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Systematic Localization of Common Disease-Associated Variation in Regulatory DNA

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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Executive Summary: Heart Disease and Stroke Statistics—2012 Update: A Report From the American Heart Association

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Inherited causes of clonal haematopoiesis in 97,691 whole genomes

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Meta-analysis identifies six new susceptibility loci for atrial fibrillation

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Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

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European Ancestry as a Risk Factor for Atrial Fibrillation in African Americans

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A Genome-Wide Association Study of Depressive Symptoms

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Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

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Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese

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Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

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Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

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Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

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