A. Kim

W. Park, B. Choi, Sun O Chang, 2015, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing

Dongsup Kim, W. Park, B. Choi, 2015, Molecules and cells.

Outcome of Cochlear Implantation in Prelingually Deafened Children According to Molecular Genetic Etiology

B. Choi, J. Koo, Joo Hyun Park, 2017, Ear and hearing.

Whole-Exome Sequencing Identifies a Novel Genotype-Phenotype Correlation in the Entactin Domain of the Known Deafness Gene TECTA

Namshin Kim, B. Choi, Juyong Chung, 2014, PloS one.

A clinical guidance to DFNA22 drawn from a Korean cohort study with an autosomal dominant deaf population: A retrospective cohort study

W. Park, Seung-ha Oh, D. Oh, 2018, The journal of gene medicine.

Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population

B. Choi, J. Koo, Seung-ha Oh, 2019, Scientific Reports.

Strong founder effect of p.P240L in CDH23 in Koreans and its significant contribution to severe-to-profound nonsyndromic hearing loss in a Korean pediatric population

W. Park, B. Choi, B. Kim, 2015, Journal of Translational Medicine.

A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation

Dongsup Kim, B. Choi, Juyong Chung, 2014, Journal of Molecular Medicine.

Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication

W. Park, B. Choi, J. Koo, 2014, Orphanet Journal of Rare Diseases.

Efficiency of Exploration of Molecular Genetic Etiology for Cochlear Implantees and Its Implication

W. Park, B. Choi, J. Koo, 2014 .

Diagnostic Application of Targeted Resequencing for Familial Nonsyndromic Hearing Loss

W. Park, B. Choi, T. Park, 2013, PloS one.

Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing Loss in Koreans

B. Choi, Soyeon Ahn, A. Kim, 2016, PloS one.

Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population

W. Park, B. Choi, Seung-ha Oh, 2015, Genetics in Medicine.

Novel TECTA Mutations Identified in Stable Sensorineural Hearing Loss and Their Clinical Implications

B. Choi, J. Koo, Seung-ha Oh, 2014, Audiology and Neurotology.

Refinement of Molecular Diagnostic Protocol of Auditory Neuropathy Spectrum Disorder

W. Park, B. Choi, Chung Lee, 2015, Medicine.

Identification of a novel splice site variant of OTOF in the Korean nonsyndromic hearing loss population with low prevalence of the OTOF mutations.

B. Choi, Y. Rah, A. Kim, 2014, International journal of pediatric otorhinolaryngology.

Clinical characteristics of patients with narrow bony cochlear nerve canal

B. Choi, J. Koo, Sun O Chang, 2013, The Laryngoscope.

Identification of a novel truncation mutation of EYA4 in moderate degree hearing loss by targeted exome sequencing

B. Choi, S. Kim, A. Kim, 2016, European Archives of Oto-Rhino-Laryngology.

De Novo Large Genomic Deletions Involving POU3F4 in Incomplete Partition Type III Inner Ear Anomaly in East Asian Populations and Implications for Genetic Counseling

W. Park, B. Choi, Juyong Chung, 2014, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Destabilization and Mislocalization of POU3F4 by C‐Terminal Frameshift Truncation and Extension Mutation

B. Choi, J. Bok, Sun O Chang, 2013, Human mutation.

Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans

W. Park, B. Choi, Seung-ha Oh, 2016, PloS one.

Mutations in TMEM43 cause autosomal dominant auditory neuropathy spectrum disorder via interaction with connexin-mediated passive conductance channels

W. Park, Eunyoung Yi, S. Blanton, 2020, bioRxiv.

Type 1 Sialidosis Patient With a Novel Deletion Mutation in the NEU1 Gene: Case Report and Literature Review

W. Park, Ji Sun Kim, J. Youn, 2019, The Cerebellum.

Downsloping High-Frequency Hearing Loss Due to Inner Ear Tricellular Tight Junction Disruption by a Novel ILDR1 Mutation in the Ig-Like Domain

Dongsup Kim, W. Park, B. Choi, 2015, PloS one.

Clarification of undiagnosed ataxia using whole-exome sequencing with clinical implications.

W. Park, Ji Sun Kim, J. Youn, 2020, Parkinsonism & related disorders.