identify platelet supervillin as an inhibitor of thrombus formation under shear stress.
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.
Common genetic determinants of intraocular pressure and primary open-angle glaucoma.
Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.
Genome-wide association study to identify genetic determinants of severe asthma.
Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
Genome-wide association and functional studies identify the DOT1L gene to be involved in cartilage thickness and hip osteoarthritis.
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
Genome-wide association study of Alzheimer's disease.
Genome-wide meta-analyses of smoking behaviors in African Americans.
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
Genome-wide association analysis identifies susceptibility loci for migraine without aura.
Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese.
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.
Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis.
Genome-wide association study confirming association of HLA-DP with protection against chronic hepatitis B and viral clearance in Japanese and Korean.
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study.
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk.
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk.
Common variants on chromosome 9p21 are associated with normal tension glaucoma.
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus.
GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers.
Genome-wide association study identifies novel loci association with fasting insulin and insulin resistance in African Americans.
Genetic associations with C-reactive protein level and white blood cell count in the KARE study.
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population.
Risk for myasthenia gravis maps to a (151) ProâAla change in TNIP1 and to human leukocyte antigen-B*08.
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.
Genetically distinct subsets within ANCA-associated vasculitis.
Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness.
Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4.
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.
Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels.
A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1.
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.
Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia.
Genome-wide association study of glioma and meta-analysis.
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome.
Genome-wide association study of Tourette's syndrome.
Genome-wide association study indicates two novel resistance loci for severe malaria.
Genome-wide association identifies genetic variants associated with lentiform nucleus volume in Nâ=â1345 young and elderly subjects.
Genetic variation in the vaspin gene affects circulating serum vaspin concentrations.
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.
Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma.
Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants.
A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population.
A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.
Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk.
Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis.
Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs.
Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions.
Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions.
FTO genotype is associated with phenotypic variability of body mass index.
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.
Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese.
Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects.
Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.
Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population.
Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.
Clinical and genetic correlates of growth differentiation factor 15 in the community.
New susceptibility loci associated with kidney disease in type 1 diabetes.
Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.
Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.
Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4.
A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.
Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis.
A genome-wide association study of circulating galectin-3.
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.
Mining the unknown: a systems approach to metabolite identification combining genetic and metabolic information.
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese.
Genome-wide association meta-analysis identifies new endometriosis risk loci.
Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations.
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.
Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.
Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene.
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts.
Preliminary evidence of genetic determinants of adiponectin response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network.
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia.
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.
Variant of TREM2 associated with the risk of Alzheimer's disease.
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.
Impact of ancestry and common genetic variants on QT interval in African Americans.
Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer.
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis.
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis.
Seven newly identified loci for autoimmune thyroid disease.
Seven newly identified loci for autoimmune thyroid disease.
Seven newly identified loci for autoimmune thyroid disease.
New loci associated with birth weight identify genetic links between intrauterine             growth and adult height and metabolism.
Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing.
Seventy-five genetic loci influencing the human red blood cell.
Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.
Genome-wide study of methotrexate clearance replicates SLCO1B1.
Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma.
Genome-wide association study pinpoints a new functional apolipoprotein B variant influencing oxidized low-density lipoprotein levels but not cardiovascular events: AtheroRemo Consortium.
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer.
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
Genome-wide association study identified novel genetic variant on SLC45A3 gene associated with serum levels prostate-specific antigen (PSA) in a Chinese population.
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians.
ImmunoChip study implicates antigen presentation to T cells in narcolepsy.
Genome-wide association study identifies loci at ATF7IP and KLK2 associated with percentage of circulating free PSA.
Genetic determinants of plasma βâ-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.
A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans.
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.
A genome wide association study of genetic loci that influence tumour biomarkers cancer antigen 19-9, carcinoembryonic antigen and α fetoprotein and their associations with cancer risk.
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India.
A genome-wide association study of early menopause and the combined impact of identified variants.
Genome-wide association study of serum albumin:globulin ratio in Korean populations.
A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).
Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.
A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region.
Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
Genome-wide significant locus of beta-trace protein, a novel kidney function biomarker, identified in European and African Americans.
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese.
Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.
Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture.
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
Novel locus including FGF21 is associated with dietary macronutrient intake.
Common variants at 12q24 are associated with drinking behavior in Han Chinese.
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population.
A genome-wide association study of a coronary artery disease risk variant.
A comprehensive family-based replication study of schizophrenia genes.
Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.
Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study.
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans.
Genetic determinants of haemolysis in sickle cell anaemia.
Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.
Genetic associations with valvular calcification and aortic stenosis.
Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts.
A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.
Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.
A genome-wide association study of recipient genotype and medium-term kidney allograft function.
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.
Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.
NKAIN1-SERINC2 is a functional, replicable and genome-wide significant risk gene region specific for alcohol dependence in subjects of European descent.
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.
Extended genetic effects of ADH cluster genes on the risk of alcohol dependence: from GWAS to replication.
Seven new loci associated with age-related macular degeneration.
Genome-wide association study in Han Chinese identifies three novel loci for human height.
A variant in FTO shows association with melanoma risk not due to BMI.
Genetic variation associated with circulating monocyte count in the eMERGE Network.
Genome-wide association study link novel loci to endometriosis.
Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
Genome-wide association study of susceptibility loci for cervical cancer.
Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction.
A genome-wide association study of central corneal thickness in Latinos.
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension.
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations.
TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk.
Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan.
Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
Genome-wide association studies identify four ER negative-specific breast cancer risk loci.
Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians.
Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
Identification of seven loci affecting mean telomere length and their association with disease.
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.
SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians.
GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease.
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm.
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.
New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population.
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
Genome-wide association study of age at menarche in African-American women.
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis.
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.
Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis.
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.
Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.
Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.
Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.
Three new single nucleotide polymorphisms identified by a genome-wide association study in Korean patients with vitiligo.
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Genome-wide association study identifies common variants in SLC39A6 associated with length of survival in esophageal squamous-cell carcinoma.
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.
Identification of genetic loci associated with Helicobacter pylori serologic status.
Meta-analysis identifies four new loci associated with testicular germ cell tumor.
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.
Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis.
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.
Genetic modifiers of cystic fibrosis-related diabetes.
Identification of KCNN2 as a susceptibility locus for coronary artery aneurysms in Kawasaki disease using genome-wide association analysis.
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.
Imputation-based meta-analysis of severe malaria in three African populations.
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
Genome-wide association study identifies a region on chromosome 11q14.3 associated with late rectal bleeding following radiation therapy for prostate cancer.
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations.
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations.
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations.
Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.
Genome-wide association study identifies two susceptibility loci for osteosarcoma.
High-density genotyping study identifies four new susceptibility loci for atopic dermatitis.
A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Genome-wide meta-analysis identifies new susceptibility loci for migraine.
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization.
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12.
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci.
Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore?
Identification of multiple genetic susceptibility loci in Takayasu arteritis.
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus.
Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls.
Genome-wide association study on differentiated thyroid cancer.
A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk.
Identification of regions associated with variation in sensitivity to food-related odors in the human genome.
Identification of regions associated with variation in sensitivity to food-related odors in the human genome.
Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies.
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study.
Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study.
A genome-wide association study of behavioral disinhibition.
Genome-wide association study identifies three novel loci for type 2 diabetes.
Genome-wide association of body fat distribution in African ancestry populations suggests new loci.
Genome-wide association of body fat distribution in African ancestry populations suggests new loci.
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics.
Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
A genome-wide association study of chronic otitis media with effusion and recurrent otitis media identifies a novel susceptibility locus on chromosome 2.
Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes.
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip.
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype.
Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis.
Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis.
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling.
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Genetic association with lipids in Filipinos: waist circumference modifies an APOA5 effect on triglyceride levels.
A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
Common variants on Xq28 conferring risk of schizophrenia in Han Chinese.
A variant in LDLR is associated with abdominal aortic aneurysm.
Genome-wide association study of sex hormones, gonadotropins and sex hormone-binding protein in Chinese men.
Genome-wide association study of sex hormones, gonadotropins and sex hormone-binding protein in Chinese men.
Genome-wide association study of ancestry-specific TB risk in the South African Coloured population.
Genome-wide association study identifies 3 genomic loci significantly associated with serum levels of homoarginine: the AtheroRemo Consortium.
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
Genome-wide association study on serum alkaline phosphatase levels in a Chinese population.
Discovery and refinement of loci associated with lipid levels.
Discovery and refinement of loci associated with lipid levels.
Discovery and refinement of loci associated with lipid levels.
Discovery and refinement of loci associated with lipid levels.
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23.
A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes.
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity.
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity.
Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant.
A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.
A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2.
Genome-wide association study of breast cancer in the Japanese population.
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia.
Genome-wide association study identifies multiple loci associated with bladder cancer risk.
Genome-wide association study identifies multiple loci associated with bladder cancer risk.
New loci associated with chronic hepatitis B virus infection in Han Chinese.
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.
Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults.
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic.
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic.
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic.
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome.
A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry.
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.
Multistage genome-wide association meta-analyses identified two new loci for bone mineral density.
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
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.
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.
A genome-wide association study identifies polymorphisms in the HLA-DR region associated with non-response to hepatitis B vaccination in Chinese Han populations.
A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians.
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children.
Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: the Long Life Family Study (LLFS).
Genome-wide association study for levels of total serum IgE identifies HLA-C in a Japanese population.
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants.
Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.
FUT2: filling the gap between genes and environment in Behçet's disease?
An integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri Lanka.
An integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri Lanka.
HLA-DQB1*03 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study.
Genetics of rheumatoid arthritis contributes to biology and drug discovery.
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.
Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study.
Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype.
A genome wide association study identifies common variants associated with lipid levels in the Chinese population.
Genome-wide association study of proneness to anger.
Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci.
Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci.
Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study.
Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis.
Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis.
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study.
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne.
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Genome-wide association study identifies a new SMAD7 risk variant associated with colorectal cancer risk in East Asians.
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Identification of a novel Parkinson's disease locus via stratified genome-wide association study.
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population.
High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci.
A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides.
Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links.
Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384.
Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384.
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.
ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma.
Genome-wide association study reveals two new risk loci for bipolar disorder.
Genetic determinants influencing human serum metabolome among African Americans.
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians.
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke.
IgA measurements in over 12 000 Swedish twins reveal sex differential heritability and regulatory locus near CD30L.
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.
A central role for GRB10 in regulation of islet function in man.
A central role for GRB10 in regulation of islet function in man.
A central role for GRB10 in regulation of islet function in man.
A central role for GRB10 in regulation of islet function in man.
A central role for GRB10 in regulation of islet function in man.
A central role for GRB10 in regulation of islet function in man.
Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study.
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
Genome-wide association scan for variants associated with early-onset prostate cancer.
Genome-wide association study of circulating vitamin D-binding protein.
A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.
A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.
Genome-wide diet-gene interaction analyses for risk of colorectal cancer.
Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies.
Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies.
Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.
New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis.
Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty.
Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty.
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology.
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans.
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans.
Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort.
An atlas of genetic influences on human blood metabolites.
An atlas of genetic influences on human blood metabolites.
Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease.
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium.
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium.
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium.
Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis.
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
Genetic determinants of P wave duration and PR segment.
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index.
GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.
Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk.
A genome-wide association study of serum levels of prostate-specific antigen in the Japanese population.
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families.
A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus.
Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
Genome-wide association analysis identifies six new loci associated with forced vital capacity.
A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese.
Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population.
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract.
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.
CMPK1 and RBP3 are associated with corneal curvature in Asian populations.
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.
A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1.
Identification of a melanoma susceptibility locus and somatic mutation in TET2.
Frontotemporal dementia and its subtypes: a genome-wide association study.
Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.
The correlation between reading and mathematics ability at age twelve has a substantial genetic component.
Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.
Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.
SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.
Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects, and an increased risk for chronic pancreatitis: a genetic association study.
Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects, and an increased risk for chronic pancreatitis: a genetic association study.
Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative.
Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians.
Genome-wide association study of hepatitis C virus- and cryoglobulin-related vasculitis.
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1.
Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3.
Biological insights from 108 schizophrenia-associated genetic loci.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing.
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine.
Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels.
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.
A genome-wide association study identifies a novel locus at 6q22.1 associated with ulcerative colitis.
Intrinsic and extrinsic risk factors for sagging eyelids.
Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis.
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer.
Genetic variation modifies risk for neurodegeneration based on biomarker status.
Trans-ethnic meta-analysis of white blood cell phenotypes.
Trans-ethnic meta-analysis of white blood cell phenotypes.
Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial.
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.
Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A.
Genome-wide association analyses identify variants in developmental genes associated with hypospadias.
A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopenia.
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
Genetic variant predicts bevacizumab-induced hypertension in ECOG-5103 and ECOG-2100.
Immunochip identifies novel, and replicates known, genetic risk loci for rheumatoid arthritis in black South Africans.
Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations.
Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations.
Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults.
Genome-wide association study identifies new susceptibility loci for epithelial ovarian cancer in Han Chinese women.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs.
Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population.
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma.
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.
Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma.
Beyond cigarettes per day. A genome-wide association study of the biomarker carbon monoxide.
Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians.
Association between antinuclear antibodies and the HLA class II locus and heterogeneous characteristics of staining patterns: the Nagahama study.
Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population.
Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis.
Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis.
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method.
Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels.
CKM and LILRB5 are associated with serum levels of creatine kinase.
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.
HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants.
Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans.
A genome-wide association study identifies a LEPR gene as a novel predisposing factor for childhood fasting plasma glucose.
Common variation near ROBO2 is associated with expressive vocabulary in infancy.
Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine.
Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine.
Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine.
Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease.
Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease.
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma.
Common variants in the CRP promoter are associated with a high C-reactive protein level in Kawasaki disease.
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region.
A novel common variant in DCST2 is associated with length in early life and height in adulthood.
A novel common variant in DCST2 is associated with length in early life and height in adulthood.
Genome-wide association study identified SNP on 15q24 associated with bladder cancer risk in Japanese population.
Defining the role of common variation in the genomic and biological architecture of adult human height.
The contribution of common genetic variation to nicotine and cotinine glucuronidation in multiple ethnic/racial populations.
The contribution of common genetic variation to nicotine and cotinine glucuronidation in multiple ethnic/racial populations.
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens.
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures.
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25.
Common variants at 1p36 are associated with superior frontal gyrus volume.
Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.
Genome-wide association study of selenium concentrations.
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk.
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk.
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk.
Common variants associated with general and MMR vaccine-related febrile seizures.
Common variants associated with general and MMR vaccine-related febrile seizures.
Common variants associated with general and MMR vaccine-related febrile seizures.
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.
Genomic predictors of combat stress vulnerability and resilience in U.S. Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene.
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.
Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
Genetic markers associated with plasma protein C level in African Americans: the atherosclerosis risk in communities (ARIC) study.
Genetic loci associated with circulating levels of very long-chain saturated fatty acids.
Genetic loci associated with circulating levels of very long-chain saturated fatty acids.
Genetic loci associated with circulating levels of very long-chain saturated fatty acids.
Variation at HLA-DRB1 is associated with resistance to enteric fever.
FASTKD2 is associated with memory and hippocampal structure in older adults.
GWAS identifies four novel eosinophilic esophagitis loci.
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci.
Identification of a Hashimoto thyroiditis susceptibility locus via a genome-wide comparison with Graves' disease.
Genetic variants at 1q32.1, 10q11.2 and 19q13.41 are associated with prostate-specific antigen for prostate cancer screening in two Korean population-based cohort studies.
Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.
A genome-wide association study of saturated, mono- and polyunsaturated red blood cell fatty acids in the Framingham Heart Offspring Study.
A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults.
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study.
T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility.
Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.
Genome-wide association study of kidney function decline in individuals of European descent.
Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin.
Genome-wide association study for endothelial growth factors.
Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study.
Genome-wide association study of hepatitis in korean populations.
Genome-wide association study identifies candidate Loci associated with platelet count in koreans.
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans.
Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study.
Genome-wide association study identified new susceptibility loci for polycystic ovary syndrome.
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms.
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms.
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms.
A genome-wide association study of marginal zone lymphoma shows association to the HLA region.
Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols.
Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols.
Pharmacogenomic determinants of the cardiovascular effects of dalcetrapib.
Identification of six new susceptibility loci for invasive epithelial ovarian cancer.
A genome-wide association study of early spontaneous preterm delivery.
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study.
Common genetic variants influence human subcortical brain structures.
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci.
Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.
Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.
Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.
New loci and coding variants confer risk for age-related macular degeneration in East Asians.
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure.
Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy.
Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes.
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease.
IKZF1, a new susceptibility gene for cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis with severe mucosal involvement.
Genetic studies of body mass index yield new insights for obesity biology.
New genetic loci link adipose and insulin biology to body fat distribution.
New genetic loci link adipose and insulin biology to body fat distribution.
New genetic loci link adipose and insulin biology to body fat distribution.
New genetic loci link adipose and insulin biology to body fat distribution.
New genetic loci link adipose and insulin biology to body fat distribution.
New genetic loci link adipose and insulin biology to body fat distribution.
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.
A Genome-Wide Association Study Identifies the Skin Color Genes IRF4, MC1R, ASIP, and BNC2 Influencing Facial Pigmented Spots.
Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia.
Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.
Novel genes for airway wall thickness identified with combined genome-wide association and expression analyses.
IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease.
IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease.
IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease.
Whole-genome sequence-based analysis of thyroid function.
Whole-genome sequence-based analysis of thyroid function.
Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking.
Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism.
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy.
Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate.
Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration.
A novel Alzheimer disease locus located near the gene encoding tau protein.
A novel Alzheimer disease locus located near the gene encoding tau protein.
A novel Alzheimer disease locus located near the gene encoding tau protein.
Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease.
A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibility.
Modulation of genetic associations with serum urate levels by body-mass-index in humans.
Modulation of genetic associations with serum urate levels by body-mass-index in humans.
Modulation of genetic associations with serum urate levels by body-mass-index in humans.
Modulation of genetic associations with serum urate levels by body-mass-index in humans.
Genome-wide association study of blood lead shows multiple associations near ALAD.
Common variation at 1q24.1 (ALDH9A1) is a potential risk factor for renal cancer.
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.
A genome-wide association study of myasthenia gravis.
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers.
Genetic and environmental factors in conjunctival UV autofluorescence.
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms.
Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development.
Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis.
New basal cell carcinoma susceptibility loci.
A common variant near TGFBR3 is associated with primary open angle glaucoma.
A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis.
Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations.
Genetics of aging, health, and survival: dynamic regulation of human longevity related traits.
GWAS for executive function and processing speed suggests involvement of the CADM2 gene.
Two new loci and gene sets related to sex determination and cancer progression are associated with susceptibility to testicular germ cell tumor.
Identification of novel genetic markers of breast cancer survival.
Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations.
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility.
Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma.
Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.
A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk.
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B.
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci.
Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity.
Effect of genetic variations on ticagrelor plasma levels and clinical outcomes.
Effect of genetic variations on ticagrelor plasma levels and clinical outcomes.
Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus.
Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci.
Two susceptibility loci identified for prostate cancer aggressiveness.
Two susceptibility loci identified for prostate cancer aggressiveness.
A genome-wide association study of body mass index across early life and childhood.
The impact of low-frequency and rare variants on lipid levels.
The impact of low-frequency and rare variants on lipid levels.
The impact of low-frequency and rare variants on lipid levels.
The impact of low-frequency and rare variants on lipid levels.
Genetic and clinical factors associated with obesity among adult survivors of childhood cancer: A report from the St. Jude Lifetime Cohort.
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.
Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults.
Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese.
Association of common variants in the calcium-sensing receptor gene with serum calcium levels in East Asians.
A polymorphism in CCR1/CCR3 is associated with narcolepsy.
Genome-wide analysis links NFATC2 with asparaginase hypersensitivity.
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder.
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.
Trans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA).
Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes.
Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study.
A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences.
Identification of new susceptibility loci for IgA nephropathy in Han Chinese.
Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma.
GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy.
A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius.
Genome-wide interaction study of gene-by-occupational exposure and effects on FEV1 levels.
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.
Genome-wide significant risk associations for mucinous ovarian carcinoma.
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
Genome-Wide Association Study Identifies Novel Pharmacogenomic Loci For Therapeutic Response to Montelukast in Asthma.
Genetics of Plasma Soluble Receptor for Advanced Glycation End-Products and Cardiovascular Outcomes in a Community-based Population: Results from the Atherosclerosis Risk in Communities Study.
A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma.
F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease.
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer.
Loss-of-function variants in ATM confer risk of gastric cancer.
Loss-of-function variants in ATM confer risk of gastric cancer.
A genome-wide association study identifies multiple loci for variation in human ear morphology.
A genome-wide association study identifies multiple loci for variation in human ear morphology.
A genome-wide association study identifies multiple loci for variation in human ear morphology.
A genome-wide association study identifies multiple loci for variation in human ear morphology.
A genome-wide association study identifies multiple loci for variation in human ear morphology.
A genome-wide association study identifies multiple loci for variation in human ear morphology.
Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours.
Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours.
Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours.
Genome-wide association study of triglyceride response to a high-fat meal among participants of the NHLBI Genetics of Lipid Lowering Drugs and Diet Network (GOLDN).
Genome-wide association study of colorectal cancer identifies six new susceptibility loci.
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.
Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample.
Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample.
Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample.
Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample.
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.
Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels.
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome.
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
Genome-wide association study of schizophrenia in Ashkenazi Jews.
Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis.
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.
Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3.
Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3.
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
Evidence of CNIH3 involvement in opioid dependence.
Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.
Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.
Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.
Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level.
GWAS of longitudinal amyloid accumulation on 18F-florbetapir PET in Alzheimer's disease implicates microglial activation gene IL1RAP.
Genome-wide association study of warfarin maintenance dose in a Brazilian sample.
An Immunochip-based interaction study of contrasting interaction effects with smoking in ACPA-positive versus ACPA-negative rheumatoid arthritis.
Common and rare variants associated with kidney stones and biochemical traits.
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations.
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations.
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes.
Genetics of long-term treatment outcome in bipolar disorder.
Genetics of long-term treatment outcome in bipolar disorder.
Genetic association analyses highlight biological pathways underlying mitral valve prolapse.
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk.
Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study.
No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity.
No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity.
No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity.
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls.
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.
Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood.
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis.
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.
A novel locus of resistance to severe malaria in a region of ancient balancing selection.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Genome-wide association study identifies multiple susceptibility loci for glioma.
Genome-wide association study identifies multiple susceptibility loci for glioma.
Genome-wide association study identifies multiple susceptibility loci for glioma.
GCKR and PPP1R3B identified as genome-wide significant loci for plasma lactate: the Atherosclerosis Risk in Communities (ARIC) study.
Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence.
Large-scale association analysis in Asians identifies new susceptibility loci for prostate cancer.
Polymorphisms in HLA Class II Genes Are Associated With Susceptibility to Staphylococcus aureus Infection in a White Population.
Polymorphisms in HLA Class II Genes Are Associated With Susceptibility to Staphylococcus aureus Infection in a White Population.
Genome-wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A, and Identification of ZBTB10 and Three Distinct HLA Associations.
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis.
Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.
Genome-wide association studies identify genetic loci for low von Willebrand factor levels.
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population.
Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.
Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.
Identification of four new susceptibility loci for testicular germ cell tumour.
Identification of four new susceptibility loci for testicular germ cell tumour.
Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians.
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis.
Genome-Wide Association Studies of the Human Gut Microbiota.
HLA-B*57:01 Confers Susceptibility to Pazopanib-Associated Liver Injury in Patients with Cancer.
Meta-analysis identifies seven susceptibility loci involved in the atopic march.
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.
Novel Genetic Loci Associated With Retinal Microvascular Diameter.
Novel Genetic Loci Associated With Retinal Microvascular Diameter.
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas.
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations.
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations.
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations.
Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis.
A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.
A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.
A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.
A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.
A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.
A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.
Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture.
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture.
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture.
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Meta analysis identifies a novel susceptibility locus associated with heel bone strength in the Korean population.
A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans.
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.
A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia.
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies.
A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry.
IDENTIFYING GENETIC ASSOCIATIONS WITH VARIABILITY IN METABOLIC HEALTH AND BLOOD COUNT LABORATORY VALUES: DIVING INTO THE QUANTITATIVE TRAITS BY LEVERAGING LONGITUDINAL DATA FROM AN EHR.
Identification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreans.
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.
Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health.
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.
HLA-B*38:02:01 predicts carbimazole/methimazole-induced agranulocytosis.
Meta-analysis of genome-wide association studies of anxiety disorders.
CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk.
Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride.
Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride.
Genome-wide association study reveals sex-specific selection signals against autosomal nucleotide variants.
A longitudinal genome-wide association study of anti-tumor necrosis factor response among Japanese patients with rheumatoid arthritis.
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome.
Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies.
Identification of IRX1 as a Risk Locus for Rheumatoid Factor Positivity in Rheumatoid Arthritis in a Genome-Wide Association Study.
Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis.
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.
Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma.
Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease.
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.
A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person.
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person.
Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies.
Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
Pharmacogenomic Study of Clozapine-Induced Agranulocytosis/Granulocytopenia in a Japanese Population.
A Genome-Wide Association Study of Cutaneous Squamous Cell Carcinoma among European Descendants.
A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.
Novel genetic predictors of venous thromboembolism risk in African Americans.
HLA-C*01 is a Risk Factor for Crohn's Disease.
Genome wide association study of uric acid in Indian population and interaction of identified variants with Type 2 diabetes.
Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies.
Novel loci and pathways significantly associated with longevity.
Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.
Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.
A Locus at 5q33.3 Confers Resistance to Tuberculosis in Highly Susceptible Individuals.
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.
Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease.
Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease.
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk.
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia.
Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank.
Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank.
Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort.
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.
Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively.
Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively.
International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents.
Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans.
Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans.
Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease.
Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokers.
Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility.
Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants.
Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants.
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.
GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.
Genome-Wide Association Study of Bladder Cancer in a Chinese Cohort Reveals a New Susceptibility Locus at 5q12.3.
Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan.
Meta-analysis of 49â549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma.
Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112â151).
Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112â151).
Identification of a new locus at 16q12 associated with time to asthma onset.
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies.
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies.
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.
Mosaic loss of chromosome Y is associated with common variation near TCL1A.
Genome-wide analysis of over 106â000 individuals identifies 9 neuroticism-associated loci.
New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins.
Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease.
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies.
Physical and neurobehavioral determinants of reproductive onset and success.
Physical and neurobehavioral determinants of reproductive onset and success.
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
The Novel ASIC2 Locus is Associated with Severe Gingival Inflammation.
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations.
Antiphospholipid antibodies in a large population-based cohort: genome-wide associations and effects on monocyte gene expression.
Clinical and Genetic Risk Factors for Acute Pancreatitis in Patients With Acute Lymphoblastic Leukemia.
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.
High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences.
High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences.
High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences.
High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences.
Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans.
Five endometrial cancer risk loci identified through genome-wide association analysis.
Five endometrial cancer risk loci identified through genome-wide association analysis.
Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.
Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.
Pharmacogenetic Discovery in CALGB (Alliance) 90401 and Mechanistic Validation of a VAC14 Polymorphism that Increases Risk of Docetaxel-Induced Neuropathy.
Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases.
An association study revealed substantial effects of dominance, epistasis and substance dependence co-morbidity on alcohol dependence symptom count.
Common genetic variation in ETV6 is associated with colorectal cancer susceptibility.
Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.
Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility.
Variation at HLA-DPB1 is associated with dermatomyositis in Chinese population.
Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease.
Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population.
Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Detection and interpretation of shared genetic influences on 42 human traits.
Multi-ethnic genome-wide association study identifies novel locus for type 2 diabetes susceptibility.
A combined large-scale meta-analysis identifies COG6 as a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus.
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.
Genome-wide association study identifies 74 loci associated with educational attainment.
Genome-wide association study identifies 74 loci associated with educational attainment.
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
Pooled analysis of genome-wide association studies of cervical intraepithelial neoplasia 3 (CIN3) identifies a new susceptibility locus.
Association of 3q13.32 variants with hip trochanter and intertrochanter bone mineral density identified by a genome-wide association study.
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci.
A Powerful Procedure for Pathway-Based Meta-analysis Using Summary Statistics Identifies 43 Pathways Associated with Type II Diabetes in European Populations.
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma.
A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies.
Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density.
Identification of genetic modifiers of age-at-onset for familial Parkinson's disease.
Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus.
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.
A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.
From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci.
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci.
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms.
Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene.
Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene.
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types.
Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma.
An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma.
Combining genomewide association study and lung eQTL analysis provides evidence for novel genes associated with asthma.
Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer.
Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer.
Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer.
KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex.
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
A thrifty variant in CREBRF strongly influences body mass index in Samoans.
An exome array study of the plasma metabolome.
Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study.
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21.
Identification of 15 genetic loci associated with risk of major depression in individuals of European descent.
Genetic associations with neuroendocrine tumor risk: results from a genome-wide association study.
Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension.
Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk.
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.
Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study.
Pooling-Based Genome-Wide Association Study Identifies Risk Loci in the Pathogenesis of Ovarian Endometrioma in Chinese Han Women.
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma.
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.
The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population.
Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma.
Genetic Analysis with the Immunochip Platform in Behçet Disease. Identification of Residues Associated in the HLA Class I Region and New Susceptibility Loci.
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.
A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD.
Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption.
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.
Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans.
Genomewide Approach Validates Thiopurine Methyltransferase Activity Is a Monogenic Pharmacogenomic Trait.
A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women.
Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin.
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins.
Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer.
Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.
Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.
Chronic Periodontitis Genome-wide Association Study in the Hispanic Community Health Study / Study of Latinos.
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.
Identification of Four Novel Loci in Asthma in European American and African American Populations.
Identification of Four Novel Loci in Asthma in European American and African American Populations.
A genome-wide association study of emotion dysregulation: Evidence for interleukin 2 receptor alpha.
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.
Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium.
Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.
African Ancestry-Specific Alleles and Kidney Disease Risk in Hispanics/Latinos.
Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels.
Genome-wide association study of plasma resistin levels identified rs1423096 and rs10401670 as possible functional variants in the Japanese population.
Genome-Wide Association Study of the Genetic Determinants of Emphysema Distribution.
Genome-wide association study identifies pharmacogenomic loci linked with specific antihypertensive drug treatment and new-onset diabetes.
Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients.
52 Genetic Loci Influencing Myocardial Mass.
52 Genetic Loci Influencing Myocardial Mass.
52 Genetic Loci Influencing Myocardial Mass.
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
The effect of host genetics on the gut microbiome.
The effect of host genetics on the gut microbiome.
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior.
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior.
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior.
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior.
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis.
Common Genetic Variation Near Melatonin Receptor 1A Gene Linked to Job-Related Exhaustion in Shift Workers.
Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer.
Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota.
Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.
Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.
Genome-wide associations for birth weight and correlations with adult disease.
Genome-wide associations for birth weight and correlations with adult disease.
GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients.
GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients.
Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.
Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.
Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.
Genome-wide association of trajectories of systolic blood pressure change.
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis.
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis.
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records.
Genome-wide association study in essential tremor identifies three new loci.
Genome-wide analysis identifies 12 loci influencing human reproductive behavior.
Genome-wide analysis identifies 12 loci influencing human reproductive behavior.
Genome-wide analysis identifies 12 loci influencing human reproductive behavior.
Genome-wide analysis identifies 12 loci influencing human reproductive behavior.
Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus.
Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants.
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Molecular Genetic Contributions to Social Deprivation and Household Income in UK Biobank.
Genome-wide association study of paliperidone efficacy.
Genetic and methylation variation in the CYP2B6 gene is related to circulating p,p'-dde levels in a population-based sample.
Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin.
Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes.
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes.
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes.
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis.
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis.
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis.
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation.
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders.
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders.
Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population.
Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications.
An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype.
Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors.
Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.
Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.
A large-scale genome-wide association and meta-analysis identified four novel susceptibility loci for leprosy.
Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits.
Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits.
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease.
Genetic variation at 16q24.2 is associated with small vessel stroke.
Genetic variation at 16q24.2 is associated with small vessel stroke.
Genetic variation at 16q24.2 is associated with small vessel stroke.
Genetic architecture of age-related cognitive decline in African Americans.
A Genome-Wide Association Study of Basal Transepidermal Water Loss Finds that Variants at 9q34.3 Are Associated with Skin Barrier Function.
The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations.
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.
Identification of novel loci affecting circulating chromogranins and related peptides.
Genome-wide association study of Parkinson's disease in East Asians.
Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.
Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.
Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.
Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma.
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis.
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis.
A genome wide association study of fast beta EEG in families of European ancestry.
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.
A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis.
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity.
Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.
Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.
Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.
Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan.
Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1.
Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1.
Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1.
Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup.
Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup.
Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup.
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.
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.
Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population.
Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.
Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry.
GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos.
Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The ARIC Study (Atherosclerosis Risk in Communities).
Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population.
Genome-Wide Study Links PNPLA3 Variant With Elevated Hepatic Transaminase After Acute Lymphoblastic Leukemia Therapy.
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
Novel genetic loci associated with hippocampal volume.
Genome-wide association study identifies MAPT locus influencing human plasma tau levels.
Genome-wide association study using the ethnicity-specific Japonica array: identification of new susceptibility loci for cold medicine-related Stevens-Johnson syndrome with severe ocular complications.
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.
A Multinational Arab Genome-Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis.
A Multinational Arab Genome-Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis.
A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder.
Genome-wide association study identiï¬es HLA-DR variants conferring risk of HBV-related acute-on-chronic liver failure.
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer.
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer.
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels.
Genome-Wide Association Study Identifies TLL1 Variant Associated With Development of Hepatocellular Carcinoma After Eradication of Hepatitis C Virus Infection.
A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability.
Transethnic genome-wide scan identifies novel Alzheimer's disease loci.
Transethnic genome-wide scan identifies novel Alzheimer's disease loci.
Transethnic genome-wide scan identifies novel Alzheimer's disease loci.
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis.
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets.
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia.
Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.
A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.
A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.
A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.
A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.
GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway.
A genome-wide association study yields five novel thyroid cancer risk loci.
Heritability and GWAS Studies for Monocyte-Lymphocyte Ratio.
Genetic prediction of male pattern baldness.
Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Genomic variants at 20p11 associated with body fat mass in the European population.
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation.
Association between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma.
Genome-wide meta-analysis identifies novel loci of plaque burden in carotid artery.
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.
GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians.
Genome-wide analyses identify common variants associated with macular telangiectasia type 2.
Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers.
Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers.
Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers.
Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis.
Common genetic variation and risk of gallbladder cancer in India: a case-control genome-wide association study.
Common coding variant in SERPINA1 increases the risk for large artery stroke.
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
A genome-wide gene-by-trauma interaction study of alcohol misuse in two independent cohorts identifies PRKG1 as a risk locus.
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.
A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus.
Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.
Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans.
Genome-wide analysis identifies an african-specific variant in SEMA4D associated with body mass index.
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations.
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations.
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations.
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations.
Identification of a novel locus associated with skin colour in African-admixed populations.
Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis.
Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes.
Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes.
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.
Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.
A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents.
Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility.
Meta-analysis of genome-wide association studies on the intolerance of angiotensin-converting enzyme inhibitors.
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.
Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.
Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.
Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.
Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.
Genome-wide analysis of clopidogrel active metabolite levels identifies novel variants that influence antiplatelet response.
Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.
Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.
Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.
GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci.
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.
Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.
Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.
Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.
Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants.
Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease.
Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci.
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.
A new locus regulating MICALL2 expression was identified for association with executive inhibition in children with attention deficit hyperactivity disorder.
SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway.
SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway.
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis.
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence.
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci.
Overexpression of the Cytokine BAFF and Autoimmunity Risk.
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.
A meta-analysis of genome-wide association studies of asthma in Puerto Ricans.
Search for genetic factor association with cancer-free prostate-specific antigen level elevation on the basis of a genome-wide association study in the Korean population.
Genetic polymorphisms associated with pancreatic cancer survival: a genome-wide association study.
Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.
Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.
Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study.
Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study.
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants.
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants.
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants.
Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin Aging.
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa.
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?
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?
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms.
A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms.
Genome-wide association study of heavy smoking and daily/nondaily smoking in the Hispanic Community Health Study / Study of Latinos (HCHS/SOL).
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma.
Genome-wide association study of subclinical interstitial lung disease in MESA.
Genome-wide association study of subclinical interstitial lung disease in MESA.
Genome-wide association study of subclinical interstitial lung disease in MESA.
Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.
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.
Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence.
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.
Genome-Wide Significance for PCLO as a Gene for Major Depressive Disorder.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
Genome-wide association study of language performance in Alzheimer's disease.
Genetic Drivers of von Willebrand Factor Levels in an Ischemic Stroke Population and Association With Risk for Recurrent Stroke.
Molecular genetic contributions to self-rated health.
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.
Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism.
Genome-wide Association Study of Susceptibility to Particulate Matter-Associated QT Prolongation.
Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth.
Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth.
Genome-wide association study identifies multiple risk loci for renal cell carcinoma.
Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.
Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits.
Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor.
Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
Genetic loci associated with heart rate variability and their effects on cardiac disease risk.
Genetic loci associated with heart rate variability and their effects on cardiac disease risk.
Genetic loci associated with heart rate variability and their effects on cardiac disease risk.
Genetic variants in ADAMTS13 as well as smoking are major determinants of plasma ADAMTS13 levels.
Identification of sequence variants influencing immunoglobulin levels.
Identification of sequence variants influencing immunoglobulin levels.
Identification of sequence variants influencing immunoglobulin levels.
Identification of sequence variants influencing immunoglobulin levels.
Identification of sequence variants influencing immunoglobulin levels.
Identification of sequence variants influencing immunoglobulin levels.
Rare coding variants associated with blood pressure variation in 15â914 individuals of African ancestry.
Rare coding variants associated with blood pressure variation in 15â914 individuals of African ancestry.
A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.
Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.
A genome-wide association study for extremely high intelligence.
Influence of common and rare genetic variation on warfarin dose among African-Americans and European-Americans using the exome array.
A genome-wide association study suggests the HLA Class II region as the major susceptibility locus for IgA vasculitis.
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.
Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer.
Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer.
Genome-wide association study of neovascular age-related macular degeneration in the Thai population.
Association analyses based on false discovery rate implicate new loci for coronary artery disease.
Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease.
Transancestral mapping and genetic load in systemic lupus erythematosus.
Transancestral mapping and genetic load in systemic lupus erythematosus.
Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis.
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass.
Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis.
Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes.
Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes.
Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes.
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.
Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis.
Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112â117).
Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112â117).
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.
Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis.
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.
Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus.
Genome-wide association analysis identifies common variants influencing infant brain volumes.
Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry.
A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration.
Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis.
Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations.
Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility.
Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study.
Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study.
Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study.
Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study.
A multi-stage genome-wide association study of uterine fibroids in African Americans.
A genome-wide association analysis identifies PDE1A|DNAJC10 locus on chromosome 2 associated with idiopathic pulmonary arterial hypertension in a Japanese population.
A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes.
Genome-wide association and functional studies identify a role for matrix Gla protein in osteoarthritis of the hand.
New variants near RHOJ and C2, HLA-DRA region and susceptibility to endometriosis in the Polish population-The genome-wide association study.
ABCG2 Polymorphism Is Associated with Hyperuricemia in a Study of a Community-Based Korean Cohort.
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.
Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis.
Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations.
Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations.
Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations.
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.
Genome-wide association study identifies 112 new loci for body mass index in the Japanese population.
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.
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.
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.
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.
Genetic Determinants of Radiographic Knee Osteoarthritis in African Americans.
Genome-wide association study of a nicotine metabolism biomarker in African American smokers: impact of chromosome 19 genetic influences.
A novel role for ciliary function in atopy: ADGRV1 and DNAH5 interactions.
Human leukocyte antigen variants and risk of hepatocellular carcinoma modified by hepatitis C virus genotypes: A genome-wide association study.
Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.
Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.
Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.
The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia.
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.
Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.
Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.
Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
Discovery of susceptibility loci associated with tuberculosis in Han Chinese.
Two genetic loci associated with ankle injury.
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.
Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence.
Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.
Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas.
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia.
Variants at HLA-A, HLA-C, and HLA-DQB1 Confer Risk of Psoriasis Vulgaris in Japanese.
Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy.
Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study.
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Exome-wide association study of plasma lipids in >300,000 individuals.
Exome-wide association study of plasma lipids in >300,000 individuals.
Exome-wide association study of plasma lipids in >300,000 individuals.
Exome-wide association study of plasma lipids in >300,000 individuals.
Exome-wide association study of plasma lipids in >300,000 individuals.
Exome-wide association study of plasma lipids in >300,000 individuals.
Exome-wide association study of plasma lipids in >300,000 individuals.
Exome-wide association study of plasma lipids in >300,000 individuals.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function.
Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function.
Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function.
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio.
2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio.
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes.
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes.
Genetic determinants of circulating GIP and GLP-1 concentrations.
Genetic determinants of circulating GIP and GLP-1 concentrations.
Genetic determinants of circulating GIP and GLP-1 concentrations.
Genetic determinants of circulating GIP and GLP-1 concentrations.
Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry.
Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry.
A common variant in ARHGEF10 alters delta-6 desaturase activity and influence susceptibility to hypertriglyceridemia.
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux.
Genome-wide Association Study of Idiopathic Osteonecrosis of the Femoral Head.
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.
Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at ID2.
A variant in PPP4R3A protects against alzheimer-related metabolic decline.
Leveraging genome characteristics to improve gene discovery for putamen subcortical brain structure.
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
Genome-wide association study of telomere length among South Asians identifies a second RTEL1 association signal.
Genome-wide association study identifies the common variants in CYP3A4 and CYP3A5 responsible for variation in tacrolimus trough concentration in Caucasian kidney transplant recipients.
Genomewide association study of HLA alloimmunization in previously pregnant blood donors.
Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density.
Genome-wide meta-analysis in Japanese populations identifies novel variants at the TMC6-TMC8 and SIX3-SIX2 loci associated with HbA1c.
Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin.
Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot.
Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot.
Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot.
Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot.
Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets.
Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets.
An Unexpectedly Complex Architecture for Skin Pigmentation in Africans.
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment.
Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia.
Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia.
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility.
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility.
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility.
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis.
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population.
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population.
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population.
Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
Heritability of Atrial Fibrillation.
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder.
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.
Genome-wide scan identifies candidate loci related to remifentanil requirements during laparoscopic-assisted colectomy.
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair.
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.
Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients.
Genome-Wide Gene-Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity).
Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry.
A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure.
Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton.
Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton.
Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton.
Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.
Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.
Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages.
Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia.
Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study.
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma.
Genetic Polymorphisms of PNPLA3 and SAMM50 Are Associated with Nonalcoholic Fatty Liver Disease in a Korean Population.
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.
Multi-trait analysis of genome-wide association summary statistics using MTAG.
Multi-trait analysis of genome-wide association summary statistics using MTAG.
Multi-trait analysis of genome-wide association summary statistics using MTAG.
Multi-trait analysis of genome-wide association summary statistics using MTAG.
Multi-trait analysis of genome-wide association summary statistics using MTAG.
Multi-trait analysis of genome-wide association summary statistics using MTAG.
Rare and Common Variants Conferring Risk of Tooth Agenesis.
Rare and Common Variants Conferring Risk of Tooth Agenesis.
Rare and Common Variants Conferring Risk of Tooth Agenesis.
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study.
Genome-wide association study of offspring birth weight in 86â577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.
Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations.
A Genome-Wide Association Study Identifies a Candidate Gene Associated With Atazanavir Exposure Measured in Hair.
Genetic Determinants of Circulating Estrogen Levels, and Evidence of a Causal Effect of Estradiol on Bone Density in Men.
Genetic Determinants of Circulating Estrogen Levels, and Evidence of a Causal Effect of Estradiol on Bone Density in Men.
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.
A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.
Real-life helping behaviours in North America: A genome-wide association approach.
Meta-analysis of exome array data identifies six novel genetic loci for lung function.
Meta-analysis of exome array data identifies six novel genetic loci for lung function.
Meta-analysis of exome array data identifies six novel genetic loci for lung function.
Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis.
Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration.
Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration.
Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration.
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels.
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21.
Genetic risk of prostate cancer in Ugandan men.
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.
A genome-wide association study in the Japanese population identifies the 12q24 locus for habitual coffee consumption: The J-MICC Study.
A genome-wide association study in the Japanese population identifies the 12q24 locus for habitual coffee consumption: The J-MICC Study.
GWAS of epigenetic aging rates in blood reveals a critical role for TERT.
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels.
Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers.
Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers.
A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N=223,773).
A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor.
A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor.
Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation: Implications in Age-Related Macular Degeneration.
Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort.
The polymorphism rs671 at ALDH2 associated with serum uric acid levels in Chinese Han males: A genome-wide association study.
Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8.
A Genome-wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos.
A Genome-wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
A genome-wide association study of corneal astigmatism: The CREAM Consortium.
A novel variant in GLIS3 is associated with osteoarthritis.
A novel variant in GLIS3 is associated with osteoarthritis.
A novel variant in GLIS3 is associated with osteoarthritis.
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer.
Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma.
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.
Genome-Wide Association Study Identifies a New Locus at 7q21.13 Associated with Hepatitis B Virus-Related Hepatocellular Carcinoma.
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma.
ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study.
Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men.
GWAS Identifies Two Novel Colorectal Cancer Loci at 16q24.1 and 20q13.12.
Genomewide association study of alcohol dependence and related traits in a Thai population.
Genome-Wide Association and Functional Studies Identify SCML4 and THSD7A as Novel Susceptibility Genes for Coronary Artery Disease.
Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to β-Blockers.
Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to β-Blockers.
A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans.
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population.
Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density.
Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density.
Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.
Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.
Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.
Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.
Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes.
Genome-wide association study identifies three novel susceptibility loci for systemic lupus erythematosus in Han Chinese.
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials.
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials.
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials.
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials.
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.
Genome-Wide Association Study of Serum 25-Hydroxyvitamin D in US Women.
Genetic study links components of the autonomous nervous system to heart-rate profile during exercise.
Genetic study links components of the autonomous nervous system to heart-rate profile during exercise.
Genetic study links components of the autonomous nervous system to heart-rate profile during exercise.
Genetic study links components of the autonomous nervous system to heart-rate profile during exercise.
Genetic study links components of the autonomous nervous system to heart-rate profile during exercise.
Genetic study links components of the autonomous nervous system to heart-rate profile during exercise.
Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
Item-level analyses reveal genetic heterogeneity in neuroticism.
A large electronic-health-record-based genome-wide study of serum lipids.
A large electronic-health-record-based genome-wide study of serum lipids.
A large electronic-health-record-based genome-wide study of serum lipids.
A large electronic-health-record-based genome-wide study of serum lipids.
A large electronic-health-record-based genome-wide study of serum lipids.
A large electronic-health-record-based genome-wide study of serum lipids.
A large electronic-health-record-based genome-wide study of serum lipids.
A large electronic-health-record-based genome-wide study of serum lipids.
Genome-wide analysis yields new loci associating with aortic valve stenosis.
A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis.
Genome-wide analysis of insomnia disorder.
Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals.
Genome Wide Association Study Identifies the HMGCS2 Locus to be Associated With Chlorthalidone Induced Glucose Increase in Hypertensive Patients.
Risk of nontyphoidal Salmonella bacteraemia in African children is modified by STAT4.
Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population.
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.
Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway.
Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway.
Key HLA-DRB1-DQB1 haplotypes and role of the BTNL2 gene for response to a hepatitis B vaccine.
Two Genetic Variants Associated with Plantar Fascial Disorders.
A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relation to chronic lymphocytic leukemia.
Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.
Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.
Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.
Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.
Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.
Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study.
Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study.
Facial Wrinkles in Europeans: a Genome-Wide Association Study.
Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations.
A genome-wide association study on photic sneeze syndrome in a Japanese population.
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis.
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis.
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis.
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum.
Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum.
Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians.
Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians.
A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood.
A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood.
Genome-Wide Association Analyses Identify New Loci Influencing Intraocular Pressure.
Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia.
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses.
Genome-Wide Associations of Global Electrical Heterogeneity ECG Phenotype: The ARIC (Atherosclerosis Risk in Communities) Study and CHS (Cardiovascular Health Study).
Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey.
Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia.
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
The genetics of smoking in individuals with chronic obstructive pulmonary disease.
The genetics of smoking in individuals with chronic obstructive pulmonary disease.
Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level.
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.
Novel association between CDKAL1 and cholesterol efflux capacity: Replication after GWAS-based discovery.
A Genome-Wide Association Study identifies new genes potentially associated with eyelid sagging.
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways.
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability.
Biological Insights Into Muscular Strength: Genetic Findings in the UK Biobank.
Biological Insights Into Muscular Strength: Genetic Findings in the UK Biobank.
Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Common variants on 6q16.2, 12q24.31 and 16p13.3 are associated with major depressive disorder.
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
Genetic Regulation of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Plasma Levels and Its Impact on Atherosclerotic Vascular Disease Phenotypes.
Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.
Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.
CETP (Cholesteryl Ester Transfer Protein) Concentration: A Genome-Wide Association Study Followed by Mendelian Randomization on Coronary Artery Disease.
Genome-wide association study for risk taking propensity indicates shared pathways with body mass index.
Genome-wide association study for risk taking propensity indicates shared pathways with body mass index.
Genome-wide association study for risk taking propensity indicates shared pathways with body mass index.
CCDC102B confers risk of low vision and blindness in high myopia.
Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium.
Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure.
Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure.
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21.
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21.
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21.
Population-specific genetic modification of Huntington's disease in Venezuela.
Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia.
Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia.
Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia.
Genome-wide association analysis identifies a meningioma risk locus at 11p15.5.
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
Common and rare variants genetic association analysis of cigarettes per day among ever smokers in COPD cases and controls.
Genetic variant for behavioral regulation factor of executive function and its possible brain mechanism in attention deficit hyperactivity disorder.
Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system.
A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica.
A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica.
Elucidating the genetic architecture of reproductive ageing in the Japanese population.
Elucidating the genetic architecture of reproductive ageing in the Japanese population.
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin.
Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study.
Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study.
GWAS on family history of Alzheimer's disease.
GWAS on family history of Alzheimer's disease.
GWAS on family history of Alzheimer's disease.
GWAS on family history of Alzheimer's disease.
Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma.
A locus at 7p14.3 predisposes to refractory celiac disease progression from celiac disease.
Genome-wide association study identified new susceptible genetic variants in HLA class I region for hepatitis B virus-related hepatocellular carcinoma.
Evaluation and application of summary statistic imputation to discover new height-associated loci.
A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases.
A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases.
A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases.
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.
Identification of nine genes as novel susceptibility loci for early-onset ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage.
CFH and VIPR2 as susceptibility loci in choroidal thickness and pachychoroid disease central serous chorioretinopathy.
Association study and fine-mapping major histocompatibility complex analysis of pemphigus vulgaris in a Han Chinese population.
Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study.
Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study.
Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study.
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
Genome-wide association study meta-analysis identifies five new loci for systemic lupus erythematosus.
Genetic study of multimodal imaging Alzheimer's disease progression score implicates novel loci.
Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.
Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.
Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.
Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs.
Genome-wide association study of developmental dysplasia of the hip identifies an association with GDF5.
GWAS reveals loci associated with velopharyngeal dysfunction.
Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes.
Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis.
Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer.
Multi-ethnic genome-wide association study for atrial fibrillation.
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.
Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.
Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia.
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.
Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.
Genome-Wide Association Study of Erosive Tooth Wear in a Finnish Cohort.
Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE.
Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE.
Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE.
Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Novel Common Genetic Susceptibility Loci for Colorectal Cancer.
Genome-Wide Association Study of Familial Lung Cancer.
Genome-Wide Association Study of Familial Lung Cancer.
Identification of five novel genetic loci related to facial morphology by genome-wide association studies.
Identification of five novel genetic loci related to facial morphology by genome-wide association studies.
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.
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.
Consortium genome-wide meta-analysis for childhood dental caries traits.
Consortium genome-wide meta-analysis for childhood dental caries traits.
Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic population.
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity.
A Genome-Wide Association Study of α-Synuclein Levels in Cerebrospinal Fluid.
Genetic variants in systemic lupus erythematosus susceptibility loci, XKR6 and GLT1D1 are associated with childhood-onset SLE in a Korean cohort.
Elucidating the genetic basis of social interaction and isolation.
Elucidating the genetic basis of social interaction and isolation.
Elucidating the genetic basis of social interaction and isolation.
Elucidating the genetic basis of social interaction and isolation.
Elucidating the genetic basis of social interaction and isolation.
Elucidating the genetic basis of social interaction and isolation.
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium.
Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.
GENOME-WIDE ASSOCIATION META-ANALYSIS OF AGE AT FIRST CANNABIS USE.
Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosis.
Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy.
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.
Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant.
Genome-Wide Association Study in Vestibular Neuritis: Involvement of the Host Factor for HSV-1 Replication.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
Heritability and genome-wide association study of diffusing capacity of the lung.
Identification of 613 new loci associated with heel bone mineral density and a polygenic risk score for bone mineral density, osteoporosis and fracture.
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.
Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines.
Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines.
Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines.
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma.
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma.
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
Variation at the TRIM11 locus modifies Progressive Supranuclear Palsy phenotype.
Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.
Genome-wide association study of lung function and clinical implication in heavy smokers.
Genome-wide association study of lung function and clinical implication in heavy smokers.
An Intergenic Variant rs9268877 Between HLA-DRA and HLA-DRB Contributes to the Clinical Course and Long-term Outcome of Ulcerative Colitis.
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology.
Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactions.
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol.
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol.
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol.
Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol.
Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.
A genome-wide association study of energy intake and expenditure.
A genome-wide association study of energy intake and expenditure.
Genome-wide analysis of genetic determinants of circulating factor VII activating protease (FSAP) activity.
Role of the Complement System in Chronic Central Serous Chorioretinopathy: A Genome-Wide Association Study.
Genome-wide Association Study Reveals Distinct Genetic Susceptibility of Thyroid Nodules from Thyroid Cancer.
Identification of nine new susceptibility loci for endometrial cancer.
Identification of nine new susceptibility loci for endometrial cancer.
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility.
Genome-wide Association Study of Leisure-Time Exercise Behavior in Japanese Adults.
Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk.
Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk.
A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1.
A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure.
Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.
Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.
Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability.
Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability.
A Large Multi-ethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci.
Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction.
Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction.
Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.
Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study.
Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia.
Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia.
Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia.
Identification of novel loci associated with infant cognitive ability.
Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population.
Cross-genetic determination of maternal and neonatal immune mediators during pregnancy.
Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age.
GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia.
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study.
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.
Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis.
Investigation of the Predisposing Factor of Pemphigus and its clinical subtype through a Genome-wide association and next generation sequence analysis.
An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels.
Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease.
Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease.
Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression.
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes.
Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease.
Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease.
Genome-Wide Association of Genetic Variation in the PSCA Gene with Gastric Cancer Susceptibility in a Korean Population.
Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal.
Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal.
Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal.
Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal.
Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure.
Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure.
Large scale meta-analysis highlights the hypothalamic-pituitary-gonadal (HPG) axis in the genetic regulation of menstrual cycle length.
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma.
GWAS for Interleukin-1β levels in gingival crevicular fluid identifies IL37 variants in periodontal inflammation.
Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations.
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma.
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.
Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.
Genetic Variants Associated with Circulating Fibroblast Growth Factor 23.
Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci.
Gamma-aminobutyric acid transaminase genetic polymorphism is a candidate locus for responsiveness to opioid analgesics in patients with cancer pain: An exploratory study.
Genome-wide Association Study for Tumour Stage, Grade, Size, and Age at Diagnosis of Non-muscle-invasive Bladder Cancer.
Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste.
Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population.
Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships.
Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships.
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort
Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort
Genome-Wide Association Study Reveals Genetic Link between Diarrhea-Associated Entamoeba histolytica Infection and Inflammatory Bowel Disease.
Subtype-Specific Inherited Predisposition to Pemphigus in Chinese Population.
Subtype-Specific Inherited Predisposition to Pemphigus in Chinese Population.
Genome-wide association analysis of common genetic variants of resistant hypertension.
Genome-Wide Association and Mechanistic Studies Indicate That Immune Response Contributes to Alzheimer's Disease Development.
Genome-Wide Association and Mechanistic Studies Indicate That Immune Response Contributes to Alzheimer's Disease Development.
Genome-Wide Association and Mechanistic Studies Indicate That Immune Response Contributes to Alzheimer's Disease Development.
Genome-Wide Association and Mechanistic Studies Indicate That Immune Response Contributes to Alzheimer's Disease Development.
A genome-wide association study identifies a 3'UTR genetic variant of RARB associated with carotid intima-media thickness in rheumatoid arthritis.
Risk locus identification ties alcohol withdrawal symptoms to SORCS2.
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes.
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes.
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes.
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume.
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain.
Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery.
A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia.
Common variants at 5q33.1 predispose to migraine in African-American children.
Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin.
Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease.
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
Association of Genetic Variants With Warfarin-Associated Bleeding Among Patients of African Descent.
A genetic perspective on the relationship between eudaimonic -and hedonic well-being.
A genetic perspective on the relationship between eudaimonic -and hedonic well-being.
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes.
A GWAS identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21.
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population.
Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time.
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese.
Plasticity-related gene 3 (LPPR1) and age at diagnosis of Parkinson disease.
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Genome-Wide Association Study of Susceptibility Loci for Radiation-Induced Brain Injury.
The eMERGE genotype set of 83,717 subjects imputed to ~40âmillion variants genome wide and association with the herpes zoster medical record phenotype.
Genetic variation in the SIM1 locus is associated with erectile dysfunction.
Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci.
Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci.
Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci.
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia.
Genome-wide association studies of brain imaging phenotypes in UK Biobank.
Genetic Variants Related to Cardiometabolic Traits Are Associated to B Cell Function, Insulin Resistance, and Diabetes Among AmeriCan Indians: The Strong Heart Family Study.
Identification of novel loci associated with hip shape: a meta-analysis of genome-wide association studies.
BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts.
Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women.
Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women.
Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women.
Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women.
Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women.
The 677CâT variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population.
The 677CâT variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population.
The 677CâT variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population.
Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts.
Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts.
Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts.
Genotype effects contribute to variation in longitudinal methylome patterns in older people.
Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging.
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation.
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis.
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis.
Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study.
Genome-Wide Association Study to Identify a New Susceptibility Locus for Central Serous Chorioretinopathy in the Japanese Population.
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.
Genome-Wide Meta-analysis identifies three novel loci associated with stroke.
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
DNA Sequence Variation in ACVR1C Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes.
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.
Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection.
Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records.
Genetic Influences on Susceptibility to Rheumatoid Arthritis in African-Americans.
Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008.
Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.
Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.
Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia.
Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia.
Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia.
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.
A genome-wide association study identifying RAP1A as a novel susceptibility gene for Crohn's disease in Japanese individuals.
Genetic determinants and an epistasis of LILRA3 and HLA-B*52 in Takayasu arteritis.
Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.
Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors.
A locus on chromosome 5 shows African ancestry-limited association with alloimmunization in sickle cell disease.
Discovery of common and rare genetic risk variants for colorectal cancer.
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.
GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes.
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.
Association of Genetic Variation at AQP4 Locus with Vascular Depression.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use.
Large-scale Genome-wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer.
Common-variant associations with fragile X syndrome.
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.
Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.
Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.
Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.
GWAS identifies 14 loci for device-measured physical activity and sleep duration.
GWAS identifies 14 loci for device-measured physical activity and sleep duration.
GWAS identifies 14 loci for device-measured physical activity and sleep duration.
GWAS identifies 14 loci for device-measured physical activity and sleep duration.
GWAS identifies 14 loci for device-measured physical activity and sleep duration.
Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study.
Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne.
Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis.
A genome-Wide Association Study Confirming a Strong Effect of HLA and Identifying Variants in CSAD/lnc-ITGB7-1 on Chromosome 12q13.13 Associated with Susceptibility to Fulminant Type 1 Diabetes.
A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene.
Large-scale, multi-ethnic genome-wide association study identifies novel loci contributing to asthma susceptibility in adults.
Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes.
A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes.
Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases.
Dissection of genetic variation and evidence for pleiotropy in male pattern baldness.
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations.
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations.
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations.
Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations.
GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology.
The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma.
The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma.
Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population.
Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus.
Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus.
Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus.
Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus.
Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers.
Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers.
Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers.
Genomics of body fat percentage may contribute to sex bias in anorexia nervosa.
An atlas of genetic influences on osteoporosis in humans and mice.
An atlas of genetic influences on osteoporosis in humans and mice.
PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome.
Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide.
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.
Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality.
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
Genome-wide analysis of genetic predisposition to Alzheimer's disease and related sex disparities.
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis.
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis.
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.
Multivariate genome-wide analyses of the well-being spectrum.
Multivariate genome-wide analyses of the well-being spectrum.
Multivariate genome-wide analyses of the well-being spectrum.
Multivariate genome-wide analyses of the well-being spectrum.
Multivariate genome-wide analyses of the well-being spectrum.
POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33.
Genome-wide association study of anti-Müllerian hormone levels in pre-menopausal women of late reproductive age and relationship with genetic determinants of reproductive lifespan.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Genetic associations with suicide attempt severity and genetic overlap with major depression.
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population.
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population.
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population.
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population.
Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score.
Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226).
Drug-induced injury due to flucloxacillin: relevance of multiple HLA alleles.
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms.
Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects.
Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects.
Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects.
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data.
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data.
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data.
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data.
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
Early-onset autoimmune vitiligo associated with an enhancer variant haplotype that upregulates class II HLA expression.
Early-onset autoimmune vitiligo associated with an enhancer variant haplotype that upregulates class II HLA expression.
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.
Genetic architecture of human thinness compared to severe obesity.
Genetic architecture of human thinness compared to severe obesity.
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits.
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits.
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits.
Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry.
Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms.
Genome-Wide Association Analysis of Single Breath Diffusing Capacity of Carbon Monoxide (DLCO).
Identification of 12 genetic loci associated with human healthspan.
A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.
A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.
Genome-wide association study identifies a novel locus associated with psychological distress in the Japanese population.
Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease.
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.
Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.
Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.
Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility.
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.
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.
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.
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.
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.
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population.
Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide.
GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy.
GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy.
GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy.
A genome-wide association study identifies single nucleotide polymorphisms associated with time-to-metastasis in colorectal cancer.
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Biological insights into multiple birth: genetic findings from UK Biobank.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Genetic Variants Associated with Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome Wide Association Studies.
A meta-analysis of genome-wide association studies identifies three loci associated with stiffness index of the calcaneus.
Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Identification of common genetic risk variants for autism spectrum disorder.
Identification of common genetic risk variants for autism spectrum disorder.
Identification of common genetic risk variants for autism spectrum disorder.
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations.
Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population.
Biological and clinical insights from genetics of insomnia symptoms.
Biological and clinical insights from genetics of insomnia symptoms.
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.
Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci.
Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes.
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci.
Joint Association Analysis Identified 18 New Loci for Bone Mineral Density.
Joint Association Analysis Identified 18 New Loci for Bone Mineral Density.
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population.
Genetic Markers of ADHD-Related Variations in Intracranial Volume.
Genetic Markers of ADHD-Related Variations in Intracranial Volume.
Genetic Markers of ADHD-Related Variations in Intracranial Volume.
Genetic Markers of ADHD-Related Variations in Intracranial Volume.
A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome.
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci.
Assessing the causal association of glycine with risk of cardio-metabolic diseases.
Analysis of pleiotropic genetic effects on cognitive impairment, systemic inflammation, and plasma lipids in the Health and Retirement Study.
Circulating Chemerin Levels, but not the RARRES2 Polymorphisms, Predict the Long-Term Outcome of Angiographically Confirmed Coronary Artery Disease.
Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.
Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates.
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates.
Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02.
Genome Wide Association Studies of Specific Antinuclear Autoantibody Sub-phenotypes in Primary Biliary Cholangitis.
Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain.
Identification of genetic heterogeneity of Alzheimer's disease across age.
Identification of genetic heterogeneity of Alzheimer's disease across age.
Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion.
Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion.
Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion.
Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion.
Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life.
Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life.
Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life.
Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry.
Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry.
Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women.
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.
A genome-wide association study on photic sneeze reflex in the Chinese population.
Integrative Genome-Wide Association Studies of eQTL and GWAS Data for Gout Disease Susceptibility.
GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture.
GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture.
GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture.
GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture.
Genome-wide association study of blood lipids in Indians confirms universality of established variants.
Genome-wide association study of blood lipids in Indians confirms universality of established variants.
Genome-wide association study of blood lipids in Indians confirms universality of established variants.
Genome-wide association study of blood lipids in Indians confirms universality of established variants.
Genome-wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol.
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct.
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct.
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct.
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct.
Genome-wide association study of psoriasis in an Egyptian population.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids.
Genetic variants in the ST6GAL1 gene are associated with thyroglobulin plasma level in healthy individuals.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Sequence variants associating with urinary biomarkers.
Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations.
Novel genetic locus of visceral fat and systemic inflammation.
Common genetic variants have associations with human cortical brain regions and risk of schizophrenia.
Protein and fat intake interacts with the haplotype of PTPN11_rs11066325, RPH3A_rs886477, and OAS3_rs2072134 to modulate serum HDL concentrations in middle-aged people.
Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness.
Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness.
Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis.
Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour.
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals.
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals.
Heritability estimates of individual psychological distress symptoms from genetic variation.
Genetic Association of Finger Photoplethysmography-Derived Arterial Stiffness Index With Blood Pressure and Coronary Artery Disease.
Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population.
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy.
Varicose veins of lower extremities: Insights from the first large-scale genetic study.
Lung Cancer Risk in Never Smokers of European Descent is Associated with Genetic Variation in the 5P15.33 TERT-CLPTM1L Region.
Lung Cancer Risk in Never Smokers of European Descent is Associated with Genetic Variation in the 5P15.33 TERT-CLPTM1L Region.
A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Genome-wide association study of medication-use and associated disease in the UK Biobank.
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.
Integrative genome analysis identified the KANNO blood group antigen as prion protein.
Cardiac Troponin T and Troponin I in the General Population: Comparing and Contrasting their Genetic Determinants and Associations with Outcomes.
Cardiac Troponin T and Troponin I in the General Population: Comparing and Contrasting their Genetic Determinants and Associations with Outcomes.
Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies.
Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies.
Genome-wide association study identifies 30 loci associated with bipolar disorder.
Genome-wide association study identifies 30 loci associated with bipolar disorder.
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.
A genome-wide association study of bitter and sweet beverage consumption.
A genome-wide association study of bitter and sweet beverage consumption.
A genome-wide association study of bitter and sweet beverage consumption.
A genome-wide association study of bitter and sweet beverage consumption.
A genome-wide association study of bitter and sweet beverage consumption.
A genome-wide association study of bitter and sweet beverage consumption.
A genome-wide association study of bitter and sweet beverage consumption.
Genetic association between CD96 locus and immunogenicity to anti-TNF therapy in Crohn's disease.
Genome-wide association study of type 2 diabetes in Africa.
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study.
Genetic heterogeneity of Alzheimer's disease in subjects with and without hypertension.
Genetic heterogeneity of Alzheimer's disease in subjects with and without hypertension.
Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy.
Shared genetic risk factors across carbamazepine-induced hypersensitivity reactions.
GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study.
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.
A commonly occurring genetic variant within the NPLOC4-TSPAN10-PDE6G gene cluster is associated with the risk of strabismus.
Genome-wide analyses of psychological resilience in U.S. Army soldiers.
Genome-wide analyses of psychological resilience in U.S. Army soldiers.
Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups.
Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups.
Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis.
Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis.
Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans.
Association between birth weight and refractive error in adulthood: a Mendelian randomisation study.
Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy.
Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy.
Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy.
Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy.
A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC network study.
Genome-Wide Association Study Confirming the Association of NAT2 with Susceptibility to Anti-tuberculosis Drug-Induced Liver Injury in Thai Patients.
Genetics of heart rate in heart failure patients (GenHRate).
Genome-wide association study identifies Alzheimer's risk variant in MS4A6A influencing cerebrospinal fluid sTREM2 levels.
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.
Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.
Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.
Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.
Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study.
Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration.
Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study.
Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study.
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study.
Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization.
Dentate gyrus volume deficit in schizophrenia.
GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.
The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function.
Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease.
Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease.
Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease.
Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease.
Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease.
Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease.
Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females.
Loci for human leukocyte telomere length in the Singaporean Chinese population and trans-ethnic genetic studies.
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
A genome wide association study on lipoprotein(a) levels and coronary artery disease severity in a Chinese population.
A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.
GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort.
GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort.
GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort.
Genome-wide association study of multisite chronic pain in UK Biobank.
Genome-wide association study of breakfast skipping links clock regulation with food timing.
Genome-wide association study of breakfast skipping links clock regulation with food timing.
Single nucleotide polymorphisms in HLA alleles are associated with HIV-1 viral load in demographically diverse, ART-naïve participants from the START trial.
Influence of Genetic and Non-Genetic Risk Factors for Serum Uric Acid Levels and Hyperuricemia in Mexicans.
Genome-wide association study implicates CHRNA2 in cannabis use disorder.
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genetic analyses of diverse populations improves discovery for complex traits.
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns.
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns.
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns.
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns.
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns.
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns.
Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink.
A Genome-wide Association Study of Prostate Cancer in Latinos.
Sex specific associations in genome wide association analysis of renal cell carcinoma.
Sex specific associations in genome wide association analysis of renal cell carcinoma.
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data.
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data.
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data.
Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants.
Genetic Variants Associated With Corneal Biomechanical Properties and Potentially Conferring Susceptibility to Keratoconus in a Genome-Wide Association Study.
Genetic Variants Associated With Corneal Biomechanical Properties and Potentially Conferring Susceptibility to Keratoconus in a Genome-Wide Association Study.
GWAS identifying HLA-DPB1 gene variants associated with responsiveness to hepatitis B virus vaccination in Koreans: Independent association of HLA-DPB1*04:02 possessing rs1042169 G - rs9277355 C - rs9277356 A.
Impact of IFNL4 Genetic Variants on Sustained Virologic Response and Viremia in Hepatitis C Virus Genotype 3 Patients.
Correlation between eosinophil count, its genetic background and body mass index: The Nagahama Study.
Correlation between eosinophil count, its genetic background and body mass index: The Nagahama Study.
Factors associated with sharing e-mail information and mental health survey participation in large population cohorts.
Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.
Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study.
Genome-wide association studies of the self-rating of effects of ethanol (SRE).
A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process.
Identification of the 12q24 locus associated with fish intake frequency by genome-wide meta-analysis in Japanese populations.
Genome-wide association study of peripheral artery disease in the Million Veteran Program.
Genome-wide association study of peripheral artery disease in the Million Veteran Program.
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout.
HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy.
Clinical and Genome-Wide Analysis of Serum Platinum Levels after Cisplatin-Based Chemotherapy.
Genome-wide association study identifies CD1A associated with rate of increase in plasma neurofilament light in non-demented elders.
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes.
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes.
Bilirubin and risk of ischemic heart disease in Korea: A two-sample Mendelian randomization study.
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.
Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations.
Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations.
Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations.
Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations.
Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations.
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.
ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response.
ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response.
Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis.
Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis.
GWAS of habitual coffee consumption reveals a sex difference in the genetic effect of the 12q24 locus in the Japanese population.
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders.
The Genetic Architecture of Chronic Mountain Sickness in Peru.
Genome-wide association analysis of 350â000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema.
Genome-wide association analysis of 350â000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema.
Genome-wide association analysis of 350â000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema.
Genome-wide association analysis of 350â000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema.
Genome-wide scan identifies opioid overdose risk locus close to MCOLN1.
Circulating oxytocin is genetically determined and associated with obesity and impaired glucose tolerance.
Exome-Wide Rare Loss-of-Function Variant Enrichment Study of 21,347 Han Chinese Individuals Identifies Four Susceptibility Genes for Psoriasis.
The MS4A gene cluster is a key modulator of soluble TREM2 and Alzheimer's disease risk.
Very low-depth whole-genome sequencing in complex trait association studies.
Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.
Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior.
Genome-wide association study identifies CBFA2T3 affecting the rate of CSF Aβ42 decline in non-demented elders.
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes.
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes.
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes.
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes.
Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures.
Molecular mimicry between Anoctamin 2 and Epstein-Barr virus nuclear antigen 1 associates with multiple sclerosis risk.
Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood.
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations.
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.
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.
Genetically regulated gene expression underlies lipid traits in Hispanic cohorts.
Genetically regulated gene expression underlies lipid traits in Hispanic cohorts.
Genetically regulated gene expression underlies lipid traits in Hispanic cohorts.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes.
GWAS for urinary sodium and potassium excretion highlights pathways shared with cardiovascular traits.
GWAS for urinary sodium and potassium excretion highlights pathways shared with cardiovascular traits.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project.
A meta-analysis of genome-wide association studies identifies multiple longevity genes.
A meta-analysis of genome-wide association studies identifies multiple longevity genes.
A meta-analysis of genome-wide association studies identifies multiple longevity genes.
A meta-analysis of genome-wide association studies identifies multiple longevity genes.
Genome-wide association study reveals two novel risk alleles for incident obstructive sleep apnea in the EPISONO cohort.
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese.
Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism.
Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism.
Genome-wide association study of cerebral small vessel disease reveals established and novel loci.
Genome-wide association study of cerebral small vessel disease reveals established and novel loci.
Early progression to active tuberculosis is a highly heritable trait driven by 3q23 in Peruvians.
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
Identification of novel risk loci with shared effects on alcoholism, heroin, and methamphetamine dependence.
Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank.
Epigenetic aging is accelerated in alcohol use disorder and regulated by genetic variation in APOL2.
Genome-wide association study for proliferative diabetic retinopathy in Africans.
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility.
Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population.
Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration.
Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration.
A Prospective Analysis of Genetic Variants Associated with Human Lifespan.
A Prospective Analysis of Genetic Variants Associated with Human Lifespan.
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI.
GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI.
Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics.
Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics.
GWAS of five gynecologic diseases and cross-trait analysis in Japanese.
GWAS of five gynecologic diseases and cross-trait analysis in Japanese.
GWAS of five gynecologic diseases and cross-trait analysis in Japanese.
GWAS of five gynecologic diseases and cross-trait analysis in Japanese.
GWAS of five gynecologic diseases and cross-trait analysis in Japanese.
GWAS of five gynecologic diseases and cross-trait analysis in Japanese.
Genome-wide scan identified genetic variants associated with skin aging in a Chinese female population.
Genome-wide scan identified genetic variants associated with skin aging in a Chinese female population.
A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and geneâenvironment interaction
A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and geneâenvironment interaction
Genome-wide association analysis of 95â549 individuals identifies novel loci and genes influencing optic disc morphology.
Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene.
Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease.
Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease.
Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease.
Genome-wide association study of circulating folate one-carbon metabolites.
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals.
A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals.
A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals.
Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness.
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group.
Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group.
Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Genetic architecture of human plasma lipidome and its link to cardiovascular disease.
Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits.
Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits.
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies.
GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.
Characterizing rare and low-frequency height-associated variants in the Japanese population.
12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population.
Quantitative and qualitative role of antagonistic heterogeneity in genetics of blood lipids.
Quantitative and qualitative role of antagonistic heterogeneity in genetics of blood lipids.
Quantitative and qualitative role of antagonistic heterogeneity in genetics of blood lipids.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth.
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
The Assessment of Interleukin-18 on the Risk of Coronary Heart Disease.
Genome-Wide Association Study of the Metabolic Syndrome in UK Biobank.
Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison.
Genome-Wide Association Study of White Blood Cell Counts in Patients With Ischemic Stroke.
Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease.
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.
Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.
Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.
Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease.
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern.
Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.
Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1.
Three Novel Loci for Infant Head Circumference Identified by a Joint Association Analysis.
Three Novel Loci for Infant Head Circumference Identified by a Joint Association Analysis.
Three Novel Loci for Infant Head Circumference Identified by a Joint Association Analysis.
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft.
Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft.
Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics.
Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics.
Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics.
Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics.
Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis.
GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation.
GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation.
Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis.
Associations with metabolites in Chinese suggest new metabolic roles in Alzheimer's and Parkinson's diseases.
A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio.
Genetic architecture of subcortical brain structures in 38,851 individuals.
Genetic architecture of subcortical brain structures in 38,851 individuals.
Genetic architecture of subcortical brain structures in 38,851 individuals.
Genetic architecture of subcortical brain structures in 38,851 individuals.
Genetic architecture of subcortical brain structures in 38,851 individuals.
Genetic architecture of subcortical brain structures in 38,851 individuals.
Genetic architecture of subcortical brain structures in 38,851 individuals.
A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.
A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.
A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.
A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study.
Genome-Wide Association Studies for Cerebrospinal Fluid Soluble TREM2 in Alzheimer's Disease.
HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype.
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
First genome-wide association study of non-severe malaria in two birth cohorts in Benin.
Common and rare sequence variants influencing tumor biomarkers in blood.
Common and rare sequence variants influencing tumor biomarkers in blood.
Common and rare sequence variants influencing tumor biomarkers in blood.
Common and rare sequence variants influencing tumor biomarkers in blood.
Common and rare sequence variants influencing tumor biomarkers in blood.
GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways.
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease.
Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls.
Genome-wide association study of cerebrospinal fluid neurofilament light levels in non-demented elders.
The interaction between ABCA1 polymorphism and physical activity on the HDL-cholesterol levels in a Japanese population.
The interaction between ABCA1 polymorphism and physical activity on the HDL-cholesterol levels in a Japanese population.
Evidence for causal effects of lifetime smoking on risk for depression and schizophrenia: a Mendelian randomisation study.
Identification of TYW3/CRYZ and FGD4 as susceptibility genes for amyotrophic lateral sclerosis.
Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis.
Genome-wide association study identifies SIAH3 locus influencing the rate of ventricular enlargement in non-demented elders.
Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status.
Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status.
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.
Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.
Genetic variants of calcium and vitamin D metabolism in kidney stone disease.
Genetic variants of calcium and vitamin D metabolism in kidney stone disease.
A meta-analysis of genome-wide association studies of epigenetic age acceleration.
A regulatory variant of CHRM3 is associated with cannabis-induced hallucinations in European Americans.
Comparative genetic architectures of schizophrenia in East Asian and European populations.
Comparative genetic architectures of schizophrenia in East Asian and European populations.
Genome-Wide Association Study of Body Mass Index and Body Fat in Mexican-Mestizo Children.
Genome-Wide Association Study of Body Mass Index and Body Fat in Mexican-Mestizo Children.
A major role for common genetic variation in anxiety disorders.
Evidence that genes involved in hedgehog signaling are associated with both bipolar disorder and high BMI.
Evidence that genes involved in hedgehog signaling are associated with both bipolar disorder and high BMI.
Genome Wide Analysis Approach Suggests Chromosome 2 Locus to be Associated with Thiazide and Thiazide Like-Diuretics Blood Pressure Response.
Genome Wide Analysis Approach Suggests Chromosome 2 Locus to be Associated with Thiazide and Thiazide Like-Diuretics Blood Pressure Response.
Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2.
Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2.
Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population.
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.
Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid.
Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid.
Genome-wide association study of hippocampal atrophy rate in non-demented elders.
Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk.
Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk.
Novel genetic loci affecting facial shape variation in humans.
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment.
Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment.
Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment.
Fine mapping and identification of serum urate loci in American Indians: The Strong Heart Family Study.
Coffee Consumption and Kidney Function: A Mendelian Randomization Study.
Genomewide Gene-by-Sex Interaction Scans Identify ADGRV1 for Sex Differences in Opioid Dependent African Americans.
Genome-wide analysis identifies two susceptibility loci for positive thyroid peroxidase and thyroglobulin antibodies.
Genetic Variant Associated with Survival of Patients with Stage II-III Colon Cancer.
Causal Associations Between Serum Bilirubin Levels and Decreased Stroke Risk: A Two-Sample Mendelian Randomization Study.
Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UKB.
Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UKB.
Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UKB.
Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.
Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.
Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.
Genetic variants that associate with liver cirrhosis have pleiotropic effects on human traits.
Insights into the genetic basis of retinal detachment.
Insights into the genetic basis of retinal detachment.
Insights into the genetic basis of retinal detachment.
Insights into the genetic basis of retinal detachment.
Insights into the genetic basis of retinal detachment.
Identification of novel loci and new risk variant in known loci for colorectal cancer risk in East Asians.
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy.
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income.
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income.
Refining genome-wide associated loci for serum uric acid in individuals with African ancestry.
Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children.
Genome-wide association study of morbid obesity in Han Chinese.
Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13.
Association of Genetic Variation With Keratoconus.
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.
Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study in multiple populations.
Ordered multinomial regression for genetic association analysis of ordinal phenotypes at Biobank scale.
Genome-wide association study of shared liability to anxiety disorders in Army STARRS.
A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort.
Genetic Architecture of Circulating Very-Long-Chain (C24:0 and C22:0) Ceramide Concentrations.
Genetic Architecture of Circulating Very-Long-Chain (C24:0 and C22:0) Ceramide Concentrations.
Using Mendelian randomization to evaluate the causal relationship between serum C-reactive protein levels and age-related macular degeneration.
Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.
Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.
Genome-wide association study of metabolic syndrome in Korean populations.
Genome-wide association study of metabolic syndrome in Korean populations.
Genome-wide association study of metabolic syndrome in Korean populations.
Genome-wide association study of metabolic syndrome in Korean populations.
Genome-wide association study of metabolic syndrome in Korean populations.
Genome-wide association study of metabolic syndrome in Korean populations.
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure.
Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population.
Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank.
Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank.
Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank.
Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank.
Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank.
Functional validity, role, and implications of heavy alcohol consumption genetic loci.
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change.
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change.
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change.
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change.
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression.
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans.
Genome-Wide Association Study Identifies SLAMF1 Affecting the Rate of Memory Decline.
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits.
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis.
Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels.
Sepsis-associated acute respiratory distress syndrome in individuals of European ancestry: a genome-wide association study.
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.
Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank.
Genome-wide association study of the sensitivity to environmental stress and adversity (SESA) neuroticism cluster.
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.
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.
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.
Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort.
Genomic influences on self-reported childhood maltreatment.
Genomic dissection of 43 serum urate-associated loci provides multiple insights into molecular mechanisms of urate control.
Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease.
Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.
Genome-Wide Association Study of Cryptosporidiosis in Infants Implicates PRKCA.
AATF and SMARCA2 are associated with thyroid volume in Hashimoto's thyroiditis patients.
Genome-wide study of immune biomarkers in cerebrospinal fluid and serum from patients with bipolar disorder and controls.
Genome-wide study of immune biomarkers in cerebrospinal fluid and serum from patients with bipolar disorder and controls.
Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci.
Novel and Known Gene-Smoking Interactions With cIMT Identified as Potential Drivers for Atherosclerosis Risk in West-African Populations of the AWI-Gen Study.
Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci.
Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Using human genetics to understand the disease impacts of testosterone in men and women.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke.
Genetic Contributions to Maternal and Neonatal Vitamin D Levels.
Genetic Association and Expression Correlation between Colony-Stimulating Factor 1 Gene Encoding M-CSF and Adult-Onset Still's Disease.
Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank.
Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank.
Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank.
Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank.
Gene discovery for high-density lipoprotein cholesterol level change over time in prospective family studies.
Genetic Analysis of Ulcerative Colitis in Japanese Individuals Using Population-specific SNP Array.
Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases.
GWAS for time to failure of kidney transplants from African American deceased donors.
Genome-Wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length.
A genome-wide association study on liver enzymes in Korean population.
A genome-wide association study on liver enzymes in Korean population.
A genome-wide association study on liver enzymes in Korean population.
Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.
Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium.
Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium.
The genetic architecture of the human cerebral cortex.
The genetic architecture of the human cerebral cortex.
Genome-wide interaction study reveals age-dependent determinants of responsiveness to inhaled corticosteroids in individuals with asthma.
Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians.
Genome-Wide Association Study of Ocular Sarcoidosis Confirms HLA Associations and Implicates Barrier Function and Autoimmunity in African Americans.
A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness.
Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.
Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.
Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.
Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.
Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.
Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.
A Variation in FGF14 Is Associated with Downbeat Nystagmus in a Genome-Wide Association Study.
Polygenic Hyperlipidemias and Coronary Artery Disease Risk.
Polygenic Hyperlipidemias and Coronary Artery Disease Risk.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response.
Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response.
A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels.
Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.
Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis.
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
Replication of FTO Gene associated with lean mass in a Meta-Analysis of Genome-Wide Association Studies.
Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes.
Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis.
Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis.
Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis.
Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis.
Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis.
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan.
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan.
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan.
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan.
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan.
Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures.
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.
Common variation at 16p11.2 is associated with glycosuria in pregnancy: Findings from a genome-wide association study in European women.
Common variation at 16p11.2 is associated with glycosuria in pregnancy: Findings from a genome-wide association study in European women.
Common variation at 16p11.2 is associated with glycosuria in pregnancy: Findings from a genome-wide association study in European women.
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Minimal phenotyping yields genome-wide association signals of low specificity for major depression.
Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients.
Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients.
Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients.
Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients.
Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients.
A Family-Based Genome Wide Association Study of Externalizing Behaviors.
Genome-wide and Mendelian randomisation studies of liver MRI yield insights into the pathogenesis of steatohepatitis.
Genome-wide and Mendelian randomisation studies of liver MRI yield insights into the pathogenesis of steatohepatitis.
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration.
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration.
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration.
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration.
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration.
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration.
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration.
A genome-wide association study finds genetic variants associated with neck or shoulder pain in UK Biobank.
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
A population-specific low-frequency variant of SLC22A12 (p.W258*) explains nearby genome-wide association signals for serum uric acid concentrations among Koreans.
A genome-wide association study identifies two novel susceptible regions for squamous cell carcinoma of the head and neck.
A genome-wide association study identifies two novel susceptible regions for squamous cell carcinoma of the head and neck.
A genome-wide association study identifies two novel susceptible regions for squamous cell carcinoma of the head and neck.
A genome-wide association study identifies two novel susceptible regions for squamous cell carcinoma of the head and neck.
Genome-wide meta-analysis identifies novel loci associated with age-related macular degeneration.
Genome-wide association study identifies new loci for albuminuria in the Japanese population.
Shared genetic background between children and adults with attention deficit/hyperactivity disorder.
Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort.
Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort.
Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma.
Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis.
Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis.
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.
Genome-wide association studies and Mendelian randomization analyses for leisure sedentary behaviours.
Genome-wide association studies and Mendelian randomization analyses for leisure sedentary behaviours.
Genome-wide association studies and Mendelian randomization analyses for leisure sedentary behaviours.
Alcohol, Carbohydrate, and Calcium Intakes and Smoking Interactions with APOA5 rs662799 and rs2266788 were Associated with Elevated Plasma Triglyceride Concentrations in a Cross-Sectional Study of Korean Adults.
Twelve New Genomic Loci Associated With Bone Mineral Density.
Twelve New Genomic Loci Associated With Bone Mineral Density.
A genome-wide association study identifies key modulators of complement factor H binding to malondialdehyde-epitopes.
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.
Genome-Wide Association Study of Diabetogenic Adipose Morphology in the GENetics of Adipocyte Lipolysis (GENiAL) Cohort.
Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval.
Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval.
Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval.
Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study.
Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study.
Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study.
Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients.
Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants.
Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants.
Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants.
Multifaceted genome-wide study identifies novel regulatory loci in SLC22A11 and ZNF45 for body mass index in Indians.
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.
Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian-randomization study.
Identification of type 2 diabetes loci in 433,540 East Asian individuals.
Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study.
Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study.
Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection.
Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C.
Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C.
Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C.
Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C.
Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C.
Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C.
Genomic analysis of diet composition finds novel loci and associations with health and lifestyle.
Genomic analysis of diet composition finds novel loci and associations with health and lifestyle.
Genomic analysis of diet composition finds novel loci and associations with health and lifestyle.
Genomic analysis of diet composition finds novel loci and associations with health and lifestyle.
A positively selected FBN1 missense variant reduces height in Peruvian individuals.
Genome-wide association study in Asians identifies novel loci for high myopia and highlights a nervous system role in its pathogenesis.
Family-based genome-wide association study of leprosy in Vietnam.
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.
CDH6 and HAGH protein levels in plasma associate with Alzheimer's disease in APOE ε4 carriers.
Pharmacogenetic assessment of tafenoquine efficacy in patients with Plasmodium vivax malaria.
Remote modulation of lncRNA GCLET by risk variant at 16p13 underlying genetic susceptibility to gastric cancer.
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits.
Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits.
Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits.
Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits.
Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study.
Association of TIM-1 (T-Cell Immunoglobulin and Mucin Domain 1) With Incidence of Stroke.
Transethnic Meta-analysis of Genome-wide Association Studies Identifies Three New Loci and Characterizes Population-specific Differences for Coronary Artery Disease.
Transethnic Meta-analysis of Genome-wide Association Studies Identifies Three New Loci and Characterizes Population-specific Differences for Coronary Artery Disease.
Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men.
Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men.
Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance.
The Human Leukocyte Antigen Locus and Rheumatic Heart Disease Susceptibility in South Asians and Europeans.
Association of OPRM1 Functional Coding Variant With Opioid Use Disorder: A Genome-Wide Association Study.
Phenotypic and Genetic Characterization of Lower LDL-C and Increased Type-2 Diabetes Risk in the UK Biobank.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
Clonal myelopoiesis in the UK Biobank cohort: ASXL1 mutations are strongly associated with smoking.
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study.
A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness.
Genetic Basis and Prognostic Value of Exercise QT Dynamics.
Genetic Basis and Prognostic Value of Exercise QT Dynamics.
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.
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.
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.
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.
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.
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.
Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1.
Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1.
Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1.
Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1.
Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1.
Genomewide Association Study of Severe Covid-19 with Respiratory Failure.
Metabolomic and genetic associations with insulin resistance in pregnancy.
Strong association between the 12q24 locus and sweet taste preference in the Japanese population revealed by genome-wide meta-analysis.
Four Loci Are Associated with Cardiorespiratory Fitness and Endurance Performance in Young Chinese Females.
Urine 6-Bromotryptophan: Associations with Genetic Variants and Incident End-Stage Kidney Disease.
Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis.
Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis.
Large-scale genome-wide association study identifies HLA class II variants associated with chronic HBV infection: a study from Taiwan Biobank.
An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn's Disease in Japanese Populations.
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease.
Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study.
Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study.
Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study.
Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study.
Genome-Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study.
Meta-analysis of 26,638 Individuals Identifies Two Genetic Loci Associated with Left Ventricular Ejection Fraction.
Meta-analysis of 26,638 Individuals Identifies Two Genetic Loci Associated with Left Ventricular Ejection Fraction.
Genome-wide Association Study of the Postprandial Triglyceride Response Yields Common Genetic Variation in Hepatic Lipase (LIPC).
Genome-wide Association Study of the Postprandial Triglyceride Response Yields Common Genetic Variation in Hepatic Lipase (LIPC).
Genome-wide Association Study of the Postprandial Triglyceride Response Yields Common Genetic Variation in Hepatic Lipase (LIPC).
Common and rare susceptibility genetic variants predisposing to Brugada Syndrome in Thailand.
Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling.
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Mood Stabilizing Antiepileptic Treatment Response in Bipolar Disorder: A Genome-Wide Association Study.
Genomic Analysis Identifies New Loci Associated With Motor Complications in Parkinson's Disease.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults.
A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish population.
PPARGC1B Is Associated with Nontraumatic Osteonecrosis of the Femoral Head: A Genomewide Association Study on a Chart-Reviewed Cohort.
Pharmacogenomics of aromatase inhibitors in postmenopausal breast cancer and additional mechanisms of anastrozole action.
Discovery and Mediation Analysis of Cross-Phenotype Associations With Asthma and Body Mass Index in 12q13.2.
Discovery and Mediation Analysis of Cross-Phenotype Associations With Asthma and Body Mass Index in 12q13.2.
Genome-wide association study of corneal biomechanical properties identifies over 200 loci providing insight into the genetic aetiology of ocular diseases.
Four pleiotropic loci associated with fat mass and lean mass.
Exome Chip Analysis of 14,026 Koreans Reve-als Known and Newly Discovered Genetic Loci Associated with Type 2 Diabetes Mellitus.
Genome-wide association study and polygenic risk score analysis of esketamine treatment response.
Genome-wide association study identifies a novel maternal geneâÃâstress interaction associated with spontaneous preterm birth.
Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections.
Genetic Risk of Trigger Finger: Results of a Genomewide Association Study.
Genetic variants and functional pathways associated with resilience to Alzheimer's disease.
Chances and challenges of machine learning-based disease classification in genetic association studies illustrated on age-related macular degeneration.
Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism.
Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels.
Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels.
Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels.
Association Between ABCB1 Genetic Variants and Persistent Chemotherapy-Induced Alopecia in Women With Breast Cancer.
Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging.
Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging.
Common susceptibility loci for male breast cancer.
Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure.
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus.
Native American ancestry significantly contributes to neuromyelitis optica susceptibility in the admixed Mexican population.
Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study.
Genetic and functional insights into the fractal structure of the heart.
Genetic and functional insights into the fractal structure of the heart.
Genetic and functional insights into the fractal structure of the heart.
Genetic and functional insights into the fractal structure of the heart.
Genetic and functional insights into the fractal structure of the heart.
Genetic and functional insights into the fractal structure of the heart.
Genetic and functional insights into the fractal structure of the heart.
Genetic control of CCL24, POR, and IL23R contributes to the pathogenesis of sarcoidosis.
Protective effect of club cell secretory protein (CC-16) on COPD risk and progression: a Mendelian randomisation study.
Genome-wide association study reveals a novel locus for asthma with severe exacerbations in diverse populations.
Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease.
Genome-wide association study and meta-analysis on alcohol-related liver cirrhosis identifies novel genetic risk factors.
Identification of new susceptibility loci associated with rheumatoid arthritis.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Polygenic and Monogenic Basis of Blood Traits and Diseases.
The Genetic Makeup of the Electrocardiogram.
Genome-wide association study for circulating fibroblast growth factor 21 and 23.
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.
A genome-wide association study on fish consumption in a Japanese population-the Japan Multi-Institutional Collaborative Cohort study.
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.
Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.
Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy.
Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences.
Association of genetic variants in migraineurs with and without restless legs syndrome.
Identification of pleiotropic loci underlying hip bone mineral density and trunk lean mass.
Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.
Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.
Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.
Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.
Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.
Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study.
Genome-wide association analysis of opioid use disorder: A novel approach using clinical data.
Genome-wide association analysis of opioid use disorder: A novel approach using clinical data.
Genome-wide association for HbA1c in Malay identified deletion on SLC4A1 that influences HbA1c independent of glycemia.
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
Genome-Wide Association Analysis of Pancreatic Beta Cell Glucose Sensitivity.
Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality.
Pleiotropic genomic variants at 17q21.31 associated with bone mineral density and body fat mass: a bivariate genome-wide association analysis.
Pleiotropic genomic variants at 17q21.31 associated with bone mineral density and body fat mass: a bivariate genome-wide association analysis.
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis.
Three pleiotropic loci associated with bone mineral density and lean body mass.
Three pleiotropic loci associated with bone mineral density and lean body mass.
Novel Risk Loci in Tinnitus and Causal Inference With Neuropsychiatric Disorders Among Adults of European Ancestry.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study.
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming.
Variants in <i>PPP2R2B</i> and <i>IGF2BP3</i> are associated with higher tau deposition.
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.
Biological insights from multi-omic analysis of 31 genomic risk loci for adult hearing difficulty.
Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study.
Genetic basis of falling risk susceptibility in the UK Biobank Study.
A Genome-wide Association Study for Concussion Risk.
Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents.
ALDH2 genotype modulates the association between alcohol consumption and AST/ALT ratio among middle-aged Japanese men: a genome-wide GâÃâE interaction analysis.
Comparison of Genome-Wide Association Scans for Quantitative and Observational Measures of Human Hair Curvature.
Comparison of Genome-Wide Association Scans for Quantitative and Observational Measures of Human Hair Curvature.
Genome-Wide Association Analysis of Neonatal White Matter Microstructure.
Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.
Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk.
Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk.
Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk.
Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells.
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.
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.
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene.
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene.
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene.
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells.
Exome-wide association analysis suggests LRP2BP as a susceptibility gene for endothelial injury in systemic sclerosis in Han Chinese population.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.
A Genome-Wide Association Study Identifies the Association between the 12q24 Locus and Black Tea Consumption in Japanese Populations.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms.
Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals.
Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals.
Genome-wide association study of high-sensitivity C-reactive protein, D-dimer and Interleukin-6 levels in multi-ethnic HIV+ cohorts.
Genome-wide association study of high-sensitivity C-reactive protein, D-dimer and Interleukin-6 levels in multi-ethnic HIV+ cohorts.
A genome-wide association study of severe asthma exacerbations in Latino children and adolescents.
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk.
The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study.
The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study.
The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study.
Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms.
An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease.
Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.
Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease.
Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease.
Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease.
Genome-wide association study of non-tuberculous mycobacterial pulmonary disease.
Genome-Wide Association Study Highlights APOH as a Novel Locus for Lipoprotein(a) Levels.
Secondary Genome-Wide Association Study Using Novel Analytical Strategies Disentangle Genetic Components of Cleft Lip and/or Cleft Palate in 1q32.2.
Genome-wide association study of self-reported walking pace suggests beneficial effects of brisk walking on health and survival.
Effect of plasma polyunsaturated fatty acid levels on leukocyte telomere lengths in the Singaporean Chinese population.
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Genetic risk factors in drug-induced liver injury due to isoniazid-containing anti-tuberculosis drug regimens.
Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans.
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans.
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans.
Genome-wide search for genes affecting the age at diagnosis of type 1 diabetes.
Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome.
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Congenital heart disease risk loci identified by genome-wide association study in European patients.
Congenital heart disease risk loci identified by genome-wide association study in European patients.
Congenital heart disease risk loci identified by genome-wide association study in European patients.
Genetic predictors of severe skin toxicity in stage III colon cancer patients treated with cetuximab: NCCTG N0147 (Alliance).
Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations.
Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band.
Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset.
Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset.
Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset.
Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset.
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
The genetic architecture of sporadic and multiple consecutive miscarriage.
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.
Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health.
Urinary metabolite quantitative trait loci in children and their interaction with dietary factors.
Urinary metabolite quantitative trait loci in children and their interaction with dietary factors.
Urinary metabolite quantitative trait loci in children and their interaction with dietary factors.
Urinary metabolite quantitative trait loci in children and their interaction with dietary factors.
A genome-wide association study in Japanese identified one variant associated with a preference for a Japanese dietary pattern.
Associations of Observational and Genetically Determined Caffeine Intake With Coronary Artery Disease and Diabetes Mellitus.
Associations of Observational and Genetically Determined Caffeine Intake With Coronary Artery Disease and Diabetes Mellitus.
Associations of Observational and Genetically Determined Caffeine Intake With Coronary Artery Disease and Diabetes Mellitus.
Cerebral small vessel disease genomics and its implications across the lifespan.
Cerebral small vessel disease genomics and its implications across the lifespan.
Cerebral small vessel disease genomics and its implications across the lifespan.
Cerebral small vessel disease genomics and its implications across the lifespan.
Cerebral small vessel disease genomics and its implications across the lifespan.
Cerebral small vessel disease genomics and its implications across the lifespan.
A large-scale association study detects novel rare variants, risk genes, functional elements, and polygenic architecture of prostate cancer susceptibility.
Genetic mechanisms of critical illness in Covid-19.
Genetic mechanisms of critical illness in Covid-19.
Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract.
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.
Genome-wide Association Studies Reveal Novel Locus With Sex-/Therapy-Specific Fracture Risk Effects in Childhood Cancer Survivors.
Urate, Blood Pressure, and Cardiovascular Disease: Evidence From Mendelian Randomization and Meta-Analysis of Clinical Trials.
Causal relationship and shared genetic loci between psoriasis and type 2 diabetes through trans-disease meta-analysis.
Causal relationship and shared genetic loci between psoriasis and type 2 diabetes through trans-disease meta-analysis.
Genome-wide association study identifying novel variant for fasting insulin and allelic heterogeneity in known glycemic loci in Chilean adolescents: The Santiago Longitudinal Study.
Deciphering the genetic and epidemiological landscape of mitochondrial DNA abundance.
Genetic Risk Score for Serum 25-Hydroxyvitamin D Concentration Helps to Guide Personalized Vitamin D Supplementation in Healthy Finnish Adults.
Germline variants are associated with increased primary melanoma tumor thickness at diagnosis.
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
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.
No evidence that vitamin D is able to prevent or affect the severity of COVID-19 in individuals with European ancestry: a Mendelian randomisation study of open data.
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction.
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction.
Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia.
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations.
Identification of genetic loci associated with nocturnal enuresis: a genome-wide association study.
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.
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.
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.
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.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Large-scale association analyses identify host factors influencing human gut microbiome composition.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Genetics of 35 blood and urine biomarkers in the UK Biobank.
Circulating chemerin levels are determined through circulating platelet counts in nondiabetic Taiwanese people: A bidirectional Mendelian randomization study.
Circulating chemerin levels are determined through circulating platelet counts in nondiabetic Taiwanese people: A bidirectional Mendelian randomization study.
Variation in the SERPINA6/SERPINA1 locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease.
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.
Associations between COVID-19 and skin conditions identified through epidemiology and genomic studies.
The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium.
The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium.
Functional Haplotype of <i>LIPC</i> Induces Triglyceride-Mediated Suppression of HDL-C Levels According to Genome-Wide Association Studies.
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder.
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder.
Genetic determinants of ferritin, haemoglobin levels and haemoglobin trajectories: results from Donor InSight.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect.
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.
Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus.
CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.
Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel Disease.
Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel Disease.
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women.
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women.
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women.
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women.
Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia.
Genome-Wide Association Study of Circulating Interleukin 6 Levels Identifies Novel Loci.
A Genome-Wide Association Study of Childhood Body Fatness.
Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder.
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction.
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction.
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
Genome-wide association study in patients with pulmonary <i>Mycobacterium avium</i> complex disease.
Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology.
Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology.
Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology.
Genetic and functional interaction network analysis reveals global enrichment of regulatory T cell genes influencing basal cell carcinoma susceptibility.
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.
Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT.
Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach.
Genetic determinants of daytime napping and effects on cardiometabolic health.
Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations.
Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations.
Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations.
Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations.
GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility.
Genetic insight into sick sinus syndrome.
Genetic determinants of risk in autoimmune pulmonary alveolar proteinosis.
"The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20âyears after assessment.
Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence.
Interaction between <i>G</i> <i>ALNT12</i> and <i>C1GALT1</i> Associates with Galactose-Deficient IgA1 and IgA Nephropathy.
Genetic loci associated with skin pigmentation in African Americans and their effects on vitamin D deficiency.
Genome-Wide Association Studies Identify Two Novel Loci Conferring Susceptibility to Diabetic Retinopathy in Japanese Patients with Type 2 Diabetes.
The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial Variation.
Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children.
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.
Genetic architectures of proximal and distal colorectal cancer are partly distinct.
Genetic architectures of proximal and distal colorectal cancer are partly distinct.
Genetic architectures of proximal and distal colorectal cancer are partly distinct.
Genetic architectures of proximal and distal colorectal cancer are partly distinct.
A Genome-wide Association Study on Confection Consumption in a Japanese Population- The Japan Multi-Institutional Collaborative Cohort study.
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.
Kleine-Levin syndrome is associated with birth difficulties and genetic variants in the <i>TRANK1</i> gene loci.
Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk.
Integrated genetic analyses revealed novel human longevity loci and reduced risks of multiple diseases in a cohort study of 15,651 Chinese individuals.
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.
Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Variants in NEB and RIF1 genes on chr2q23 are associated with skeletal muscle index in Koreans: genome-wide association study.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS.
Genetic discovery and risk characterization in type 2 diabetes across diverse populations.
Observational or Genetically Predicted Higher Vegetable Intake and Kidney Function Impairment: An Integrated Population-Scale Cross-Sectional Analysis and Mendelian Randomization Study.
Genetic variation in WNT9B increases relapse hazard in multiple sclerosis.
Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function.
Gene-environment correlations and causal effects of childhood maltreatment on physical and mental health: a genetically informed approach.
Nuclear genome-wide associations with mitochondrial heteroplasmy.
Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression.
Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank.
Identification of common genetic variants associated with serum concentrations of p, p'-DDE in non-occupational populations in eastern China.
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci.
Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci.
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity.
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity.
Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity.
Genetic factors influencing a neurobiological substrate for psychiatric disorders.
Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study.
Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study.
Genome-wide association and transcriptome analysis suggests total serum ghrelin to be linked with GFRAL.
Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.
Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.
Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.
Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study.
The association of genetically determined serum glycine with cardiovascular risk in East Asians.
Analysis of overlapping genetic association in type 1 and type 2 diabetes.
Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia.
Sex-stratified genome-wide association study of multisite chronic pain in UK Biobank.
Sex-stratified genome-wide association study of multisite chronic pain in UK Biobank.
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions.
Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose.
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression.
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression.
The Impact of Removing Former Drinkers from Genome-wide Association Studies of AUDIT-C.
Germline variants at SOHLH2 influence multiple myeloma risk.
Germline variants at SOHLH2 influence multiple myeloma risk.
Genetically-Determined Serum Calcium Levels and Markers of Ventricular Repolarisation: A Mendelian Randomization Study in the UK Biobank.
Genetic analyses identify widespread sex-differential participation bias.
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.
Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity.
Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia.
Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity.
Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity.
Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity.
Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity.
A Systematic Analysis of Protein-altering Exonic Variants in Chronic Obstructive Pulmonary Disease.
Medical Records-Based Genetic Studies of the Complement System.
Medical Records-Based Genetic Studies of the Complement System.
Low frequency variants associated with leukocyte telomere length in the Singapore Chinese population.
A genome-wide association study of plasma phosphorylated tau181.
Effect of longevity genetic variants on the molecular aging rate.
A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans.
A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans.
A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans.
Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease.
Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD.
Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD.
Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD.
Genome-wide association study of cardiac troponin I in the general population.
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes.
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes.
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes.
Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease.
Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease.
Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease.
Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease.
Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease.
Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease.
Identification of a Novel Genetic Marker for Risk of Degenerative Rotator Cuff Disease Surgery in the UK Biobank.
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans.
A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans.
A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans.
A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans.
Ethnic similarities in genetic polymorphisms associated with atrial fibrillation: Far East Asian vs European populations.
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology.
The genetic architecture of the human thalamus and its overlap with ten common brain disorders.
The genetic architecture of the human thalamus and its overlap with ten common brain disorders.
The genetic architecture of the human thalamus and its overlap with ten common brain disorders.
The genetic architecture of the human thalamus and its overlap with ten common brain disorders.
Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants.
Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants.
Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants.
Genome-wide association study of early-onset bipolar I disorder in the Han Taiwanese population.
Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study.
Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study.
Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease.
Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche.
Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche.
<i>ALDH2</i> p.E504K Variation and Sex Are Major Factors Associated with Current and Quitting Alcohol Drinking in Japanese Oldest Old.
Genetic Susceptibility for Low Testosterone in Men and Its Implications in Biology and Screening: Data from the UK Biobank.
Genetics of symptom remission in outpatients with COVID-19.
Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions.
Joint genome-wide association analyses identified 49 novel loci for age at natural menopause.
Joint genome-wide association analyses identified 49 novel loci for age at natural menopause.
Genetic underpinnings of sociability in the general population.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
The trans-ancestral genomic architecture of glycemic traits.
Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study.
Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
A UGT1A1 variant is associated with serum total bilirubin levels, which are causal for hypertension in African-ancestry individuals.
Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.
Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.
Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.
Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning.
Genome-Wide Association Analyses Identify Variants in <i>IRF4</i> Associated With Acute Myeloid Leukemia and Myelodysplastic Syndrome Susceptibility.
Genome-Wide Association Analyses Identify Variants in <i>IRF4</i> Associated With Acute Myeloid Leukemia and Myelodysplastic Syndrome Susceptibility.
Potential Novel Genes for Late-Onset Alzheimer's Disease in East-Asian Descent Identified by APOE-Stratified Genome-Wide Association Study.
Identifying novel genetic variants for brain amyloid deposition: a genome-wide association study in the Korean population.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study.
Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia.
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging.
Genome Wide Association Study Identifies Risk Loci For Cluster Headache.
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis.
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis.
Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty.
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour.
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour.
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour.
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour.
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour.
Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.
Functional multigenic variations associated with hodgkin lymphoma.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses.
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.
Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.
Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.
Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.
Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration.
TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study.
Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank.
Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank.
Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank.
Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank.
Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank.
Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank.
Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank.
Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition.
A Genome-Wide Association Study Identifying SVEP1 Variant as a Predictor of Response to Tolvaptan for Cirrhotic Ascites.
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms.
Association Between NEDD4L Variation and the Genetic Risk of Acute Appendicitis: A Multi-institutional Genome-Wide Association Study.
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
Genetic Susceptibility to Pneumonia: A GWAS Meta-Analysis Between the UK Biobank and FinnGen.
Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan.
Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan.
Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan.
Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy.
Genome-wide Association Study Identified Chromosome 8 Locus Associated with Medication-related Osteonecrosis of the Jaw.
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.
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.
Genetics of PlGF plasma levels highlights a role of its receptors and supports the link between angiogenesis and immunity.
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
A genome-wide association study of the frailty index highlights brain pathways in ageing.
Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability.
Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability.
Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability.
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction.
Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort.
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions.
A genome-wide association meta-analysis identifies new Eosinophilic esophagitis loci.
Genome-wide association study of liver enzyme elevation in rheumatoid arthritis patients starting methotrexate.
Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.
Kallikrein augments the anticoagulant function of the protein C system in thrombin generation.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
A cross-population atlas of genetic associations for 220 human phenotypes.
Genome-wide association study identifies multiple genetic loci for skin color in Korean women.