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Author: L. Adrienne Cupples

Rankings

  • All-time downloads: 28,664 (rank: 1,380 out of 360,568)
  • Categories:
    • bioinformatics: 827 (rank: 12,301 (tie) out of 31,200)
    • epidemiology: 208 (rank: 7,541 (tie) out of 9,541)
    • genetics: 15,983 (rank: 650 out of 33,839)
    • genomics: 11,646 (rank: 1,071 out of 39,015)

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Preprints

Recovery of trait heritability from whole genome sequence data

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

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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

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Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

genetics more details view paper
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Personalized genetic assessment of age associated Alzheimers disease risk

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Hardy Weinberg Exact Test In Large Scale Variant Calling Quality Control

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A Fully-Adjusted Two-Stage Procedure for Rank Normalization in Genetic Association Studies

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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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Novel genetic determinants of telomere length from a multi-ethnic analysis of 75,000 whole genome sequences in TOPMed

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Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer's Disease Sequencing Project

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Large-scale multivariate multi-ancestry Interaction analyses point towards different genetic mechanisms by population and exposure

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

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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
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Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

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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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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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Methylome-Wide Association Study Of Central Adiposity Implicates Genes Involved In Immune And Endocrine Systems

genomics 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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Population Stratification at the Phenotypic Variance level and Implication for the Analysis of Whole Genome Sequencing Data from Multiple Studies

genetics more details view paper
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