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Annals of Clinical and Translational Neurology|November 24, 2022
A KCNC1-related neurological disorder due to gain of Kv3.1 functionJerome Clatot, Natalie Ginn, Gregory Costain, et al.The Journal of General Physiology|June 25, 2026
An epilepsy-associated KV3.1 potassium channel variant acts via dominant-positive effectJerome Clatot, Hubert Monnerie, Axel Panzer, et al.Frontiers in Physiology|June 25, 2019
Mutations in NaV1.5 Reveal Calcium-Calmodulin Regulation of Sodium ChannelEyal Nof, Leonid Vysochek, Eshcar Meisel, et al.Proceedings of the National Academy of Sciences of the United States of America|January 9, 2024
A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunctionJerome Clatot, Christopher B Currin, Qiansheng Liang, et al.Elife|February 18, 2026
Impaired excitability of fast-spiking neurons in a novel mouse model of KCNC1 epileptic encephalopathyEric R Wengert, Sophie R Liebergall, Teresa Jimenez, et al.Journal of the American College of Cardiology|October 15, 2021
Distinct Features of Probands With Early Repolarization and Brugada Syndromes Carrying SCN5A Pathogenic VariantsZhong-He Zhang, Hector Barajas-Martínez, Hao Xia, et al.Cell Reports. Medicine|January 24, 2024
Targeted therapy improves cellular dysfunction, ataxia, and seizure susceptibility in a model of a progressive myoclonus epilepsyHuijie Feng, Jerome Clatot, Keisuke Kaneko, et al.Pageof 1