Jil C. Tardiff, MD, PhD

Professor, Biomedical Engineering
Professor, Cellular and Molecular Medicine
Professor, Medicine
Steven M. Gootter Endowed Chair for the Prevention of Sudden Cardiac Death
Member, Sarver Heart Center and BIO5 Institute

Dr. Tardiff joined our faculty in 2012. As a physician-scientist, Dr. Tardiff focuses on hypertrophic cardiomyopathy. These complex disorders affect one in 500 individuals of all ages and represent the most common cause of sudden cardiac death in the field. Her studies detailing the mechanisms of disease pathogenesis at the level of individual cells using transgenic mouse models has been continuously funded by the NIH since 2001 and the work has been cited in support of new clinical trials to evaluate novel treatment modalities for this challenging cardiomyopathy. More recently, in collaboration with Steven Schwartz in the Department of Chemistry at the University of Arizona, her lab has developed computational approaches to modeling and eventually predicting disease severity based on protein structure. To fully translate these basic research findings to the clinical realm, one of her main goals remains the development of an HCM Center of Excellence at the University of Arizona where patients from all over the southwest can obtain lifelong cutting-edge medical care for this complex and often devastating disorder. Dr. Tardiff was awarded $1.4 million to continue her lab’s study to improve the understanding of how independent mutations cause this complex disorder and discover better therapeutic options, especially in young people.

Degree(s)

  • MD: Albert Einstein College of Medicine, New York City, 1992
  • PhD: Cell Biology, Albert Einstein College of Medicine, New York City, 1992
  • BA: Genetics, University of California, Berkeley, 1984
Residency
Columbia-Presbyterian Medical Center, Internal Medicine, New York City
Fellowship
Columbia-Presbyterian Medical Center, Clinical Research in Cardiovascular Medicine, New York City
Honors and Awards
College of Medicine Faculty Mentoring Awards, 2017
Research Interests

mechanisms that underlie the development of the most common form of genetic cardiomyopathy, those caused by mutations in proteins of the cardiac sarcomere, hypertrophic cardiomyopathy (HCM)