Over the past two decades, the study of cancer genetics has provided new insights into the biological diversity of human cancers through high-throughput technologies. Research in this area has improved our understanding of the diversity of somatic variation in DNA and how these sequence changes (as well as epigenetic changes) lead to oncogenic phenotypes.
Cancer genetics can be subdivided into three main areas of study: analysis of patient populations; the impact chromosome biology on phenotypes; and mutagenesis and the impact of variation on gene function. Through these studies, we obtain knowledge on the molecular underpinnings of cancer and avenues through which therapeutics may be developed. Please browse the profiles of the cancer genetics faculty below to explore the research of individual laboratories.
Director, University of Michigan Rogel Cancer Center
Associate Dean for Cancer Programs
Professor of Internal Medicine
Professor of Pathology
Professor of Human Genetics
Medical School
Professor of Pediatrics
Professor of Pathology
Medical School
Associate Chair, Department of Human Genetics
Associate Professor of Computational Medicine and Bioinformatics, Medical School
Medical School
Medical School
Professor of Internal Medicine
Professor of Human Genetics and Program Assistant
Internal Medicine
Medical School
Professor of Computational Medicine and Bioinformatics
Professor of Internal Medicine
Professor of Human Genetics
Medical School
Professor of Environmental Health Sciences
School of Public Health
Associate Professor of Human Genetics
Associate Chair, Department of Human Genetics and Program Director, Human Genetics, Medical School
Professor of Human Genetics
Associate Medical Director
Molecular Diagnostics Laboratory
Program Assistant
MGP Fellowship Director
Medical School
