Yamamoto Hidenori 山本英範

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YAMAMOTO Hidenori 山本英範

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Researcher Number	80801662
Other IDs
Affiliation (Current)	2025: 名古屋大学, 医学部附属病院, 病院助教
Affiliation (based on the past Project Information) *help	2019 – 2023: 名古屋大学, 医学部附属病院, 医員
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator チロシンキナーゼ / プロテオーム解析 / 先天性心疾患 / 成長障害 / 骨格異常 / CRISPR-Cas9 / 次世代シークエンサー / 房室中隔欠損症 / 心室中隔欠損症 / エクソーム解析 / リン酸化プロテオーム解析 / 22q11.2欠失症候群 / 全エクソーム解析 … More Except Principal Investigator … More 閉塞性病変 / プロテオーム解析 / レーザーマイクロダイセクション / 形質変換 / 平滑筋細胞 / 肺高血圧症 / メタゲノム解析 / 単心室症 / Fontan手術 / 腸内細菌叢 / 蛋白漏出性胃腸症 Less

網羅的プロテオーム解析に基づいた肺高血圧症病変における新規治療ターゲットの検証
- Principal Investigator
  
  加藤太一
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya University
メタゲノム解析とオミクス解析を用いたFontan術後蛋白漏出性胃腸症の病態解明
- Principal Investigator
  
  郷清貴
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya University
Mechanism analysis of a syndrome with congenital heart disease due to tyrosine kinase gene abnormalityPrincipal Investigator
- Principal Investigator
  
  Yamamoto Hidenori
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya University
proteomic analysis of smooth muscle cell transformation in obstructive lesions of pulmonary hypertension.
- Principal Investigator
  
  Kato Taichi
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya University
Comprehensive analysis of causative gene in familial congenital heart disease by whole exome analysisPrincipal Investigator
- Principal Investigator
  
  YAMAMOTO Hidenori
- Project Period (FY)
  2019 – 2020
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nagoya University

All 2024 2023 2022 2021 2020 2019

All Journal Article Presentation

[Journal Article] Dysbiosis of gut microbiota in patients with protein-losing enteropathy after the Fontan procedure2024
- Author(s)
  Go Kiyotaka、Horiba Kazuhiro、Yamamoto Hidenori、Morimoto Yoshihito、Fukasawa Yoshie、Ohashi Naoki、Yasuda Kazushi、Ishikawa Yuichi、Kuraishi Kenji、Suzuki Kazutaka、Ito Yoshinori、Takahashi Yoshiyuki、Kato Taichi
- Journal Title
  
  International Journal of Cardiology
  
  Volume: 396 Pages: 131554-131554
- DOI
  10.1016/j.ijcard.2023.131554
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K19584, KAKENHI-PROJECT-22K07912, KAKENHI-PROJECT-23K07329, KAKENHI-PROJECT-21K15900
[Journal Article] Effects of General Anesthesia on the Results of Cardiac Catheterization in Pediatric Patients with Ventricular Septal Defect2023
- Author(s)
  Kiyotaka Go, Taichi Kato, Machiko Kito, et al.
- Journal Title
  
  Congenital Heart Disease
  
  Volume: 18 Issue: 2 Pages: 235-243
- DOI
  10.32604/chd.2023.027590
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K07912, KAKENHI-PROJECT-20K08155
[Journal Article] Case report: High-dose epoprostenol therapy in pediatric patients with pulmonary hypertension and developmental lung disease2023
- Author(s)
  Fukasawa Yoshie、Yamamoto Hidenori、Ito Miharu、Saito Akiko、Go Kiyotaka、Morimoto Yoshihito、Yasuda Kazushi、Sato Yoshiaki、Hayakawa Masahiro、Kato Taichi
- Journal Title
  
  Frontiers in Pediatrics
  
  Volume: 11 Pages: 1-7
- DOI
  10.3389/fped.2023.1116434
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K15900, KAKENHI-PROJECT-20K08155, KAKENHI-PROJECT-23K07329
[Journal Article] Conception by assisted reproductive technology in infants with critical congenital heart disease in Japan2022
- Author(s)
  Morimoto Yoshihito、Go Kiyotaka、Yamamoto Hidenori、Fukasawa Yoshie、Nakai Michikazu、Morihana Eiji、Yasuda Kazushi、Nishikawa Hiroshi、Ohashi Naoki、Takahashi Yoshiyuki、Kato Taichi
- Journal Title
  
  Reproductive BioMedicine Online
  
  Volume: 44 Issue: 1 Pages: 163-170
- DOI
  10.1016/j.rbmo.2021.10.005
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08319, KAKENHI-PROJECT-21K15900
[Journal Article] Familial cardiac septal defect due to a novel nine‐base deletion in TBX202022
- Author(s)
  Yamamoto Hidenori、Inagaki Hidehito、Hayano Satoshi、Kurahashi Hiroki、Kato Taichi
- Journal Title
  
  Pediatrics International
  
  Volume: 64 Issue: 1
- DOI
  10.1111/ped.14995
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K15900
[Journal Article] Tension hemothorax 1 week after pericardiocentesis associated with thrombocytopenia2022
- Author(s)
  Yamamoto Hidenori、Go Kiyotaka、Morimoto Yoshihito、Fukasawa Yoshie、Kato Taichi
- Journal Title
  
  Pediatrics International
  
  Volume: 64 Issue: 1 Pages: 1-2
- DOI
  10.1111/ped.15395
- Data Source
  KAKENHI-PROJECT-21K15900
[Journal Article] Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor2021
- Author(s)
  Kataoka S, Kawashima N, Okuno Y, Muramatsu H, Miwata S, Narita K, Hamada M, Murakami N, Taniguchi R, Ichikawa D, Kitazawa H, Suzuki K, Nishikawa E, Narita A, Nishio N, Yamamoto H, Fukasawa Y, Kato T, Yamamoto H, Natsume J, Kojima S, Nishio I, Taketani T, Ohnishi H, Tahakashi Y.
- Journal Title
  
  Journal of Allergy and Clinical Immunology
  
  Volume: - Issue: 2 Pages: 639-644
- DOI
  10.1016/j.jaci.2021.03.010
- NAID
  120007192018
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K08155, KAKENHI-PROJECT-18K07840, KAKENHI-PROJECT-19K17357, KAKENHI-PROJECT-19K08297, KAKENHI-PROJECT-19K08319, KAKENHI-PROJECT-21K00249, KAKENHI-PROJECT-21K07770
[Journal Article] Phosphorylated proteome analysis of a novel germline ABL1 mutation causing an autosomal dominant syndrome with ventricular septal defect2021
- Author(s)
  Yamamoto Hidenori、Hayano Satoshi、Okuno Yusuke、Onoda Atsuto、Kato Kohji、Nagai Noriko、Fukasawa Yoshie、Saitoh Shinji、Takahashi Yoshiyuki、Kato Taichi
- Journal Title
  
  International Journal of Cardiology
  
  Volume: 326 Pages: 81-87
- DOI
  10.1016/j.ijcard.2020.10.032
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08319, KAKENHI-PROJECT-20K08155, KAKENHI-PROJECT-20K21583, KAKENHI-PROJECT-19K17324, KAKENHI-PROJECT-20H05700, KAKENHI-PROJECT-19K17357, KAKENHI-PROJECT-20K16897, KAKENHI-PROJECT-19K23823
[Journal Article] Influence of Percutaneous Occlusion of Atrial Septal Defect on Left Atrial Function Evaluated Using 2D Speckle Tracking Echocardiography2020
- Author(s)
  Suzuki Kazutaka、Kato Taichi、Koyama Satoshi、Shinohara Tsutomu、Inukai Sachiko、Sato Jun、Yamamoto Hidenori、Omori Daisuke、Yoshida Shuichiro、Takeda Sho、Nishikawa Hiroshi、Ohashi Naoki、Sakurai Hajime、Saitoh Shinji
- Journal Title
  
  Int. Heart J.
  
  Volume: 61 Issue: 1 Pages: 83-88
- DOI
  10.1536/ihj.19-173
- NAID
  130007792792
- ISSN
  1349-2365, 1349-3299
- Year and Date
  2020-01-31
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K17357
[Journal Article] Mesenchymal stem/stromal cells stably transduced with an inhibitor of CC chemokine ligand 2 ameliorate bronchopulmonary dysplasia and pulmonary hypertension2020
- Author(s)
  Suzuki Toshihiko、Sato Yoshiaki、Yamamoto Hidenori、Kato Taichi、Kitase Yuma、Ueda Kazuto、Mimatsu Haruka、Sugiyama Yuichiro、Onoda Atsuto、Saito Shigeki、Takahashi Yoshiyuki、Nakayama Takayuki、Hayakawa Masahiro
- Journal Title
  
  Cytotherapy
  
  Volume: - Issue: 4 Pages: 180-192
- DOI
  10.1016/j.jcyt.2020.01.009
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K17357, KAKENHI-PROJECT-18J01110, KAKENHI-PROJECT-17K09944, KAKENHI-PROJECT-18K15667, KAKENHI-PROJECT-19K08341, KAKENHI-PROJECT-19K17324
[Journal Article] Ventricular tachycardia and chest pain due to foreign body in the pericardium caused by self-injurious behaviour2019
- Author(s)
  Yamamoto Hidenori、Fukasawa Yoshie、Kato Taichi
- Journal Title
  
  Cardiology in the Young
  
  Volume: 29 Issue: 09 Pages: 1217-1218
- DOI
  10.1017/s1047951119001744
- NAID
  120006847450
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08319, KAKENHI-PROJECT-19K17357
[Journal Article] Prediction of postnatal clinical course in primary congenital dilated cardiomyopathy2019
- Author(s)
  Yamamoto Hidenori、Fukasawa Yoshie、Ohashi Naoki、Yokoyama Takehiko、Suzuki Kazutaka、Ota Takaya、Yasuda Kazushi、Omoya Kentaro、Takahashi Yoshiyuki、Kato Taichi
- Journal Title
  
  Pediatrics International
  
  Volume: 61 Issue: 12 Pages: 1196-1201
- DOI
  10.1111/ped.14029
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08319, KAKENHI-PROJECT-19K17357
[Journal Article] Severe fetal cardiomegaly caused by multiple non-giant placental chorioangiomas2019
- Author(s)
  Yamamoto Hidenori、Fukasawa Yoshie、Kato Taichi
- Journal Title
  
  Cardiology in the Young
  
  Volume: 29 Issue: 12 Pages: 1559-1560
- DOI
  10.1017/s1047951119002567
- NAID
  120006847449
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08319, KAKENHI-PROJECT-19K17357
[Presentation] Comprehensive genetic analysis of 9 families with hereditary WPW syndrome2023
- Author(s)
  Hidenori Yamamoto, Hidehito Inagaki, Kiyotaka Go, Yoshihito Morimoto, Yoshie Fukasawa, Hiroko Goto, Sayaka Mii, Hiroki Kurahashi, and Taichi Kato
- Organizer
  Human Genetics Asia 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K15900
[Presentation] Proteomic Analysis for the Formation of the Plexiform Lesions of a Rat Pulmonary Arterial Hypertension Model2023
- Author(s)
  Morimoto Y, Yamamoto H, Go K, Fukasawa Y, Ohashi N, Takahashi Y, Kato T.
- Organizer
  American Heart Association Scientific Sessions 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K07329
[Presentation] 長期生存し肺移植を行った非典型ACD/MPVの一例2022
- Author(s)
  齊藤明子、脇田浩正、郷清貴、森本美仁、山本英範、伊藤美春、村松友佳子、深澤佳絵、佐藤義朗、加藤太一、高橋義行、早川昌弘、安田和志、伊藤諒一
- Organizer
  第125回日本小児科学会
- Data Source
  KAKENHI-PROJECT-20K08155
[Presentation] ZC4H2機能喪失は遺伝子Xの発現調節を介して徐脈性不整脈を呈する～プロテオーム解析を用いた遺伝性不整脈の機能解析～2022
- Author(s)
  山本英範, 郷清貴, 森本美仁, 深澤佳絵, 加藤太一
- Organizer
  第55回日本小児循環器学会
- Data Source
  KAKENHI-PROJECT-21K15900
[Presentation] TBX20新規9塩基欠失が確認された遺伝性心中隔欠損の1家系2021
- Author(s)
  山本英範、早野聡、森本美仁、郷清貴、深澤佳絵、加藤太一
- Organizer
  第130回東海小児循環器談話会
- Data Source
  KAKENHI-PROJECT-19K17357
[Presentation] 新生児慢性肺疾患に合併する肺高血圧症に対する治療の検討2020
- Author(s)
  加藤太一、森本美仁、山本英範、深澤佳絵、沼口敦、伊藤美春、齊藤明子、佐藤義朗、早川昌弘
- Organizer
  第5回日本肺高血圧・肺循環学会
- Data Source
  KAKENHI-PROJECT-20K08155
[Presentation] ABL1変異は先天性心疾患を伴う症候群の原因となる～エクソーム解析と質量分析法を応用した遺伝性心室中隔欠損症の網羅的病態解明～2020
- Author(s)
  山本英範、早野聡、奥野友介、小野田淳人、加藤耕治、長井典子、深澤佳絵、齋藤伸治、高橋義行、加藤太一
- Organizer
  第56回日本小児循環器学会総会・学術集会
- Data Source
  KAKENHI-PROJECT-19K17357
[Presentation] 小児３群肺高血圧症に対する治療内容と効果の検討2020
- Author(s)
  加藤太一、深澤佳絵、山本英範、沼口敦、伊藤美春、齊藤明子、佐藤義朗、内田広夫、早川昌弘
- Organizer
  第56回日本小児循環器学会
- Data Source
  KAKENHI-PROJECT-20K08155
[Presentation] 早産児慢性肺疾患に合併する肺高血圧症のモデルラット作成および網羅的病態解明2019
- Author(s)
  山本英範、深澤佳絵、小野田淳人、三浦良介、呉尚治、沼口敦、佐藤義朗、加藤太一
- Organizer
  第55回日本小児循環器学会
- Data Source
  KAKENHI-PROJECT-19K17357

1. Kato Taichi (20422777)

# of Collaborated Projects: 3 results

# of Collaborated Products: 11 results
2. 佐藤義朗 (30435862)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
3. 郷清貴 (40908779)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
4. 深澤佳絵

# of Collaborated Projects: 0 results

# of Collaborated Products: 5 results
5. 大橋直樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Yamamoto Hidenori 山本 英範

YAMAMOTO Hidenori 山本 英範

Research Projects

Research Products

Co-Researchers

網羅的プロテオーム解析に基づいた肺高血圧症病変における新規治療ターゲットの検証

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

メタゲノム解析とオミクス解析を用いたFontan術後蛋白漏出性胃腸症の病態解明

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Mechanism analysis of a syndrome with congenital heart disease due to tyrosine kinase gene abnormalityPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

proteomic analysis of smooth muscle cell transformation in obstructive lesions of pulmonary hypertension.

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Comprehensive analysis of causative gene in familial congenital heart disease by whole exome analysisPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Dysbiosis of gut microbiota in patients with protein-losing enteropathy after the Fontan procedure2024

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Effects of General Anesthesia on the Results of Cardiac Catheterization in Pediatric Patients with Ventricular Septal Defect2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Case report: High-dose epoprostenol therapy in pediatric patients with pulmonary hypertension and developmental lung disease2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Conception by assisted reproductive technology in infants with critical congenital heart disease in Japan2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Familial cardiac septal defect due to a novel nine‐base deletion in TBX202022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Tension hemothorax 1 week after pericardiocentesis associated with thrombocytopenia2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor2021

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Phosphorylated proteome analysis of a novel germline ABL1 mutation causing an autosomal dominant syndrome with ventricular septal defect2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Influence of Percutaneous Occlusion of Atrial Septal Defect on Left Atrial Function Evaluated Using 2D Speckle Tracking Echocardiography2020

Author(s)

Journal Title

DOI

Yamamoto Hidenori 山本英範

YAMAMOTO Hidenori 山本英範