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: 970
  • In genomics: 94
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  • Site-wide: 1,038
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  • Site-wide: 2,233

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

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  • Site-wide: 3,581
  • In genetics: 164
• Year to date:
  • Site-wide: 27,626
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  • Site-wide: 41,956

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

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  • Site-wide: 6,182
  • In genetics: 309
• Year to date:
  • Site-wide: 10,605
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The Polygenic and Monogenic Basis of Blood Traits and Diseases

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  • Site-wide: 7,026
  • In genetic and genomic medicine: 18
• Year to date:
  • Site-wide: 15,741
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  • Site-wide: 14,486

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

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  • Site-wide: 8,435
  • In genetics: 425
• Year to date:
  • Site-wide: 54,587
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  • Site-wide: 59,742

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

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  • Site-wide: 13,689
  • In epidemiology: 864
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  • Site-wide: 56,037
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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: 24,700
  • In genetics: 1,242
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  • Site-wide: 99,256

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

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  • Site-wide: 28,782
  • In genomics: 2,663
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  • Site-wide: 109,607

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: 33,196
  • In genetics: 1,655
• Year to date:
  • Site-wide: 119,640
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  • Site-wide: 59,599

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: 33,955
  • In genomics: 2,995
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  • Site-wide: 49,609

Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

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  • Site-wide: 48,646
  • In genomics: 3,868
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  • Site-wide: 25,045
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  • Site-wide: 64,644

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

• Downloaded 363 times
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  • Site-wide: 66,091
  • In genetics: 3,129
• Year to date:
  • Site-wide: 64,937
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  • Site-wide: 119,278

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: 74,791
  • In genomics: 5,053
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  • Site-wide: 84,133
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Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

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  • Site-wide: 80,605
  • In hematology: 50
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  • Site-wide: 2,900
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  • Site-wide: 2,473

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

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  • Site-wide: 85,353
  • In genetics: 3,953
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  • Site-wide: 21,296
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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: 85,751
  • In genetics: 3,960
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  • Site-wide: 101,432
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  • Site-wide: 108,060

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

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  • Site-wide: 116,665
  • In genetic and genomic medicine: 501
• Year to date:
  • Site-wide: 2,889
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  • Site-wide: None