J-GLOBAL ID:201801008681123309   Update date: Nov. 25, 2021

KATO Koichi

カトウ コウイチ | KATO Koichi
Affiliation and department:
Research field  (1): Cardiology
Research keywords  (3): Long QT syndrome ,  Laminopathy ,  遺伝性不整脈
Research theme for competitive and other funds  (4):
  • 2021 - 2024 The elucidation of complicated genetic backgrounds and pathogenicity in patients with inherited primary arrhythmia syndromes caused by unknown etiology
  • 2020 - 2023 The genetic analysis and underlying function of the endoplasmic reticulum membrane protein targeting inherited arrhythmogenic syndromes
  • 2020 - 2023 SNTA1変異による早期再分極症候群発症メカニズムの解明に関する研究
  • 2018 - 2020 Research project for SCN5A dominant-negative mechanism
Papers (19):
  • Sayako Hirose, Takashi Murayama, Naoyuki Tetsuo, Minako Hoshiai, Hiroaki Kise, Masao Yoshinaga, Hisaaki Aoki, Megumi Fukuyama, Yimin Wuriyanghai, Yuko Wada, et al. Loss-of-function mutations in cardiac ryanodine receptor channel cause various types of arrhythmias including long QT syndrome. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology. 2021
  • Daisuke Tomioka, Koichi Kato, Tomoya Ozawa, Kenji Kodama, Hiroaki Takahashi, Kenichi Dochi, Yoshiki Ueno, Yoshihisa Nakagawa. Diverse phenotypic expression associated with the same genetic variant in female heterozygote patients of Anderson-Fabry disease: a case series. European Heart Journal - Case Reports. 2021. 5. 2. ytaa538
  • 小野 朱美, 森 一博, 武井 美貴子, 岡田 朝美, 佐々木 亜由美, 庄野 実希, 木下 ゆき子, 早渕 康信, 大野 聖子, 加藤 浩一. compound heterozygoteのため若年発症した重症不整脈源性右室心筋症の1例. 日本小児科学会雑誌. 2020. 124. 12. 1795-1795
  • Koichi Kato, Seiko Ohno, Keiko Sonoda, Megumi Fukuyama, Takeru Makiyama, Tomoya Ozawa, Minoru Horie. LMNA Missense Mutation Causes Nonsense-mediated mRNA Decay and Severe Dilated Cardiomyopathy. Circulation: Genomic and Precision Medicine. 2020
  • Kato K, Ozawa T, Ohno S, Nakagawa Y, Horie M. Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose. BMC cardiovascular disorders. 2020. 20. 1. 315-315
Lectures and oral presentations  (13):
  • LMNA missense mutation causes nonsense-mediated mRNA decay and severe dilated cardiomyopathy.
  • Splice site mutation of LMNA causes severe dilated cardiomyopathy via strong dominant reduction of total lamin expression
  • A Novel CALM3 Variant Associated With a Mild LQTS Phenotype
  • 致死性遺伝性不整脈に対する遺伝子診断 -当院における現状と課題-
    (日本心臓病学会 2019)
  • A Novel SCN5A Frameshift Mutation Caused Progressive Cardiac Conduction Disorder and Multiform Ventricular Arrhythmia in A Case with A Surgical-Repair History of Congenital Heart Disease.
Association Membership(s) (4):
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