TAKAYAMA Koichiro

Affiliation and department：
Job title： Postdoctoral fellow
Other affiliations (1)：

Shiga University of Medical Science Department of Cardiovascular Medicine Visiting Resercher

Research field (2)： Genetics , Cardiology

Research theme for competitive and other funds (3)：

2021 - 2024 The elucidation of complicated genetic backgrounds and pathogenicity in patients with inherited primary arrhythmia syndromes caused by unknown etiology
2021 - 2023 疾患モデルiPS細胞を用いたKCND3変異による早期再分極症候群の病態解明
2019 - 2021 Electrophysiological analysis of pathogenesis and effective therapy for early repolarization syndrome

Papers (7)：

Shimamoto Keiko, Ohno Seiko, Kato Koichi, Takayama Koichiro, Sonoda Keiko, Fukuyama Megumi, Makiyama Takeru, Okamura Satomi, Asakura Koko, Imanishi Noriaki, et al. RYR2遺伝子変異を有する家族性CPVT患者とde Novo CPVT患者の表現型の違い(Phenotypic Differences between Familial and De Novo CPVT Patient Carrying RYR2 Variants). 日本循環器学会学術集会抄録集. 2022. 86回. OE18-7
Keiko Shimamoto, Seiko Ohno, Koichi Kato, Koichiro Takayama, Keiko Sonoda, Megumi Fukuyama, Takeru Makiyama, Satomi Okamura, Koko Asakura, Noriaki Imanishi, et al. Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1. Heart (British Cardiac Society). 2022. 108. 11. 840-847
Fukuyama Megumi, Ohno Seiko, Kato Koichi, Fujii Yusuke, Takayama Koichiro, Makiyama Takeru, Horie Minoru, Nakagawa Yoshihisa. RYR2変異を有する遺伝性特発性不整脈症候群患者における重度表現型(Severe Phenotype in RYR2 Variant Carriers with Idiopathic Primary Arrhythmia Syndromes). 日本循環器学会学術集会抄録集. 2020. 84回. FRS2-4
Fukuyama Megumi, Ohno Seiko, Ozawa Junichi, Yamamoto Yuta, Kato Koichi, Takayama Koichiro, Yagi Noriaki, Makiyama Takeru, Horie Minoru, Nakagawa Yoshihisa. カルシウムハンドリング関連遺伝子に変異を有する先天性QT延長症候群患者の重症度の変化(Variable Severity in Long QT Syndrome Patients with Mutations in Genes Related with Calcium Handling). 日本循環器学会学術集会抄録集. 2020. 84回. PE44-4
Koichiro Takayama, Seiko Ohno, Wei-Guang Ding, Takashi Ashihara, Daisuke Fukumoto, Yuko Wada, Takeru Makiyama, Hiroaki Kise, Minako Hoshiai, Hiroshi Matsuura, et al. A de novo gain-of-function KCND3 mutation in early repolarization syndrome. Heart rhythm. 2019. 16. 11. 1698-1706

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MISC (13)：

福山恵, 大野聖子, 小澤淳一, 高山幸一郎, 加藤浩一, 伊藤英樹, 青木寿明, 牧山武, 堀江稔. 学校心臓検診の問題点と課題・金沢宣言も踏まえて(Usefulness of Genetic Screening for Long QT Syndrome in the School-Based Electrocardiographic Screening Programs). 日本循環器学会学術集会抄録集. 2019. 83回. SY23-4
伊藤英樹, 村山尚, 呉林なごみ, 大野聖子, 藤居祐介, 加藤浩一, 福山恵, 高山幸一郎, 渡邉昌也, 安斉俊久, et al. Excessive Ca2+ Release from Ryanodine Receptors Underlying a RyR2 Mutation Associated with Catecholaminergic Polymorphic Ventricular Tachycardia(和訳中). 日本循環器学会学術集会抄録集. 2019. 83回. OJ05-4
福山恵, 大野聖子, 小澤淳一, 高山幸一郎, 加藤浩一, 伊藤英樹, 青木寿明, 牧山武, 堀江稔. 学校心臓検診の問題点と課題・金沢宣言も踏まえて心電図による学校検診プログラムにおけるQT延長症候群の遺伝学的スクリーニングの有用性(Usefulness of Genetic Screening for Long QT Syndrome in the School-Based Electrocardiographic Screening Programs). 日本循環器学会学術集会抄録集. 2019. 83回. SY23-4
高山幸一郎, 大野聖子, 堀江稔, 喜瀬広亮, 星合美奈子. 徐脈化によって早期再分極症候群が顕在化し、薬物治療にてVFストームを鎮静化しえた1例. 心臓. 2018. 50. Suppl.2. 244-244
高山幸一郎, 大野聖子, 芦原貴司, 喜瀬広亮, 星合美奈子, 松浦博, 堀江稔. 心臓突然死の病態解明と予知・予防(Early Repolarization Syndrome Caused by a De Novo KCND3 Gain-of-Function Mutation). 日本循環器学会学術集会抄録集. 2018. 82回. SY05-3

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Education (2)：

2015 - 2019 Shiga University of Medical Science
2001 - 2007 Shiga University of Medical Science

Professional career (1)：

Doctor of Medical Science (Shiga University of Medical Science)

Work history (4)：

2019/04 - 現在国立循環器病研究センター分子生物学部
2016/06 - 2019/03 Shiga University of Medical Science
2015/04 - 2016/05 長浜赤十字病院循環器内科
2012/04 - 2015/03 国立循環器病研究センター心臓血管内科

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