Amel Bahloul

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 7

Top Topics

Spectrum Disorder

Top Venues

Journal of clinical medicine

Proceedings of the National Academy of Sciences of the United States of America

This page only lists publications with an associated author ORCID identifier.

Publications

Anissa Rym Saidia, Jérôme Ruel, Amel Bahloul, Benjamin Chaix, Frédéric Venail, Jing Wang
Current Advances in Gene Therapies of Genetic Auditory Neuropathy Spectrum Disorder. Journal of clinical medicine 12 (3) (2023)
Anissa Rym Saidia, Jérôme Ruel, Amel Bahloul, Benjamin Chaix, Frédéric Venail, Jing Wang
Current Advances in Gene Therapies of Genetic Auditory Neuropathy Spectrum Disorder. Journal of clinical medicine 12 (3) (2023)
Anissa Rym Saidia, Jérôme Ruel, Amel Bahloul, Benjamin Chaix, Frédéric Venail, Jing Wang
Current Advances in Gene Therapies of Genetic Auditory Neuropathy Spectrum Disorder. Journal of clinical medicine 12 (3) (2023)
Ju Sun Song, Amel Bahloul, Christine Petit, Sang Jin Kim, Il Joon Moon, Jinhyuk Lee, Change Seok Ki
A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in USH1C That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss. Annals of laboratory medicine 40 (3) (2020)
Sophie Boucher, Fabienne Wong Jun Tai, Sedigheh Delmaghani, Andrea Lelli, Amrit Singh-Estivalet, Typhaine Dupont, Magali Niasme-Grare, Vincent Michel, Nicolas Wolff, Amel Bahloul, Yosra Bouyacoub, Didier Bouccara, Bernard Fraysse, Olivier Deguine, Lionel Collet, Hung Thai-Van, Eugen Ionescu, Jean-Louis Kemeny, Fabrice Giraudet, Jean-Pierre Lavieille, Arnaud Deveze, Anne-Laure Roudevitch-Pujol, Christophe Vincent, Christian Renard, Valerie Franco-Vidal, Claire Thibult-Apt, Vincent Darrouzet, Eric Bizaguet, Arnaud Coez, Hugues Aschard, Nicolas Michalski, Gaëlle M Lefevre, Anne Aubois, Paul Avan, Crystel Bonnet, Christine Petit
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis. Proceedings of the National Academy of Sciences of the United States of America 117 (49) (2020)
Nicolas Michalski, Juan D Goutman, Sarah Marie Auclair, Jacques Boutet de Monvel, Margot Tertrais, Alice Emptoz, Alexandre Parrin, Sylvie Nouaille, Marc Guillon, Martin Sachse, Danica Ciric, Amel Bahloul, Jean-Pierre Hardelin, Roger Bryan Sutton, Paul Avan, Shyam S Krishnakumar, Gregory Lavieu, Didier Dulon, Saaid Safieddine, Christine Petit
Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses. eLife 6 (2017)
Amel Bahloul, Elise Pepermans, Bertrand Raynal, Nicolas Wolff, Florence Cordier, Patrick England, Sylvie Nouaille, Bruno Baron, Aziz El-Amraoui, Jean-Pierre Hardelin, Dominique Durand, Christine Petit
Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery. FEBS letters 591 (15) (2017)