日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Phenotypic Severity of SCN5A-Related Bradycardia Is Independent of Dominant-Negative and Coupled Gating Effects

SCN5A相关性心动过缓的表型严重程度与显性负效应和耦合门控效应无关。

期刊:Circulation-Arrhythmia and Electrophysiology
影响因子:9.8
doi:10.1161/CIRCEP.125.014270
Tano, Ayami; Kato, Koichi; Yamauchi, Kohei; Jinzai, Hideyuki; Iguchi, Takafumi; Toyoda, Futoshi; Baba, Yuichi; Kubo, Toru; Ohno, Seiko; Makiyama, Takeru; Nakagawa, Yoshihisa; Horie, Minoru
发表日期：2026
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A Genome-Wide Association Study Reveals Desmoglein-2 Predominance in Japanese Arrhythmogenic Cardiomyopathy

全基因组关联研究揭示，桥粒芯蛋白-2在日本致心律失常性心肌病中占主导地位

期刊:Journal of Arrhythmia
影响因子:1.7
doi:10.1002/joa3.70273
Ishikawa, Taisuke; Sonehara, Kyuto; Sonoda, Keiko; Hayashi, Kenshi; Kato, Koichi; Nagase, Satoshi; Kusano, Kengo; Aiba, Takeshi; Horie, Minoru; Ohno, Seiko; Okada, Yukinori; Makita, Naomasa
心血管
心肌病
发表日期：2026
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A diagnostic challenge of advanced-stage cardiac Fabry disease without left ventricular hypertrophy: a case report

晚期心脏法布里病伴无左心室肥厚的诊断挑战：病例报告

期刊:European Heart Journal - Case Reports
影响因子:0.8
doi:10.1093/ehjcr/ytag234
Suzuki, Masataka; Yoshigai, Yuko; Hashimura, Hiromi; Aiba, Takeshi; Ohno, Seiko; Osue, Tsuyoshi; Eizawa, Hiroshi; Tanaka, Hidekazu
发表日期：2026
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Novel KCNH2 and SLC4A3 variants in short QT syndrome: Clinical phenotypes and antiarrhythmic drug response

短QT综合征中新型KCNH2和SLC4A3变异：临床表型和抗心律失常药物反应

期刊:HeartRhythm Case Reports
影响因子:
doi:10.1016/j.hrcr.2026.01.015
Fukue, Noriko; Ueyama, Takeshi; Ohno, Seiko; Kanemoto, Masashi; Kato, Koichi; Akase, Hideaki; Okuda, Shinichi; Nakao, Fumiaki; Ikeda, Yasuhiro
KCNH2
发表日期：2026
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Long-term follow-up of patients with catecholaminergic polymorphic ventricular tachycardia related to a novel CALM2 variant

对患有与新型 CALM2 变异相关的儿茶酚胺敏感性多形性室性心动过速的患者进行长期随访

期刊:Journal of Cardiology Cases
影响因子:
doi:10.1016/j.jccase.2025.09.003
Ohno, Seiko; Kato, Koichi; Fukuyama, Megumi; Hirono, Keiichi; Nishida, Kunihiro; Horie, Minoru
发表日期：2026
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SCN5A variant type-dependent risk prediction in Brugada syndrome

SCN5A变异类型依赖性风险预测在布鲁加达综合征中的作用

期刊:Europace
影响因子:7.4
doi:10.1093/europace/euaf024
Aizawa, Takanori; Makiyama, Takeru; Huang, Hai; Imamura, Tomohiko; Fukuyama, Megumi; Sonoda, Keiko; Kato, Koichi; Hisamatsu, Takashi; Nakamura, Yuko; Hoshino, Kenji; Ozawa, Junichi; Suzuki, Hiroshi; Yasuda, Kazushi; Aoki, Hisaaki; Kurita, Takashi; Yoshida, Yoko; Suzuki, Tsugutoshi; Nakamura, Yoshihide; Ogawa, Yoshiharu; Yamagami, Shintaro; Morita, Hiroshi; Yuasa, Shinsuke; Fukuda, Masakazu; Ono, Makoto; Kondo, Hidekazu; Takahashi, Naohiko; Ohno, Seiko; Nakagawa, Yoshihisa; Ono, Koh; Horie, Minoru
发表日期：2025
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Case report: Severe arrhythmogenic cardiomyopathy in a young girl with compound heterozygous DSG2 and MYBPC3 variants with a 6-year follow-up

病例报告：一名年轻女孩患有严重的致心律失常性心肌病，其携带DSG2和MYBPC3复合杂合变异，并进行了6年随访。

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2025.1545561
Hashizume, Ryotaro; Imai, Hiroshi; Ohashi, Hiroyuki; Sawada, Hirofumi; Yodoya, Noriko; Okamoto, Ryuji; Dohi, Kaoru; Kasai, Chika; Kitajima, Takahito; Fujiwara, Takumi; Mochiki, Ikuyo; Nakatani, Kaname; Wakita, Sachiko; Ohno, Seiko; Kato, Koichi; Okugawa, Yoshinaga; Mitani, Yoshihide; Hirayama, Masahiro
心血管
心肌病
发表日期：2025
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Episodic long-lasting atrial standstill associated with an SCN5A variant resulting in atrial pacing failure: Is an atrial lead necessary for familial atrial standstill?

与 SCN5A 变异相关的阵发性长期心房静止导致心房起搏失败：家族性心房静止是否需要心房导线？

期刊:HeartRhythm Case Reports
影响因子:
doi:10.1016/j.hrcr.2024.10.004
Ohya, Hiroaki; Inaba, Osamu; Inamura, Yukihiro; Kato, Koichi; Ohno, Seiko; Sasano, Tetsuo
发表日期：2025
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SCN5A mutation-associated sick sinus syndrome revealed by atrial flutter in a pediatric patient

儿童患者出现心房扑动，揭示了SCN5A基因突变相关的病态窦房结综合征

期刊:Journal of Cardiology Cases
影响因子:
doi:10.1016/j.jccase.2025.03.001
Takeda, Yoshikatsu; Fujita, Shuhei; Yachi, Yusuke; Honda, Mariko; Iwata, Mayu; Sakumura, Naoto; Ueno, Kazuyuki; Miyashita, Kengo; Futatani, Takeshi; Usuda, Keisuke; Chikata, Akio; Usuda, Kazuo; Nishida, Keigo; Araki, Raita; Kato, Koichi; Ohno, Seiko
发表日期：2025
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Atypical Holt-Oram syndrome: Early-onset sick sinus syndrome in a Japanese family with a novel TBX5 mutation, Q469

非典型霍尔特-奥拉姆综合征：日本一个家族中出现早发性病态鼻窦综合征，该家族携带一种新的TBX5基因突变，Q469

期刊:Journal of Cardiology Cases
影响因子:
doi:10.1016/j.jccase.2025.03.003
Nomura, Yoshihiro; Ishikawa, Taisuke; Ohno, Seiko; Makita, Naomasa; Horie, Minoru; Naruse, Hiroyuki; Koshikawa, Masayuki; Nishimura, Asuka; Motoike, Yuji; Harada, Masahide; Sobue, Yoshihiro; Watanabe, Eiichi; Izawa, Hideo
TBX5
发表日期：2025
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