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Author: Braxton D Mitchell

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  • All-time downloads: 17,742 (rank: 2,389 out of 336,720)
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    • genetics: 14,103 (rank: 729 out of 32,488)
    • genomics: 2,612 (rank: 6,310 (tie) out of 36,988)
    • neuroscience: 1,027 (rank: 13,111 (tie) out of 56,752)

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Preprints

Recovery of trait heritability from whole genome sequence data

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

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Genome-wide Meta-analysis of 158,000 Individuals of European Ancestry Identifies Three Loci Associated with Chronic Back Pain

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

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Do Candidate Genes Affect the Brain's White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans

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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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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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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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De novo mutations across 1,465 diverse genomes reveal novel mutational insights and reductions in the Amish founder population.

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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

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Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

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The Subtype Specificity of Genetic Loci Associated with Stroke in 16,664 cases and 32,792 controls

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White Matter Hyperintensity Quantification in Large-Scale Clinical Acute Ischemic Stroke Cohorts - The MRI-GENIE Study

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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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Genetic and functional evidence relates a missense variant in B4GALT1 to lower LDL-C and fibrinogen

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A genome-wide association study identifies that the GDF5 and COL27A1 genes are associated with knee pain in UK Biobank (N = 171, 516)

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Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke

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