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Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.
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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
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A saturated map of common genetic variants associated with human height.
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
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Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
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Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.
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Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.
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Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus
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Genetic variation in CADM2 as a link between psychological traits and obesity
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Associations of autozygosity with a broad range of human phenotypes.
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A key role for the novel coronary artery disease gene JCAD in atherosclerosis via shear stress mechanotransduction
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A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure
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Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease
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Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
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Multi-ancestry genome-wide gene–smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
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Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets
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