| KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness C Kubisch, BC Schroeder, T Friedrich, B Lütjohann, A El-Amraoui, ... Cell 96 (3), 437-446, 1999 | 1079 | 1999 |
| A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness S Yasunaga, M Cohen-Salmon, A El-Amraoui, M Mustapha, N Salem, ... Nature genetics 21 (4), 363-369, 1999 | 680 | 1999 |
| KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway T Kharkovets, JP Hardelin, S Safieddine, M Schweizer, A El-Amraoui, ... Proceedings of the National Academy of Sciences 97 (8), 4333-4338, 2000 | 503 | 2000 |
| Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle B Boëda, A El‐Amraoui, A Bahloul, R Goodyear, L Daviet, S Blanchard, ... The EMBO journal, 2002 | 494 | 2002 |
| Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31 P Mburu, M Mustapha, A Varela, D Weil, A El-Amraoui, RH Holme, ... Nature genetics 34 (4), 421-428, 2003 | 371 | 2003 |
| Usher syndrome type IG (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin D Weil, A El-Amraoui, S Masmoudi, M Mustapha, Y Kikkawa, S Lainé, ... Human molecular genetics 12 (5), 463-471, 2003 | 345 | 2003 |
| Interactions in the network of Usher syndrome type 1 proteins A Adato, V Michel, Y Kikkawa, J Reiners, KN Alagramam, D Weil, ... Human molecular genetics 14 (3), 347-356, 2005 | 281 | 2005 |
| Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin–catenins complex P Küssel-Andermann, A El-Amraoui, S Safieddine, S Nouaille, I Perfettini, ... The EMBO journal 19 (22), 6020-6029, 2000 | 266 | 2000 |
| Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells A El-Amraoui, C Petit Journal of cell science 118 (20), 4593-4603, 2005 | 225 | 2005 |
| Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells A Adato, G Lefevre, B Delprat, V Michel, N Michalski, S Chardenoux, ... Human molecular genetics 14 (24), 3921-3932, 2005 | 213 | 2005 |
| Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly B Delprat, V Michel, R Goodyear, Y Yamasaki, N Michalski, A El-Amraoui, ... Human molecular genetics 14 (3), 401-410, 2005 | 207 | 2005 |
| The auditory hair cell ribbon synapse: from assembly to function S Safieddine, A El-Amraoui, C Petit Annual review of neuroscience 35, 509-528, 2012 | 205 | 2012 |
| MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes A El‐Amraoui, JS Schonn, P Küssel‐Andermann, S Blanchard, C Desnos, ... EMBO reports, 2002 | 204 | 2002 |
| Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia. D Weil, G Levy, I Sahly, F Levi-Acobas, S Blanchard, A El-Amraoui, ... Proceedings of the National Academy of Sciences 93 (8), 3232-3237, 1996 | 203 | 1996 |
| Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites C Desnos, JS Schonn, S Huet, VS Tran, A El-Amraoui, G Raposo, ... The Journal of cell biology 163 (3), 559-570, 2003 | 193 | 2003 |
| Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice I Sahly, E Dufour, C Schietroma, V Michel, A Bahloul, I Perfettini, ... Journal of Cell Biology 199 (2), 381-399, 2012 | 189 | 2012 |
| Otogelin: a glycoprotein specific to the acellular membranes of the inner ear M Cohen-Salmon, A El-Amraoui, M Leibovici, C Petit Proceedings of the National Academy of Sciences 94 (26), 14450-14455, 1997 | 182 | 1997 |
| Human Usher 1B/Mouse shaker-1 : The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor … A El-Amraoui, I Sahly, S Picaud, J Sahel, M Abitbol, C Petit Human molecular genetics 5 (8), 1171-1178, 1996 | 171 | 1996 |
| Involvement of the Rab27 binding protein Slac2c/MyRIP in insulin exocytosis L Waselle, T Coppola, M Fukuda, M Iezzi, A El-Amraoui, C Petit, ... Molecular biology of the cell 14 (10), 4103-4113, 2003 | 170 | 2003 |
| Targeted disruption of otog results in deafness and severe imbalance MC Simmler, M Cohen-Salmon, A El-Amraoui, L Guillaud, JC Benichou, ... Nature genetics 24 (2), 139-143, 2000 | 169 | 2000 |
