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Author: Paul S. de Vries

  • ORCiD: http://orcid.org/0000-0003-0964-0111
  • Most recently observed institution: Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston

Rankings

  • All-time downloads: 6,393 (rank: 25,343 (tie) out of 513,978)
  • Categories:
    • bioinformatics: 234 (rank: 31,407 (tie) out of 37,097)
    • epidemiology: 265 (rank: 17,358 (tie) out of 23,860)
    • genetic and genomic medicine: 541 (rank: 2,274 out of 6,816)
    • genetics: 4,067 (rank: 4,044 out of 38,823)
    • genomics: 1,286 (rank: 15,854 (tie) out of 45,850)

Downloads per author, site-wide

Preprints

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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

genetics more details view paper
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Large-scale multivariate multi-ancestry Interaction analyses point towards different genetic mechanisms by population and exposure

genetics more details view paper
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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

genomics more details view paper
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Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

genomics more details view paper
  • Downloaded 487 times
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Elucidating mechanisms of genetic cross-disease associations: an integrative approach implicates protein C as a causal pathway in arterial and venous diseases

genetic and genomic medicine more details view paper
  • Downloaded 421 times
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    • In genetic and genomic medicine: 122 out of 497
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Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: The Trans-Omics for Precision Medicine Program.

genetics more details view paper
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Role of Rare and Low Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

epidemiology more details view paper
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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

genetics more details view paper
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    • In genetics: 3,835 out of 5,153
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Deriving stratified effects from joint models investigating Gene-Environment Interactions

bioinformatics more details view paper
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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

genetics more details view paper
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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

genomics more details view paper
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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

genetic and genomic medicine more details view paper
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    • In genetic and genomic medicine: 393 out of 497
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    • Site-wide: 3,556 out of 119,207

Lifestyle Risk Score for aggregating multiple lifestyle factors: Handling missingness of individual lifestyle components in meta-analysis of gene-by-lifestyle interactions

genetics more details view paper
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