Author: Russell P Tracy

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Preprints

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

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SARS-CoV-2 seropositivity and subsequent infection risk in healthy young adults: a prospective cohort study

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  • Site-wide: 3,909
  • In infectious diseases: 684
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Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

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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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  • Site-wide: 9,923
  • In genetics: 477
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Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

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  • In genetic and genomic medicine: 89
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Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

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  • In genomics: 2,836
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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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Whole-Genome Association Analyses of Sleep-disordered Breathing Phenotypes in the NHLBI TOPMed Program

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  • In genetics: 2,833
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Combined protein and transcript single cell RNA sequencing reveals cardiovascular disease and HIV signatures

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  • In immunology: 1,787
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Collaborative Cohort of Cohorts for COVID-19 Research (C4R) Study: Study Design

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  • In epidemiology: 2,786
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Bidirectional Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of intermediate potential

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  • In genetic and genomic medicine: 484
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