Marie‐Madeleine Eliot
Hôpitaux Universitaires de Strasbourg(FR)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, RNA and protein synthesis mechanisms, Mitochondrial Function and Pathology, Vestibular and auditory disorders, Connexins and lens biology
Most-Cited Works
- → Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates(2005)549 cited
- → GJB2 and GJB6 Mutations(2005)103 cited
- → Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip(2007)95 cited
- → Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome(2014)69 cited
- → Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor(2002)53 cited
- → Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: Genotypic and phenotypic analysis(2004)49 cited
- [Autistic-like behavioural disorders and deafness in children].(2005)
- Complete exon sequencing of all known Usher syndrome genes greatly improves molecular(2011)
- → Suivi auditif et prise en charge de la surdité après méningite bactérienne chez le nourrisson(2012)