M'hamed Grati
M'hamed Grati
Research Assistant Professor - Principal Investigator
Verified email at med.miami.edu
TitleCited byYear
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene
F Denoyelle, D Weil, MA Maw, SA Wilcox, NJ Lench, DR Allen-Powell, ...
Human molecular genetics 6 (12), 2173-2177, 1997
7721997
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness
S Yasunaga, M Grati, M Cohen-Salmon, A El-Amraoui, M Mustapha, ...
Nature genetics 21 (4), 363, 1999
5141999
Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse
I Roux, S Safieddine, R Nouvian, M Grati, MC Simmler, A Bahloul, ...
Cell 127 (2), 277-289, 2006
4832006
Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse
I Roux, S Safieddine, R Nouvian, M Grati, MC Simmler, A Bahloul, ...
Cell 127 (2), 277-289, 2006
4832006
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9
S Yasunaga, M Grati, S Chardenoux, TN Smith, TB Friedman, AK Lalwani, ...
The American Journal of Human Genetics 67 (3), 591-600, 2000
1832000
Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction
M Grati, B Kachar
Proceedings of the National Academy of Sciences 108 (28), 11476-11481, 2011
1252011
Regulation of stereocilia length by myosin XVa and whirlin depends on the actin-regulatory protein Eps8
U Manor, A Disanza, MH Grati, L Andrade, H Lin, PP Di Fiore, G Scita, ...
Current Biology 21 (2), 167-172, 2011
1152011
Mutation of the ATP-gated P2X2 receptor leads to progressive hearing loss and increased susceptibility to noise
D Yan, Y Zhu, T Walsh, D Xie, H Yuan, A Sirmaci, T Fujikawa, ACY Wong, ...
Proceedings of the National Academy of Sciences 110 (6), 2228-2233, 2013
932013
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
C Bonnet, M Grati, S Marlin, J Levilliers, JP Hardelin, M Parodi, ...
Orphanet journal of rare diseases 6 (1), 21, 2011
872011
Pendred syndrome: Phenotypic variability in two families carrying the same PDS missense mutation
S Masmoudi, I Charfedine, M Hmani, M Grati, AM Ghorbel, ...
American journal of medical genetics 90 (1), 38-44, 2000
872000
Neurotransmitters: The critical modulators regulating gut–brain axis
R Mittal, LH Debs, AP Patel, D Nguyen, K Patel, G O'Connor, M Grati, ...
Journal of cellular physiology 232 (9), 2359-2372, 2017
812017
Current concepts in the pathogenesis and treatment of chronic suppurative otitis media
R Mittal, CV Lisi, R Gerring, J Mittal, K Mathee, G Narasimhan, RK Azad, ...
Journal of medical microbiology 64 (Pt 10), 1103, 2015
772015
Intricate functions of matrix metalloproteinases in physiological and pathological conditions
R Mittal, AP Patel, LH Debs, D Nguyen, K Patel, M Grati, J Mittal, D Yan, ...
Journal of cellular physiology 231 (12), 2599-2621, 2016
692016
Molecular determinants for differential membrane trafficking of PMCA1 and PMCA2 in mammalian hair cells
M Grati, N Aggarwal, EE Strehler, RJ Wenthold
J Cell Sci 119 (14), 2995-3007, 2006
672006
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non‐syndromic autosomal recessive deafness
S Masmoudi, SE Antonarakis, T Schwede, AM Ghorbel, M Gratri, ...
Human mutation 18 (2), 101-108, 2001
582001
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation
M Grati, I Chakchouk, Q Ma, M Bensaid, A Desmidt, N Turki, D Yan, ...
Human molecular genetics 24 (9), 2482-2491, 2015
542015
A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E
L Jonard, D Feldmann, C Parsy, S Freitag, M Sinico, C Koval, M Grati, ...
European journal of medical genetics 51 (1), 35-43, 2008
542008
Rapid turnover of stereocilia membrane proteins: evidence from the trafficking and mobility of plasma membrane Ca2+-ATPase 2
M Grati, ME Schneider, K Lipkow, EE Strehler, RJ Wenthold, B Kachar
Journal of Neuroscience 26 (23), 6386-6395, 2006
532006
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents
D Yan, D Tekin, G Bademci, J Foster, FB Cengiz, A Kannan-Sundhari, ...
Human genetics 135 (8), 953-961, 2016
492016
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing
O Diaz-Horta, A Subasioglu-Uzak, M Grati, A DeSmidt, J Foster, L Cao, ...
Proceedings of the National Academy of Sciences 111 (27), 9864-9868, 2014
462014
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