Nahid G. Robertson
Edinburgh Napier University(GB)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Vestibular and auditory disorders, Hearing Loss and Rehabilitation, Connexins and lens biology, Cancer-related molecular mechanisms research
Most-Cited Works
- → Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction(1998)336 cited
- → Isolation of Novel and Known Genes from a Human Fetal Cochlear cDNA Library Using Subtractive Hybridization and Differential Screening(1994)187 cited
- → Proteomics Reveal Cochlin Deposits Associated with Glaucomatous Trabecular Meshwork(2004)161 cited
- → High Prevalence of Symptoms of Meniere's Disease in three Families With a Mutation in the COCH Gene(1999)146 cited
- → Mapping and Characterization of a Novel Cochlear Gene in Human and in Mouse: A Positional Candidate Gene for a Deafness Disorder, DFNA9(1997)141 cited
- → Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction(2006)115 cited
- → Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9(2001)107 cited
- → Increased Frequencies of Cochlin-Specific T Cells in Patients with Autoimmune Sensorineural Hearing Loss(2006)97 cited
- → Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9(2003)82 cited
- → A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site‐specific vestibular and central oculomotor dysfunction(2005)57 cited