Wayne Giles
External collaborator
Publications
Simula-affiliated publications listed
2021
Journal Articles
K. H. Jæger, A. G. Edwards, W. R. Giles and A. Tveito
A computational method for identifying an optimal combination of existing drugs to repair the action potentials of SQT1 ventricular myocytes
PLoS Computational Biology
K. H. Jæger, A. G. Edwards, W. R. Giles and A. Tveito
From Millimeters to Micrometers; Re-introducing Myocytes in Models of Cardiac Electrophysiology
Frontiers in Physiology
2020
Journal Articles
A. Tveito, K. H. Jæger, M. Maleckar, W. R. Giles and S. Wall
Computational translation of drug effects from animal experiments to human ventricular myocytes
Nature Scientific Reports
2014
Journal Articles
J. Koivumäki, R. Clark, D. Belke, C. Kondo, P. Fedak, M. Maleckar and W. R. Giles
Na+ Current Expression in Human Atrial Myofibroblasts: Its Identity and Functional Consequences
Frontiers in Physiology
2012
Journal Articles
R. A. Rose, D. Belke, M. Maleckar and W. R. Giles
Ca(2+) Entry Through TRP-C Channels Regulates Fibroblast Biology in Chronic Atrial Fibrillation
Circulation
2009
Journal Articles
M. Maleckar, J. L. Greenstein, W. R. Giles and N. A. Trayanova
Electrotonic Coupling Between Human Atrial Myocytes and Fibroblasts Alters Excitability and Repolarization
Biophysical Journal
M. Maleckar, J. L. Greenstein, W. R. Giles and N. A. Trayanova
K+ Current Changes Account for the Rate Dependence of the Action Potential in the Human Atrial Myocyte
American Journal of Physiology - Heart and Circulatory Physiology
2008
Journal Articles
M. Maleckar, J. L. Greenstein, N. A. Trayanova and W. R. Giles
Mathematical Simulations of Ligand-Gated and Specific Cell-Type Effects in the Human Atrium
Progress in Biophysics and Molecular Biology
Talks, contributed
M. Maleckar, J. L. Greenstein, W. R. Giles and N. A. Trayanova
Coupling of Human Atrial Myocytes and Myofibroblasts Can Lead to Conduction Disturbances
HRS Scientific Sessions 2008
2007
Journal Articles
S. N. Flaim, W. R. Giles and A. D. McCulloch
Arrhythmogenic Consequences of Na+ Channel Mutations in the Transmurally Heterogeneous Mammalian Left Ventricle: Analysis of the I1768V SCN5A Mutation
Heart Rhythm