Ayadi, Hammadi

Top Publications

Top Publications Authored or Co-Authored by "Ayadi, Hammadi"

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

  Human Molecular Genetics, Volume 6, No. 12, Year 1997, Citations 646
• 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
• Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin

  Human Molecular Genetics, Volume 12, No. 5, Year 2003, Citations 306
• Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in usher 1B families from diverse origins

  American Journal of Human Genetics, Volume 61, No. 4, Year 1997, Citations 123
• A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21

  Human Molecular Genetics, Volume 6, No. 1, Year 1997, Citations 122