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Author: Ramachandran S Vasan

  • ORCiD: http://orcid.org/0000-0001-7357-5970
  • Most recently observed institution: Evans Department of Medicine, Whitaker Cardiovascular Institute and Cardiology Section, Boston University School of Medicine

Rankings

  • All-time downloads: 33,868 (rank: 3,516 (tie) out of 510,677)
  • Categories:
    • cardiovascular medicine: 687 (rank: 473 out of 2,276)
    • epidemiology: 201 (rank: 19,493 (tie) out of 23,903)
    • genetic and genomic medicine: 787 (rank: 1,305 (tie) out of 6,821)
    • genetics: 18,575 (rank: 627 out of 38,674)
    • genomics: 12,571 (rank: 1,130 out of 45,521)
    • infectious diseases: 1,047 (rank: 15,187 (tie) out of 32,290)

Downloads per author, site-wide

Preprints

Recovery of trait heritability from whole genome sequence data

genetics more details view paper
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

genomics more details view paper
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Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

genomics more details view paper
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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

genomics more details view paper
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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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    • In genetics: 441 out of 5,138
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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

genetics more details view paper
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Proteomic Profiling in Biracial Cohorts Implicates DC-SIGN as a Mediator of Genetic Risk in COVID-19

infectious diseases more details view paper
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Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed

genetics more details view paper
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A Fully-Adjusted Two-Stage Procedure for Rank Normalization in Genetic Association Studies

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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Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

genomics more details view paper
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Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

genetic and genomic medicine more details view paper
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    • In genetic and genomic medicine: 64 out of 488
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    • Site-wide: 9,736 out of 118,387
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De novo mutations across 1,465 diverse genomes reveal novel mutational insights and reductions in the Amish founder population.

genetics more details view paper
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    • In genetics: 1,592 out of 5,138
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Whole-Genome Association Analyses of Sleep-disordered Breathing Phenotypes in the NHLBI TOPMed Program

genetics more details view paper
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    • In genetics: 2,774 out of 5,138
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EDEM3 modulates plasma triglyceride level through its regulation of LRP1 expression

genetics more details view paper
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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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Eicosanoid Inflammatory Mediators Are Robustly Associated with Blood Pressure in the General Population

cardiovascular medicine more details view paper
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    • In cardiovascular medicine: 87 out of 282
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Cardiac Microstructural Abnormalities Identify Women at Risk of Incident Heart Failure

cardiovascular medicine more details view paper
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    • In cardiovascular medicine: 130 out of 282
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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 211 times
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Association of mitochondrial DNA copy number with cardiometabolic diseases in a large cross-sectional study of multiple ancestries

epidemiology more details view paper
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High-Throughput Digitization of Analog Human Echocardiography Data

cardiovascular medicine 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 488
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Presence and Transmission of Mitochondrial Heteroplasmic Mutations in Human Populations of European and African Ancestry

genetics more details view paper
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    • In genetics: 4,919 out of 5,138
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