Kato Koichi 加藤浩一

Researcher Number	70736983
Other IDs
Affiliation (Current)	2025: 滋賀医科大学, 医学部, 助教
Affiliation (based on the past Project Information) *help	2018 – 2024: 滋賀医科大学, 医学部, 助教
Review Section/Research Field	Principal Investigator Basic Section 53020:Cardiology-related Except Principal Investigator Basic Section 53020:Cardiology-related / Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator ブルガダ症候群 / QT延長症候群 / 心臓突然死 / SCN5A / L型カルシウムチャネル / 先天性QT延長症候群 / イオンチャネル / カルシウム電流 / 早期再分極症候群 / 機能喪失型変異 … More / 心臓ナトリウム電流 / 心臓イオンチャネル / 遺伝性不整脈 / カルモジュリン / CALM3 / 遺伝性QT延長症候群 / SNTA1 / Brugada症候群 / ナトリウムチャネル / 心臓ナトリウムチャネル / 細胞膜イオンチャネル発現量不変 / ドミナントネガティブ効果 … More Except Principal Investigator 遺伝性不整脈 / 家族性心房細動 / 若年性心房細動 / 洞不全症候群 / 心臓突然死 / エピジェネティクス / 全ゲノムシークエンス / バイオインフォマティクス / DNA構造多型 / DNA構造異常 / long read sequencer / ゲノム構造多型 / ゲノムDNA構造異常 / 遺伝子 / 筋小胞体 / 特発性心室細動 / リアノジン / 小胞体 / 突然死 / 不整脈 / カルシウム / シミュレーション / 心室細動 / リアノジン受容体 Less

若年性/家族性心房細動における心臓関連遺伝子多型に基づいた治療アルゴリズムの構築
- Principal Investigator
  
  小澤友哉
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Shiga University of Medical Science
QT延長とブルガダ症候群の合併を来すCa2+チャネル変異の機序解明を目指す研究Principal Investigator
- Principal Investigator
  
  加藤浩一
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Shiga University of Medical Science
バイオインフォマティクスを用いた非コードDNA解析による若年突然死の発症機序解明
- Principal Investigator
  
  村田広茂
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Nippon Medical School
The elucidation of complicated genetic backgrounds and pathogenicity in patients with inherited primary arrhythmia syndromes caused by unknown etiology
- Principal Investigator
  
  大野聖子
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  National Cardiovascular Center Research Institute
The genetic analysis and underlying function of the endoplasmic reticulum membrane protein targeting inherited arrhythmogenic syndromes
- Principal Investigator
  
  Itoh Hideki
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Hiroshima University
The research project about the association between SNTA variant and Early depolarisation syndromePrincipal Investigator
- Principal Investigator
  
  Kato Koichi
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Shiga University of Medical Science
Research project for SCN5A dominant-negative mechanismPrincipal Investigator
- Principal Investigator
  
  Kato Koichi
- Project Period (FY)
  2018 – 2019
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Shiga University of Medical Science

All 2024 2023 2022 2021

All Journal Article Presentation

[Journal Article] Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome2024
- Author(s)
  Yoshinaga M, Ninomiya Y, Tanaka Y, Fukuyama M, Kato K, Ohno S, Horie M, Ogata H.
- Journal Title
  
  Circ J
  
  Volume: 88 Issue: 7 Pages: 1176-1184
- DOI
  10.1253/circj.CJ-23-0409
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2024-06-25
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-23K07528
[Journal Article] Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants2024
- Author(s)
  Kashiwa A, Itoh H, Makiyama T, Wada Y, Ozawa J, Kato K, Fukuyama M, Nakajima T, Ohno S, Horie M.
- Journal Title
  
  Heart Rhythm
  
  Volume: In press Issue: 7 Pages: 1113-1120
- DOI
  10.1016/j.hrthm.2024.02.021
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-23K06845, KAKENHI-PROJECT-23K07528, KAKENHI-PROJECT-20K08473
[Journal Article] Non-missense variants of <i>KCNH2</i> show better outcomes in type 2 long QT syndrome2023
- Author(s)
  Aizawa Takanori、Wada Yuko、Hasegawa Kanae、Huang Hai、Imamura Tomohiko、Gao Jingshan、Kashiwa Asami、Kohjitani Hirohiko、Fukuyama Megumi、Kato Koichi、Kato Eri Toda、Hisamatsu Takashi、Ohno Seiko、Makiyama Takeru、Kimura Takeshi、Horie Minoru
- Journal Title
  
  EP Europace
  
  Volume: 25 Issue: 4 Pages: 1491-1499
- DOI
  10.1093/europace/euac269
- Data Source
  KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-20K17113, KAKENHI-PROJECT-23K07575
[Journal Article] Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.2023
- Author(s)
  Gao J, Makiyama T, Yamamoto Y, Kobayashi T, Aoki H, Maurissen TL, Wuriyanghai Y, Kashiwa A, Imamura T, Aizawa T, Huang H, Kohjitani H, Nishikawa M, Chonabayashi K, Fukuyama M, Manabe H, Nakau K, Wada T, Kato K, Toyoda F, Yoshida Y, Makita N, Woltjen K, Ohno S, Kurebayashi N, Murayama T, Sakurai T, Horie M, Kimura T.
- Journal Title
  
  Circulation: Arrhythmia and Electrophysiology
  
  Volume: 16 Issue: 3 Pages: 9999-9999
- DOI
  10.1161/circep.122.011387
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K11368, KAKENHI-PROJECT-21K06781, KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-20K17113, KAKENHI-PROJECT-22K06652, KAKENHI-PROJECT-21H02920
[Journal Article] Calmodulinopathy in Japanese Children　― Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy ―2023
- Author(s)
  Megumi Fukuyama, Minoru Horie, Koichi Kato, Seiko Ohno, et al.
- Journal Title
  
  Circ J
  
  Volume: 87 Issue: 12 Pages: 1828-1835
- DOI
  10.1253/circj.CJ-23-0195
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2023-11-24
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-23K07528, KAKENHI-PROJECT-23K07575
[Journal Article] School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome2022
- Author(s)
  Fukuyama Megumi、Horie Minoru、Aoki Hisaaki、Ozawa Junichi、Kato Koichi、Sawayama Yuichi、Tanaka-Mizuno Sachiko、Makiyama Takeru、Yoshinaga Masao、Nakagawa Yoshihisa、Ohno Seiko
- Journal Title
  
  EP Europace
  
  Volume: - Issue: 9 Pages: 1496-1503
- DOI
  10.1093/europace/euab320
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-19K08555, KAKENHI-PROJECT-20K17113, KAKENHI-PROJECT-21H02888
[Journal Article] Novel CALM3 Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation Family2022
- Author(s)
  Kato Koichi、Isbell Holly M.、Fressart Veronique、Denjoy Isabelle、Debbiche Amal、Itoh Hideki、Poinsot Jacques、George Alfred L.、Coulombe Alain、Shea Madeline A.、Guicheney Pascale
- Journal Title
  
  Circulation: Arrhythmia and Electrophysiology
  
  Volume: 15 Issue: 3
- DOI
  10.1161/circep.121.010572
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-20K17113
[Journal Article] Successful Management of a Young Athlete with Type 2 Long QT Syndrome by Genotype-specific Risk Stratification and Bridging Therapy with a Wearable Cardioverter Defibrillator2022
- Author(s)
  Kojima Katsumi、Kato Koichi、Fujii Yusuke、Okuyama Yusuke、Ohno Seiko、Ozawa Tomoya、Horie Minoru、Nakagawa Yoshihisa
- Journal Title
  
  Intern. Med.
  
  Volume: 61 Issue: 8 Pages: 1179-1182
- DOI
  10.2169/internalmedicine.8093-21
- NAID
  130008150341
- ISSN
  0918-2918, 1349-7235
- Year and Date
  2022-04-15
- Language
  English
- Data Source
  KAKENHI-PROJECT-20K17113, KAKENHI-PROJECT-20K17146
[Journal Article] Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 12022
- Author(s)
  Shimamoto K, Ohno S, Kato K, Takayama K, Sonoda K, Fukuyama M, Makiyama T, Okamura S, Asakura K, Imanishi N, Kato Y, Sakaguchi H, Kamakura T, Wada M, Yamagata K, Ishibashi K, Inoue Y, Miyamoto K, Nagase S, Kusano K, Horie M, Aiba T.
- Journal Title
  
  Heart
  
  Volume: - Issue: 11 Pages: 2021-320220
- DOI
  10.1136/heartjnl-2021-320220
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-19K08555, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-21K07765, KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-19K17581
[Journal Article] An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia2022
- Author(s)
  Peltenburg, P. J. Kallas, D. Bos, J. M. Lieve, K. V. V. Franciosi, S. Roston, T. M. Denjoy, I. Sorensen, K. B. Ohno, S. Shimizu, W. Horie, M. Leenhardt, A. Ackerman, M. J. Sanatani, S. van der Werf, C. Wilde, A. A. M.
- Journal Title
  
  Circulation
  
  Volume: 145 Issue: 5 Pages: 333-344
- DOI
  10.1161/circulationaha.121.056018
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-20K17113, KAKENHI-PROJECT-19K08505
[Journal Article] Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome2022
- Author(s)
  Suzuki Keisuke、Sonoda Keiko、Aoki Hisaaki、Nakamura Yuko、Watanabe Seiichi、Yoshida Yoko、Hoshino Kenji、Ozawa Junichi、Imamura Tomohiko、Aiba Takeshi、Kato Koichi、Makiyama Takeru、Kusano Kengo、Horie Minoru、Ohno Seiko
- Journal Title
  
  JACC: Clinical Electrophysiology
  
  Volume: 8 Issue: 3 Pages: 297-305
- DOI
  10.1016/j.jacep.2022.01.007
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-19K17581
[Journal Article] Case report: Vascular graft infection due to Aspergillus species presenting with recurrent vascular occlusion2022
- Author(s)
  Tano Ayami、Kato Koichi、Seike Yoshimasa、Matsuda Hitoshi、Suzue Takashi、Kaneko Yoshihiro、Kodama Misato、Sawayama Yuichi、Miyamoto Akashi、Yagi Noriaki、Nakagawa Yoshihisa
- Journal Title
  
  BMC Cardiovascular Disorders
  
  Volume: 22 Issue: 1 Pages: 02571-73
- DOI
  10.1186/s12872-022-02571-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K17520, KAKENHI-PROJECT-20K17113
[Journal Article] Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome2021
- Author(s)
  Hirose Sayako、Murayama Takashi、Tetsuo Naoyuki、Hoshiai Minako、Kise Hiroaki、Yoshinaga Masao、Aoki Hisaaki、Fukuyama Megumi、Wuriyanghai Yimin、Wada Yuko、Kato Koichi、Makiyama Takeru、Kimura Takeshi、Sakurai Takashi、Horie Minoru、Kurebayashi Nagomi、Ohno Seiko
- Journal Title
  
  EP Europace
  
  Volume: 24 Issue: 3 Pages: 497-510
- DOI
  10.1093/europace/euab250
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-19K08555, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-19K07105, KAKENHI-PROJECT-20K17113, KAKENHI-PROJECT-19H03404
[Presentation] The dominant-negative effect of Nav 1.5 variants through channel dimerization does not play a crucial role in determining a phenotype severity2024
- Author(s)
  Koichi Kato, Ayami Tano, Hideyuki Jinzai, Daisuke Fukumoto, Toru Kubo, Seiko Ohno, Yoshihisa Nakagawa, Minoru Horie
- Organizer
  日本生理学会
- Data Source
  KAKENHI-PROJECT-23K07528
[Presentation] Genetic Aspects of Drug-induced Long QT syndrome: Ion Channel Genes and Race-Specific Variants of CYP genes2023
- Author(s)
  伊藤英樹, 加藤浩一, 中野由紀子, 平塚真弘
- Organizer
  第87回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-20K08473
[Presentation] Compound heterozygous SCN5A variants caused severe bradyarrhythmia via complex channel-channel interaction.2023
- Author(s)
  Ayami Tano1), Koichi Kato2), Hideyuki Jinzai2), Daisuke Fukumoto2), Toru Kubo 3), Seiko Ohno4), Yoshihisa Nakagawa2), Minoru Horie2)
- Organizer
  2023 日本循環器学会
- Data Source
  KAKENHI-PROJECT-20K17113
[Presentation] Correction of cryptic donor site splicing by antisense oligo nucleotides in a case of Brugada syndrome.2023
- Author(s)
  Hideyuki Jinzai1, Koichi Kato1, Takeru Makiyama2, Yuichi Sawayama1, Seiko Ohno4, Yoshihisa Nakagawa1, Minoru Horie1
- Organizer
  2023 日本循環器学会
- Data Source
  KAKENHI-PROJECT-20K17113
[Presentation] The dominant-negative effect of Loss of function Nav 1.5 variants is not a critical determinant of phenotype severity2023
- Author(s)
  K. Kato, A. Tano, H. Jinzai, T. Kubo, S. Ohno, Y. Nakagawa, M. Horie
- Organizer
  ESC Congress 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K07528
[Presentation] Calmodulinopathy is a common cause of critical cardiac phenotypes in2022
- Author(s)
  Fukuyama M, Horie M, Kato K, Ozawa T, Fujii Y, Okuyama Y, Makiyama T, Ohno S, Nakagawa Y.
- Organizer
  ESC Congress 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] Mutant Nav1.5 with dominant-negative effect does not correspond to the severe phenotype2022
- Author(s)
  Ayami Tano1), Koichi Kato2), Hideyuki Jinzai2), Daisuke Fukumoto2), Seiko Ohno3), Yoshihisa Nakagawa2), Minoru Horie2)
- Organizer
  Asia Pacific Heart Rhythm Society 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K17113
[Presentation] デスモゾーム関連遺伝子変異キャリアの小児期の特徴2022
- Author(s)
  大野　聖子, 園田桂子, 加藤浩一, 堀江稔
- Organizer
  第58回日本小児循環器学会総会・学術集会
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] Correction of SCN5A splicing error of Brugada syndrome patient by antisense oligo nucleotides2022
- Author(s)
  Koichi Kato1, Hideyuki Jinzai1, Takeru Makiyama2, Yuichi Sawayama1, Ryotaro Kida1, Ryo Kurosawa3, Masahiko Ajiro3, Seiko Ohno4, Yoshihisa Nakagawa1, Minoru Horie1
- Organizer
  Asia Pacific Heart Rhythm Society 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K17113
[Presentation] Genetic Analysis for Inherited Primary Arrhythmia Syndrome Speaker2022
- Author(s)
  Koichi Kato 1、Co-author：Megumi Fukuyama 1、Co-author：Ayami Tano 1、Co-author：Keiko Sonoda 2、Co-author： Koichiro Takayama 2、Co-author：Dimitar P Zankov 2、Co-author：Minoru Horie 1、Co-author：Takeru Makiyama 3、Co- author：Yoshihisa Nakagawa 1、Co-author：Seiko Ohno 2
- Organizer
  日本不整脈心電学会　2022
- Data Source
  KAKENHI-PROJECT-20K17113
[Presentation] Different prognosis of ARVC patients between DSG2 and PKP2 variant carriers2022
- Author(s)
  Sonoda K, Nagase S, Aiba T, Kato K, Shiga T, Kusano K, Horie M, Ohno S.
- Organizer
  ESC Congress 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] Haploinsufficient Variant of KCNH2 Cause Better Arrhythmia Outcome in Patients with Type 2 Long QT Syndrome2022
- Author(s)
  Aizawa Takanori , Wada Yuko , Makiyama Takeru , Huang Hai , Imamura Tomohiko , Gao Jingshan , Kashiwa Asami , Kohjitani Hirohiko , Kato Koichi , Ohno Seiko , Kimura Takeshi , Horie Minoru
- Organizer
  日本循環器学会
- Data Source
  KAKENHI-PROJECT-20K17113
[Presentation] Early onset of heart failure in Japanese ARVC patients with pathogenic desmosomal gene variants2021
- Author(s)
  Sonoda K, Nagase S, Aiba T, Fukuyama M, Kato K, Kusano K, Horie M, Ohno S
- Organizer
  European Society of Cardiology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] A Synonymous SCN5A Variant p.E446E Causing Brugada Syndrome via Cryptic Donor Site Splicing2021
- Author(s)
  Yuichi Sawayama、Koichi Kato、Masahiko Ajiro、 Ryo Kurosawa、Megumi Fukuyama、Seiko Ohno、 Yoshihisa Nakagawa、Minoru Horie
- Organizer
  第85回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-20K17113
[Presentation] LMNA missense mutation causes nonsense-mediated mRNA decay and severe dilated cardiomyopathy.2021
- Author(s)
  Koichi Kato , Seiko Ohno , Keiko Sonoda , Takeru Makiyama , Tomoya Ozawa , Yoshihisa Nakagawa , Minoru Horie
- Organizer
  日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-20K17113
[Presentation] 日本人カテコラミン誘発多形性心室頻拍患者における遺伝子変異頻度とその特徴2021
- Author(s)
  大野聖子、園田桂子、福山恵、加藤浩一、堀江稔.
- Organizer
  日本人類遺伝学会第66回大会
- Data Source
  KAKENHI-PROJECT-21H02888

1. 大野聖子 (20610025)

# of Collaborated Projects: 3 results

# of Collaborated Products: 8 results
2. 牧山武 (30528302)

# of Collaborated Projects: 3 results

# of Collaborated Products: 6 results
3. 堀江稔 (90183938)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
4. 相庭武司 (40574348)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
5. 福山恵 (60625771)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
6. Itoh Hideki (30402738)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
7. 竹島浩 (70212024)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. ZANKOV DimitarP (20631295)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. 園田桂子 (90824417)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
10. 高山幸一郎 (20816988)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. Wang Qi (70756767)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. 村田広茂 (30594014)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. 清水渉 (50399606)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 小澤友哉 (20584395)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 豊田太 (90324574)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. KOBAYASHI Takuya

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
17. 国広なごみ

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. 八木典章

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kato Koichi 加藤 浩一

Research Projects

Research Products

Co-Researchers

若年性/家族性心房細動における心臓関連遺伝子多型に基づいた治療アルゴリズムの構築

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

QT延長とブルガダ症候群の合併を来すCa2+チャネル変異の機序解明を目指す研究Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

バイオインフォマティクスを用いた非コードDNA解析による若年突然死の発症機序解明

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

The elucidation of complicated genetic backgrounds and pathogenicity in patients with inherited primary arrhythmia syndromes caused by unknown etiology

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

The genetic analysis and underlying function of the endoplasmic reticulum membrane protein targeting inherited arrhythmogenic syndromes

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

The research project about the association between SNTA variant and Early depolarisation syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Research project for SCN5A dominant-negative mechanismPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome2024

Author(s)

Journal Title

DOI

ISSN

Year and Date

Language

Data Source

[Journal Article] Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants2024

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Non-missense variants of <i>KCNH2</i> show better outcomes in type 2 long QT syndrome2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Calmodulinopathy in Japanese Children ― Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy ―2023

Author(s)

Journal Title

DOI

ISSN

Year and Date

Language

Data Source

[Journal Article] School-based routine screenings of electrocardiograms for the diagnosis of long QT syndrome2022

Author(s)

Journal Title

Kato Koichi 加藤浩一

[Journal Article] Calmodulinopathy in Japanese Children　― Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy ―2023