Jayoung Oh

Analysis of Lateral Decubitus Position During Sleep in Patients With Obstructive Sleep Apnea Using WatchPAT Device

Dong-Young Kim, Jayoung Oh, Y. Cho, 2022, Journal of Rhinology.

Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness

W. Park, B. Choi, Sejoon Lee, 2019, Human mutation.

Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach

B. Choi, J. Jang, Y. Choung, 2020, Genetics in Medicine.

Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach

B. Choi, J. Jang, Y. Choung, 2020, Genetics in Medicine.

Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation

B. Choi, D. Oh, Kwangsic Joo, 2019, Clinical and experimental otorhinolaryngology.

The Impact of Lateral Relaxing Incision on Middle Ear Function in Cleft Palate Repair.

M. Park, Sukwha Kim, Sungmi Jeon, 2023, The Journal of craniofacial surgery.

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.

Enhanced Type 2 Immune Reactions by Increased IL-22/IL-22Ra1 Signaling in Chronic Rhinosinusitis With Nasal Polyps

Ara Jo, Dae Woo Kim, Dong Kyu Kim, 2020, Allergy, asthma & immunology research.

Audiogram Configuration, Molecular Etiology, and Outcome of Cochlear Implantation in Postlingual Auditory Neuropathy Spectrum Disorder

J. J. Han, J. Choi, Yehree Kim, 2023, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder

W. Park, Eunyoung Yi, S. Blanton, 2021, Proceedings of the National Academy of Sciences.

Rising of LOXHD1 as a signature causative gene of down-sloping hearing loss in people in their teens and 20s

Dongsup Kim, B. Choi, J. Koo, 2021, Journal of Medical Genetics.

Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human DIAPH1-related cytoskeletopathy

W. Park, B. Choi, D. Oh, 2019, Journal of Medical Genetics.