Author: Andrew D. Johnson

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Preprints

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

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  • Site-wide: 1,049
  • In genomics: 95
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  • Site-wide: 2,365
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  • Site-wide: 5,830

Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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  • Site-wide: 4,004
  • In genetics: 168
• Year to date:
  • Site-wide: 55,879
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  • Site-wide: 75,377

Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations

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  • Site-wide: 5,734
  • In genetics: 267
• Year to date:
  • Site-wide: 5,219
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The Polygenic and Monogenic Basis of Blood Traits and Diseases

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  • Site-wide: 7,441
  • In genetic and genomic medicine: 25
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  • Site-wide: 22,568
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  • Site-wide: 20,061

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

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  • Site-wide: 9,478
  • In genetics: 450
• Year to date:
  • Site-wide: 85,161
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  • Site-wide: 94,473

Genome-wide Association Study Of Plasma Proteins Identifies Putatively Causal Genes, Proteins, And Pathways For Cardiovascular Disease

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  • Site-wide: 14,913
  • In epidemiology: 968
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  • Site-wide: 59,066
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  • Site-wide: 86,478

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: 27,072
  • In genetics: 1,306
• Year to date:
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  • Site-wide: 103,244

Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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  • Site-wide: 31,634
  • In genomics: 2,819
• Year to date:
  • Site-wide: 94,590
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  • Site-wide: 108,192

De novo mutations across 1,465 diverse genomes reveal novel mutational insights and reductions in the Amish founder population.

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  • Site-wide: 34,832
  • In genetics: 1,668
• Year to date:
  • Site-wide: 68,521
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  • Site-wide: 54,253

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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  • Site-wide: 37,193
  • In genomics: 3,164
• Year to date:
  • Site-wide: 78,284
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  • Site-wide: 108,612

Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

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  • In genomics: 3,797
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  • Site-wide: 32,668

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

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  • Site-wide: 50,959
  • In hematology: 33
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  • Site-wide: 5,592
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  • Site-wide: 7,203

Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program.

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  • Site-wide: 67,473
  • In genetics: 3,102
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  • Site-wide: 61,002
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Integrative Genomic Analysis and Functional Studies Reveal GP5, GRN, MPO and MCAM as Causal Protein Biomarkers for Platelet Traits

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  • Site-wide: 78,678
  • In genomics: 5,204
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  • Site-wide: 86,078
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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

• Downloaded 292 times
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  • Site-wide: 87,458
  • In genetics: 3,944
• Year to date:
  • Site-wide: 51,145
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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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  • Site-wide: 92,293
  • In genetics: 4,142
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  • Site-wide: 123,207
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  • Site-wide: 106,961

BinomiRare: A carriers-only test for association of rare genetic variants with a binary outcome for mixed models and any case-control proportion

• Downloaded 173 times
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  • Site-wide: 113,636
  • In genetic and genomic medicine: 518
• Year to date:
  • Site-wide: 14,095
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  • Site-wide: 42,683