Studies
NHLBI TOPMed: Australian Familial Atrial Fibrillation Study
NHLBI TOPMed: Australian Familial Atrial Fibrillation Study
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Overview
Selected Publications (6)
Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation?
R. Otway, J. Vandenberg, J. Vandenberg, et al.. (2007). Journal of the American College of Cardiology. Cited 158 times.
https://doi.org/10.1016/J.JACC.2006.09.044
Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis.
Bo Liang, M. Soka, A. Christensen, et al.. (2014). Journal of molecular and cellular cardiology. Cited 68 times.
https://doi.org/10.1016/j.yjmcc.2013.12.014
Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk.
Stefan A. Mann, R. Otway, G. Guo, et al.. (2012). Journal of the American College of Cardiology. Cited 68 times.
https://doi.org/10.1016/j.jacc.2011.11.039
Genes and atrial fibrillation: a new look at an old problem.
D. Fatkin, R. Otway, J. Vandenberg. (2007). Circulation. Cited 68 times.
https://doi.org/10.1161/CIRCULATIONAHA.106.688889
The two-pore domain potassium channel, TWIK-1, has a role in the regulation of heart rate and atrial size.
A. Christensen, F. Chatelain, I. Huttner, et al.. (2016). Journal of molecular and cellular cardiology. Cited 35 times.
https://doi.org/10.1016/j.yjmcc.2016.04.006
Atrial fibrillation--a new cardiac channelopathy.
R. Otway, J. Vandenberg, D. Fatkin. (2007). Heart, lung & circulation. Cited 14 times.
https://doi.org/10.1016/J.HLC.2007.07.003
