Journal of Audiology & Otology

A 250-kb Microdeletion Identified in Chromosome 16 Is Associated With Non-Syndromic Sensorineural Hearing Loss in a South Indian Consanguineous Family: Jayakumar Swetha, Arulmozhi Sakthignanavel, Aarthi Manoharan, Jayakumar Rangarajalu, Priyadharshini Arunagiri, Chandramohan Govindasamy, Sambandam Ravikumar; J Audiol Otol. 2025;29(1):31-37. Published online January 20, 2025; DOI: https://doi.org/10.7874/jao.2024.00038; Full text PubReader ePub PDF Supplementary Materials

Application of Genetic Information to Cochlear Implantation in Clinical Practice: Chen-Chi Wu; J Audiol Otol. 2024;28(2):93-99. Published online April 10, 2024; DOI: https://doi.org/10.7874/jao.2024.00080
Web of Science 2 Crossref 2; Full text PubReader ePub PDF

Updates on Genetic Hearing Loss: From Diagnosis to Targeted Therapies: Yejin Yun, Sang-Yeon Lee; J Audiol Otol. 2024;28(2):88-92. Published online April 10, 2024; DOI: https://doi.org/10.7874/jao.2024.00157
Web of Science 3 Crossref 4; Full text PubReader ePub PDF

Tone-Burst Auditory Brainstem Response and Cortical Potentials in Diagnosis of Syndromic Auditory Neuropathy Spectrum Disorder: Wafaa A. Kaf, Samantha Reiter, Amanda Brodeur, Letitia White-Minnis, William Deal; J Audiol Otol. 2023;27(3):153-160. Published online November 24, 2022; DOI: https://doi.org/10.7874/jao.2022.00192; Full text PubReader ePub PDF

One Genetic Defect and Two Related Entities in Monozygotic Twins: Otosclerosis and Superior Semicircular Canal Near Dehiscence Syndrome: F Ceyda Akin Ocal, Haluk Kavus, Bulent Satar, Davut Pehli̇van; J Audiol Otol. 2022;26(2):97-102. Published online November 9, 2021; DOI: https://doi.org/10.7874/jao.2021.00381; Full text PubReader ePub PDF Supplementary Materials

Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations: Mahbobeh Koohiyan, Fatemeh Azadegan-Dehkordi, Farideh Koohian, Morteza Hashemzadeh-Chaleshtori; J Audiol Otol. 2019;23(4):175-180. Published online June 27, 2019; DOI: https://doi.org/10.7874/jao.2019.00059
Web of Science 10 Crossref 9; Full text PubReader ePub PDF

Strategy for the Customized Mass Screening of Genetic Sensorineural Hearing Loss in Koreans: Mun Young Chang, Byung Yoon Choi; J Audiol Otol. 2014;18(2):45-49. Published online September 16, 2014; DOI: https://doi.org/10.7874/kja.2014.18.2.45
Crossref 8; Full text PubReader ePub PDF

Pathophysiology of Age-Related Hearing Loss (Peripheral and Central): Kyu-Yup Lee; J Audiol Otol. 2013;17(2):45-49. Published online September 24, 2013; DOI: https://doi.org/10.7874/kja.2013.17.2.45
Crossref 75; Full text PubReader ePub PDF

Familial Multiple Recurrence of Benign Paroxysmal Positional Vertigo: Sungdo Jung, Jae Yun Jung, Chung-Ku Rhee, Myung-Whan Suh; J Audiol Otol. 2010;14(3):233-236.; PDF

Advances in Understanding the Molecular Dynamics of Autosomal Dominant Auditory Neuropathy: Unveiling a Novel DIAPH3 Gene Variant Associated With Sensorineural Hearing Loss and Bilateral Vestibular Aqueduct Enlargement: Gianmaria Miolo, Francesco Margiotta, Alessandra Murgia, Lara Della Puppa, Giuseppe Corona; Received February 19, 2024 Accepted March 6, 2025; [Epub ahead of print]; PDF

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