Nahid G. Robertson - Concepedia

Author

Nahid G. Robertson

Brigham and Women's Hospital

Also Known As

N G Robertson, N ROBERTSON, N. G. Robertson, Nahid G Robertson, Nahid G. Robertson, Nahid Robertson

Publications

Citations

H-Index

Concepts

All Affiliations

Brigham and Women's Hospital Harvard University Massachusetts Eye and Ear Infirmary Broad Institute University of Manchester

About

Nahid G. Robertson is an author at Brigham and Women's Hospital specializing in medicine, genetics, and hearing loss.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	1.1K
2	Health Sciences	4	4	516
3	Arts	3	3	202
4	Natural Sciences	3	3	248
5	Public Health	1	1	18

Nahid G. Robertson

Publications

Citations

H-Index

Page 1

	Year	Citations
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction Nahid G. Robertson, Leonard Lu, Stefan Heller, Nature Genetics Vestibular DysfunctionDevelopmental BiologyVestibular SystemHealth SciencesGenetics	1998	336
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, Genomics Known GenesNatural SciencesGeneticsMolecular BiologyNucleic Acid Amplification Test	1994	187
Proteomics Reveal Cochlin Deposits Associated with Glaucomatous Trabecular Meshwork Sanjoy K. Bhattacharya, Edward J. Rockwood, Scott D. Smith, Journal of Biological Chemistry	2004	160
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, Human Molecular Genetics	1999	145
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, Genomics Developmental BiologyGeneticsAudiologyArtsNovel Cochlear Gene	1997	141
Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction Nahid G. Robertson, Cor W. R. J. Cremers, P.L.M. Huygen, Human Molecular Genetics	2006	114
Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9 Nahid G. Robertson Human Molecular Genetics GeneticsProtein ProductsNeurotologySensorineural DeafnessInner Ear	2001	107
Increased Frequencies of Cochlin-Specific T Cells in Patients with Autoimmune Sensorineural Hearing Loss Moo-Jin Baek, Hyun-Min Park, Justin M. Johnson, The Journal of Immunology	2006	97
Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9 Nahid G. Robertson Journal of Medical Genetics	2003	82
A novel <i>DFNA9</i> mutation in the vWFA2 domain of <i>COCH</i> alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site‐specific vestibular and central oculomotor dysfunction Valerie A. Street, Jeremy C. Kallman, Nahid G. Robertson, American Journal of Medical Genetics Part A	2005	57

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