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Author: Joshua C Bis

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    • bioinformatics: 643 (rank: 13,848 (tie) out of 28,935)
    • genetics: 18,717 (rank: 396 out of 32,531)
    • genomics: 2,606 (rank: 6,326 out of 37,049)
    • neuroscience: 2,233 (rank: 5,582 (tie) out of 56,826)

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Preprints

The genetic architecture of the human cerebral cortex

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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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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

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Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

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

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Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

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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 blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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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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Partial derivatives meta-analysis: pooled analyses when individual participant data cannot be shared

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Planar cell polarity pathway and development of the human visual cortex

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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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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

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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

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