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National Cancer Institute, National Institutes of Health
Rockville, Maryland
The Permanente Medical Group, Inc. (Kaiser Permanente Northern California)
Modesto & Oakland, California
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University of Arkansas for Medical Sciences @ Arkansas Children's Hospital
Little Rock, Arkansas
NIH National Human Genome Research Institute & FDA Office of Minority Health and Health Equity
Bethesda, Maryland
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Yale University School of Medicine, Department of Genetics
New Haven, Connecticut
Washington University School of Medicine in St. Louis
Saint Louis , Missouri
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Zucker School of Medicine at Hofstra/Northwell
New York, New York
Boston Children’s Hospital (a Harvard Teaching Hospital)
Boston, Massachusetts
Boston Children’s Hospital (a Harvard Teaching Hospital)
Boston, Massachusetts
Assistant Professor, Clinical Statistical Geneticist/Epidemiologist, Division of Genomic Diagnostics
Children's Hospital of Philadelphia | Perelman School of Medicine, University of Pennsylvania
Philadelphia, Pennsylvania
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Virginia Commonwealth University Health System
Richmond, Virginia
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Stanford University
Stanford, California
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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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