Michel Leibovici
Centre National de la Recherche Scientifique(FR)Inserm(FR)Université Paris Cité(FR)Institut Necker Enfants Malades(FR)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Hearing Loss and Rehabilitation, Vestibular and auditory disorders, RNA Research and Splicing, Connexins and lens biology
Most-Cited Works
- → A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome(1997)881 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
- → A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C(2000)466 cited
- → Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy(2006)326 cited
- → Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes(2015)214 cited
- → Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus(2001)191 cited