A. Amraoui

KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness

Christian Kubisch, Björn C. Schroeder, Thomas Friedrich et al. · Cell · 1999 · 868 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

Shin’ichiro Yasunaga, M’hamed Grati, Martine Cohen‐Salmon et al. · Nature Genetics · 1999 · 585 citations

Medicine, Genetics, Molecular Genetics +13

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

Batiste Boëda, A. Amraoui, Amel Bahloul et al. · The EMBO Journal · 2002 · 444 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +16

KCNQ4, a K ⁺ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway

Tatjana Kharkovets, Jean‐Pierre Hardelin, Saaïd Safieddine et al. · Proceedings of the National Academy of Sciences · 2000 · 406 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Philomena Mburu, Mirna Mustapha, Anabel Varela et al. · Nature Genetics · 2003 · 342 citations

Life Sciences, Genetics, Neuroscience +11