NAITO Takehiko 内藤武彦

Researcher Number	50467164
Affiliation (based on the past Project Information) *help	2015 – 2016: 信州大学, 医学部附属病院, 医員 2014: 信州大学, 医学部附属病院, 助教(特定雇用) 2013: 信州大学, 医学部附属病院, 医員 2012: 信州大学, 医学部附属病院, 助教(特定雇用)
Review Section/Research Field	Principal Investigator Otorhinolaryngology Except Principal Investigator Otorhinolaryngology
Keywords	Principal Investigator 聴力型 / ゲノム / KCNQ4 / 遺伝子 / 難聴 Except Principal Investigator 難聴 / 遺伝子 / 聴覚医学 / KCNQ4 / 細胞外マトリソクス … More / 感音難聴 / 内耳 / 次世代シークエンサー / 耳科学 Less

High frequency and mid frequency hearing loss caused by KCNQ4 gene mutationsPrincipal Investigator
- Principal Investigator
  
  NAITO Takehiko
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Shinshu University
Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort
- Principal Investigator
  
  NISHIO Shin-ya
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Shinshu University
Comprehensive genetic analysis of hearing loss using next generation sequencer.
- Principal Investigator
  
  USAMI Shinichi
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Shinshu University

All 2015 2013 2012 2011

All Journal Article Presentation

[Journal Article] Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation2013
- Author(s)
  aito T, Nishio SY, Iwasa Y, Yano T,Kumakawa K, Abe S, Ishikawa K, Kojima H, Namba A, Oshikawa C, Usami S
- Journal Title
  
  PLoS One
  
  Volume: 8(5) Issue: 5 Pages: e63231-e63231
- DOI
  10.1371/journal.pone.0063231
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22249057, KAKENHI-PROJECT-25462633
[Journal Article] Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations2011
- Author(s)
  Moteki H, Naito Y, Fujiwara K, Kitoh R, Nishio S Y, Oguchi K, Takumi Y, Usami SI
- Journal Title
  
  Acta Oto-Laryngol
  
  Volume: 131 Issue: 11 Pages: 1232-1236
- DOI
  10.3109/00016489.2011.593719
- NAID
  120007110633
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21592153, KAKENHI-PROJECT-22249057, KAKENHI-PROJECT-22591894, KAKENHI-PROJECT-22791587
[Journal Article] 残存聴力活用型人工内耳(electric acoustic stimulation) ～手術法と聴力保存成績について～2011
- Author(s)
  宇佐美真一、茂木英明、宮川麻衣子、内藤武彦、西尾信哉、工穣、岩崎聡
- Journal Title
  
  Otol Jpn
  
  Volume: 21(5) Pages: 763-770
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22249057
[Presentation] 次世代シーケンサーを用いた日本人難聴患者1120例の網羅的遺伝子解析2015
- Author(s)
  西尾信哉、宮川麻衣子、内藤武彦、岩佐陽一郎、市瀬彩、宇佐美真一
- Organizer
  第25回日本耳科学会
- Place of Presentation
  長崎ブリックホール（長崎県長崎市）
- Year and Date
  2015-10-08
- Data Source
  KAKENHI-PROJECT-25462633
[Presentation] 特発性両側性感音難聴患者に対する遺伝学的検査～次世代シーケンサーを用いた検査～2015
- Author(s)
  西尾信哉、宮川麻衣子、池園哲郎、石川浩太郎、岩崎聡、岡本牧人、小川郁、加我君孝、熊川孝三、小橋元、坂田英明、佐藤宏昭、佐野肇、曾根三千彦、高橋晴雄、武田英彦、東野哲也、内藤泰、中川尚志、西崎和則、野口佳裕、羽藤直人、原　晃、福田諭、松永達雄、山岨達也、宇佐美真一
- Organizer
  第60回　日本聴覚医学会総会・学術講演会
- Place of Presentation
  京王プラザホテル（東京都新宿区）
- Year and Date
  2015-10-22
- Data Source
  KAKENHI-PROJECT-25462633
[Presentation] Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort; genotype-phenotype correlations and a founder mutation.2013
- Author(s)
  Naito T, Nishio S, Usami S
- Organizer
  9th Molecular Biology of Hearing and Deafness Conference
- Place of Presentation
  Stanford University
- Data Source
  KAKENHI-PROJECT-25462633
[Presentation] Comprehensive genetic screening of hearing loss for efficient clinical molecular diagnosis.2013
- Author(s)
  Nishio S, Naito T, Miyagawa M, Usami S.
- Organizer
  Life Technologies Asia Pacific Japan 2013 Genetic Analysis Summit
- Place of Presentation
  Bali
- Invited
- Data Source
  KAKENHI-PROJECT-25462633
[Presentation] 次世代シーケンサーによる難聴の遺伝子解析（2）～見出された原因遺伝子および表現型について～2012
- Author(s)
  宮川麻衣子、内藤武彦、西尾信哉、宇佐美真一
- Organizer
  第22回日本耳科学会総会
- Place of Presentation
  名古屋国際会議場
- Data Source
  KAKENHI-PROJECT-22249057
[Presentation] 次世代シーケンサーによる難聴の遺伝子解析(2)～見出された原因遺伝子および表現型について～2012
- Author(s)
  宮川麻衣子、内藤武彦、西尾信哉、宇佐美真一
- Organizer
  第22回日本耳科学会総会
- Place of Presentation
  名古屋国際会議場
- Data Source
  KAKENHI-PROJECT-22249057
[Presentation] 次世代シーケンサーによる難聴の遺伝子解析(1)～方法論および変異検出アルゴリズムについて～2012
- Author(s)
  西尾信哉、宮川麻衣子、内藤武彦、宇佐美真一
- Organizer
  第22回日本耳科学会総会
- Place of Presentation
  名古屋国際会議場
- Data Source
  KAKENHI-PROJECT-22249057
[Presentation] 次世代シーケンサーによる難聴の遺伝子解析（1）～方法論および変異検出アルゴリズムについて～2012
- Author(s)
  西尾信哉、宮川麻衣子、内藤武彦、宇佐美真一
- Organizer
  第22回日本耳科学会総会
- Place of Presentation
  名古屋国際会議場
- Data Source
  KAKENHI-PROJECT-22249057
[Presentation] 先進医療「先天性難聴の遺伝子診断」の現状2011
- Author(s)
  工穣、岩佐陽一郎、吉村豪兼、矢野卓也、内藤武彦、宮川麻衣子、茂木英明、西尾信哉、宇佐美真一
- Organizer
  第56回日本聴覚医学会総会・学術講演会
- Place of Presentation
  福岡
- Year and Date
  2011-10-27
- Data Source
  KAKENHI-PROJECT-22249057

1. USAMI Shinichi (10184996)

# of Collaborated Projects: 3 results

# of Collaborated Products: 11 results
2. NISHIO Shinya (70467166)

# of Collaborated Projects: 3 results

# of Collaborated Products: 11 results
3. KUMAKAWA Kozo (40142252)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
4. SATO Hiroaki (40215827)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. TONO Tetsuya (80145424)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. FURUYA Nobuhiko (80107606)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. NAGAI Kyoko (50302469)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. TAKUMI Yutaka (70312501)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
9. MOTEKI Hideaki (60422698)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
10. MIYAKAWA Maiko (60467165)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results

NAITO Takehiko 内藤 武彦

Research Projects

Research Products

Co-Researchers

High frequency and mid frequency hearing loss caused by KCNQ4 gene mutationsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Comprehensive genetic analysis of hearing loss using next generation sequencer.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation2013

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations2011

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] 残存聴力活用型人工内耳(electric acoustic stimulation) ～手術法と聴力保存成績について～2011

Author(s)

Journal Title

Data Source

[Presentation] 次世代シーケンサーを用いた日本人難聴患者1120例の網羅的遺伝子解析2015

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] 特発性両側性感音難聴患者に対する遺伝学的検査～次世代シーケンサーを用いた検査～2015

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort; genotype-phenotype correlations and a founder mutation.2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Comprehensive genetic screening of hearing loss for efficient clinical molecular diagnosis.2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] 次世代シーケンサーによる難聴の遺伝子解析（2）～見出された原因遺伝子および表現型について～2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] 次世代シーケンサーによる難聴の遺伝子解析(2)～見出された原因遺伝子および表現型について～2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] 次世代シーケンサーによる難聴の遺伝子解析(1)～方法論および変異検出アルゴリズムについて～2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] 次世代シーケンサーによる難聴の遺伝子解析（1）～方法論および変異検出アルゴリズムについて～2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] 先進医療「先天性難聴の遺伝子診断」の現状2011

NAITO Takehiko 内藤武彦