UNIVERSITY OF WISCONSIN River Falls
Professor - College of Business and Economics
member of graduate faculty
Start Year: 2002
Computer Science and Information Systems
Office: 127c South Hall
Ph.D. University of Minnesota, Minneapolis, MN, Biomedical Engineering, 1992
M.S. University of Minnesota, Minneapolis, MN, Electrical Engineering, 1987
B.S. University of Wisconsin Platteville, Platteville, WI, Electrical Engineering, 1983
Dr. Varghese's research involves the simulation of biological systems, specifically cellular electrophysiology. He uses the tools of Mathematical Modeling, Numerical Methods for Differential Equations, and High-Performance Computing to address research problems in the area of Cellular Electrophysiology. With the help of numerous collaborators in academia and industry, he also uses the techniques of Cell culture, Immunochemistry, and Molecular Biology: PCR, siRNA. He started using C++ and Java as soon as they were available and developed object-oriented code for a startup named Physiome Sciences while in the UK in the 1990s followed by stints developing code at Medtronic Inc. and Endocardial Solutions Inc. (now part of St Jude Medical).
Varghese, A., Mann, S., Benn, D., Tan, P., Vandenberg, J. I., Hill, A. P. (in press). A hERG gating model incorporating mode-shift and the effects of N-terminal LQTS2 mutations. Biophisical Journal, Cell Press.
Zlesak, DC,, Van Schaick, J, Varghese, A, et al. (2019) SNP markers linked to sex in dioecious Rosa setigera Michx. Acta Horticulturae, 1232, 33-39. https://doi.org/10.17660/ActaHortic.2019.1232.6
Varghese, A et al. (2018) A hERG gating model incorporating mode-shift and the effects of N-terminal LQTS2 mutations. In: The Heart by Numbers, Biophysical Society.
Varghese, A. (2016). Reciprocal modulation of IK1-INa extends excitability in cardiac ventricular cells. Frontiers in Physiology, 7, 542. http://journal.frontiersin.org/article/10.3389/fphys.2016.00542/full
Varghese, A., Spindler, A. J., Paterson, D., Noble, D. (2015). Rate Dependent Activation Failure in Single Cells and Tissue due to Na Channel Block. American Journal of Physiology, 309(10), H1753–H1763.
Zhao JT, Hill AP, Varghese A, Cooper AA, Swan HP, Laitenen J, Rees M., Skinner JR, Campbell TF, and Vandenberg JI (2009). Not All Pore Domain Mutations Have a Severe Phenotype: G584S Has an Inactivation Gating Defect with Mild Phenotype Compared to G572S, Which Has a Dominant Negative Trafficking Defect and a Severe Phenotype. Journal of Cardiovascular hERG, 20, 923-930.