1. Evaluation of the Contribution of the EYA4 and GRHL2 Genes in Korean Patients with Autosomal Dominant Non-Syndromic Hearing Loss
   Ye-Ri Kim et al, 2015, PLOS ONE CrossRef
2. Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss
   Songqun Hu et al, 2018, Neural Plasticity CrossRef
3. Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults
   null null et al, 2021, Human Genetics CrossRef
4. Phenotypic variability in a seven-generation Swedish family segregating autosomal dominant hearing impairment due to a novel EYA4 frameshift mutation
   Carina Frykholm et al, 2015, Gene CrossRef
5. Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case report
   Lukas Varga et al, 2019, BMC Medical Genetics CrossRef
6. Insights into the pathophysiology of DFNA10 hearing loss associated with novel EYA4 variants
   Matias Morín et al, 2020, Scientific Reports CrossRef
7. Prevalence and clinical features of hearing loss caused by EYA4 variants
   Jun Shinagawa et al, 2020, Scientific Reports CrossRef
8. Eya4 Induces Hypertrophy via Regulation of p27 kip1
   Tatjana Williams et al, 2015, Circulation: Cardiovascular Genetics CrossRef
9. Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation
   Satoko Abe et al, 2018, Human Genome Variation CrossRef
10. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review
    Mirko Aldè et al, 2023, Biomedicines CrossRef
11. A combined genome-wide association and molecular study of age-related hearing loss in H. sapiens
    Wei Liu et al, 2021, BMC Medicine CrossRef
12. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options
    Nandita Sharma et al, 2023, Clinical Genetics CrossRef
13. Detection and Functional Verification of Noncanonical Splice Site Mutations in Hereditary Deafness
    Penghui Chen et al, 2021, Frontiers in Genetics CrossRef
14. A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafness
    Aiping Huang et al, 2015, Journal of Translational Medicine CrossRef
15. Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss
    Weixun Zhang et al, 2022, BMC Medical Genomics CrossRef