Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss

Cochlear Implants — Science, Serendipity, and Success

(2013) Gerard O'Donoghue   NEW ENGLAND JOURNAL OF MEDICINE

EYA1 and SIX1 drive the neuronal developmental program in cooperation with the SWI/SNF chromatin-remodeling complex and SOX2 in the mammalian inner ear

(2012) M. Ahmed et al.   DEVELOPMENT

Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families

(2012) Jeong-In Baek et al.   Orphanet Journal of Rare Diseases

Cilia Motility and Structure in Primary and Secondary Ciliary Dyskinesia

(2010) Miguel Armengot et al.   American Journal of Rhinology & Allergy

The epidemiology of hearing impairment in the United States: Newborns, children, and adolescents

(2009) Saral Mehra et al.   OTOLARYNGOLOGY-HEAD AND NECK SURGERY

Eya4 regulation of Na+/K+-ATPase is required for sensory system development in zebrafish

(2008) L. Wang et al.   DEVELOPMENT