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National Cancer Institute, National Institutes of Health Logo
National Cancer Institute, National Institutes of Health

Rockville, Maryland

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Moffitt Cancer Center

Tampa, Florida

Midwestern University

Glendale, Arizona

University of Arkansas for Medical Sciences @ Arkansas Children's Hospital

Little Rock, Arkansas

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Yale University School of Medicine, Department of Genetics

New Haven, Connecticut

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Saint Louis , Missouri

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New York, New York

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Boston Children’s Hospital (a Harvard Teaching Hospital)

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Boston Children’s Hospital (a Harvard Teaching Hospital)

Boston, Massachusetts

Axia Women's Health

Oaks, Pennsylvania

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Children's Hospital of Philadelphia | Perelman School of Medicine, University of Pennsylvania

Philadelphia, Pennsylvania

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Staff Research Associate
Human genetics has long been appreciated as source of understanding the molecular factors that underlie differences observed between individuals. In particular, patient-derived cell lines, such as induced pluripotent stem cells (iPSCs), represent a unique opportunity to leverage inter-individual human variation for the discovery of novel genetic and molecular contributors to disease risk. Cardiometabolic diseases such as atherosclerotic cardiovascular disease (ASCVD) and nonalcoholic fatty liver disease (NAFLD) are well known to be heritable within families, but the genetic determinants that contribute to individual level risk for these diseases is not entirely known. As iPSCs retain the genetic


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