Author: Donald W Bowden

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Preprints

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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

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Identification of type 2 diabetes loci in 433,540 East Asian individuals

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Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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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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Rare coding variants in 35 genes associate with circulating lipid levels: a multi-ancestry analysis of 170,000 exomes

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

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Rare Non-coding Variation Identified by Large Scale Whole Genome Sequencing Reveals Unexplained Heritability of Type 2 Diabetes: Trans-Omics for Precision Medicine (TOPMed) Program

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Genetic variants for head size share genes and pathways with cancer

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Progression of chronic kidney disease in African American with type 2 diabetes mellitus using topology learning in electronic medical records

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

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Whole genome sequence analysis of blood lipid levels in >66,000 individuals

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A framework for detecting noncoding rare variant associations of large-scale whole-genome sequencing studies

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