Levin Lab

We use human genetics and bioinformatics to identify therapeutic targets, predict cardiovascular risk, and bring both into clinical care.

University of Pennsylvania · Philadelphia VA Medical Center

Research

Drug target identification and validation. Which genes cause cardiovascular disease, and which of them are promising drug targets? We run large-scale genetic discovery across common and rare variants, then use fine-mapping, colocalization, and Mendelian randomization to nominate candidate genes and test whether they play a causal role in disease.

Cardiovascular risk prediction. How well can genetics predict a person’s cardiovascular risk, and when is that prediction reliable enough to guide care? We build, benchmark, and clinically evaluate polygenic risk scores in deeply phenotyped biobank and clinical cohorts.

Clinical translation. Do treatments act in patients the way human genetics predicts? We run genetically informed clinical trials and mechanistic clinical studies to test what genetic findings imply about human biology, such as a mechanistic trial of colchicine in peripheral artery disease.

Deep phenotyping. What do diagnosis codes miss about cardiovascular disease, and what do risk variants do among carriers? We measure disease endophenotypes, such as the extent of coronary atherosclerosis and changes in cardiac structure and function, from clinical notes and imaging across whole biobanks and health systems. We also run recall-by-genotype studies, which invite participants back for detailed measurement based on the variants they carry.

Our work draws on the Million Veteran Program, Penn Medicine BioBank, UK Biobank, and All of Us, with a focus on atherosclerosis, lipoproteins including lipoprotein(a), and heart failure and cardiomyopathy.

People

Portrait of Michael G. Levin, MD

Michael G. Levin, MD, MSTR

Principal Investigator

Assistant Professor of Medicine and Genetics, University of Pennsylvania
Staff Cardiologist, Philadelphia VA Medical Center

Publications

The lab has published 146 papers and preprints, including work in JAMA, Nature Genetics, and Circulation. Recent work:

Shared additive- and variance-associated genetic architecture of cardiac structure and function
Tsaggaris JC, Mimouni N, Judy RL, Xue D, Morley MP, Wang X, Cotney JL, Kelly DP, Day SM, Cappola TP, Penn Medicine BioBank, Damrauer SM, Levin MG
medRxiv. Preprint. 2026. doi:10.64898/2026.11.04.26367193
A Common CD36 Variant and the Genetic Landscape of Dilated Cardiomyopathy in Individuals of African Ancestry
Challa SP, Biddinger KJ, Abramowitz SA, Zheng A, Mead JO, Judy RL, Jurgens SJ, Gaziano L, Wang X, Choi SH, Halford J, Jordan E, Liu J, Chang K-M, Vest A, Tang WHW, Tsao PS, Kinnamon DD, Damrauer SM, Ellinor PT, Levin M, Hershberger RE, Huffman JE, Aragam KG
JAMA. 2026. doi:10.1001/jama.2026.18449
Polygenic Risk Scores for Cardiovascular Disease: Closing the Gap Between Prediction and Practice
Clark MG, Levin MG
JACC. 2026;88(10):1090-1092. doi:10.1016/j.jacc.2026.03.089
Multi-population genome-wide association meta-analysis of acute and chronic pancreatitis
Khodursky S, Judy R, Abramowitz S, Levin MG, Damrauer SM
medRxiv. Preprint. 2026. doi:10.64898/2026.09.16.26363222
Expanding the Genetic Architecture of Severe Hypercholesterolemia
Levin MG
JACC. 2026;88(10):1104-1106. doi:10.1016/j.jacc.2026.04.035

All publications

Contact

We welcome research collaborations, industry partnerships, and prospective trainees. Email Michael.Levin@pennmedicine.upenn.edu.

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Publications updated November 12, 2026