Christine Petit
Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut Pasteur(FR)Collège de France(FR)Université Paris Cité(FR)Assistance Publique – Hôpitaux de Paris(FR)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Connexins and lens biology, Vestibular and auditory disorders, Hearing Loss and Rehabilitation, RNA and protein synthesis mechanisms
Most-Cited Works
- → Defective myosin VIIA gene responsible for Usher syndrome type IB(1995)1,065 cited
- → A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome(1997)881 cited
- → KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness(1999)863 cited
- → Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome(2003)827 cited
- → Otoferlin, Defective in a Human Deafness Form, Is Essential for Exocytosis at the Auditory Ribbon Synapse(2006)729 cited
- → A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family(1997)678 cited