ShearerAEHildebrandMSSloanCMSmithRJ. Deafness in the genomics era. Hear Res. 2011;282:1-9.
2.
HildebrandMSTackDMcMordieSJ. Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus. Genet Med. 2008;10:797-804.
3.
HildebrandMSDeLucaAPTaylorKR. A contemporary review of AudioGene audioprofiling: a machine-based candidate gene prediction tool for autosomal dominant nonsyndromic hearing loss. Laryngoscope. 2009;119:2211-2215.
4.
ShearerAEDeLucaAPHildebrandMS. Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing. Proc Natl Acad Sci U S A. 2010;107:21104-21109.
5.
LuijendijkMWVan WijkEBischoffAM. Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). Hum Genet. 2004;115:149-156.