Author: Henry J Lin

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Preprints

An open resource of structural variation for medical and population genetics

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A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.

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Loss-of-function in IRF2BPL is associated with neurological phenotypes

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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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

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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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Multi-ethnic genome-wide association study of decomposed cardioelectric phenotypes illustrates strategies to identify and characterize evidence of shared genetic effects for complex traits

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GWAS of QRS Duration Identifies New Loci Specific to Hispanic/Latino Populations

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Monogenic and Polygenic Contributions to QTc Prolongation in the Population

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Mitochondrial DNA Copy Number and Incident Atrial Fibrillation

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Endophenotype Effect Sizes Provide Evidence Supporting Variant Pathogenicity in Monogenic Disease Susceptibility Genes

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