Editorial: Christine Petit-Jean-Genaz Receives the 2012 Robert H. Siemann Award by Frank Zimmermann

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Spontaneous Mouse Behavior in Presence of Dissonance and Acoustic Roughness by Olivier Postal, Olivier Postal, Typhaine Dupont, Warren Bakay, Noémi Dominique, Christine Petit, Christine Petit, Christine Petit, Nicolas Michalski, Boris Gourévitch, Boris Gourévitch

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Contributions of Age-Related and Audibility-Related Deficits to Aided Consonant Identification in Presbycusis: A Causal-Inference Analysis by Léo Varnet, Agnès C. Léger, Sophie Boucher, Sophie Boucher, Sophie Boucher, Crystel Bonnet, Crystel Bonnet, Christine Petit, Christine Petit, Christian Lorenzi

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A synaptic F-actin network controls otoferlin-dependent exocytosis in auditory inner hair cells by Philippe FY Vincent, Yohan Bouleau, Christine Petit, Didier Dulon

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Phylogenetic analysis of Harmonin homology domains by Baptiste Colcombet-Cazenave, Karen Druart, Crystel Bonnet, Christine Petit, Olivier Spérandio, Julien Guglielmini, Nicolas Wolff

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Methicillin-resistant Staphylococcus aureus in Saarland, Germany: a statewide admission prevalence screening study. by Mathias Herrmann, Christine Petit, Alik Dawson, Judith Biechele, Alexander Halfmann, Lutz von Müller, Stefan Gräber, Stefan Wagenpfeil, Renate Klein, Barbara Gärtner

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SponGee: A Genetic Tool for Subcellular and Cell-Specific cGMP Manipulation by Oriol Ros, Yvrick Zagar, Solène Ribes, Sarah Baudet, Karine Loulier, Sandrine Couvet, Delphine Ladarre, Alain Aghaie, Alice Louail, Christine Petit, Yves Mechulam, Zsolt Lenkei, Xavier Nicol

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Characteristics of Retinitis Pigmentosa Associated with <i>ADGRV1</i> and Comparison with <i>USH2A</i> in Patients from a Multicentric Usher Syndrome Study Treatrush by Ana Fakin, Crystel Bonnet, Anne Kurtenbach, Saddek Mohand-Said, Ditta Zobor, Katarina Stingl, Francesco Testa, Francesca Simonelli, José-Alain Sahel, Isabelle Audo, Eberhart Zrenner, Marko Hawlina, Christine Petit

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Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation by Laura F. Corns, Stuart L. Johnson, Terri Roberts, Kishani M. Ranatunga, Aenea Hendry, Federico Ceriani, Saaid Safieddine, Karen P. Steel, Andy Forge, Christine Petit, David N. Furness, Corné J. Kros, Walter Marcotti

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Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome. by Samia Abdi, Amel Bahloul, Asma Behlouli, Jean-Pierre Hardelin, Mohamed Makrelouf, Kamel Boudjelida, Malek Louha, Ahmed Cheknene, Rachid Belouni, Yahia Rous, Zahida Merad, Djamel Selmane, Mokhtar Hasbelaoui, Crystel Bonnet, Akila Zenati, Christine Petit

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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients. by Zied Riahi, Crystel Bonnet, Rim Zainine, Saida Lahbib, Yosra Bouyacoub, Rym Bechraoui, Jihène Marrakchi, Jean-Pierre Hardelin, Malek Louha, Leila Largueche, Salim Ben Yahia, Moncef Kheirallah, Leila Elmatri, Ghazi Besbes, Sonia Abdelhak, Christine Petit

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The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses by Charlotte Calvet, Thibault Peineau, Najate Benamer, Maxence Cornille, Andrea Lelli, Baptiste Plion, Ghizlène Lahlou, Julia Fanchette, Sylvie Nouaille, Jacques Boutet de Monvel, Amrit Estivalet, Philippe Jean, Vincent Michel, Martin Sachse, Nicolas Michalski, Paul Avan, Christine Petit, Didier Dulon, Saaid Safieddine

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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness. by Zied Riahi, Crystel Bonnet, Rim Zainine, Malek Louha, Yosra Bouyacoub, Nadia Laroussi, Mariem Chargui, Rym Kefi, Laurence Jonard, Imen Dorboz, Jean-Pierre Hardelin, Sihem Belhaj Salah, Jacqueline Levilliers, Dominique Weil, Kenneth McElreavey, Odile Tanguy Boespflug, Ghazi Besbes, Sonia Abdelhak, Christine Petit

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Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss. by Hongyang Wang, Yali Zhao, Yuting Yi, Yun Gao, Qiong Liu, Dayong Wang, Qian Li, Lan Lan, Na Li, Jing Guan, Zifang Yin, Bing Han, Feifan Zhao, Liang Zong, Wenping Xiong, Lan Yu, Lijie Song, Xin Yi, Ling Yang, Christine Petit, Qiuju Wang

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Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses by 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, James E Rothman, Didier Dulon, Saaid Safieddine, Christine Petit

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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health by Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Jihene Marrakchi, Nessrine Mezzi, Nessrine Mezzi, Lilia Romdhane, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hager Jaouadi, Hager Jaouadi, Hela Boudabbous, Hela Boudabbous, Hela Boudabbous, Lotfi Zekri, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Meriem Elyounsi, Ichraf Kraoua, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Ilhem Turki, Mourad Mokni, Sophie Boucher, Sophie Boucher, Christine Petit, Christine Petit, Fabrice Giraudet, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Soumeyya Halayem, Rim Zainine, Rim Zainine, Hamida Turki, Amel Tounsi, Crystel Bonnet, Ridha Mrad, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Mediha Trabelsi, Cherine Charfeddine

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Exome sequencing and linkage analysis identified tenascin-C (TNC) as a novel causative gene in nonsyndromic hearing loss. by Yali Zhao, Feifan Zhao, Liang Zong, Peng Zhang, Liping Guan, Jianguo Zhang, Dayong Wang, Jing Wang, Wei Chai, Lan Lan, Qian Li, Bing Han, Ling Yang, Xin Jin, Weiyan Yang, Xiaoxiang Hu, Xiaoning Wang, Ning Li, Yingrui Li, Christine Petit, Jun Wang, Huanming Yang Jian Wang, Qiuju Wang

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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment. by Rahma Mkaouar, Zied Riahi, Cherine Charfeddine, Imen Chelly, Hela Boudabbous, Hamza Dallali, Crystel Bonnet, Meriem Hechmi, Soumeya Bekri, Nadia Zitouna, Lotfi Zekri, Amel Tounsi, Rym Kefi, Jihene Marrakchi, Olfa Messaoud, Ichraf Kraoua, Sonia Maalej, Ilhem Turki Ben Youssef, Ahlem Ben Hmid, Fabrice Giraudet, Sami Bouchoucha, Neji Tebib, Ghazi Besbes, Christine Petit, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi

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Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function by Lucy A Dunbar, Pranav Patni, Carlos Aguilar, Philomena Mburu, Laura Corns, Helena RR Wells, Sedigheh Delmaghani, Andrew Parker, Stuart Johnson, Debbie Williams, Christopher T Esapa, Michelle M Simon, Lauren Chessum, Sherylanne Newton, Joanne Dorning, Prashanthini Jeyarajan, Susan Morse, Andrea Lelli, Gemma F Codner, Thibault Peineau, Suhasini R Gopal, Kumar N Alagramam, Ronna Hertzano, Didier Dulon, Sara Wells, Frances M Williams, Christine Petit, Sally J Dawson, Steve DM Brown, Walter Marcotti, Aziz El‐Amraoui, Michael R Bowl

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