Dodé, Catheriné

Top Publications

Top Publications Authored or Co-Authored by "Dodé, Catheriné"

• 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 comparative phenotypic study of Kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes

  Journal of Clinical Endocrinology and Metabolism, Volume 95, No. 2, Year 2010, Citations 131
• Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions

  Journal of Clinical Investigation, Volume 120, No. 10, Year 2010, Citations 88
• Mapping of DFNB12 a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22

  Human Molecular Genetics, Volume 5, No. 7, Year 1996, Citations 82
• Familial Mediterranean fever in Lebanon: Mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694l mutations

  European Journal of Human Genetics, Volume 9, No. 1, Year 2001, Citations 78