Nahid G. Robertson

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

Nahid G. Robertson, Leonard Lu, Stefan Heller et al. · Nature Genetics · 1998 · 340 citations

Medicine, Genetics, Molecular Genetics +16

Isolation of Novel and Known Genes from a Human Fetal Cochlear cDNA Library Using Subtractive Hybridization and Differential Screening

Nahid G. Robertson, U. Khetarpal, Gustavo A. Gutiérrez‐Espeleta et al. · Genomics · 1994 · 187 citations · Full text

Life Sciences, Genetics, Molecular Biology +12

Proteomics Reveal Cochlin Deposits Associated with Glaucomatous Trabecular Meshwork

Sanjoy K. Bhattacharya, Edward J. Rockwood, Scott D. Smith et al. · Journal of Biological Chemistry · 2004 · 161 citations · Full text

Health Professions, Molecular Biology, Ophthalmology +15

High Prevalence of Symptoms of Meniere's Disease in three Families With a Mutation in the COCH Gene

Erik Fransén, Margriet Verstreken, W. I. M. Verhagen et al. · Human Molecular Genetics · 1999 · 146 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Mapping and Characterization of a Novel Cochlear Gene in Human and in Mouse: A Positional Candidate Gene for a Deafness Disorder, DFNA9

Nahid G. Robertson, Anne B. Skvorak, Yi Yin et al. · Genomics · 1997 · 141 citations

Medicine, Genetics, Molecular Genetics +15