Iwasa Youichirou 岩佐陽一郎

… Alternative Names

IWASA Yohichirou 岩佐陽一郎

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Researcher Number	10613002
Affiliation (Current)	2022: 信州大学, 学術研究院医学系(医学部附属病院), 助教 2022: 信州大学, 学術研究院医学系, 助教
Affiliation (based on the past Project Information) *help	2015 – 2019: 信州大学, 医学部, 助教(特定雇用) 2015: 信州大学, 医学部, 助教 2014: 信州大学, 医学部附属病院, 医員
Review Section/Research Field	Principal Investigator Otorhinolaryngology Except Principal Investigator Otorhinolaryngology
Keywords	Principal Investigator 遺伝子 / 難聴 / 先天性難聴 / ANSD / OTOF / 耳科学 / Auditory neuropathy / 聴覚 / 内耳 / 常染色体優性遺伝 / 次世代シークエンサー / ゲノム … More Except Principal Investigator … More 難聴 / 遺伝子 / OTOF / 聴覚医学 / 内耳 / 人工内耳 / オーディとリーニューロパチー / Auditory Neuropathy Less

Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss PatientsPrincipal Investigator
- Principal Investigator
  
  Yoh-ichiro Iwasa
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Shinshu University
Genetic analysis and clinical features of auditory neuropathy spectrum disorder patientsPrincipal Investigator
- Principal Investigator
  
  IWASA Yoh-ishiro
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Shinshu University
OTOF mutation screening in Japanese sensorineural hearing loss patients
- Principal Investigator
  
  SUZUKI Hiroaki
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Shinshu University

All 2020 2019 2018 2017 2016 2013

All Journal Article Presentation

[Journal Article] A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations2020
- Author(s)
  Walls WD, Moteki H, Thomas TR, Nishio SY, Yoshimura H, Iwasa Y, et al
- Journal Title
  
  Human Genetics
  
  Volume: NA Pages: 1315-1323
- DOI
  10.1007/s00439-020-02174-y
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K16900, KAKENHI-PROJECT-19K18727
[Journal Article] OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients2019
- Author(s)
  Iwasa YI, Nishio SY, Sugaya A, Kataoka Y, Kanda Y, Taniguchi M, Nagai K, Naito Y, Ikezono T, Horie R, Sakurai Y, Matsuoka R, Takeda H, Abe S, Kihara C, Ishino T, Morita SY, Iwasaki S, Takahashi M, Ito T, Arai Y, Usami SI.
- Journal Title
  
  PLOS ONE
  
  Volume: 14 Pages: 0215932-0215932
- DOI
  10.1371/journal.pone.0215932
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K11322, KAKENHI-PROJECT-17K16900, KAKENHI-PROJECT-15K20209, KAKENHI-PROJECT-18K16890, KAKENHI-PROJECT-18K16905
[Journal Article] OTOF mutation screening in Japanese severe to profound recessive hearing loss patients2013
- Author(s)
  Iwasa Y, Nishio S, Yoshimura H, Kanda Y, Kumakawa K, Abe S, Naito Y, Nagai K, Usami S.
- Journal Title
  
  BMC Med Genet
  
  Volume: 14 Pages: 1-5
- DOI
  10.1186/1471-2350-14-95
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25861544
[Presentation] OTOF mutation analysis with massively parallel DNA sequencing in 2135 Japanese sensorineural hearing loss patients2018
- Author(s)
  Iwasa Y, Usami S
- Organizer
  Association for Research in Otolaryngology 2018
- Data Source
  KAKENHI-PROJECT-17K16900
[Presentation] OTOF遺伝子p.R1172Q変異による難聴発症機序の解析2018
- Author(s)
  岩佐陽一郎、北尻真一郎、西尾信哉、吉村豪兼、宇佐美真一
- Organizer
  第63回日本聴覚医学会総会
- Data Source
  KAKENHI-PROJECT-17K16900
[Presentation] 次世代シーケンサーを用いたAuditory neuropathy spectrum disorderに対する遺伝子解析2017
- Author(s)
  岩佐陽一郎、西尾信哉、宇佐美真一
- Organizer
  第27回　日本耳科学会
- Data Source
  KAKENHI-PROJECT-17K16900
[Presentation] COL11A2遺伝子変異によるStickler症候群３型の２症例2017
- Author(s)
  岡晋一郎、岩佐陽一郎、西尾信哉、茂木英明、宇佐美真一
- Organizer
  第63回　日本聴覚医学会総会
- Data Source
  KAKENHI-PROJECT-17K16900
[Presentation] 当科データベースにおける次世代シーケンサーを用いたOTOF遺伝子の変異解析2016
- Author(s)
  岩佐陽一郎、西尾信哉、宇佐美真一
- Organizer
  第26回日本耳科学会
- Place of Presentation
  長野市ホテル国際２１
- Year and Date
  2016-10-05
- Data Source
  KAKENHI-PROJECT-26861364
[Presentation] OTOF mutation screening in Japanese severe to profound recessive hearing loss patients2013
- Author(s)
  Iwasa Y, Suzuki H, Usami S
- Organizer
  12th Taiwan-Japan Conference on Otolaryngology Head and Neck surgery
- Place of Presentation
  Taiwan University Hospital
- Data Source
  KAKENHI-PROJECT-25861544
[Presentation] OTOF遺伝子変異によるAuditory neuropathy症例の臨床像と人工内耳の効果に関する検討2013
- Author(s)
  岩佐陽一郎、吉村豪兼、工　穣、宇佐美真一
- Organizer
  第8回　日本小児耳鼻咽喉科学会総会
- Place of Presentation
  前橋
- Data Source
  KAKENHI-PROJECT-25861544

1. USAMI Shin-ichi (10184996)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
2. NISHIO Shin-ya (70467166)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
3. SUZUKI Hiroaki (00419368)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
4. MATSUOKA Rina

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
5. 吉村豪兼

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. 菅谷明子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Iwasa Youichirou 岩佐 陽一郎

IWASA Yohichirou 岩佐 陽一郎

Research Projects

Research Products

Co-Researchers

Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss PatientsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Genetic analysis and clinical features of auditory neuropathy spectrum disorder patientsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

OTOF mutation screening in Japanese sensorineural hearing loss patients

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] OTOF mutation screening in Japanese severe to profound recessive hearing loss patients2013

Author(s)

Journal Title

DOI

Data Source

[Presentation] OTOF mutation analysis with massively parallel DNA sequencing in 2135 Japanese sensorineural hearing loss patients2018

Author(s)

Organizer

Data Source

[Presentation] OTOF遺伝子p.R1172Q変異による難聴発症機序の解析2018

Author(s)

Organizer

Data Source

[Presentation] 次世代シーケンサーを用いたAuditory neuropathy spectrum disorderに対する遺伝子解析2017

Author(s)

Organizer

Data Source

[Presentation] COL11A2遺伝子変異によるStickler症候群３型の２症例2017

Author(s)

Organizer

Data Source

[Presentation] 当科データベースにおける次世代シーケンサーを用いたOTOF遺伝子の変異解析2016

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] OTOF mutation screening in Japanese severe to profound recessive hearing loss patients2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] OTOF遺伝子変異によるAuditory neuropathy症例の臨床像と人工内耳の効果に関する検討2013

Author(s)

Organizer

Place of Presentation

Data Source

Iwasa Youichirou 岩佐陽一郎

IWASA Yohichirou 岩佐陽一郎