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Fulminant Myocarditis with Combination Immune Checkpoint Blockade

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Drug-induced prolongation of the QT interval

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A genomic mutational constraint map using variation in 76,156 human genomes

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Cardiovascular toxicities associated with immune checkpoint inhibitors: an observational, retrospective, pharmacovigilance study

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A structural variation reference for medical and population genetics

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A saturated map of common genetic variants associated with human height

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Prevention of Torsade de Pointes in Hospital Settings: A Scientific Statement From the American Heart Association and the American College of Cardiology Foundation

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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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Recovery of trait heritability from whole genome sequence data

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A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

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Common variants in KCNN3 are associated with lone atrial fibrillation

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A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose

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Metabolic Syndrome and Risk of Development of Atrial Fibrillation: The Niigata Preventive Medicine Study

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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

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Cardiac Sodium Channel ( SCN5A ) Variants Associated with Atrial Fibrillation

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The phenotypic legacy of admixture between modern humans and Neandertals

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Association of step counts over time with the risk of chronic disease in the All of Us Research Program

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Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes

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