Rchr
J-GLOBAL ID：201801008681123309   Update date: May. 06, 2025

KATO Koichi

カトウ コウイチ | KATO Koichi
Affiliation and department：
Shiga University of Medical Science

About Shiga University of Medical Science


Research field  (1)： Cardiology
Research keywords  (4)： Brugada syndrome ,  Long QT syndrome ,  Laminopathy ,  遺伝性不整脈
Research theme for competitive and other funds  (9)：
  • 2023 - 2026 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
  • 2022 - 2025 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
  • 2023 - 2024 Naチャネルのカップリングが及ぼす心臓興奮伝導への影響に関する 研究
  • 2023 - 2024 山内進循環器病研究助成
  • 2021 - 2024 The elucidation of complicated genetic backgrounds and pathogenicity in patients with inherited primary arrhythmia syndromes caused by unknown etiology
Show all
Papers (59)：
  • Takanori Aizawa, Takeru Makiyama, Hai Huang, Tomohiko Imamura, Megumi Fukuyama, Keiko Sonoda, Koichi Kato, Takashi Hisamatsu, Yuko Nakamura, Kenji Hoshino, et al. SCN5A variant type-dependent risk prediction in Brugada syndrome. Europace. 2025
  • Tomohiko Imamura, Takeru Makiyama, Junichi Ozawa, Keiko Sonoda, Koichi Kato, Takanori Aizawa, Asami Kashiwa, Jingshan Gao, Hai Huang, Yuta Yamamoto, et al. Sex-specific clinical course of young patients with Brugada syndrome. European Heart Journal. 2025
  • Toshika Hata, Koichi Kato, Kenichi Kamiya, Yusuke Okuyama, Yusuke Fujii, Noriaki Yagi, Tomoya Ozawa, Yoshihisa Nakagawa. Author's reply to Optimal Pacemaker Implantation in Patients with Isolated Persistent Left Superior Vena Cava. Internal medicine (Tokyo, Japan). 2024. 63. 17. 2479-2479
  • Makiyama Takeru, Gao Jingshan, Yamamoto Yuta, Kobayashi Takuya, Takanori Aizawa, Huang Hai, Kasahiwa Asami, Imamura Tomohiko, Aoki Hisaaki, Kato Koichi, et al. 心疾患の発症機構解明と新たな治療戦略 iPS細胞を用いたカルモジュリン遺伝子異常による致死性不整脈疾患の病態解明(Elucidation of the pathogenesis of heart diseases and development of new therapeutic strategies Modeling calmodulin-related life-threatening arrhythmias using iPS cells). The Journal of Physiological Sciences. 2024. 74. Suppl.2. 99-99
  • Aizawa Takanori, Makiyama Takeru, Huang Hai, Imamura Tomohiko, Fukuyama Megumi, Sonoda Keiko, Kato Koichi, Ohno Seiko, Horie Minoru, Ono Koh. Fatal Arrhythmic Events are Higher in Non-missense than in Missense Variants in SCN5A-positive Brugada Syndrome(タイトル和訳中). 日本循環器学会学術集会抄録集. 2024. 88回. FRS5-3
ｍore...
MISC (20)：
  • HUANG Hai, MAKIYAMA Takeru, SHIRAI Manabu, WAKABAYASHI Masaki, YOSHIDA Morikatsu, NISHIUCHI Suguru, MORIUCHI Kenji, GAO Jing Shan, KASHIWA Asami, IMAMURA Tomohiko, et al. Histological Characteristics of a Rat Model of Cardiac Laminopathy Carrying Lmna p.S143P. 日本循環器学会学術集会(Web). 2024. 88th
  • 榮智徳, 大張靖幸, 石本尚美, 吉林護, 桑形尚吾, 山原康佑, 佐々木裕紀, 山原真子, 加藤浩一, 中川義久, et al. ペースメーカー留置により腎機能の回復が見られた薬剤誘発徐脈性心房細動の1例. 日本腎臓学会誌(Web). 2022. 64. 6-W
  • GAO Jingshan, MAKIYAMA Takeru, YAMAMOTO Yuta, KOBAYASHI Takuya, AOKI Hisaaki, MAURISSEN L Thomas, KASHIWA Asami, IMAMURA Tomohiko, AIZAWA Takanori, HUANG Hai, et al. Novel CPVT-Associated Calmodulin Mutation Activating RyR2 Channels Causes Robust Arrhythmogenicity in iPS Cell Model. 日本不整脈心電学会学術大会プログラム・抄録集(Web). 2022. 68th
  • IMAMURA Tomohiko, MAKIYAMA Takeru, OZAWA Junichi, HUANG Hai, AIZAWA Takanori, GAO Jingshan, KASHIWA Asami, KOHJITANI Hirohiko, KATO Koichi, AOKI Hisaaki, et al. Clinical Characteristics and Risk Stratification in Pediatric Brugada Syndrome. 日本不整脈心電学会学術大会プログラム・抄録集(Web). 2022. 68th
  • 今村知彦, 牧山武, 小澤淳一, 相澤卓範, 柏麻美, 糀谷泰彦, 加藤浩一, 青木寿明, 鈴木博, 園田桂子, et al. Clinical Aspects of Brugada Syndrome in Children: The Impact of Gender and Age on the Prognosis. 日本循環器学会学術集会(Web). 2022. 86th
ｍore...
Lectures and oral presentations  (24)：
  • Variable penetrance of KCNJ2 pathogenic variants in Japanese Andersen-Tawil syndrome patients: Insights into the molecular mechanism
    (Japanese Circulation Society annual meeting 2025)
  • 若手教育セッション:初めてみる遺伝性不整脈
    (日本不整脈心電学会 2024)
  • A long-term follow-up study of Japanese Andersen-Tawil syndrome patients.
    (Japanese Heart Rhythm Society Annual MeetingSociety 2024)
  • Is Andersen-Tawil syndrome a malignant arrhythmic disease? A long-term follow-up study of Japanese ATS patients.
    (2024)
  • The dominant-negative effect of Nav 1.5 variants through channel dimerization does not play a crucial role in determining a phenotype severity
    (2024)
ｍore...
Education (2)：
  • 2010 - 2014 Shiga University of Medical Science Graduate School of Medicine
  • 1999 - 2005 Shiga University of Medical Science Undergraduate School of Medicine Faculty of Medicine
Professional career (1)：
  • Ph. D (Shiga University of Medical Science)
Work history (8)：
  • 2018/04 - 現在 Shiga University of Medical Science
  • 2016/03 - 2018/03 INSERM, Université Pierre et Marie Curie UMRS1166 Ingénieur de recherche
  • 2015/10 - 2016/02 Shiga University of Medical Science
  • 2014/06 - 2015/09 Shiga University of Medical Science
  • 2014/04 - 2014/05 滋賀医科大学附属病院 循環器内科 医員
Show all
Committee career (2)：
  • 2021/12 - 現在 日本不整脈心電学会 不整脈専門医試験問題作成委員
  • 2020 - 現在 日本循環器学会近畿支部 評議員
Awards (3)：
  • 2023/05 - 公益財団法人循環器病研究振興財団 山内進循環器病研究助成
  • 2016 - l’Institut de France Le Foulon Delalande bourse de recherche Etude de variants de la protéine SAP97 dans le syndrome de Brugada.
  • 2015 - 日本心電学会 海外留学助成
Association Membership(s) (4)：
日本人類遺伝学会 ,  JAPANESE HEART RHYTHM SOCIETY ,  THE JAPANESE SOCIETY OF INTERNAL MEDICINE ,  The Japanese Circulation Society
※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

Return to Previous Page

TOP

BOTTOM