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Mohamed Yassine Amarouch - Publications

Affiliations: 
2011-2014 University of Bern, Bern, Bern, Switzerland 
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26 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Amarouch MY, El Hilaly J. Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies. Cardiovascular Therapeutics. 2020: 6615038. PMID 33381229 DOI: 10.1155/2020/6615038  0.508
2020 Amarouch MY, Kurt H, Delemotte L, Abriel H. Biophysical Characterization of Epigallocatechin-3-Gallate Effect on the Cardiac Sodium Channel Na1.5. Molecules (Basel, Switzerland). 25. PMID 32085432 DOI: 10.3390/Molecules25040902  0.615
2016 Boukhabza M, El Hilaly J, Attiya N, El-Haidani A, Filali-Zegzouti Y, Mazouzi D, Amarouch MY. Evaluation of the Potential Antiarrhythmic Effect of Epigallocatechin-3-Gallate on Cardiac Channelopathies. Computational and Mathematical Methods in Medicine. 2016: 7861653. PMID 27882075 DOI: 10.1155/2016/7861653  0.468
2016 Syam N, Chatel S, Ozhathil LC, Sottas V, Rougier JS, Baruteau A, Baron E, Amarouch MY, Daumy X, Probst V, Schott JJ, Abriel H. Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block. Journal of the American Heart Association. 5. PMID 27207958 DOI: 10.1161/Jaha.114.001625  0.639
2016 Amarouch MY, Swan H, Leinonen J, Marjamaa A, Lahtinen AM, Kontula K, Toivonen L, Widen E, Abriel H. Antiarrhythmic Action of Flecainide in Polymorphic Ventricular Arrhythmias Caused by a Gain-of-Function Mutation in the Nav 1.5 Sodium Channel. Annals of Noninvasive Electrocardiology : the Official Journal of the International Society For Holter and Noninvasive Electrocardiology, Inc. 21: 343-51. PMID 26965448 DOI: 10.1111/Anec.12312  0.691
2016 Daumy X, Amarouch MY, Lindenbaum P, Bonnaud S, Charpentier E, Bianchi B, Nafzger S, Baron E, Fouchard S, Thollet A, Kyndt F, Barc J, Le Scouarnec S, Makita N, Le Marec H, et al. Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I. International Journal of Cardiology. 207: 349-58. PMID 26820365 DOI: 10.1016/J.Ijcard.2016.01.052  0.757
2016 Daumy X, Amarouch MY, Lindenbaum P, Bonnaud S, Charpentier E, Bianchi B, Nafzger S, Baron E, Fouchard S, Thollet A, Kyndt F, Barc J, Le Scouarnec S, Makita N, Le Marec H, et al. Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type i International Journal of Cardiology. 207: 349-358. DOI: 10.1016/j.ijcard.2016.01.052  0.716
2015 Amarouch MY, Abriel H. Cellular hyper-excitability caused by mutations that alter the activation process of voltage-gated sodium channels. Frontiers in Physiology. 6: 45. PMID 25741286 DOI: 10.3389/Fphys.2015.00045  0.68
2015 Ossola D, Amarouch MY, Behr P, Vörös J, Abriel H, Zambelli T. Force-controlled patch clamp of beating cardiac cells. Nano Letters. 15: 1743-50. PMID 25639960 DOI: 10.1021/Nl504438Z  0.602
2015 Saber S, Amarouch MY, Fazelifar AF, Haghjoo M, Emkanjoo Z, Alizadeh A, Houshmand M, Gavrilenko AV, Abriel H, Zaklyazminskaya EV. Complex genetic background in a large family with Brugada syndrome. Physiological Reports. 3. PMID 25626866 DOI: 10.14814/Phy2.12256  0.646
2015 Amarouch MY, Swan H, Leinonen J, Marjamaa A, Lahtinen AM, Kontula K, Toivonen L, Widen E, Abriel H. Antiarrhythmic Action of Flecainide in Polymorphic Ventricular Arrhythmias Caused by a Gain-of-Function Mutation in the Nav1.5 Sodium Channel Annals of Noninvasive Electrocardiology. DOI: 10.1016/S1878-6480(16)30436-0  0.66
2014 Amarouch MY, Kasimova MA, Tarek M, Abriel H. Functional interaction between S1 and S4 segments in voltage-gated sodium channels revealed by human channelopathies. Channels (Austin, Tex.). 8: 414-20. PMID 25483584 DOI: 10.4161/19336950.2014.958922  0.589
2014 Béziau DM, Barc J, O'Hara T, Le Gloan L, Amarouch MY, Solnon A, Pavin D, Lecointe S, Bouillet P, Gourraud JB, Guicheney P, Denjoy I, Redon R, Mabo P, le Marec H, et al. Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations. Basic Research in Cardiology. 109: 446. PMID 25341504 DOI: 10.1007/s00395-014-0446-5  0.454
2014 Swan H, Amarouch MY, Leinonen J, Marjamaa A, Kucera JP, Laitinen-Forsblom PJ, Lahtinen AM, Palotie A, Kontula K, Toivonen L, Abriel H, Widen E. Gain-of-function mutation of the SCN5A gene causes exercise-induced polymorphic ventricular arrhythmias. Circulation. Cardiovascular Genetics. 7: 771-81. PMID 25210054 DOI: 10.1161/Circgenetics.114.000703  0.66
2014 Coyan FC, Abderemane-Ali F, Amarouch MY, Piron J, Mordel J, Nicolas CS, Steenman M, Mérot J, Marionneau C, Thomas A, Brasseur R, Baró I, Loussouarn G. A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation. Plos One. 9: e93255. PMID 24681627 DOI: 10.1371/journal.pone.0093255  0.435
2014 Amarouch MY, Leinonen J, Marjamaa A, Kucera JP, Laitinen-Forsblom PJ, Lahtinen AM, Palotie A, Kontula K, Toivonen L, Abriel H, Widen E, Swan H. 0265: A novel SCN5A mutation associated with exercise-induced polymorphic ventricular arrhythmias resembling CPVT Archives of Cardiovascular Diseases Supplements. 6: 41-42. DOI: 10.1016/S1878-6480(14)71376-X  0.64
2014 Coyan FC, Amarouch M, Abderemane Ali F, Piron J, Mordel J, Nicolas CS, Steenman M, Mérot J, Marionneau C, Thomas A, Brasseur R, Baró I, Loussouarn G. In KCNQ1 Channels, a Long QT Mutation Induces a Regulation by Cholesterol Instead of Phosphatidylinositol-4,5-Bisphosphate Biophysical Journal. 106: 140a. DOI: 10.1016/J.BPJ.2013.11.814  0.372
2013 Amarouch MY, Syam N, Abriel H. Biochemical, single-channel, whole-cell patch clamp, and pharmacological analyses of endogenous TRPM4 channels in HEK293 cells. Neuroscience Letters. 541: 105-10. PMID 23428507 DOI: 10.1016/J.Neulet.2013.02.011  0.752
2013 Ossola D, Behr P, Amarouch M, Abriel H, Vörös J, Zambelli T. Fluidfm for Force Controlled Electrophysiology Biophysical Journal. 104: 502a. DOI: 10.1016/J.Bpj.2012.11.2771  0.479
2012 Laurent G, Saal S, Amarouch MY, Béziau DM, Marsman RF, Faivre L, Barc J, Dina C, Bertaux G, Barthez O, Thauvin-Robinet C, Charron P, Fressart V, Maltret A, Villain E, et al. Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy. Journal of the American College of Cardiology. 60: 144-56. PMID 22766342 DOI: 10.1016/j.jacc.2012.02.052  0.337
2012 Abriel H, Syam N, Sottas V, Amarouch MY, Rougier JS. TRPM4 channels in the cardiovascular system: physiology, pathophysiology, and pharmacology. Biochemical Pharmacology. 84: 873-81. PMID 22750058 DOI: 10.1016/J.Bcp.2012.06.021  0.645
2011 Piron J, Amarouch MY, Mordel J, Nicolas CS, Thomas A, Brasseur R, Charpentier F, Mérot J, Baró I, Loussouarn G. KCNQ1-R539W Mutation Substitutes Cholesterol for Phosphatidylinositol-4, 5-Bisphosphate in Channel Regulation Biophysical Journal. 100: 428a. DOI: 10.1016/j.bpj.2010.12.2530  0.376
2010 Rodriguez N, Amarouch MY, Montnach J, Piron J, Labro AJ, Charpentier F, Mérot J, Baró I, Loussouarn G. Phosphatidylinositol-4,5-bisphosphate (PIP(2)) stabilizes the open pore conformation of the Kv11.1 (hERG) channel. Biophysical Journal. 99: 1110-8. PMID 20712994 DOI: 10.1016/j.bpj.2010.06.013  0.442
2010 Piron J, Choveau FS, Amarouch MY, Rodriguez N, Charpentier F, Mérot J, Baró I, Loussouarn G. KCNE1-KCNQ1 osmoregulation by interaction of phosphatidylinositol-4,5-bisphosphate with Mg2+ and polyamines. The Journal of Physiology. 588: 3471-83. PMID 20660559 DOI: 10.1113/jphysiol.2010.195313  0.418
2010 Amarouch M, Saal S, Bertaux G, Faivre L, Baró I, Schott j, Kyndt F, Loussouarn G, Laurent G. Mutation of Cardiac Nav1.5 in an Hisian-Type Arrhythmia, Associated with Dilated Cardiomayopathy Biophysical Journal. 98: 311a. DOI: 10.1016/J.BPJ.2009.12.1688  0.334
2009 Amarouch M, Barc J, Béziau D, Kyndt F, Le Marec H, Babuty D, Probst V, Schott J, Baro I. G022 Loss-of-function mutation of the cardiac CAV1.2 channel in the short QT syndrome Archives of Cardiovascular Diseases. 102: S70. DOI: 10.1016/S1875-2136(09)72297-1  0.428
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