Author: Christopher J. O’Donnell

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Preprints

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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  • In genetics: 449
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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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  • Site-wide: 9,967
  • In genetic and genomic medicine: 28
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Genetic predisposition to myeloproliferative neoplasms implicates hematopoietic stem cell biology

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  • In genetics: 780
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Measuring genetic variation in the multi-ethnic Million Veteran Program (MVP)

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  • In genetics: 1,286
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Machine learning identifies SNPs predictive of advanced coronary artery calcium in ClinSeq® and Framingham Heart Study cohorts

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  • In genomics: 2,809
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High-throughput Multimodal Automated Phenotyping (MAP) with Application to PheWAS

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  • In bioinformatics: 4,436
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A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

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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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  • In genetic and genomic medicine: 139
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Genetics of fasting indices of glucose homeostasis using GWIS unravels tight relationships with inflammatory markers

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  • In genetics: 3,358
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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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  • In genetics: 3,944
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Actionable druggable genome-wide Mendelian randomization identifies repurposingopportunities for COVID-19

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  • In epidemiology: 3,908
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