Thematic program focuses on understanding the mechanisms cells use to access the information in their genomes to grow and develop, to respond to the environment, to safeguard their genetic information, and how errors in these processes can lead to genetic disease. The program includes study of DNA sequence and genetic variation, chromatin dynamics, gene regulation, epigenetic modification and inheritance, nuclear organization, and genome stability. Investigators use a variety of established and cutting-edge approaches to interrogate genome function in multiple organisms including flies, mice, and humans. Our interests include: 1) fine-scale mapping of non-coding genetic variation that affects enhancer function to determine the mechanisms by which disease-associated alleles induce atherosclerosis and hypertension, 2) examining how chromatin compaction alters nuclear shape and gene expression in laminopathies such as Emery-Driefuss Muscular Dystrophy and Hutchinson Gilford Progeria Syndrome, and 3) understanding how epigenetic changes cause hyper-mutation and chromosome damage, pushing healthy cells toward a cancer disease state.
Associate Professor, Cellular and Molecular Medicine
Associate Department Head, Faculty Development, Cellular and Molecular Medicine
Associate Professor, Molecular and Cellular Biology
Associate Professor, BIO5 Institute
Understanding cellular mechanisms that regulate centrosome duplication, nuclear organization, and genomic integrity.
Assistant Professor, Cellular and Molecular Medicine
BIO5 Fellow, BIO5 Institute
Faculty, Genetics Graduate Interdisciplinary Program
Member, Center for Applied Genetics and Genomic Medicine
Systems genetics approaches to identify mechanisms of complex disease.
Professor, Cellular and Molecular Medicine
Professor, BIO5 Institute
Associate Director, Asthma and Airway Disease Research Center
Director, Arizona Center for the Biology of Complex Diseases
Genetic, epigenetic and environmental mechanisms that control susceptibility to complex lung diseases