Hélène Catros

Association pour l'Utilisation du Rein Artificiel — France

Neuroscience · Life Sciences

7h-index691citations7works0.02yr avg
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Research Topics

Hearing, Cochlea, Tinnitus, Genetics(6), Vestibular and auditory disorders(4), Ear Surgery and Otitis Media(3), Connexins and lens biology(3), Genomics and Phylogenetic Studies(1)

Publications7 total

Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct
International Journal of Pediatric Otorhinolaryngology·2010· 51 cited
Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip
European Journal of Human Genetics·2007· 95 citedOpen Access
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations
European Journal of Human Genetics·2006· 240 citedOpen Access
GJB2 and GJB6 Mutations
Archives of Otolaryngology - Head and Neck Surgery·2005· 103 cited
Screening of <i>SLC26A4</i> (<i>PDS</i>) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity
Clinical Genetics·2004· 98 cited
Large deletion of the <i>GJB6</i> gene in deaf patients heterozygous for the <i>GJB2</i> gene mutation: Genotypic and phenotypic analysis
American Journal of Medical Genetics Part A·2004· 49 cited
Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene
European Journal of Human Genetics·2003· 55 citedOpen Access

Frequent Co-authors

Hubert Journel(7), Valérie Drouin‐Garraud(7), Sandrine Marlin(7), Françoise Denoyelle(7), Delphine Feldmann(6), F Duriez(6), Christine Petit(6), Rémy Couderc(6), Jacques Leman(5), Hélène Dollfus(5), Marie-Françoise Obstoy(5), Alain Joannard(4), S. Schmerber(4), Bruno Delobel(4), Albert David(4), C. Calais(4), Éréa-Noël Garabédian(4), Natalie Loundon(4), Hélène Blons(3), Laurence Jonard(3)