A. Amraoui
Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut Pasteur(FR)Université Paris Cité(FR)Assistance Publique – Hôpitaux de Paris(FR)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Ocular Diseases and Behçet’s Syndrome, Intraocular Surgery and Lenses, Retinal and Optic Conditions, Retinal Development and Disorders
Most-Cited Works
- → KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness(1999)863 cited
- → A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness(1999)580 cited
- → KCNQ4, a K + channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway(2000)403 cited
- → Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31(2003)339 cited
- → Interactions in the network of Usher syndrome type 1 proteins(2004)239 cited
- → The Auditory Hair Cell Ribbon Synapse: From Assembly to Function(2012)189 cited