Ori Rokach, Ph.D.🎗️🇮🇱🇺🇲🏳️‍🌈

🏳️‍🌈🇮🇱🇺🇲 (He/Him)🎗️

🇮🇱🇺🇲🏳️‍🌈

🎗️🇮🇱🇺🇲 #BRINGTHEMHOME

Education

Doctor of Philosophy, Cell Biology

Master of Business Administration, Marketing

Master of Science, Biotechnology

Bachelor of Science, Life Science, Molecular Cellular and Medical Biology

Publications

Rokach O, Sekulic-Jablanovic M, Voermans N, Wilmshurst J, Pillay K, Heytens L, Zhou H, Muntoni F, Gautel M, Nevo Y, Mitrani-Rosenbaum S, Attali R, Finotti A, Gambari R, Mosca B, Jungbluth H, Zorzato F, Treves S. Epigenetic changes as a common trigger of muscle weakness in congenital myopathies. Hum Mol Genet. 2015 Aug 15;24(16):4636-47. doi: 10.1093/hmg/ddv195. Epub 2015 May 27. PMID: 26019235.CopyDownload .nbibFor

Ori Rokach, Nina D. Ullrich, Martin Rausch, Vincent Mouly, Haiyan Zhou, Francesco Muntoni, Francesco Zorzato, Susan Treves; Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization. Biochem J 15 October 2013; 455 (2): 169–177. doi: https://doi.org/10.1042/BJ20130698

 Attali R, Aharoni S, Treves S, Rokach O, Becker Cohen M, Fellig Y, et al. (2013) Variable Myopathic Presentation in a Single Family with Novel Skeletal RYR1 Mutation. PLoS ONE 8(7): e69296. https://doi.org/10.1371/journal.pone.0069296

Zhou, H.; Rokach, O.; Feng, L.; Munteanu, I.; Mamchaoui, K.; Wilmshurst, J.M.; Sewry, C.; Manzur, A.Y.; Pillay, K.; Mouly, V.; et al.
RyR1 deficiency in congenital myopathies disrupts excitation-contraction coupling. Hum. Mutat. 2013, 34, 986–996.