Author: Lisa R Yanek

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Preprints

Recovery of trait heritability from whole genome sequence data

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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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  • Site-wide: 18,782
  • In genetic and genomic medicine: 69
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  • Site-wide: 11,151

Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies

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  • In genetics: 1,306
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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: 2,831
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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 coding variants in 35 genes associate with circulating lipid levels: a multi-ancestry analysis of 170,000 exomes

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  • In genetics: 1,896
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Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

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  • In genomics: 3,797
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Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

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  • In hematology: 33
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Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities

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  • In neuroscience: 9,111
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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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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

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  • Site-wide: 87,458
  • In genetics: 3,944
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  • Site-wide: 51,145
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Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

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  • In genetics: 4,106
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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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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: 470
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Whole Genome Sequence Association Analysis of Fasting Glucose and Fasting Insulin Levels in Diverse Cohorts from the NHLBI TOPMed Program

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  • In genetic and genomic medicine: 490
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