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Christine Petit

Centre National de la Recherche Scientifique

Publishes on Hearing, Cochlea, Tinnitus, Genetics, Vestibular and auditory disorders, Connexins and lens biology. 495 papers and 33k citations.

495Publications

33kTotal Citations

Hearing, Cochlea, Tinnitus, Genetics Vestibular and auditory disorders Connexins and lens biology Hearing Loss and Rehabilitation RNA and protein synthesis mechanisms

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Top publicationsby citations

Defective myosin VIIA gene responsible for Usher syndrome type IB

Dominique Well, Stéphane Blanchard, Josseline Kaplan et al.|Nature|1995

Cited by 1.1k

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy et al.|Nature Genetics|1997

Cited by 883

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

Cited by 867Open Access

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont et al.|Nature Genetics|2003

Cited by 829Open Access

Otoferlin, Defective in a Human Deafness Form, Is Essential for Exocytosis at the Auditory Ribbon Synapse

Isabelle Roux, Saaïd Safieddine, Régis Nouvian et al.|Cell|2006

Cited by 740Open Access