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

Associations Between TGFA/TGFB3/MSX1 Gene Polymorphisms and Congenital Non-Syndromic Hearing Impairment in a Chinese Population. Med Sci Monit (2016) 0.75

Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation. PLoS One (2017) 0.75

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nat Genet (1997) 2.68

1002 protein phosphatases? Annu Rev Cell Biol (1992) 2.27

Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode. Development (1997) 2.18

Cochlear implants--science, serendipity, and success. N Engl J Med (2013) 2.16

Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation. Genes Dev (1999) 2.08

Eyes absent represents a class of protein tyrosine phosphatases. Nature (2003) 2.05

Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya. Mol Cell Biol (1999) 1.96

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss. Nat Genet (2005) 1.80

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus. Hum Mol Genet (2001) 1.68

Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families. Orphanet J Rare Dis (2012) 1.49

Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid. Development (2002) 1.49

The epidemiology of hearing impairment in the United States: newborns, children, and adolescents. Otolaryngol Head Neck Surg (2009) 1.42

Mutations of a human homologue of the Drosophila eyes absent gene (EYA1) detected in patients with congenital cataracts and ocular anterior segment anomalies. Hum Mol Genet (2000) 1.38

EYA4, a novel vertebrate gene related to Drosophila eyes absent. Hum Mol Genet (1999) 1.32

Eye development: governed by a dictator or a junta? Cell (1997) 1.27

Eya4-deficient mice are a model for heritable otitis media. J Clin Invest (2008) 1.16

A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10. Mol Med (2002) 1.14

A novel splice site mutation in EYA4 causes DFNA10 hearing loss. Am J Med Genet A (2007) 1.10

EYA1 and SIX1 drive the neuronal developmental program in cooperation with the SWI/SNF chromatin-remodeling complex and SOX2 in the mammalian inner ear. Development (2012) 1.06

Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain. Am J Med Genet A (2007) 1.02

Cilia motility and structure in primary and secondary ciliary dyskinesia. Am J Rhinol Allergy (2010) 0.90

Audiometric analysis of a Belgian family linked to the DFNA10 locus. Am J Otol (2000) 0.89

Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non‑syndromic hearing loss. Int J Mol Med (2014) 0.87

Eya4 regulation of Na+/K+-ATPase is required for sensory system development in zebrafish. Development (2008) 0.85

Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish. PLoS One (2015) 0.75

Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss. Clin Genet (2019) 0.75

New role of LRP5, associated with non-syndromic autosomal recessive hereditary hearing loss. Hum Mutat (2017) 0.75