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Author: Paul S. de Vries

  • ORCiD: http://orcid.org/0000-0003-0964-0111
  • Most recently observed institution: Human Genetics Center, Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA, 77030.

Rankings

  • All-time downloads: 11,275 (rank: 20,125 (tie) )
  • Categories:
    • bioinformatics: 262 (rank: 36,936 (tie) )
    • cardiovascular medicine: 145 (rank: 3,493 (tie) )
    • epidemiology: 430 (rank: 19,601 (tie) )
    • genetic and genomic medicine: 2,658 (rank: 1,235 )
    • genetics: 5,583 (rank: 3,622 )
    • genomics: 1,499 (rank: 16,844 (tie) )
    • hematology: 698 (rank: 487 (tie) )

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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Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants.

genetic and genomic medicine more details view paper
  • Downloaded 1,351 times
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    • Site-wide: 15,942
    • In genetic and genomic medicine: 69
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    • Site-wide: 2,231
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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
  • Downloaded 874 times
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    • Site-wide: 30,115
    • In genetics: 1,378
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    • Site-wide: 57,407
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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
  • Downloaded 858 times
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    • In genetics: 1,420
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Rare coding variants in 35 genes associate with circulating lipid levels: a multi-ancestry analysis of 170,000 exomes

genetics more details view paper
  • Downloaded 848 times
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    • Site-wide: 31,461
    • In genetics: 1,447
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    • Site-wide: 7,471
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    • Site-wide: 4,474

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

hematology more details view paper
  • Downloaded 698 times
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    • Site-wide: 41,185
    • In hematology: 34
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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
  • Downloaded 692 times
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    • In genomics: 3,358
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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 557 times
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    • Site-wide: 54,880
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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 518 times
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    • In genomics: 4,377
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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

genetics more details view paper
  • Downloaded 499 times
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    • Site-wide: 62,408
    • In genetics: 2,758
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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
  • Downloaded 460 times
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    • Site-wide: 68,185
    • In genetic and genomic medicine: 281
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    • Site-wide: 24,960
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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
  • Downloaded 412 times
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    • Site-wide: 76,338
    • In genetics: 3,328
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    • Site-wide: 104,137

Role of Rare and Low Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

epidemiology more details view paper
  • Downloaded 332 times
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    • In epidemiology: 3,893
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Whole Genome Sequence Association Analysis of Fasting Glucose and Fasting Insulin Levels in Diverse Cohorts from the NHLBI TOPMed Program

genetic and genomic medicine more details view paper
  • Downloaded 290 times
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    • Site-wide: 101,913
    • In genetic and genomic medicine: 488
  • Year to date:
    • Site-wide: 20,255
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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

genomics more details view paper
  • Downloaded 289 times
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    • Site-wide: 102,059
    • In genomics: 6,123
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    • Site-wide: 68,550
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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

genetics more details view paper
  • Downloaded 275 times
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    • In genetics: 4,475
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Deriving stratified effects from joint models investigating Gene-Environment Interactions

bioinformatics more details view paper
  • Downloaded 262 times
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    • Site-wide: 108,676
    • In bioinformatics: 9,108
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A multi-omics study of circulating phospholipid markers of blood pressure

cardiovascular medicine more details view paper
  • Downloaded 145 times
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    • Site-wide: 136,892
    • In cardiovascular medicine: 409
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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
  • Downloaded 127 times
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    • Site-wide: 140,885
    • In genetics: 5,635
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Multi-omics insights into the biological mechanisms underlying gene-by-lifestyle interactions with smoking and alcohol consumption detected by genome-wide trans-ancestry meta-analysis

epidemiology more details view paper
  • Downloaded 98 times
  • Download rankings, all-time:
    • Site-wide: 146,315
    • In epidemiology: 6,043
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    • Site-wide: 70,156
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    • Site-wide: 4,306

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