| Biallelic variants in TMIE and PDE6B genes mimic Usher syndrome S Abdi, M Makrelouf, IN Rous, K Ounnoughi, A Zenati, C Petit, C Bonnet Gene Reports, 101954, 2024 | | 2024 |
| Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health R Mkaouar, Z Riahi, J Marrakchi, N Mezzi, L Romdhane, M Boujemaa, ... Frontiers in Genetics 15, 1384094, 2024 | | 2024 |
| Gene therapy for treating usher syndrome G Lahlou, S Safieddine, C Petit US Patent App. 18/257,727, 2024 | | 2024 |
| Extended time frame for restoring inner ear function through gene therapy in Usher1G preclinical model G Lahlou, C Calvet, F Simon, V Michel, L Alciato, B Plion, JB de Monvel, ... JCI insight 9 (3), 2024 | | 2024 |
| Prevention and/or treatment of hearing loss or impairment C Petit, A Paul, S Delmaghani, J Defourny, A Aghaie, S Safieddine, ... US Patent App. 18/313,124, 2023 | | 2023 |
| Novel pathogenic WHRN variant causing hearing loss in a moroccan family I AitRaise, G Amalou, S Redouane, H Charoute, K Snoussi, ... Molecular Biology Reports 50 (12), 10663-10669, 2023 | | 2023 |
| Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families I AitRaise, G Amalou, A Bakhchane, A Bousfiha, H Abdelghaffar, C Majida, ... Biochemical Genetics, 1-11, 2023 | 1 | 2023 |
| Deafness: From genetic architecture to gene therapy C Petit, C Bonnet, S Safieddine Nature Reviews Genetics 24 (10), 665-686, 2023 | 27 | 2023 |
| Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness M Salame, C Bonnet, ECM Moctar, SM Brahim, A Dedy, LA Vetah, ... European Archives of Oto-Rhino-Laryngology 280 (9), 4057-4063, 2023 | | 2023 |
| Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies P Jean, F Wong Jun Tai, A Singh-Estivalet, A Lelli, C Scandola, ... Proceedings of the National Academy of Sciences 120 (26), e2221744120, 2023 | 13 | 2023 |
| Prevention and/or treatment of hearing loss or impairment C Petit, A Paul, S Delmaghani, J Defourny, A Aghaie, S Safieddine, ... US Patent 11,679,140, 2023 | | 2023 |
| François Gros (1925–2022) C Petit, P Kourilsky Comptes Rendus. Biologies 346 (S2), 3-8, 2023 | | 2023 |
| The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses C Calvet, T Peineau, N Benamer, M Cornille, A Lelli, B Plion, G Lahlou, ... Iscience 25 (12), 2022 | 9 | 2022 |
| Adeno Associated Vector-Based Gene Therapy for the Autosomal Recessive Non-Syndromic Deafness 9 (DFNB9) G Olivier, CT Van Ba, APJ Giese, P Vidal, L Barrot, P Rambeau, ... HUMAN GENE THERAPY 33 (23-24), A80-A80, 2022 | | 2022 |
| Audition: hearing and deafness C Petit, A El-Amraoui, P Avan Neuroscience in the 21st Century: From Basic to Clinical, 1075-1142, 2022 | 15 | 2022 |
| Characterizing subcutaneous cortical auditory evoked potentials in mice O Postal, W Bakay, T Dupont, A Buck, É Daoud, C Petit, N Michalski, ... Hearing Research 422, 108566, 2022 | 4 | 2022 |
| Otologie et audiologie, un parcours de soin en pleine mutation à la lumière des avancées scientifiques P Avan, C Petit médecine/sciences 38 (8-9), 621-622, 2022 | | 2022 |
| Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco I AitRaise, G Amalou, A Bousfiha, H Charoute, H Rouba, H Abdelghaffar, ... Molecular Biology Reports 49 (5), 3949-3954, 2022 | 6 | 2022 |
| Aav-mediated gene therapy restoring the otoferlin gene S Safieddine, C Petit US Patent App. 17/422,737, 2022 | | 2022 |
| Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort VM Smirnov, M Nassisi, S Mohand-Saïd, C Bonnet, A Aubois, C Devisme, ... Investigative ophthalmology & visual science 63 (4), 25-25, 2022 | | 2022 |
