Author: Dan M. Roden

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Preprints

Arrhythmia variant associations and reclassifications in the eMERGE-III sequencing study

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Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

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The All of Us Research Program: data quality, utility, and diversity

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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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Genetic determinants of risk and survival in pulmonary arterial hypertension

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Deep Mutational Scan of a cardiac sodium channel voltage sensor

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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High-throughput reclassification of SCN5A variants

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

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Mutations in RPL3L and MYZAP increase risk of atrial fibrillation

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A rare variant on a common risk haplotype of HFE causes increased risk of hereditary hemochromatosis

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A Bayesian method using sparse data to estimate penetrance of disease-associated genetic variants

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High-throughput discovery of trafficking-deficient variants in the cardiac potassium channel KCNH2

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Temporal changes in genetic admixture are linked to heterozygosity and health diagnoses in humans

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Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

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Bidirectional Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of intermediate potential

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A scalable EHR-based approach for phenotype discovery and variant interpretation for hereditary cancer genes

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