Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss-Reference-Cited by-同舟云学术

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Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss

Published:2014-12 Issue:1 Volume:15 Page:
ISSN:1471-2164
Container-title:BMC Genomics
language:en
Short-container-title:BMC Genomics

Author:

Haraksingh Rajini R,Jahanbani Fereshteh,Rodriguez-Paris Juan,Gelernter Joel,Nadeau Kari C,Oghalai John S,Schrijver Iris,Snyder Michael P

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Biotechnology

Link

https://link.springer.com/content/pdf/10.1186/1471-2164-15-1155.pdf

Reference43 articles.

1. Hilgert N, Smith RJ, Van Camp G: Forty-Six Genes Causing Nonsyndromic Hearing Impairment: Which Ones Should Be Analyzed in Dna Diagnostics?. Mutat Res. 2009, 681 (2-3): 189-196. 10.1016/j.mrrev.2008.08.002.

2. Petit C, Levilliers J, Hardelin JP: Molecular Genetics of Hearing Loss. Annu Rev Genet. 2001, 35: 589-646. 10.1146/annurev.genet.35.102401.091224.

3. Morton CC, Nance WE: Newborn Hearing Screening--a Silent Revolution. N Engl J Med. 2006, 354 (20): 2151-2164. 10.1056/NEJMra050700.

4. Dror AA, Avraham KB: Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology. Annu Rev Genet. 2009, 43: 411-137. 10.1146/annurev-genet-102108-134135.

5. Girotto G, Pirastu N, Sorice R, Biino G, Campbell H, D'Adamo AP, Hastie ND, Nutile T, Polasek O, Portas L, Rudan I, Ulivi S, Zemunik T, Wright AF, Ciullo M, Hayward C, Pirastu M, Gasparini P: Hearing Function and Thresholds: A Genome-Wide Association Study in European Isolated Populations Identifies New Loci and Pathways. J Med Genet. 2011, 48 (6): 369-74. 10.1136/jmg.2010.088310.

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