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Syam, Ninda Ratna Maharani; Chatel, Stéphanie; Ozhathil, Lijo Cherian; Sottas, Valentin; Rougier, Jean-Sébastien; Baruteau, Alban; Baron, Estelle; Amarouch, Mohamed Yassine; Daumy, Xavier; Probst, Vincent; Schott, Jean-Jacques; Abriel, Hugues (2016). Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block. Journal of the American Heart Association, 5(5) American Heart Association 10.1161/JAHA.114.001625
Daumy, Xavier; Amarouch, Mohamed Yassine; Lindenbaum, Pierre; Bonnaud, Stéphanie; Charpentier, Eric; Bianchi, Beatrice; Nafzger, Sabine Naomi; Baron, Estelle; Fouchard, Swanny; Thollet, Aurélie; Kyndt, Florence; Barc, Julien; Le Scouarnec, Solena; Makita, Naomasa; Le Marec, Hervé; Dina, Christian; Gourraud, Jean-Baptiste; Probst, Vincent; Abriel, Hugues; Redon, Richard; ... (2016). Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I. International journal of cardiology, 207, pp. 349-358. Elsevier 10.1016/j.ijcard.2016.01.052
Amarouch, Mohamed Yassine; Swan, Heikki; Leinonen, Jaakko; Marjamaa, Annukka; Lahtinen, Annukka M.; Kontula, Kimmo; Toivonen, Lauri; Widen, Elisabeth; Abriel, Hugues (2016). Antiarrhythmic Action of Flecainide in Polymorphic Ventricular Arrhythmias Caused by a Gain-of-Function Mutation in the Na v 1.5 Sodium Channel. Annals of noninvasive electrocardiology, 21(4), pp. 343-351. Wiley 10.1111/anec.12312
Ossola, Dario; Amarouch, Mohamed Yassine; Behr, Pascal; Vörös, János; Abriel, Hugues; Zambelli, Tomaso (2015). Force-controlled patch clamp of beating cardiac cells. Nano letters, 15(3), pp. 1743-1750. American Chemical Society 10.1021/nl504438z
Saber, Siamak; Amarouch, Mohamed Yassine; Fazelifar, Amir-Farjam; Haghjoo, Majid; Emkanjoo, Zahra; Alizadeh, Abolfath; Houshmand, Massoud; Gavrilenko, Alexander V; Abriel, Hugues; Zaklyazminskaya, Elena V (2015). Complex genetic background in a large family with Brugada syndrome. Physiological reports, 3(1) The American Physiological Society 10.14814/phy2.12256
Amarouch, Mohamed Yassine; Abriel, Hugues (2015). Cellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channels. Frontiers in physiology, 6(45), p. 45. Frontiers Research Foundation 10.3389/fphys.2015.00045
Swan, H.; Amarouch, Mohamed Yassine; Leinonen, J.; Marjamaa, A.; Kucera, Jan; Laitinen-Forsblom, P. J.; Lahtinen, A. M.; Palotie, A.; Kontula, K.; Toivonen, L.; Abriel, Hugues; Widen, E. (2014). Gain-of-Function Mutation of the SCN5A Gene Causes Exercise-Induced Polymorphic Ventricular Arrhythmias. Circulation - cardiovascular genetics, 7(6), pp. 771-781. Lippincott Williams & Wilkins 10.1161/CIRCGENETICS.114.000703
Amarouch, Mohamed Yassine; Syam, Ninda Ratna Maharani; Abriel, Hugues (2013). Biochemical, single-channel, whole-cell patch clamp, and pharmacological analyses of endogenous TRPM4 channels in HEK293 cells. Neuroscience letters, 541, pp. 105-110. Elsevier 10.1016/j.neulet.2013.02.011
