Martine Cohen‐Salmon

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

Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death

Martine Cohen‐Salmon, Thomas Ott, Vincent Michel et al. · Current Biology · 2002 · 443 citations · Full text

Cell Death, Cochlear Development, Systems Biology +4

Connexin 30 sets synaptic strength by controlling astroglial synapse invasion

Ulrike Pannasch, Dominik Freche, Glenn Dallérac et al. · Nature Neuroscience · 2014 · 324 citations · Full text

Synaptic Plasticity, Cellular Neurobiology, Molecular Neuroscience +10

Deletion of Astroglial Connexins Weakens the Blood–Brain Barrier

Pascal Ezan, Pascal André, Salvatore Cisternino et al. · Journal of Cerebral Blood Flow & Metabolism · 2012 · 213 citations · Full text

X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene.

Jean‐Pierre Hardelin, Jacqueline Levilliers, Ignacio del Castillo et al. · Proceedings of the National Academy of Sciences · 1992 · 189 citations · Full text

Cytogenetics, Genetics, Pathology +16