M’hamed Grati

Otoferlin, Defective in a Human Deafness Form, Is Essential for Exocytosis at the Auditory Ribbon Synapse

Isabelle Roux, Saaïd Safieddine, Régis Nouvian et al. · Cell · 2006 · 723 citations · Full text

Neuroanatomy, Medicine, Audiology +10

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 635 citations · Full text

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

Shin’ichiro Yasunaga, M’hamed Grati, Martine Cohen‐Salmon et al. · Nature Genetics · 1999 · 575 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

Regulation of Stereocilia Length by Myosin XVa and Whirlin Depends on the Actin-Regulatory Protein Eps8

Uri Manor, Andrea Disanza, M’hamed Grati et al. · Current Biology · 2011 · 208 citations · Full text

Signal Transduction, Molecular Physiology, Molecular Regulation +14

OTOF Encodes Multiple Long and Short Isoforms: Genetic Evidence That the Long Ones Underlie Recessive Deafness DFNB9

Shin’ichiro Yasunaga, M’hamed Grati, Sébastien Chardenoux et al. · The American Journal of Human Genetics · 2000 · 203 citations · Full text

Developmental Biology, Short Isoforms, Genetic Disorder +11