N G Robertson
Overview
Explore the profile of N G Robertson including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
18
Citations
576
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Robertson N, Hamaker S, Patriub V, Aster J, Morton C
J Med Genet
. 2003 Jul;
40(7):479-86.
PMID: 12843317
Five missense mutations in the FCH/LCCL domain of the COCH gene, encoding the protein cochlin, are pathogenic for the autosomal dominant hearing loss and vestibular dysfunction disorder, DFNA9. To date,...
2.
Robertson N, Resendes B, Lin J, Lee C, Aster J, Adams J, et al.
Hum Mol Genet
. 2001 Nov;
10(22):2493-500.
PMID: 11709536
Missense mutations in the COCH gene, which is expressed preferentially at high levels in the inner ear, cause the autosomal dominant sensorineural deafness and vestibular disorder, DFNA9 (OMIM 601369). By...
3.
Ahituv N, Sobe T, Robertson N, Morton C, Taggart R, Avraham K
Gene
. 2001 Feb;
261(2):269-75.
PMID: 11167014
Mutations in myosin VI (Myo6) cause deafness and vestibular dysfunction in Snell's waltzer mice. Mutations in two other unconventional myosins cause deafness in both humans and mice, making myosin VI...
4.
Wayne S, Robertson N, Declau F, Chen N, Verhoeven K, Prasad S, et al.
Hum Mol Genet
. 2001 Feb;
10(3):195-200.
PMID: 11159937
We identified Eyes absent 4 (EYA4), a member of the vertebrate Eya family of transcriptional activators, as the causative gene of postlingual, progressive, autosomal dominant hearing loss at the DFNA10...
5.
Robertson N, Heller S, Lin J, Resendes B, Weremowicz S, Denis C, et al.
Genomics
. 2000 Jun;
66(3):242-8.
PMID: 10873378
We have identified a novel cochlear gene, designated OTOR, from a comparative sequence analysis of over 4000 clones from a human fetal cochlear cDNA library. Northern blot analysis of human...
6.
Fransen E, Verstreken M, Verhagen W, Wuyts F, Huygen P, DHaese P, et al.
Hum Mol Genet
. 1999 Jul;
8(8):1425-9.
PMID: 10400989
We report the genetic analysis of one large Belgian and two small Dutch families with autosomal dominant non-syndromic progressive sensorineural hearing loss associated with vestibular dysfunction. Linkage studies in the...
7.
8.
Skvorak A, Weng Z, Yee A, Robertson N, Morton C
Hum Mol Genet
. 1999 Feb;
8(3):439-52.
PMID: 9949203
To identify candidate genes for human hearing disorders and to understand better human hearing at the molecular level, we constructed a human cochlear cDNA library. An aliquot of the unsubtracted...
9.
de Kok Y, Bom S, Brunt T, Kemperman M, van Beusekom E, Robertson N, et al.
Hum Mol Genet
. 1999 Feb;
8(2):361-6.
PMID: 9931344
We analysed a Dutch family with autosomal dominant non-syndromic progressive sensorineural hearing loss and mapped the underlying gene defect by genetic linkage analysis to a 11.0 cM region overlapping the...
10.
Robertson N, Lu L, Heller S, Merchant S, Eavey R, McKenna M, et al.
Nat Genet
. 1998 Nov;
20(3):299-303.
PMID: 9806553
DFNA9 is an autosomal dominant, nonsyndromic, progressive sensorineural hearing loss with vestibular pathology. Here we report three missense mutations in human COCH (previously described as Coch5b2), a novel cochlear gene,...