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Deafness in the genomics era
Journal article   Peer reviewed

Deafness in the genomics era

A. Eliot Shearer, Michael S Hildebrand, Christina M Sloan and Richard J.H Smith
Hearing research, Vol.282(1), pp.1-9
2011
DOI: 10.1016/j.heares.2011.10.001
PMCID: PMC3230685
PMID: 22016077

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Abstract

Our understanding of hereditary hearing loss has greatly improved since the discovery of the first human deafness gene. These discoveries have only accelerated due to the great strides in DNA sequencing technology since the completion of the human genome project. Here, we review the immense impact that these developments have had in both deafness research and clinical arenas. We review commonly used genomic technologies as well as the application of these technologies to the genetic diagnosis of hereditary hearing loss and to the discovery of novel deafness genes. ► Genomic technologies have greatly improved our understanding of deafness. ► Genomic technologies can provide comprehensive genetic diagnosis for hearing loss for the first time. ► Eight new deafness genes have been discovered using next-generation sequencing.

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