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Author: Sharon LR Kardia

  • Most recently observed institution: Department of Epidemiology, School of Public Health, University of Michigan

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  • All-time downloads: 27,486 (rank: 1,647 out of 383,552)
  • Categories:
    • epidemiology: 231 (rank: 7,324 (tie) out of 9,545)
    • genetics: 15,510 (rank: 700 out of 35,367)
    • genomics: 11,745 (rank: 1,143 out of 40,785)

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Preprints

Genome-wide association studies identify 137 loci for DNA methylation biomarkers of ageing

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

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Heterogeneity in polygenic scores for common human traits

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

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

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism

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

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Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

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Population sequencing data reveal a compendium of mutational processes in human germline

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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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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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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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Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior

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

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

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