Author: Stephanie M Gogarten

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Preprints

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

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

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

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Integrated Computing And Tracking System For Centralized High-Throughput Genetic Analysis: A Case Study

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  • In bioinformatics: 8,410
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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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BinomiRare: A carriers-only test for association of rare genetic variants with a binary outcome for mixed models and any case-control proportion

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  • In genetic and genomic medicine: 512
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Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL Study

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