B. Choi

B. Choi, Sun O Chang, Seung-ha Oh, 2008, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Management of intractable Ménière's disease after intratympanic injection of Gentamicin

B. Choi, J. Koo, J. J. Han, 2015, The Laryngoscope.

Prenatal electroporation-mediated gene transfer restores Slc26a4 knock-out mouse hearing and vestibular function

R. Minoda, B. Choi, T. Miwa, 2019, Scientific Reports.

Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition.

R. Petralia, A. Griffith, T. Friedman, 2011, The Journal of clinical investigation.

Modiolar Proximity of Slim Modiolar Electrodes and Cochlear Duct Length: Correlation for Potential Basis of Customized Cochlear Implantation With Perimodiolar Electrodes.

Jae-Jin Song, B. Choi, J. Koo, 2020, Ear and hearing.

SLC26A4 Genotypes and Phenotypes Associated with Enlargement of the Vestibular Aqueduct

T. Shawker, J. Butman, A. Griffith, 2011, Cellular Physiology and Biochemistry.

SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct

J. Niparko, J. Butman, A. Griffith, 2010, The Laryngoscope.

Head-shaking and Vibration-induced Nystagmus During and Between the Attacks of Unilateral Ménière’s Disease

B. Choi, Ji-Soo Kim, Sun-Uk Lee, 2015, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Early combination treatment with intratympanic steroid injection in severe to profound sudden sensorineural hearing loss improves speech discrimination performance

B. Choi, Sun O Chang, Seung-ha Oh, 2012, European Archives of Oto-Rhino-Laryngology.

Response to: The c.−103T>C variant in the 5′‐UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?

A. Griffith, B. Choi, S. Alper, 2009 .

TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia.

J. R. Holt, Bryan A. Millis, H. Nakanishi, 2015, Cell reports.

Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population

B. Choi, J. Koo, Seung-ha Oh, 2015, PloS one.

Novel genotype–phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing loss

B. Choi, J. Koo, Seung-ha Oh, 2020, Human mutation.

Relation between amniotic fluid infection or cytokine levels and hearing screen failure in infants at 32 wk gestation or less

B. Choi, K. Park, J. Rhee, 2017, Pediatric Research.

Tauroursodeoxycholic acid attenuates cisplatin-induced hearing loss in rats

B. Choi, Da-Hye Lee, So Min Lee, 2020, Neuroscience Letters.

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

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

Molecular Etiology of Hereditary Single-Side Deafness

B. Choi, Seung-ha Oh, S. Kim, 2015, Medicine.

Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness

W. Park, B. Choi, D. Oh, 2018, BMC Medical Genetics.

Prediction of the Outcome of Cochlear Implantation in the Patients with Congenital Cytomegalovirus Infection based on Magnetic Resonance Imaging Characteristics

Jae-Jin Song, B. Choi, J. Koo, 2019, Journal of clinical medicine.

Development of novel noninvasive prenatal testing protocol for whole autosomal recessive disease using picodroplet digital PCR

B. Choi, J. J. Han, C. Kang, 2016, Scientific Reports.

Molecular Genetic Diagnosis of Deafness: Current and Future

B. Choi, Seung-ha Oh, 2014 .

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.

Tight modiolar proximity and feasibility of slim modiolar cochlear implant electrode array insertion in diverse etiologies of hearing loss

B. Choi, Sang-yeon Lee, Yoonjoong Kim, 2021, European Archives of Oto-Rhino-Laryngology.

Novel Splice Site Pathogenic Variant of EFTUD2 Is Associated with Mandibulofacial Dysostosis with Microcephaly and Extracranial Symptoms in Korea

B. Choi, Da-Hye Lee, S. Y. Kim, 2020, Diagnostics.

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

B. Choi, D. Oh, C. Kang, 2018, 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, S. Y. Kim, 2015, Journal of Translational Medicine.

Distinct vestibular phenotypes in DFNA9 families with COCH variants

B. Choi, J. Koo, Y. Rah, 2016, European Archives of Oto-Rhino-Laryngology.

Clinical observations and molecular variables of patients with hearing loss and incomplete partition type III

Jae-Jin Song, B. Choi, J. Koo, 2016, The Laryngoscope.

Head Position Dependency of Induced Nystagmus to Ice-Water Irrigation in Peripheral Vestibulopathy

B. Choi, J. Koo, Sun O Chang, 2005, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Cerebrospinal Fluid Gusher in Cochlear Implantation

B. Choi, Hyo-Jeong Lee, Sun O Chang, 2004 .

CSF gusher in cochlear implantation

B. Choi, Hyo-Jeong Lee, Sun O Chang, 2004, Cochlear implants international.

Dopamine increases Na+ absorption in the Reissner's membrane of the gerbil cochlea.

B. Choi, Chang-Hee Kim, Sun O Chang, 2013, Auris, nasus, larynx.

Is the posterior cingulate cortex an on-off switch for tinnitus?: A comparison between hearing loss subjects with and without tinnitus

D. De Ridder, S. Vanneste, B. Choi, 2021, Hearing Research.

Central auditory maturation and behavioral outcomes after cochlear implantation in prelingual auditory neuropathy spectrum disorder related to OTOF variants (DFNB9): Lessons from pilot study

B. Choi, Sang-yeon Lee, N. Kim, 2021, PloS one.

Natural Course of Residual Hearing with Reference to GJB2 and SLC26A4 Genotypes: Clinical Implications for Hearing Rehabilitation

B. Choi, J. Koo, Seung-ha Oh, 2021, Ear and hearing.

Identification of Novel Functional Null Allele of SLC26A4 Associated with Enlarged Vestibular Aqueduct and Its Possible Implication

Jeong Hun Jang, Sang Yeon Lee, Byung Yoon Choi, 2014, Audiology and Neurotology.

Hypo‐Functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype‐phenotype correlation or coincidental polymorphisms?

Rick Kittles, James Thomsen, John Niparko, 2009, Human mutation.

Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction

A. Griffith, B. Choi, P. Wangemann, 2014, Neurobiology of Disease.

Targeted Exome Sequencing of Deafness Genes After Failure of Auditory Phenotype-Driven Candidate Gene Screening

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.

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.

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.

Cerebrospinal Fluid Rhinorrhea-Clinical Manifestations and Endoscopic Repair

B. Choi, S. Oh, C. Rhee, 2004 .

Silent Vestibulopathy in Asymmetric Hearing Loss Can Be a Sign of a Cerebellopontine Angle Tumor

B. Choi, J. Koo, W. Sunwoo, 2018 .

Genetic Information and Precision Medicine in Hearing Loss

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

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 .

Strategy for the Customized Mass Screening of Genetic Sensorineural Hearing Loss in Koreans

B. Choi, M. Chang, 2014, Korean journal of audiology.

Diagnostic Application of Targeted Resequencing for Familial Nonsyndromic Hearing Loss

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

Application of Next Generation Sequencing Upon the Molecular Genetic Diagnosis of Deafness

B. Choi, B. Kim, 2012, Korean journal of audiology.

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.

Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis.

S. Jacobson, A. D. den Hollander, A. Swaroop, 2012, The Journal of clinical investigation.

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.

Maternal and Placental Factors Associated with Congenital Hearing Loss in Very Preterm Neonates.

B. Choi, K. Park, S. Kim, 2017, Pediatrics and neonatology.

Appropriate Imaging Modality for the Etiologic Diagnosis of Congenital Single-Sided Deafness in Children

B. Choi, J. Koo, Sang-yeon Lee, 2018, Journal of clinical medicine.

A Case with the Bilateral Narrow Bony Cochlear Nerve Canals Associated with Near Normal Hearing Thresholds

B. Choi, S. Kim, Jae-Cheul Ahn, 2012, Korean journal of audiology.

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.

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.

Diverse etiologies manifesting auditory neuropathy characteristics from infants with profound hearing loss and clinical implications.

B. Choi, S. Kim, H. Choi, 2016, International journal of pediatric otorhinolaryngology.

Outcomes and limitations of hospital-based newborn hearing screening.

Jae Hyun Lim, B. Choi, J. Koo, 2017, International journal of pediatric otorhinolaryngology.

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.

Characterization of Detailed Audiological Features of Cytomegalovirus Infection: A Composite Cohort Study from Groups with Distinct Demographics

B. Choi, J. Koo, Seung-ha Oh, 2018, BioMed research international.

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

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

Objectification and Differential Diagnosis of Vascular Pulsatile Tinnitus by Transcanal Sound Recording and Spectrotemporal Analysis: A Preliminary Study

D. De Ridder, Kyogu Lee, B. Choi, 2016, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Involvement of the Internal Auditory Canal in Subjects With Cochlear Otosclerosis: A Less Acknowledged Third Window That Affects Surgical Outcome.

Kyogu Lee, B. Choi, J. H. Kim, 2019, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Jugular Bulb Resurfacing With Bone Cement for Patients With High Dehiscent Jugular Bulb and Ipsilateral Pulsatile Tinnitus.

B. Choi, J. Koo, Sang-yeon Lee, 2019, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Longitudinal analysis of surgical outcome in subjects with pulsatile tinnitus originating from the sigmoid sinus

Kyogu Lee, B. Choi, J. Koo, 2020, Scientific Reports.

Beware of a Fragile Footplate: Lessons from Ossiculoplasty in Patients with Ossicular Anomalies Related to Second Pharyngeal Arch Defects

B. Choi, J. Koo, Yoonjoong Kim, 2019, Journal of clinical medicine.

Electrocochleographic findings in superior canal dehiscence syndrome

B. Choi, J. Koo, Joo Hyun Park, 2015, Hearing Research.

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.

Postoperative Results of Congenital Middle Ear Cholesteatoma According to Location, Type and Stage

B. Choi, M. Lee, Hyo-Jeong Lee, 2003 .

Dizziness and vestibular function before and after cochlear implantation

B. Choi, J. Koo, Y. Rah, 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.

A New Technique for Correcting Cryptotia: V-Y Swing Flap

B. Choi, Sun O Chang, Myung-Whan Suh, 2007, Plastic and reconstructive surgery.

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

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

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.

Cochlear reimplantation in device failure: effectiveness and safety

B. Choi, Hyo-Jeong Lee, Sun O Chang, 2004, Cochlear Implants International.

Simpler and effective radiological evaluations for modiolar proximity of a slim modiolar cochlear implant electrode

Sang-Yeon Lee, Jin Hee Han, Marge Carandang, 2020, Scientific Reports.

Nasopharyngeal carcinoma with skull base invasion: a necessity of staging subdivision.

J. Roh, B. Choi, Seung-ha Oh, 2004, American journal of otolaryngology.

CHARGE syndrome with oculomotor nerve palsy.

B. Choi, J. H. Kim, J. Koo, 2015, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Etiology of Hearing Loss and Genetic Hearing Loss

B. Choi, So Young Kim, 2015 .

Prevalence of p.V37I Variant of GJB2 in Mild or Moderate Hearing Loss in a Pediatric Population and the Interpretation of Its Pathogenicity

W. Park, B. Choi, J. Koo, 2013, PloS one.

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.

Functional characterization of a novel loss‐of‐function mutation of PRPS1 related to early‐onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic intervention

W. Park, B. Choi, D. Yan, 2016, The journal of gene medicine.

Unraveling of Enigmatic Hearing-Impaired GJB2 Single Heterozygotes by Massive Parallel Sequencing: DFNB1 or Not?

W. Park, B. Choi, Chung Lee, 2016, Medicine.

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

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

Risk factors for failure in the newborn hearing screen test in very preterm twins.

B. Choi, K. Park, S. Y. Kim, 2018, Pediatrics and neonatology.

Inflammatory and Immune Proteins in Umbilical Cord Blood: Association with Hearing Screening Test Failure in Preterm Neonates

B. Choi, Y. Jung, K. Park, 2018, Mediators of inflammation.

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 comparison study of audiological outcome and compliance of bone conduction implantable hearing implants

B. Choi, J. Koo, J. J. Han, 2020, European Archives of Oto-Rhino-Laryngology.

Atlantoaxial Rotary Subluxation After Tympanoplasty

B. Choi, J. Koo, So Young Kim, 2011, 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.

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.

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.

Cochlear implantation in chronic ear disease

B. Choi, Hyo-Jeong Lee, Sun O Chang, 2004, Cochlear implants international.

Outcome of cochlear implantation in the worse ear of post-lingual asymmetric hearing loss: elucidation of prognostic markers

B. Choi, Seung-ha Oh, J. Lee, 2021, Acta oto-laryngologica.