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A saturated map of common genetic variants associated with human height
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외 610명 — 모두 보기
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23andMe Research Team · VA Million Veteran Program 외 컨소시엄 5곳
Nature · 2022 · PMID 36224396 · open access
페이지 12개+
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
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외 279명 — 모두 보기
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페이지 12개+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
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외 135명 — 모두 보기
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Million Veteran Program · Lifelines Cohort Study 외 컨소시엄 2곳
Nature genetics · 2024 · PMID 38689001 · open access
페이지 12개+
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
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외 180명 — 모두 보기
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페이지 7개
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외 137명 — 모두 보기
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Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
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A genome- and phenome-wide association study of plasma procalcitonin concentrations in individuals of European ancestry
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외 1명 — 모두 보기
EBioMedicine · 2026 · PMID 41406505 · open access
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Meta-analysis of genome-wide association studies of anxiety disorders
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외 35명 — 모두 보기
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Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
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LifeLines Cohort Study · CHARGE Lipids Working Group
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Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci
Thio CHL,
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외 6명 — 모두 보기
Lifelines Cohort Study group
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