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List of works by Chen-Chi Wu

Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment.

scientific article published in December 2009

Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment

scientific article

Aspirin intake correlates with halted growth of sporadic vestibular schwannoma in vivo.

scientific article published on February 2014

Can Nutritional Intervention for Obesity and Comorbidities Slow Down Age-Related Hearing Impairment?

scientific article published on 21 July 2019

Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter Study

scientific article published in 2022

Cochlear implantation in LEOPARD syndrome: Our experience with three patients

scientific article published in 2021

Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas

scientific article published on 25 September 2011

Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical Implications

scientific article published in 2022

Determinants of bilateral audiometric notches in noise-induced hearing loss.

scientific article published in April 2013

Differences in the pathogenicity of the p.H723R mutation of the common deafness-associated SLC26A4 gene in humans and mice

scientific article

Establishment of a knock-in mouse model with the SLC26A4 c.919-2A>G mutation and characterization of its pathology

scientific article

Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing Loss

scientific article

Gene therapy with a synthetic adeno-associated viral vector improves audiovestibular phenotypes in Pjvk-mutant mice

scientific article published in 2022

Generation of a human iPS cell line (CGMH.SLC26A4919-2) from a Pendred syndrome patient carrying SLC26A4 c.919-2A>G splice-site mutation

scientific article published on 31 July 2019

Generation of induced pluripotent stem cells from a patient with hearing loss carrying GJB2 p.V37I mutation

scientific article published on 03 October 2018

In response to Determinants of bilateral audiometric notches in noise-induced hearing loss.

scientific article published on 9 July 2013

Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome.

scientific article published on 23 March 2012

Mutations in the OTOF gene in Taiwanese patients with auditory neuropathy

scientific article published on 11 March 2010

Newborn genetic screening for hearing impairment: a population-based longitudinal study.

scientific article published on 16 June 2016

Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center

scientific article

Otoprotective Effects of Fucoidan Reduce Cisplatin-Induced Ototoxicity in Mouse Cochlear UB/OC-2 Cells

scientific article published in 2023

Patients with positive allergen test have less favorable outcome after endoscopic microdebrider-assisted inferior turbinoplasty.

scientific article

Phenotypic Analyses and Mutation Screening of the SLC26A4 and FOXI1 Genes in 101 Taiwanese Families with Bilateral Nonsyndromic Enlarged Vestibular Aqueduct (DFNB4) or Pendred Syndrome

article

Positive perilymph fistula test with semicircular canal dehiscence from cholesteatoma

scientific article published on 01 January 2019

Prediction Model for Audiological Outcomes in Patients With GJB2 Mutations

scientific article published on 01 January 2020

Predominance of genetic diagnosis and imaging results as predictors in determining the speech perception performance outcome after cochlear implantation in children.

scientific article published in March 2008

Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment

scientific article published in 2021

Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation

scientific article published on 17 February 2010

Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population

scientific article published in 2023

Specificity of SLC26A4 mutations in the pathogenesis of inner ear malformations

scientific article published on 18 May 2005

Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct

scientific article published on 28 September 2018

The grainyhead-like 2 gene (GRHL2) single nucleotide polymorphism is not associated with age-related hearing impairment in Han Chinese.

scientific article published on 6 May 2011

Timing of cochlear implantation in auditory neuropathy patients with OTOF mutations: Our experience with 10 patients.

scientific article

Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations

scientific article published in PLoS ONE

Using endoscopy to locate the round window membrane during cochlear implantation: Our experience with 25 patients.

scientific article published on 14 August 2017

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