Jean-Pierre Hardelin

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Catherine Dodé, Luís Teixeira, Jacqueline Levilliers et al. · PLoS Genetics · 2006 · 452 citations · Full text

Life Sciences, Endocrinology, Genetics +16

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 · 447 citations · Full text

Life Sciences, Cell Biology, Otolaryngology +12

Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes

Sedigheh Delmaghani, Jean Defourny, Asadollah Aghaie et al. · Cell · 2015 · 217 citations · Full text

Life Sciences, Physiology, Acoustics +8

SEMA3A, a Gene Involved in Axonal Pathfinding, Is Mutated in Patients with Kallmann Syndrome

Naresh K. Hanchate, Paolo Giacobini, Pierre Lhuillier et al. · PLoS Genetics · 2012 · 216 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Molecular Characterization of the Ankle-Link Complex in Cochlear Hair Cells and Its Role in the Hair Bundle Functioning

Nicolas Michalski, Vincent Michel, Amel Bahloul et al. · Journal of Neuroscience · 2007 · 213 citations · Full text

Life Sciences, Molecular Biology, Neuroscience +12