Author: Daniel J. Rader

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Preprints

A genome-first approach to rare variants in hypertrophic cardiomyopathy genes MYBPC3 and MYH7 in a medical biobank

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Seasonal human coronavirus antibodies are boosted upon SARS-CoV-2 infection but not associated with protection

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Discovery of 318 novel loci for type-2 diabetes and related micro- and macrovascular outcomes among 1.4 million participants in a multi-ethnic meta-analysis.

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SARS-CoV-2 seropositivity and seroconversion in patients undergoing active cancer-directed therapy

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Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease

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A Mendelian randomization study of the role of lipoprotein subfractions in coronary artery disease

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A genome-wide association study for nonalcoholic fatty liver disease identifies novel genetic loci and trait-relevant candidate genes in the Million Veteran Program.

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SARS-CoV-2 Seroprevalence Among Parturient Women

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Sero-monitoring of health care workers reveals complex relationships between common coronavirus antibodies and SARS-CoV-2 severity

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Exome-by-phenome-wide rare variant gene burden association with electronic health record phenotypes

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Genome-wide Association Study of Alcohol Consumption and Use Disorder in Multiple Populations (N = 274,424)

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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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Genetic And Epigenetic Fine Mapping Of Complex Trait Associated Loci In The Human Liver

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Disrupting upstream translation in mRNAs leads to loss-of-function associated with human disease

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RNA-binding protein A1CF modulates plasma triglyceride levels through posttranscriptional regulation of stress-induced VLDL secretion

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Genetic regulatory mechanisms of smooth muscle cells map to coronary artery disease risk loci

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Polygenic risk of psychiatric disorders exhibits cross-trait associations in electronic health record data

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Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

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Genetics of Height and Risk of Atrial Fibrillation: A Mendelian Randomization Study

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Multiplexed targeted resequencing identifies coding and regulatory variation underlying phenotypic extremes of HDL-cholesterol in humans

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Genetics of Smoking and Risk of Atherosclerotic Cardiovascular Diseases: A Mendelian Randomization Study

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Targeting the Coronavirus Nucleocapsid Protein through GSK-3 Inhibition

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Coronary Artery Disease Risk of Familial Hypercholesterolemia Genetic Variants Independent of Historical Cholesterol Exposure

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Myeloid Tribbles 1 induces early atherosclerosis via enhanced foam cell expansion

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Linking abdominal imaging traits to electronic health record phenotypes

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ApoC-III helical structure determines its ability to bind plasma lipoproteins and inhibit Lipoprotein Lipase-mediated triglyceride lipolysis.

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Association of the Transthyretin Variant V122I With Polyneuropathy Among Individuals of African Descent

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Genetic Variation in Blood Pressure and Lifetime Risk of Peripheral Artery Disease: A Mendelian Randomization Study

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Multi-trait GWAS of atherosclerosis detects novel pleiotropic loci

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