Petit, Christine

Top Publications

Top Publications Authored or Co-Authored by "Petit, Christine"

• Prelingual deafness: High prevalence of a 30delG mutation in the connexin 26 gene

  Human Molecular Genetics, Volume 6, No. 12, Year 1997, Citations 646
• A human homologue of the Drosophila eyes absent gene underlies branchio- oto-renal (BOR) syndrome and identifies a novel gene family

  Nature Genetics, Volume 15, No. 2, Year 1997, Citations 643
• A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

  Nature Genetics, Volume 21, No. 4, Year 1999, Citations 528
• A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

  Nature Genetics, Volume 26, No. 1, Year 2000, Citations 471
• The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

  Nature Genetics, Volume 16, No. 2, Year 1997, Citations 420