Togawa Takao 戸川貴夫

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Takao Togawa 戸川貴夫

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Researcher Number	10792814
Other IDs
Affiliation (Current)	2025: 名古屋市立大学, 医薬学総合研究院(医学), 研究員
Affiliation (based on the past Project Information) *help	2023 – 2024: 名古屋市立大学, 医薬学総合研究院(医学), 研究員 2020 – 2022: 名古屋市立大学, 医薬学総合研究院(医学), 講師 2019: 名古屋市立大学, 医薬学総合研究院(医学), 助教 2018: 名古屋市立大学, 大学院医学研究科, 助教 2017: 名古屋市立大学, 大学院医学研究科, 臨床研究医
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics Except Principal Investigator Medium-sized Section 47:Pharmaceutical sciences and related fields / Pediatric surgery
Keywords	Principal Investigator トランスクリプトーム解析 / 全エクソーム解析 / 染色体構造異常 / 全エクソン解析 / 全ゲノム解析 / 遺伝性肝内胆汁うっ滞症 / 胆汁うっ滞 / 次世代高速シークエンサー / 遺伝子解析 / 体質性黄疸 … More / 遺伝学的解析 / 新生児胆汁うっ滞 / Rotor症候群 / Dubin-Johnson症候群 / 遺伝性抱合型高ビリルビン血症 … More Except Principal Investigator 胆汁酸 / 小児肝疾患 / 病態モデル / 胆汁うっ滞 / iPS細胞由来肝細胞 / オミクスデータ解析 / 肝内胆汁うっ滞 / 早期鑑別システム / 次世代シークエンサー / マイクロアレイCGH解析 / MLPA解析 / マイクロアレイCGH / 次世代シーケンサー / 胆道閉鎖症 / アラジール症候群 Less

Study to simplify disease models for pediatric liver diseases
- Principal Investigator
  
  林久允
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Fund for the Promotion of Joint International Research (International Collaborative Research)
- Review Section
  
  Medium-sized Section 47:Pharmaceutical sciences and related fields
- Research Institution
  The University of Tokyo
遺伝性胆汁うっ滞疾患に対する全ゲノム解析による新規分子病態の発見と診断率の向上Principal Investigator
- Principal Investigator
  
  戸川貴夫
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya City University
Analysis of molecular mechanisms in the development of pediatric cholestatic liver disease
- Principal Investigator
  
  Hayashi Hisamitsu
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
- Review Section
  
  Medium-sized Section 47:Pharmaceutical sciences and related fields
- Research Institution
  The University of Tokyo
A study of molecular genetic analysis to hereditary conjugated hyperbilirubinemia with next-generation sequencingPrincipal Investigator
- Principal Investigator
  
  Takao Togawa
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Nagoya City University
Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome
- Principal Investigator
  
  Sugiura Tokio
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatric surgery
- Research Institution
  Nagoya City University

All 2023 2022 2021 2019 2018 2017

All Journal Article Presentation

[Journal Article] Clinicopathologic Features, Genetics, Treatment, and Long-Term Outcomes in Japanese Children and Young Adults with Benign Recurrent Intrahepatic Cholestasis: A Multicenter Study2023
- Author(s)
  Kato Ken、Umetsu Shuichiro、Togawa Takao、Ito Koichi、Kawabata Takayoshi、Arinaga-Hino Teruko、Tsumura Naoya、Yasuda Ryosuke、Mihara Yutaro、Kusano Hironori、Ito Shogo、Imagawa Kazuo、Hayashi Hisamitsu、Inui Ayano、Yamashita Yushiro、Mizuochi Tatsuki
- Journal Title
  
  Journal of Clinical Medicine
  
  Volume: 12 Issue: 18 Pages: 5979-5979
- DOI
  10.3390/jcm12185979
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20KK0172
[Journal Article] Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis2022
- Author(s)
  Ito Shogo、Togawa Takao、Imagawa Kazuo、Ito Koichi、Endo Takeshi、Sugiura Tokio、Saitoh Shinji
- Journal Title
  
  JPGN Reports
  
  Volume: 3 Issue: 2
- DOI
  10.1097/pg9.0000000000000196
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07854
[Journal Article] Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages.2018
- Author(s)
  Hayashi H, Naoi S, Togawa T, Hirose Y, Kondou H, Hasegawa Y, Abukawa D, Sasaki M, Muroya K, Watanabe S, Nakano S, Minowa K, Inui A, Fukuda A, Kasahara M, Nagasaka H, Bessho K, Suzuki M, Kusuhara H
- Journal Title
  
  EBioMedicine
  
  Volume: 27
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K10148
[Journal Article] Alagille症候群2018
- Author(s)
  戸川貴夫
- Journal Title
  
  小児内科
  
  Volume: 50 Pages: 446-447
- Data Source
  KAKENHI-PROJECT-17K10148
[Journal Article] 胆道閉鎖症との鑑別が必要であった新生児Dubin-Johnson症候群の1例2018
- Author(s)
  清松光貴，水落建輝，石原　潤，髙木祐吾，靏久士保理，深堀　優，八木　実，草野弘宣，戸川貴夫，山下裕史朗
- Journal Title
  
  日本小児栄養消化器肝臓学会雑誌
  
  Volume: 32
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10148
[Journal Article] Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan.2018
- Author(s)
  Togawa T, Tatsuki Mizuochi, Tokio Sugiura, Hironori Kusano, Ken Tanikawa, Takato Sasaki, Fumio Ichinose, Seiichi Kagimoto, Takahisa Tainaka, Hiroo Uchida, Shinji Saitoh
- Journal Title
  
  The Journal of Pediatrics
  
  Volume: - Pages: 161-167
- DOI
  10.1016/j.jpeds.2017.12.058
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10148, KAKENHI-PROJECT-16K19096, KAKENHI-PROJECT-17K11516
[Journal Article] Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g.2018
- Author(s)
  Nagara S, Kouwaki M, Togawa T, Sugiura T, Okada M, Koyama N.
- Journal Title
  
  Pediatr Neonatol.
  
  Volume: 59 Issue: 3 Pages: 274-280
- DOI
  10.1016/j.pedneo.2017.09.005
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11516
[Journal Article] Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome.2017
- Author(s)
  Ohashi K, Togawa T, Sugiura T, Ito K, Endo T, Aoyama K, Negishi Y, Kudo T, Ito R, Saitoh S.
- Journal Title
  
  Acta Paediatr.
  
  Volume: 106 Issue: 11 Pages: 1717-1824
- DOI
  10.1111/apa.13981
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K11516
[Presentation] 成人期に遺伝子診断された進行性家族性肝内胆汁うっ滞症１型の１例2023
- Author(s)
  齋藤博大、今川和生、須磨崎亮、伊藤彰悟、戸川貴夫、林久允
- Organizer
  第39回日本小児肝臓研究会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] 小児期発症胆汁うっ滞疾患レジストリCIRCLe報告1：現在までの進捗状況2023
- Author(s)
  中野聡, 今川和生, 伊藤彰悟, 戸川貴夫, 三原勇太郎, 草野弘宣, 入戸野博, 林久允
- Organizer
  第50回日本小児栄養消化器肝臓学会学術集会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] Clinical and Genetic Features of 22 Neonatal Dubin-Johnson Syndrome in Japan2023
- Author(s)
  戸川貴夫
- Organizer
  American Society of Human Genetics Annual Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07854
[Presentation] 小児期発症胆汁うっ滞疾患レジストリCIRCLe報告2：遺伝子パネルの改良と未診断症例に対する全エクソーム解析2023
- Author(s)
  今川和生、鈴木寿人、伊藤彰悟、戸川貴夫、中野聡、小崎健次郎、林久允
- Organizer
  第50回日本小児栄養消化器肝臓学会学術集会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] 未診断の小児期発症胆汁うっ滞性疾患における全エクソーム解析及びRNAseqの有用性2023
- Author(s)
  今川和生、伊藤彰悟、戸川貴夫、鈴木寿人、東良紘、谷川健、林久允
- Organizer
  第39回日本小児肝臓研究会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] MYO5Bに複合ヘテロ変異を認めたγGTP正常胆汁うっ滞の１例2023
- Author(s)
  伊藤彰悟、伊藤孝一、谷村知繁、戸川貴夫、今川和生、林久允
- Organizer
  第39回日本小児肝臓研究会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] 小児期発症胆汁うっ滞疾患レジストリCIRCLe報告3：全エクソーム解析が診断の一助となったミオチュブラーミオパチー肝紫斑病の1例2023
- Author(s)
  伊藤彰悟、伊藤孝一、谷村知繁、戸川貴夫、今川和生、林久允
- Organizer
  第50回日本小児栄養消化器肝臓学会学術集会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] 本邦における良性反復性肝内胆汁うっ滞症の臨床像：多施設共同研究2022
- Author(s)
  加藤健，梅津守一郎, 乾あやの, 伊藤孝一, 河畑孝佳, 坂本理恵子, 別所一彦, 安田亮輔, 今川和生, 戸川貴夫, 林久允, 水落建輝
- Organizer
  第49回日本小児栄養消化器肝臓学会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] 小児期発症の胆汁うっ滞性肝疾患を対象とした多施設前向きレジストリ研究(CIRCLe)2022
- Author(s)
  小西健一郎、中野聡、戸川貴夫、今川和生、伊藤彰悟、三原勇太郎、草野弘宣、鹿毛政義、入戸野博、林久允
- Organizer
  第49回日本胆道閉鎖症研究会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] リファンピシン投与におけるグルクロン酸抱合型胆汁酸の体内動態2021
- Author(s)
  鈴木光幸、武井一、林久允、田村隆太郎、武藤大和、平井沙依子、今川和生、戸川貴夫、村井毅、木村昭彦、入戸野博、清水俊明
- Organizer
  第48回日本小児栄養消化器肝臓学会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] PFIC type2に対するフェニル酪酸Na初回導入時の治療戦略2021
- Author(s)
  武藤大和、鈴木光幸、中野聡、今川和生、田川学、戸川貴夫、三原勇太郎、草野弘宣、林久允、清水俊明
- Organizer
  第37回日本小児肝臓研究会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] 胆汁うっ滞を伴う早産児・低出生体重児における遺伝学的解析2021
- Author(s)
  今川和生、戸川貴夫、伊藤彰悟、伊藤孝一、林久允、高田英俊、斎藤伸治
- Organizer
  第124回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] 進行性家族性肝内胆汁うっ滞症2型に合併する掻痒症に対する薬物療法2021
- Author(s)
  武藤大和，鈴木光幸，中野聡，箕輪圭，今川和生，戸川貴夫，三原勇太郎，草野弘宣，林久允，清水俊明
- Organizer
  第48回日本小児栄養消化器肝臓学会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] 東南アジア地域における原因不明胆汁うっ滞小児に対する次世代シークエンサー解析2021
- Author(s)
  今川和生、伊藤彰悟、戸川貴夫、伊藤孝一、林久允
- Organizer
  第48回日本小児栄養消化器肝臓学会
- Data Source
  KAKENHI-PROJECT-20KK0172
[Presentation] Inherited Disorders of Neonatal/Infantile Intrahepatic Cholestasis and Molecular Genetic Testing.2019
- Author(s)
  戸川貴夫
- Organizer
  The 4th international Conference for Paediatric Gastroenterology & Nutrition.
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10148
[Presentation] 遺伝性新生児乳児胆汁うっ滞と分子遺伝学的解析2019
- Author(s)
  戸川貴夫
- Organizer
  日本小児栄養消化器肝臓学会第14回卒後教育セミナー
- Invited
- Data Source
  KAKENHI-PROJECT-17K10148
[Presentation] DIVERSITY OF ATP8B1 MUTATIONS IN JAPANESE PATIENTS WITH INTRAHEPATIC CHOLESTASIS ASSOCIATED WITH LOW GAMMA-GLUTAMYL TRANSPEPTIDASE LEVEL2018
- Author(s)
  戸川貴夫
- Organizer
  North American Society for Pediatric Gastroenterology, Hepatology and Nutrition 2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10148
[Presentation] 小児稀少難病，進行性家族性肝内胆汁うっ滞症2型への遺伝子解析とABCB11日本人高頻度変異:フェニル酪酸ナトリウム治療適応を見据えて2018
- Author(s)
  戸川貴夫
- Organizer
  第63回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-17K10148
[Presentation] Inherited Disorders of Neonatal/Infantile Intrahepatic Cholestasis and Molecular Genetic Testing in an Era of Precision Medicine2018
- Author(s)
  戸川貴夫
- Organizer
  The 2nd Vinmec international Conference on Cell and Gene Therapy Conference
- Invited
- Data Source
  KAKENHI-PROJECT-17K10148
[Presentation] Diversity of JAG1 mutations in Japanese patients with Alagille syndrome2017
- Author(s)
  戸川貴夫
- Organizer
  The 67th Annual Meeting of the American Society of Human Genetics
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10148
[Presentation] アラジール症候群と胆道閉鎖症に対する体系的遺伝学的解析2017
- Author(s)
  杉浦時雄, 大橋圭、戸川貴夫、伊藤孝一、遠藤剛、齋藤伸治
- Organizer
  第44回日本小児栄養消化器肝臓学会
- Data Source
  KAKENHI-PROJECT-17K11516
[Presentation] DIVERSITY OF ABCB11 MUTATIONS IN JAPANESE PATIENTS WITH INTRAHEPATIC CHOLESTASIS ASSOCIATED WITH LOW GAMMA-GLUTAMYL TRANSPEPTIDASE LEVEL2017
- Author(s)
  戸川貴夫
- Organizer
  North American Society for Pediatric Gastroenterology, Hepatology and Nutrition 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10148
[Presentation] 新生児Dubin-Johnson症候群の全国多施設研究：遺伝子解析と臨床像の検討2017
- Author(s)
  戸川貴夫
- Organizer
  第34回小児肝臓研究会
- Data Source
  KAKENHI-PROJECT-17K10148

1. Sugiura Tokio (10381881)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
2. Hayashi Hisamitsu (10451858)

# of Collaborated Projects: 2 results

# of Collaborated Products: 14 results
3. 今川和生 (40708509)

# of Collaborated Projects: 2 results

# of Collaborated Products: 14 results
4. 齋藤伸治 (00281824)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 田井中貴久 (30378195)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 水野忠快 (90736050)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. 斉藤伸治

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Togawa Takao 戸川 貴夫

Takao Togawa 戸川 貴夫

Research Projects

Research Products

Co-Researchers

Study to simplify disease models for pediatric liver diseases

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

遺伝性胆汁うっ滞疾患に対する全ゲノム解析による新規分子病態の発見と診断率の向上Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Analysis of molecular mechanisms in the development of pediatric cholestatic liver disease

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

A study of molecular genetic analysis to hereditary conjugated hyperbilirubinemia with next-generation sequencingPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Clinicopathologic Features, Genetics, Treatment, and Long-Term Outcomes in Japanese Children and Young Adults with Benign Recurrent Intrahepatic Cholestasis: A Multicenter Study2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Real-life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages.2018

Author(s)

Journal Title

Data Source

[Journal Article] Alagille症候群2018

Author(s)

Journal Title

Data Source

[Journal Article] 胆道閉鎖症との鑑別が必要であった新生児Dubin-Johnson症候群の1例2018

Author(s)

Journal Title

Data Source

[Journal Article] Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan.2018

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g.2018

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome.2017

Author(s)

Journal Title

DOI

Data Source

[Presentation] 成人期に遺伝子診断された進行性家族性肝内胆汁うっ滞症１型の１例2023

Author(s)

Organizer

Data Source

[Presentation] 小児期発症胆汁うっ滞疾患レジストリCIRCLe報告1：現在までの進捗状況2023

Author(s)

Organizer

Data Source

Togawa Takao 戸川貴夫

Takao Togawa 戸川貴夫