The University of Arizona
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Casey Romanoski

Associate Professor, Genetics - GIDP | Associate Professor, Cellular and Molecular Medicine | Associate Professor, BIO5 Institute | Member of the Graduate Faculty | Associate Professor, Clinical Translational Sciences

Cellular & Molecular Medicine

About

Casey received her B.A. in 2004 from the Arizona International College at the University of Arizona where she concentrated in Math and Science. She then received her Ph.D. from UCLA in Human Genetics from the laboratory of Dr. Aldons (Jake) Lusis. In the Lusis Lab, Casey demonstrated that gene regulation in human endothelial cells is genetically and environmentally determined. She then completed her postdoctoral research at UCSD in the laboratory of Dr. Christopher Glass. There, Casey used natural genetic variation between inbred mouse strains to demonstrate the hierarchical and collaborative nature of enhancer activity in gene regulation. Throughout her training, Casey became very interested in the interdependence between genetic sequence and molecular traits, which is the foundation of her ongoing research. In 2016, Casey accepted a position as an Assistant Professor in the Department of Cellular and Molecular Medicine and BIO5 Fellow at the University of Arizona. Her research program uses experimental and computational approaches to better understand complex disease and human biology.

Research Area

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    • The overarching goal of the Romanoski Lab is to better understand the mechanisms by which DNA sequence instructs molecular programs that underlie human biology. We are particularly interested in complex diseases such as atherosclerosis and hypertension, which are caused by combinations of environmental and genetic risk factors. While these diseases involve many cell types, our research is focused on endothelial cells, which line blood vessels and form the barrier between blood and tissue.Our laboratory is both experimental and computational. We use next-generation sequencing technologies to measure genome-wide molecular phenotypes. By leveraging the interconnected relationships between DNA sequence, transcription factor binding, chromatin modification, and gene expression, we study how cells achieve context-appropriate expression patterns and signal responsiveness.Ongoing projects in the lab include systems genetics of endothelial cells, transcriptional network determination in different endothelial beds, and functional genetics of GWAS loci.

    • Thesis

    • The Art of Scientific Communication

    • Individualized Scientific Writing

    • Principles of Cell Biology

    • Current Topics in Biomedical Sciences

    Casey Romanoski | KMap Profile - Institutional Knowledge Map (KMap)