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The Journal of Physiology|March 31, 2026
Differential negative dominance by KCNA2 variants associated with global developmental delay suggests KCNA2 haploinsufficiency in humansPei Xin Boon, Amaia Jauregi-Miguel, S Suheda Yasarbas, et al.
European Heart Journal|August 20, 2009
Exercise-induced ventricular arrhythmias and risk of sudden cardiac death in patients with hypertrophic cardiomyopathyJuan R Gimeno, Maite Tomé-Esteban, Carla Lofiego, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathyJuan Pablo Kaski, Petros Syrris, Maria Teresa Tome Esteban, et al.
Circulation. Cardiovascular Genetics|August 19, 2010
Prevalence of desmosomal protein gene mutations in patients with dilated cardiomyopathyPerry Elliott, Constantinos O'Mahony, Petros Syrris, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 18, 2008
Distinct roles for two histamine receptors (hclA and hclB) at the Drosophila photoreceptor synapseAntonios Pantazis, Ashvina Segaran, Che-Hsiung Liu, et al.
European Heart Journal|December 27, 2011
Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathyGiovanni Quarta, Petros Syrris, Michael Ashworth, et al.
The Journal of General Physiology|April 29, 2015
Targeting the late component of the cardiac L-type Ca2+ current to suppress early afterdepolarizationsRoshni V Madhvani, Marina Angelini, Yuanfang Xie, et al.
The Journal of Physiology|August 25, 2020
Tracking the motion of the KV1.2 voltage sensor reveals the molecular perturbations caused by a de novo mutation in a case of epilepsyAntonios Pantazis, Maki Kaneko, Marina Angelini, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 19, 2022
An epilepsy-associated KV1.2 charge-transfer-center mutation impairs KV1.2 and KV1.4 traffickingMichelle Nilsson, Sarah H Lindström, Maki Kaneko, et al.
Circulation|May 25, 2011
Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteriaGiovanni Quarta, Alison Muir, Antonios Pantazis, et al.
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