| 2020 | Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation | EAR AND HEARING |
| 2019 | Meta-analysis of Delayed Facial Palsy Following Middle Ear Surgery | OTOLOGY & NEUROTOLOGY |
| 2019 | Is Early Progression to Bilateral Involvement in Menière's Disease a Poor Prognostic Indicator? | OTOLOGY & NEUROTOLOGY |
| 2019 | Lessons From an Analysis of Newborn Hearing Screening Data for Children With Cochlear Implants | OTOLOGY & NEUROTOLOGY |
| 2019 | Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing
| THERANOSTICS |
| 2019 | Effect of Specific Retinoic Acid Receptor Agonists on Noise-Induced Hearing Loss
| International Journal of Environmental Research and Public Health |
| 2019 | Outcomes and Predictive Factors of Electroacoustic Stimulation Rehabilitation in Children With Limited Low-Frequency Hearing | Otology & Neurotology |
| 2019 | Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment | Experimental and Molecular Medicine |
| 2019 | Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency
| Scientific Reports |
| 2019 | Extended-duration deafness is correlated with better subjective satisfaction in CROS-tBAHI recipients | Clinical Otolaryngology |
| 2019 | Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants
| Clinical and Experimental Otorhinolaryngology |
| 2019 | Clinical Characteristics of Bilateral Meniere's Disease in a Single Asian Ethnic Group | LARYNGOSCOPE |
| 2019 | Feasibility of Revision Cochlear Implant Surgery for Better Speech Comprehension
| Journal of Audiology & Otology |
| 2019 | Effects of self-reported hearing or vision impairment on depressive symptoms: a population-based longitudinal study | EPIDEMIOLOGY AND PSYCHIATRIC SCIENCES |
| 2019 | The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report
| BMC MEDICAL GENETICS |
| 2019 | Cleaved Cochlin Sequesters Pseudomonas aeruginosa and Activates Innate Immunity in the Inner Ear | CELL HOST & MICROBE |
| 2019 | Long-Term Changes in Video Head Impulse and Caloric Tests in Patients with Unilateral Vestibular Neuritis
| Korean Journal of Otorhinolaryngology-Head and Neck Surgery |
| 2019 | A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators | HUMAN MUTATION |
| 2019 | A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction | EUROPEAN JOURNAL OF MEDICAL GENETICS |
| 2018 | Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss
| SCIENTIFIC REPORTS |
| 2018 | Benefits of Bimodal Hearing With Cochlear and Middle Ear Implants: Preliminary Results in Four Patients. | OTOLOGY & NEUROTOLOGY |
| 2018 | Vibrant Soundbridge can improve the most comfortable listening level in sensorineural hearing loss: Our experience with 61 patients. | CLINICAL OTOLARYNGOLOGY |
| 2017 | Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report
| BMC MEDICAL GENETICS |
| 2017 | ANO9/TMEM16J promotes tumourigenesis via EGFR and is a novel therapeutic target for pancreatic cancer | BRITISH JOURNAL OF CANCER |
| 2017 | Hearing Preservation During Cochlear Implantation and Electroacoustic Stimulation in Patients With SLC26A4 Mutations | OTOLOGY & NEUROTOLOGY |
| 2017 | Audiologic Gain of Incus Short Process Vibroplasty With Conventional Incus Long Process Vibroplasty: A Retrospective Analysis of 36 Patients | OTOLOGY & NEUROTOLOGY |
| 2017 | Evaluation of Maximal Speech Intelligibility With Vibrant Soundbridge in Patients With Sensorineural Hearing Loss | OTOLOGY & NEUROTOLOGY |
| 2017 | Effects of Saccular Function on Recovery of Subjective Dizziness After Vestibular Rehabilitation | OTOLOGY & NEUROTOLOGY |
| 2017 | Discrepancies between video head impulse and caloric tests in patients with enlarged vestibular aqueduct. | LARYNGOSCOPE |
| 2017 | Benefits of active middle ear implants in mixed hearing loss: Stapes versus round window | LARYNGOSCOPE |
| 2017 | Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population
| SCIENTIFIC REPORTS |
| 2017 | Resistance to hypertension and high Cl- excretion in humans with SLC26A4 mutations | CLINICAL GENETICS |
| 2017 | β1- and β2-adrenergic stimulation-induced electrogenic transport by human endolymphatic sac epithelium and its clinical implications.
| SCIENTIFIC REPORTS |
| 2016 | Vestibular function is associated with residual low-frequency hearing loss in patients with bi-allelic mutations in the SLC26A4 gene | HEARING RESEARCH |
| 2016 | Is dehydration test using isosorbide useful in Meniere's disease? | ACTA OTO-LARYNGOLOGICA |
| 2016 | Ventilation tube insertion is not effective to the treatment of hearing impairment in pediatric patients with Cornelia de Lange syndrome | AMERICAN JOURNAL OF OTOLARYNGOLOGY |
| 2016 | Audiologic limitations of Vibrant Soundbridge device: Is the contralateral hearing aid fitting indispensable? | LARYNGOSCOPE |
| 2016 | Pore dilatation increases the bicarbonate permeability of CFTR, ANO1 and glycine receptor anion channels. | JOURNAL OF PHYSIOLOGY-LONDON |
| 2016 | The HSP70 co-chaperone DNAJC14 targets misfolded pendrin for unconventional protein secretion.
| NATURE COMMUNICATIONS |
| 2015 | Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure | PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY |
| 2015 | Electrogenic transport and K(+) ion channel expression by the human endolymphatic sac epithelium
| SCIENTIFIC REPORTS |
| 2015 | Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and Secretion | HUMAN MUTATION |
| 2015 | Genetic aspects and clinical characteristics of familial Meniere's disease in a South Korean population | LARYNGOSCOPE |
| 2015 | Non-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene
| EXPERIMENTAL AND MOLECULAR MEDICINE |
| 2015 | Does calmodulin regulate the bicarbonate permeability of ANO1/TMEM16A or not?
| JOURNAL OF GENERAL PHYSIOLOGY |
| 2014 | Identification of novel functional null allele of SLC26A4 associated with enlarged vestibular aqueduct and its possible implication | AUDIOLOGY AND NEURO-OTOLOGY |
| 2014 | Correlation between genotype and phenotype in patients with bi-allelic SLC26A4 mutations | CLINICAL GENETICS |
| 2014 | Mechanisms of CFTR Functional Variants That Impair Regulated Bicarbonate Permeation and Increase Risk for Pancreatitis but Not for Cystic Fibrosis.
| PLOS GENETICS |
| 2014 | Role of calcium signaling in epithelial bicarbonate secretion | CELL CALCIUM |
| 2014 | Shank2 mutant mice display a hypersecretory response to cholera toxin | JOURNAL OF PHYSIOLOGY-LONDON |
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