Author: Lisa R Yanek

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Preprints

Recovery of trait heritability from whole genome sequence data

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  • In genetics: 16
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  • Site-wide: 2,513

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

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  • Site-wide: 23,324
  • In genetic and genomic medicine: 61
• Year to date:
  • Site-wide: 10,059
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  • Site-wide: 5,795

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

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  • Site-wide: 24,518
  • In genetics: 1,234
• Year to date:
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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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  • Site-wide: 29,390
  • In genomics: 2,710
• Year to date:
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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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  • In genomics: 2,986
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  • Site-wide: 50,871

Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

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  • Site-wide: 49,938
  • In genomics: 3,938
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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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  • Site-wide: 51,521
  • In genetics: 2,496
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Common genetic variation indicates separate etiologies for periventricular and deep white matter hyperintensities

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  • In neuroscience: 8,603
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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: 3,909
• Year to date:
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  • Site-wide: 100,476

A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

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  • Site-wide: 84,749
  • In genetics: 3,939
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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: 3,945
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  • Site-wide: 90,859
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  • Site-wide: 108,039

Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

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  • Site-wide: 89,333
  • In hematology: 50
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  • Site-wide: 3,533
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  • Site-wide: 2,468

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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  • Site-wide: 92,791
  • In genetic and genomic medicine: 305
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  • Site-wide: 37,518
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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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  • Site-wide: 119,295
  • In genetic and genomic medicine: 516
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  • Site-wide: 2,235
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