D. Oh

Y. Shin, Jhingook Kim, Mi-Sook Lee, 2017, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome Sequencing.

Yeon Jeong Kim, P. Park, R. Kucherlapati, 2016, American journal of human genetics.

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.

Identification of a Potential Founder Effect of a Novel PDZD7 Variant Involved in Moderate-to-Severe Sensorineural Hearing Loss in Koreans

B. Choi, Seung-ha Oh, D. Oh, 2019, International journal of molecular sciences.

Genetic Information and Precision Medicine in Hearing Loss

B. Choi, D. Oh, 2020, Clinical and experimental otorhinolaryngology.

Powerful use of automated prioritization of candidate variants in genetic hearing loss with extreme etiologic heterogeneity

Changwon Keum, D. Oh, M. Park, 2021, Scientific Reports.

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.

Improving genetic diagnosis by disease-specific, ACMG/AMP variant interpretation guidelines for hearing loss

Changwon Keum, D. Oh, N. Kim, 2022, Scientific Reports.

Flexible Real-Time Polymerase Chain Reaction-Based Platforms for Detecting Deafness Mutations in Koreans: A Proposed Guideline for the Etiologic Diagnosis of Auditory Neuropathy Spectrum Disorder

B. Choi, J. Koo, Seung-ha Oh, 2020, Diagnostics.

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.

POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic features

A. Tomkinson, W. Park, B. Choi, 2020, Human mutation.

Identification of a novel partner gene, KIAA1217, fused to RET: Functional characterization and inhibitor sensitivity of two isoforms in lung adenocarcinoma

Joungho Han, Jhingook Kim, Yoon-La Choi, 2016, Oncotarget.

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.

Prevalence of Mutations in Discoidin Domain-Containing Receptor Tyrosine Kinase 2 (DDR2) in Squamous Cell Lung Cancers in Korean Patients

Joungho Han, Mi-Sook Lee, Yoon-La Choi, 2017, Cancer research and treatment : official journal of Korean Cancer Association.

One-step noninvasive prenatal testing (NIPT) for autosomal recessive homozygous point mutations using digital PCR

B. Choi, D. Oh, C. Kang, 2018, Scientific Reports.

Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss

W. Park, D. Oh, T. Kang, 2021, Experimental & Molecular 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.

TM4SF4 and LRRK2 Are Potential Therapeutic Targets in Lung and Breast Cancers through Outlier Analysis

Y. Shin, Mi-Sook Lee, Yoon-La Choi, 2020, Cancer research and treatment : official journal of Korean Cancer Association.

The molecular etiology of deafness and auditory performance in the postlingually deafened cochlear implantees

B. Choi, J. Koo, Seung-ha Oh, 2020, Scientific Reports.

Precision medicine approaches to lung adenocarcinoma with concomitant MET and HER2 amplification

W. Park, Yoon-La Choi, D. Oh, 2017, BMC Cancer.

Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinics

W. Park, B. Choi, J. Jang, 2018, Journal of Translational Medicine.

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.

The Analysis of A Frequent TMPRSS3 Allele Containing P.V116M and P.V291L in A Cis Configuration among Deaf Koreans

W. Park, B. Choi, Juyong Chung, 2017, International journal of molecular sciences.

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.

Perifosine‐induced inhibition of akt attenuates brain‐derived neurotrophic factor/TrkB‐induced chemoresistance in neuroblastoma in vivo

C. Thiele, Zhijie Li, Katsuya Nakamura, 2011, Cancer.