List of works - Hideaki Moteki

A rational approach to identifying newborns with hearing loss caused by congenital cytomegalovirus infection by dried blood spot screening.

scientific article

Achievement of hearing preservation in the presence of an electrode covering the residual hearing region.

scientific article

Cochlear Implantation From the Perspective of Genetic Background

scientific article published on 06 February 2020

Comprehensive analysis of syndromic hearing loss patients in Japan

scientific article published on 19 August 2019

Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization.

scientific article published on 28 July 2016

Diagnostic pitfalls for -related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing loss

scientific article published on 21 September 2018

Etiology of single-sided deafness and asymmetrical hearing loss.

scientific article published on April 2017

Feasibility of hearing preservation for residual hearing with longer cochlear implant electrodes

scientific article published on 01 December 2018

Frequency and clinical features of hearing loss caused by STRC deletions

scientific article published on 13 March 2019

Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness

scientific article published on 26 March 2015

Hearing preservation and clinical outcome of 32 consecutive electric acoustic stimulation (EAS) surgeries

scientific article

Language development in Japanese children who receive cochlear implant and/or hearing aid.

scientific article published on 26 January 2012

Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearing.

scientific article published on 17 November 2016

Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss

scientific article published on 16 September 2019

Mutations in LOXHD1 gene cause various types and severities of hearing loss

scientific article

Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis

scientific article published on 19 March 2015

Non-ocular Stickler syndrome with a novel mutation in COL11A2 diagnosed by massively parallel sequencing in Japanese hearing loss patients

scientific article published on 16 March 2015

Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss

scientific article published on 27 April 2020

Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing loss

scientific article

Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness.

scientific article published on 23 March 2015

Novel mutations in LRTOMT associated with moderate progressive hearing loss in autosomal recessive inheritance.

scientific article published on 18 March 2015

POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss

scientific article

Prevalence and clinical features of hearing loss caused by EYA4 variants

scientific article published on 27 February 2020

Simple and efficient germline copy number variant visualization method for the Ion AmpliSeq™ custom panel

scientific article published on 06 April 2018

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients.

scientific article

The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss

scientific article published on 24 September 2019

The advantages of sound localization and speech perception of bilateral electric acoustic stimulation

scientific article

The effects of cochlear implantation in Japanese single-sided deafness patients: five case reports

journal article; published in Acta Oto-Laryngologica in 2016

The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation.

scientific article published on 13 March 2015

WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis.

scientific article published on 12 March 2018

List of works by Hideaki Moteki

A rational approach to identifying newborns with hearing loss caused by congenital cytomegalovirus infection by dried blood spot screening.

Achievement of hearing preservation in the presence of an electrode covering the residual hearing region.

Cochlear Implantation From the Perspective of Genetic Background

Comprehensive analysis of syndromic hearing loss patients in Japan

Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization.

Diagnostic pitfalls for -related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing loss

Etiology of single-sided deafness and asymmetrical hearing loss.

Feasibility of hearing preservation for residual hearing with longer cochlear implant electrodes

Frequency and clinical features of hearing loss caused by STRC deletions

Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness

Hearing preservation and clinical outcome of 32 consecutive electric acoustic stimulation (EAS) surgeries

Language development in Japanese children who receive cochlear implant and/or hearing aid.

Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearing.

Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss

Mutations in LOXHD1 gene cause various types and severities of hearing loss

Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis

Non-ocular Stickler syndrome with a novel mutation in COL11A2 diagnosed by massively parallel sequencing in Japanese hearing loss patients

Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss

Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing loss

Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness.

Novel mutations in LRTOMT associated with moderate progressive hearing loss in autosomal recessive inheritance.

POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss

Prevalence and clinical features of hearing loss caused by EYA4 variants

Simple and efficient germline copy number variant visualization method for the Ion AmpliSeq™ custom panel

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients.

The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss

The advantages of sound localization and speech perception of bilateral electric acoustic stimulation

The effects of cochlear implantation in Japanese single-sided deafness patients: five case reports

The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation.

WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis.