Elizabeth Theusch
Assistant Researcher
Pediatrics
School of Medicine

As a computational biologist with training in human genetics and molecular biology, my recent projects have focused on studying statin pharmacogenomics and transcriptomics, cholesterol metabolism, and cardiovascular disease. I am especially passionate about studying sex and genetic ancestry differences in disease risk, metabolism, and drug response.

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In addition to my involvement in ongoing collaborative projects led by other investigators, I am leading my own research projects focused on the impact of menopause on gene regulation and cardiometabolic disease risk factors.

Awards

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  • Butler-Williams Scholar, National Institute on Aging, 2022
  • Postdoctoral Fellowship (one-year), American Heart Association, 2015-2016
  • Featured Investigator (June), Pharmacogenomics Research Network, 2015
  • Postdoctoral Fellowship, American Heart Association, 2012-2014
  • Graduate Research Fellowship, National Science Foundation, 2006-2009
  • Hilldale Undergraduate Research Award, University of Wisconsin-Madison, 2004

Education & Training

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  • Diversity, Equity, and Inclusion Champion Training University of California, San Francisco 2022
  • Postdoctoral Computational Biology Children's Hospital Oakland Research Institute (CHORI) 2016
  • Ph.D. Biomedical Sciences University of California, San Francisco 2010
  • Certificate Computer Programming: C++ City College of San Francisco 2009
  • B.S. Genetics and Biochemistry University of Wisconsin-Madison 2005

Interests

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  • statin pharmacogenomics
  • sexual dimorphism
  • transcriptomics
  • computational biology
  • human genetics
  • cardiovascular disease
  • cholesterol metabolism
  • genetic ancestry
  • menopause

Grants and Projects

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Publications (35)

Top publication keywords:
Proprotein ConvertasesChitinasesCholesterolGenome-Wide Association StudyCholesterol, LDLSerine EndopeptidasesSerpinsLymphocytesHydroxymethylglutaryl-CoA Reductase InhibitorsDyslipidemiasSimvastatinPitch DiscriminationPolymorphism, Single NucleotideGenetic Association StudiesPharmacogenomic Variants

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