Hattori Tetsuhisa 服部哲久

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HATTORI Tetsuhisa 服部哲久

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Researcher Number	80638932
Other IDs
Affiliation (based on the past Project Information) *help	2019 – 2020: 国立研究開発法人国立循環器病研究センター, 研究所, 客員研究員 2018: 国立研究開発法人国立循環器病研究センター, 研究所, 研究員 2016: 滋賀医科大学, 医学部, 特任助教 2015: 滋賀医科大学, 医学部, 非常勤講師 2013 – 2014: 滋賀医科大学, 医学部, 助教
Review Section/Research Field	Principal Investigator General physiology / Basic Section 53020:Cardiology-related
Keywords	Principal Investigator 不整脈 / DNA構造多型 / ゲノムDNA構造異常 / エピゲノム / ロングリードシークエンサー / エピジェネティクス / 遺伝子 / チャネル / 疾患関連遺伝子 / 分子心臓学 … More / 生理学的機能解析 / QT延長症候群 / 心筋細胞 / 疾患特異的iPS細胞 / 分子心臓病態学 Less

Investigation of relationship between inherited arrhythmias and epigeneticsPrincipal Investigator
- Principal Investigator
  
  Hattori Tetsuhisa
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  National Cardiovascular Center Research Institute
A novel TRPM4 mutation identified in a patient with catecholaminergic polymorphic ventricular tachycardiaPrincipal Investigator
- Principal Investigator
  
  Hattori Tetsuhisa
- Project Period (FY)
  2015 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  General physiology
- Research Institution
  Shiga University of Medical Science
Modeling and analyzing of long QT syndrome using disease-specific iPS cellsPrincipal Investigator
- Principal Investigator
  
  HATTORI Tetsuhisa
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  General physiology
- Research Institution
  Shiga University of Medical Science

All 2019 2018

All Presentation

[Presentation] Lower Frequency of Classical Triad in Andersen-Tawil Syndrome Probands with De Novo KCNJ2 Mutations than Those with Familial Mutations2019
- Author(s)
  Hattori T, Sonoda K, Horie M, Ohno S
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] Lower Frequency of Classical Triad in Andersen-Tawil Syndrome Probands with De Novo KCNJ2 Mutations than Those with Familial Mutations2019
- Author(s)
  Tetsuhisa Hattori, Keiko Sonoda, Minoru Horie, Seiko Ohno
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] De novo RYR2 mutations are associated with severe phenotype of CPVT more strongly than inherited ones2019
- Author(s)
  Keiko Sonoda, Tetsuhisa Hattori, Minoru Horie, Seiko Ohno
- Organizer
  The American Society of Human Genetics 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] Functional Change of an SCN5A Mutation Identified in the Patient with Short-Coupled Variant of Torsades de Pointes2018
- Author(s)
  Keiko Sonoda, Seiko Ohno, Tetsuhisa Hattori, Minoru Horie
- Organizer
  APHRS2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] High Frequency of De Novo KCNJ2 Mutations in Andersen-Tawil Syndrome Patients2018
- Author(s)
  Tetsuhisa Hattori, Keiko Sonoda, Minoru Horie, Seiko Ohno
- Organizer
  APHRS2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08102

1. 大野聖子 (20610025)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
2. KURODA Yusuke

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. YUASA Shinsuke

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

Hattori Tetsuhisa 服部 哲久

HATTORI Tetsuhisa 服部 哲久

Research Projects

Research Products

Co-Researchers

Investigation of relationship between inherited arrhythmias and epigeneticsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

A novel TRPM4 mutation identified in a patient with catecholaminergic polymorphic ventricular tachycardiaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Modeling and analyzing of long QT syndrome using disease-specific iPS cellsPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Presentation] Lower Frequency of Classical Triad in Andersen-Tawil Syndrome Probands with De Novo KCNJ2 Mutations than Those with Familial Mutations2019

Author(s)

Organizer

Data Source

[Presentation] Lower Frequency of Classical Triad in Andersen-Tawil Syndrome Probands with De Novo KCNJ2 Mutations than Those with Familial Mutations2019

Author(s)

Organizer

Data Source

[Presentation] De novo RYR2 mutations are associated with severe phenotype of CPVT more strongly than inherited ones2019

Author(s)

Organizer

Data Source

[Presentation] Functional Change of an SCN5A Mutation Identified in the Patient with Short-Coupled Variant of Torsades de Pointes2018

Author(s)

Organizer

Data Source

[Presentation] High Frequency of De Novo KCNJ2 Mutations in Andersen-Tawil Syndrome Patients2018

Author(s)

Organizer

Data Source

Hattori Tetsuhisa 服部哲久

HATTORI Tetsuhisa 服部哲久