Ohno Seiko 大野聖子

… Alternative Names

OHNO Seiko 大野聖子

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Researcher Number	20610025
Other IDs	https://orcid.org/0000-0003-1209-8896
Affiliation (Current)	2025: 国立研究開発法人国立循環器病研究センター, オープンイノベーションセンター, 部長
Affiliation (based on the past Project Information) *help	2023 – 2024: 国立研究開発法人国立循環器病研究センター, オープンイノベーションセンター, 部長 2017 – 2023: 国立研究開発法人国立循環器病研究センター, 研究所, 部長 2017: 滋賀医科大学, 学内共同利用施設等, 特任講師 2015 – 2017: 滋賀医科大学, アジア疫学研究センター, 特任講師 2014: 滋賀医科大学, アジア疫学研究センター, 講師 … More 2014: 滋賀医科大学, 学内共同利用施設等, その他 2013: 滋賀医科大学, 医学部, 特任講師 2012: 滋賀医科大学, 医学部, 特任助教 Less
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics Except Principal Investigator Basic Section 53020:Cardiology-related / Cardiovascular medicine / Basic Section 48020:Physiology-related / Basic Section 52050:Embryonic medicine and pediatrics-related / Medium-sized Section 58:Society medicine, nursing, and related fields / Epidemiology and preventive medicine / Hygiene and public health
Keywords	Principal Investigator RYR2 / 先天性QT延長症候群 / 遺伝子変異 / 不整脈 / QT延長症候群 / 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 … More / 遺伝性不整脈 / リアノジン / カルシウムイオンチャネル / LQT15 / LQT8 / LQTS / Calmodulin / CACNA1c / CALM2 / CALM1 / CACNA1C / カルモジュリン / カルシウムチャネル / リアノジンレセプターチャネル / カテコラミン誘発性多型性心室頻拍 / 心臓リアノジンチャネル / カテコラミン誘発性多形成心室頻拍 / カテコラミン誘発性多形性心室頻拍 / 家族性突然死症候群 / パッチクランプ / 交感神経刺激 / 運動負荷 / 失神 / 運動誘発性 / カリウムチャネル … More Except Principal Investigator 遺伝性不整脈 / エピジェネティクス / QT延長症候群 / 全ゲノムシークエンス / バイオインフォマティクス / 心臓突然死 / カテコラミン誘発性多型性心室頻拍 / リアノジン受容体遺伝子 / カテコラミン誘発多型性心室頻拍 / 潜在性動脈硬化 / 脳萎縮 / 疫学 / 認知症 / 循環器・高血圧 / 遺伝子 / マウス / リモデリング / 炎症 / 徐脈 / HCN4チャネル / ジフテリア毒素 / 膜電位感受性色素 / パッチクランプ / 心房細動 / 家族性心房細動 / 若年性心房細動 / 洞不全症候群 / 機能実験 / 遺伝子検査 / 疾患遺伝子関連 / 拡張型心筋症 / モデル / 遺伝子変異 / iPS細胞 / TTN / RBM20 / TCAP / z-ライン / 心筋症 / Desmoglein 2 / Desmosome / Arrhythmia / Cardiomyopathy / Mouse model / DSG2 / knock-in mouse / dsg2 / ARVC / Cell free DNA / 胎児診断 / Speckle tracking法 / 等容拡張時間 / 先天性QT延長症候群 / 胎児心エコー / 心磁図 / 胎児 / 脳委縮 / 日本人女性 / 日本人一般女性 / ゲノム解析 / 遺伝性心疾患 / リアノジン受容体 / リアノジン受容体遺伝子異常 / 不整脈 / DNA構造多型 / ゲノムDNA構造異常 / エピゲノム / ロングリードシークエンサー / 社会医学 / 細菌 / 腸内細菌叢 / コホート研究 / 腸内細菌 / 予防 / 一般女性 / 女性 / 動脈硬化 / 後天性 / 多型 / 薬剤性 / QT延長 / 薬剤 / 突然死 / 個別化医療 / ブルガダ症候群 / SCN5A / コピー数変動 / 機能解析 / 遺伝学 / 高血圧 / 循環器 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
Electrical remodeling of atrial myocyte induced by chronic inflammation or bradycardia and its role in the atrial fibrillation.
- Principal Investigator
  
  鷹野誠
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 48020:Physiology-related
- Research Institution
  Kurume University
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
遺伝的背景が不明なカテコラミン誘発多型性心室頻拍患者における遺伝子構造多型の検索
- Principal Investigator
  
  福山恵
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Shiga University of Medical Science
The elucidation of complicated genetic backgrounds and pathogenicity in patients with inherited primary arrhythmia syndromes caused by unknown etiologyPrincipal Investigator
- 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
Development of a non-invasive early diagnosis method for fetal long QT syndrome
- Principal Investigator
  
  Kato Yoshiaki
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  National Cardiovascular Center Research Institute
Elucidation of the pathology in ARVC caused by Japanese-specific DSG2 mutations using knock-in mice models: searching for the therapeutic targets
- Principal Investigator
  
  Zankov Dimitar P
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  National Cardiovascular Center Research Institute
臨床予後予測に向けたiPS細胞由来心筋症モデルによる特発性拡張型心筋症の病態解明
- Principal Investigator
  
  藍智彦
- Project Period (FY)
  2021 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Juntendo University
Elucidation of pathology of inherited cardiac disease caused by mutations in ryanodine receptor gene
- Principal Investigator
  
  Fukuyama Megumi
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Shiga University of Medical Science
Whole-genome sequencing analysis using epigenetics databases to elucidate novel mechanisms of inherited arrhythmia syndromes
- Principal Investigator
  
  Murata Hiroshige
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Nippon Medical School
Elucidation of pathogenesis and clinical characteristics, establishment of the therapy in patients with LQTS caused by calcium related gene variantsPrincipal Investigator
- Principal Investigator
  
  Ohno Seiko
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  National Cardiovascular Center Research Institute
Investigation of relationship between inherited arrhythmias and epigenetics
- Principal Investigator
  
  Hattori Tetsuhisa
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  National Cardiovascular Center Research Institute
Subclinical atherosclerosis and brain atrophy in general Japanese women : the second phase survey
- Principal Investigator
  
  Miura Katsuyuki
- Project Period (FY)
  2018 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 58:Society medicine, nursing, and related fields
- Research Institution
  Shiga University of Medical Science
The risk stratification of drug-induced long QT syndrome upon the underlying genetics
- Principal Investigator
  
  Itoh Hideki
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Hiroshima University
  Shiga University of Medical Science
Effective diagnosis and establishment of the therapy for catecholaminergic polymorphic ventricular tachycardiaPrincipal Investigator
- Principal Investigator
  
  Ohno Seiko
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  National Cardiovascular Center Research Institute
  Shiga University of Medical Science
Multilateral Research on the Mechanisms of Inherited Arrhythmias
- Principal Investigator
  
  Horie Minoru
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Shiga University of Medical Science
Subclinical atherosclerosis and brain atrophy in the general Japanese women
- Principal Investigator
  
  Miura Katsuyuki
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Hygiene and public health
- Research Institution
  Shiga University of Medical Science
Gut microbiota and sublinical atherosclerosis in general population
- Principal Investigator
  
  Arima Hisatomi
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Epidemiology and preventive medicine
- Research Institution
  Fukuoka University
  Shiga University of Medical Science
Mechanism of arrhythmo-genesis by exercise stress in long QT syndrome patientsPrincipal Investigator
- Principal Investigator
  
  OHNO Seiko
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Shiga University of Medical Science

All 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 Other

All Journal Article Presentation Book

[Book] 循環器診療コンプリート　心筋症　「不整脈原性右室心筋症」2021
- Author(s)
  大野聖子、北岡裕章
- Total Pages
  272
- Publisher
  学研メディカル秀潤社
- ISBN
  9784780904079
- Data Source
  KAKENHI-PROJECT-18K07875
[Book] 最新ガイドラインに基づく循環器疾患診療指針2021-'22　その他の遺伝性不整脈（CPVT, QT短縮症候群, PCCD, ARVC）2020
- Author(s)
  大野聖子、清水　渉
- Total Pages
  384
- Publisher
  総合医学社
- ISBN
  9784883787241
- Data Source
  KAKENHI-PROJECT-18K07875
[Book] 循環器ジャーナル　心電図診断スキルアップ2017
- Author(s)
  大野聖子
- Total Pages
  9
- Publisher
  医学書院
- ISBN
  9784260029438
- Data Source
  KAKENHI-PROJECT-15K09689
[Book] Chapter 4: Genetic basis for Early Repolarization Syndrome. In J Wave Syndromes: Brugada and Early Repolarization Syndromes 1st ed.2017
- Author(s)
  Horie M, Sonoda K, Ohno S
- Publisher
  Antzelevitch and G-X Yan, Springer, Co
- Data Source
  KAKENHI-PROJECT-15H04818
[Book] 心筋症における心臓突然死を予測する2016
- Author(s)
  大野聖子
- Total Pages
  70
- Publisher
  医歯薬出版
- Data Source
  KAKENHI-PROJECT-15H04818
[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] 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] Continuous Bayesian variant interpretation accounts for incomplete penetrance among Mendelian cardiac channelopathies2023
- Author(s)
  O’Neill Matthew J.、Sala Luca、Denjoy Isabelle、Wada Yuko、Kozek Krystian、Crotti Lia、Dagradi Federica、Kotta Maria-Christina、Spazzolini Carla、Leenhardt Antoine、Salem Joe-Elie、Kashiwa Asami、Ohno Seiko、Tao Ran、Roden Dan M.、Horie Minoru、Extramiana Fabrice、Schwartz Peter J.、Kroncke Brett M.
- Journal Title
  
  Genetics in Medicine
  
  Volume: 25 Issue: 3 Pages: 100355-100355
- DOI
  10.1016/j.gim.2022.12.002
- Data Source
  KAKENHI-PROJECT-21H02888
[Journal Article] Non-missense variants of KCNH2 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] Pandora will never regret having opened her box: reappraisal of genes associated with CPVT and SQTS2022
- Author(s)
  Horie M, Ohno S, Ai T.
- Journal Title
  
  Eur Heart J.
  
  Volume: 43 Issue: 15 Pages: 1511-1513
- DOI
  10.1093/eurheartj/ehab794
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K08135
[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] 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] 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] 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] Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly.2022
- Author(s)
  Ozawa J, Ohno S, Melgari D, Wang Q, Fukuyama M, Toyoda F, Makiyama T, Yoshinaga M, Suzuki H, Saitoh A, Ai T, Horie M.
- Journal Title
  
  Sci Rep
  
  Volume: 12 Issue: 1 Pages: 18984-18984
- DOI
  10.1038/s41598-022-23512-2
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08900, KAKENHI-PROJECT-21K06781, KAKENHI-PROJECT-21K08135, KAKENHI-PROJECT-22K07840, KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-21H02888
[Journal Article] Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants2021
- Author(s)
 Kozek K, Wada Y, Makita N, Ishikawa T, Crotti L, Kroncke BM, et al.
- Journal Title
 
 Circulation: Genomic and Precision Medicine
 
 Volume: 14 Issue: 4
- DOI
 10.1161/circgen.120.003289
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
 KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-20K08416
[Journal Article] Impact of the T-wave characteristics on distinguishing arrhythmogenic right ventricular cardiomyopathy from healthy children2021
- Author(s)
  Imamura Tomohiko、Sumitomo Naokata、Muraji Shota、Yasuda Kazushi、Nishihara Eiki、Iwamoto Mari、Tateno Shigeru、Doi Shozaburo、Hata Tadayoshi、Kogaki Shigetoyo、Horigome Hitoshi、Ohno Seiko、Ichida Fukiko、Nagashima Masami、Makiyama Takeru、Yoshinaga Masao
- Journal Title
  
  International Journal of Cardiology
  
  Volume: 323 Pages: 168-174
- DOI
  10.1016/j.ijcard.2020.08.088
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07813, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K02505, KAKENHI-PROJECT-18K07785
[Journal Article] Familial sick sinus syndrome possibly associated with novel SCN5A mutation diagnosed in pregnancy2021
- Author(s)
  Abe Ichitaro、Wang Pu、Takahashi Masaki、Ohno Seiko、Ono Katsushige、Takahashi Naohiko
- Journal Title
  
  HeartRhythm Case Reports
  
  Volume: 7 Issue: 2 Pages: 117-122
- DOI
  10.1016/j.hrcr.2020.11.016
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Journal Article] Impact of Medical Castration on Malignant Arrhythmias in Patients With Prostate Cancer.2021
- Author(s)
  Hasegawa K, Ito H, Kaseno K, Miyazaki S, Shiomi Y, Tama N, Ikeda H, Ishida K, Uzui H, Ohno S, Horie M, Yokoyama O, Tada H.
- Journal Title
  
  J Am Heart Assoc.
  
  Volume: 10 Issue: 5
- DOI
  10.1161/jaha.120.017267
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K09521, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-19K17553
[Journal Article] Long-Read Sequence Confirmed a Large Deletion Including MYH6 and MYH7 in an Infant of Atrial Septal Defect and Atrial Arrhythmias2021
- Author(s)
 Sonoda Keiko、Ishihara Haruko、Sakazaki Hisanori、Suzuki Tsugutoshi、Horie Minoru、Ohno Seiko
- Journal Title
 
 Circulation: Genomic and Precision Medicine
 
 Volume: 14 Issue: 4
- DOI
 10.1161/circgen.120.003223
- NAID
 120007146546
- Peer Reviewed
- Data Source
 KAKENHI-PROJECT-21H02888
[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
[Journal Article] An NGS-based genotyping in LQTS; minor genes are no longer minor2020
- Author(s)
  Ohno Seiko、Ozawa Junichi、Fukuyama Megumi、Makiyama Takeru、Horie Minoru
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 65 Issue: 12 Pages: 1083-1091
- DOI
  10.1038/s10038-020-0805-z
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-19K08555, KAKENHI-PROJECT-18K07875
[Journal Article] High Prevalence of Late-Appearing T-Wave in Patients With Long QT Syndrome Type 82020
- Author(s)
  Fukuyama M, Ohno S,Ozawa J, Kato K, Makiyama T, Nakagawa Y, Horie M.
- Journal Title
  
  Circ J
  
  Volume: 84 Issue: 4 Pages: 559-568
- DOI
  10.1253/circj.CJ-19-1101
- NAID
  130007815680
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2020-03-25
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08555, KAKENHI-PROJECT-16H06277, KAKENHI-PROJECT-18K07875
[Journal Article] SCN5A mutation identified in a patient with short-coupled variant of torsades de pointes2020
- Author(s)
  Sonoda Keiko、Ohno Seiko、Shimizu Yukiko、Kaitani Kazuaki、Makiyama Takeru、Nakagawa Yoshihisa、Horie Minoru
- Journal Title
  
  Pacing and Clinical Electrophysiology
  
  Volume: - Issue: 5 Pages: 456-461
- DOI
  10.1111/pace.13924
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K17581, KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-18K07875
[Journal Article] Postoperative supraventricular tachycardia and polymorphic ventricular tachycardia due to a novel SCN5A variant: a case report of a rare comorbidity that is difficult to diagnose2020
- Author(s)
  Kato Koichi、Ozawa Tomoya、Ohno Seiko、Nakagawa Yoshihisa、Horie Minoru
- Journal Title
  
  BMC Cardiovascular Disorders
  
  Volume: 20 Issue: 1
- DOI
  10.1186/s12872-020-01601-2
- NAID
  120006871010
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07875
[Journal Article] Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome2020
- Author(s)
  Lahrouchi N, Tadros R, Crotti L, Makiyama T et al.
- Journal Title
  
  Circulation
  
  Volume: 142 Issue: 4 Pages: 324-338
- DOI
  10.1161/circulationaha.120.045956
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416
[Journal Article] Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense Mutation2020
- Author(s)
 Nozaki Y, Kato Y, Uike K, Yamamura K, Kikuchi M, Yasuda M, Ohno S, Horie M, Murayama T, Kurebayashi N, Horigome H
- Journal Title
 
 Circ J
 
 Volume: 84 Issue: 2 Pages: 226-234
- DOI
 10.1253/circj.CJ-19-0720
- NAID
 130007789920
- ISSN
 1346-9843, 1347-4820
- Year and Date
 2020-01-24
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-18K07813, KAKENHI-PROJECT-19K07105, KAKENHI-PROJECT-19K19820, KAKENHI-PROJECT-16K08507, KAKENHI-PROJECT-16H06277, KAKENHI-PROJECT-19H03404, KAKENHI-PROJECT-18K07875
[Journal Article] LMNA Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated Cardiomyopathy2020
- Author(s)
  Kato Koichi、Ohno Seiko、Sonoda Keiko、Fukuyama Megumi、Makiyama Takeru、Ozawa Tomoya、Horie Minoru
- Journal Title
  
  Circulation: Genomic and Precision Medicine
  
  Volume: 13 Issue: 5 Pages: 435-443
- DOI
  10.1161/circgen.119.002853
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-19K08555, KAKENHI-PROJECT-19K17581, KAKENHI-PROJECT-18K07875
[Journal Article] Propranolol Attenuates Late Sodium Current in a Long QT Syndrome Type 3-Human Induced Pluripotent Stem Cell Model2020
- Author(s)
  Hirose Sayako、Makiyama Takeru、Melgari Dario、Yamamoto Yuta、Wuriyanghai Yimin、Yokoi Fumika、Nishiuchi Suguru、Harita Takeshi、Hayano Mamoru、Kohjitani Hirohiko、Gao Jingshan、Kashiwa Asami、Nishikawa Misato、Wu Jie、Yoshimoto Jun、Chonabayashi Kazuhisa、Ohno Seiko、Yoshida Yoshinori、Horie Minoru、Kimura Takeshi
- Journal Title
  
  Frontiers in Cell and Developmental Biology
  
  Volume: 8 Pages: 761-761
- DOI
  10.3389/fcell.2020.00761
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-19K17595, KAKENHI-PROJECT-17H04176
[Journal Article] SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families2020
- Author(s)
  3.Wijeyeratne YD, Tanck MW, Mizusawa Y, Batchvarov V, Barc J, Crotti L, et al.
- Journal Title
  
  Circulation: Genomic and Precision Medicine
  
  Volume: 13 Issue: 6
- DOI
  10.1161/circgen.120.002911
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416
[Journal Article] Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls2020
- Author(s)
  2.Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, et al.
- Journal Title
  
  Genetics in Medicine
  
  Volume: 23 Issue: 1 Pages: 47-58
- DOI
  10.1038/s41436-020-00946-5
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08100, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18K15407, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-20K08416
[Journal Article] Identification of transmembrane protein 168 mutation in familial Brugada syndrome.2020
- Author(s)
  Shimizu A, Zankov DP, Sato A, Komeno M, Toyoda F, Yamazaki S, Makita T, Noda T, Ikawa M, Asano Y, Miyashita Y, Takashima S, Morita H, Ishikawa T, Makita N, Hitosugi M, Matsuura H, Ohno S, Horie M, Ogita H.
- Journal Title
  
  FASEB Journal
  
  Volume: 34 Issue: 5 Pages: 6399-6417
- DOI
  10.1096/fj.201902991r
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08075, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-ORGANIZER-19H05749, KAKENHI-PROJECT-17F17418, KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K08627, KAKENHI-PROJECT-17K08657, KAKENHI-PROJECT-16H06276, KAKENHI-PROJECT-19K09408, KAKENHI-PROJECT-20K08489, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08033, KAKENHI-PROJECT-19H03652, KAKENHI-PROJECT-18K19547, KAKENHI-PROJECT-21K08119
[Journal Article] Mutant KCNJ3 and KCNJ5 potassium channels as novel molecular targets in bradyarrhythmias and atrial fibrillation.2019
- Author(s)
  Yamada N, Asano Y, Fujita M, Yamazaki S, Inanobe A, Matsuura N, Kobayashi H, Ohno S, Ebana Y, Tsukamoto O, Ishino S, Takuwa A, Kioka H, Yamashita T, Hashimoto N, Zankov DP, Shimizu A, Asakura M, Asanuma H, Kato H, Nishida Y, Miyashita Y, Shinomiya H, Naiki N, Hayashi K, Makiyama T, Ogita H, et al.
- Journal Title
  
  Circulation
  
  Volume: In press Issue: 18 Pages: 2157-2169
- DOI
  10.1161/circulationaha.118.036761
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08627, KAKENHI-PROJECT-17K08657, KAKENHI-PROJECT-17K09577, KAKENHI-PROJECT-17K09578, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08100, KAKENHI-PROJECT-17F17418, KAKENHI-PROJECT-15K09111, KAKENHI-PROJECT-15KK0302, KAKENHI-PROJECT-17K07251, KAKENHI-PROJECT-18K08033, KAKENHI-PROJECT-19K08538, KAKENHI-ORGANIZER-17H06391, KAKENHI-PROJECT-17H01560, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-17H04018, KAKENHI-PROJECT-16H06276, KAKENHI-PROJECT-18H04074, KAKENHI-PROJECT-18H02803, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K19547, KAKENHI-PROJECT-19H03652
[Journal Article] Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry2019
- Author(s)
  Crotti Lia、Spazzolini Carla、Tester David J、Ohno Seiko、Ackerman Michael J、Schwartz Peter J, et al.
- Journal Title
  
  European Heart Journal
  
  Volume: 40 Issue: 35 Pages: 2964-2975
- DOI
  10.1093/eurheartj/ehz311
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-16H06277, KAKENHI-PROJECT-18H02808
[Journal Article] Transcriptional cofactor Vgll2 is required for functional adaptations of skeletal muscle induced by chronic overload2019
- Author(s)
  Honda Masahiko、Tsuchimochi Hirotsugu、Hitachi Keisuke、Ohno Seiko
- Journal Title
  
  Journal of Cellular Physiology
  
  Volume: 印刷中 Issue: 9 Pages: 15809-15824
- DOI
  10.1002/jcp.28239
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K08646, KAKENHI-PROJECT-18K07875
[Journal Article] Dynamic QT Changes in Long QT Syndrome Type 82019
- Author(s)
  Harada Mizuki、Suzuki Hiroshi、Ohno Seiko、Ozawa Junichi、Saitoh Akihiko、Horie Minoru
- Journal Title
  
  Circ J
  
  Volume: 83 Issue: 7 Pages: 1614
- DOI
  10.1253/circj.CJ-18-0984
- NAID
  130007666938
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2019-06-25
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07875
[Journal Article] Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest2019
- Author(s)
  van der Werf Christian、Lieve Krystien V、Seiko Ohno、Leenhardt Antoine、Ackerman Michael J、Wilde Arthur A、et al.
- Journal Title
  
  European Heart Journal
  
  Volume: 40 Issue: 35 Pages: 2953-2961
- DOI
  10.1093/eurheartj/ehz309
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-19K08566, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-16H06277
[Journal Article] A de novo gain-of-function KCND3 mutation in early repolarization syndrome2019
- Author(s)
  Takayama Koichiro、Ohno Seiko、Ding Wei-Guang、Ashihara Takashi、Fukumoto Daisuke、Wada Yuko、Makiyama Takeru、Kise Hiroaki、Hoshiai Minako、Matsuura Hiroshi、Horie Minoru
- Journal Title
  
  Heart Rhythm
  
  Volume: 16 Issue: 11 Pages: 1698-1706
- DOI
  10.1016/j.hrthm.2019.05.033
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-19K17593, KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-16H06277, KAKENHI-PROJECT-18H02808
[Journal Article] Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia2019
- Author(s)
  Dharmawan T, Nakajima T, Ohno S, Iizuka T, Tamura S, Kaneko Y, Horie M, Kurabayashi M.
- Journal Title
  
  Ann Noninvasive Electrocardiol
  
  Volume: - Issue: 3
- DOI
  10.1111/anec.12623
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09487, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-17K09495
[Journal Article] Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients2019
- Author(s)
  Shimizu Wataru、Makimoto Hisaki、Yamagata Kenichiro、Kamakura Tsukasa、Wada Mitsuru、Miyamoto Koji、Inoue-Yamada Yuko、Okamura Hideo、Ishibashi Kohei、Noda Takashi、Nagase Satoshi、Miyazaki Aya、Sakaguchi Heima、Shiraishi Isao、Makiyama Takeru、Ohno Seiko、Itoh Hideki、et al
- Journal Title
  
  JAMA Cardiology
  
  Volume: in press Issue: 3 Pages: 246-254
- DOI
  10.1001/jamacardio.2018.4925
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-18K08100, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15KK0302, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-17K09524, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08075, KAKENHI-PROJECT-19K08566, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18H02808
[Journal Article] Long QT syndrome with a de novo CALM2 mutation in a 4‐year‐old boy2019
- Author(s)
  Fujita Shuhei、Nakagawa Ryo、Futatani Takeshi、Igarashi Noboru、Fuchigami Takamasa、Saito Shinsuke、Ohno Seiko、Horie Minoru、Hatasaki Kiyoshi
- Journal Title
  
  Pediatrics International
  
  Volume: 61 Issue: 9 Pages: 852-858
- DOI
  10.1111/ped.13959
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-17K09495
[Journal Article] Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1: A Modified Schwartz Score2018
- Author(s)
  Ozawa J, Ohno S, Fujii Y, Makiyama T, Suzuki H, Saitoh A, Horie M
- Journal Title
  
  Circulation Journal
  
  Volume: in press
- NAID
  130007438837
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09689
[Journal Article] A hERG mutation E1039X produced a synergistic lesion on IKs together with KCNQ1-R174C mutation in a LQTS family with three compound mutations2018
- Author(s)
  Wu Jie、Mizusawa Yuka、Ohno Seiko、Ding Wei-Guang、Higaki Takashi、Wang Qi、Kohjitani Hirohiko、Makiyama Takeru、Itoh Hideki、Toyoda Futoshi、James Andrew F.、Hancox Jules C.、Matsuura Hiroshi、Horie Minoru
- Journal Title
  
  Scientific Reports
  
  Volume: 8 Issue: 1 Pages: 3129-3129
- DOI
  10.1038/s41598-018-21442-6
- NAID
  120006529715
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-18K07875
[Journal Article] Home blood pressure variability and subclinical atherosclerosis in multiple vascular beds2018
- Author(s)
  Hisamatsu Takashi、Miura Katsuyuki、Ohkubo Takayoshi、Arima Hisatomi、Fujiyoshi Akira、Satoh Atsushi、Kadota Aya、Zaid Maryam、Takashima Naoyuki、Ohno Seiko、Horie Minoru、Ueshima Hirotsugu
- Journal Title
  
  Journal of Hypertension
  
  Volume: 36 Issue: 11 Pages: 2193-2203
- DOI
  10.1097/hjh.0000000000001810
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-17K15827
[Journal Article] A challenge for mutation specific risk stratification in long QT syndrome type 12018
- Author(s)
  Yagi Noriaki、Itoh Hideki、Hisamatsu Takashi、Tomita Yukinori、Kimura Hiromi、Fujii Yusuke、Makiyama Takeru、Horie Minoru、Ohno Seiko
- Journal Title
  
  Journal of Cardiology
  
  Volume: 18 Issue: 1 Pages: 30012-1
- DOI
  10.1016/j.jjcc.2017.12.011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-18K07875
[Journal Article] Autonomic Function and QT Interval During Night-Time Sleep in Infant Long QT Syndrome2018
- Author(s)
  Yoshinaga Masao、Kucho Yu、Ushinohama Hiroya、Ishikawa Yuichi、Ohno Seiko、Ogata Hiromitsu
- Journal Title
  
  Circ J
  
  Volume: 82 Issue: 8 Pages: 2152-2159
- DOI
  10.1253/circj.CJ-18-0048
- NAID
  130007419286
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2018-07-25
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07875
[Journal Article] A tryptophan residue in the caffeine-binding site of the ryanodine receptor regulates Ca2+ sensitivity2018
- Author(s)
  Murayama Takashi、Ogawa Haruo、Kurebayashi Nagomi、Ohno Seiko、Horie Minoru、Sakurai Takashi
- Journal Title
  
  Communications Biology
  
  Volume: 1 Issue: 1 Pages: 98-98
- DOI
  10.1038/s42003-018-0103-x
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K08507, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-15K08243
[Journal Article] Differential Diagnosis Between Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome Type 1　― Modified Schwartz Score ―2018
- Author(s)
  Ozawa Junichi、Ohno Seiko、Fujii Yusuke、Makiyama Takeru、Suzuki Hiroshi、Saitoh Akihiko、Horie Minoru
- Journal Title
  
  Circ J
  
  Volume: 82 Issue: 9 Pages: 2269-2276
- DOI
  10.1253/circj.CJ-17-1032
- NAID
  130007438837
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2018-08-24
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-16K09499
[Journal Article] Association of zygotic piRNAs derived from paternal P elements with hybrid dysgenesis in Drosophila melanogaster2018
- Author(s)
  Wakisaka Keiko Tsuji、Ichiyanagi Kenji、Ohno Seiko、Itoh Masanobu
- Journal Title
  
  Mobile DNA
  
  Volume: 9 Issue: 1 Pages: 7-7
- DOI
  10.1186/s13100-018-0110-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K08098, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-16H04817
[Journal Article] Catecholaminergic polymorphic ventricular tachycardia managed as orthostatic dysregulation and epilepsy in 11‐ and 15‐year‐old sisters2018
- Author(s)
  Fujita Shuhei、Nishida Keigo、Irabu Hitoshi、Nakagawa Ryo、Futatani Takeshi、Igarashi Noboru、Usuda Kazuo、Nagata Yoshiki、Ohno Seiko、Horie Minoru、Hatasaki Kiyoshi
- Journal Title
  
  Pediatrics International
  
  Volume: 60 Issue: 11 Pages: 998-1001
- DOI
  10.1111/ped.13688
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875
[Journal Article] Novel roles of Drosophila FUS and Aub responsible for piRNA biogenesis in neuronal disorders.2018
- Author(s)
  Wakisaka KT, Tanaka R, Hirashima T, Muraoka Y, Azuma Y, Yoshida H, Tokuda T, Asada S, Suda K, Ichiyanagi K, Ohno S, Itoh M, Yamaguchi M.
- Journal Title
  
  Brain Res.
  
  Volume: 18 Pages: 30646-30652
- DOI
  10.1016/j.brainres.2018.12.028
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K07385, KAKENHI-PROJECT-17K07500, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-16K07346, KAKENHI-PROJECT-16K19519, KAKENHI-PROJECT-19K06659
[Journal Article] Copy number variations of SCN5A in Brugada syndrome2018
- Author(s)
  Sonoda Keiko、Ohno Seiko、Ozawa Junichi、Hayano Mamoru、Hattori Tetsuhisa、Kobori Atsushi、Yahata Mitsuhiko、Aburadani Isao、Watanabe Seiichi、Matsumoto Yuichi、Makiyama Takeru、Horie Minoru
- Journal Title
  
  Heart Rhythm
  
  Volume: - Issue: 8 Pages: 1179-1188
- DOI
  10.1016/j.hrthm.2018.03.033
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-18K07875
[Journal Article] Population pharmacokinetics and pharmacogenomics of apixaban in Japanese adult patients with atrial fibrillation.2018
- Author(s)
  Ueshima S, Hira D, Kimura Y, Fujii R, Tomitsuka C, Yamane T, Tabuchi Y, Ozawa T, Itoh H, Ohno S, Horie M, Terada T, Katsura T.
- Journal Title
  
  Br. J. Clin. Pharmacol.
  
  Volume: - Issue: 6 Pages: 1301-1312
- DOI
  10.1111/bcp.13561
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K15504, KAKENHI-PROJECT-17K15528, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K06766, KAKENHI-PROJECT-18K06782, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-15K08114
[Journal Article] Complex aberrant splicing in the induced pluripotent stem cell?derived cardiomyocytes from a patient with long QT syndrome carrying KCNQ1-A344Aspl mutation2018
- Author(s)
  Wuriyanghai Yimin、Makiyama Takeru、Sasaki Kenichi、Kamakura Tsukasa、Yamamoto Yuta、Hayano Mamoru、Harita Takeshi、Nishiuchi Suguru、Chen Jiarong、Kohjitani Hirohiko、Hirose Sayako、Yokoi Fumika、Gao Jingshan、Chonabayashi Kazuhisa、Watanabe Ken、Ohno Seiko、Yoshida Yoshinori、Kimura Takeshi、Horie Minoru
- Journal Title
  
  Heart Rhythm
  
  Volume: 15 Issue: 10 Pages: 1566-1574
- DOI
  10.1016/j.hrthm.2018.05.028
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K15847, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17H04176, KAKENHI-PROJECT-18H02808
[Journal Article] A novel CACNA1C mutation identified in a patient with Timothy syndrome without syndactyly exerts both marked loss-and-gain of function effects2018
- Author(s)
  Ozawa Junichi、Ohno Seiko、Saito Hideki、Saitoh Akihiko、Matsuura Hiroshi、Horie Minoru
- Journal Title
  
  HeartRhythm Case Reports
  
  Volume: in press Issue: 7 Pages: 273-277
- DOI
  10.1016/j.hrcr.2018.03.003
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875
[Journal Article] Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry2018
- Author(s)
 14.Nakajima K, Aiba T, Makiyama T, Nishiuchi S, Ohno S, Kato K, Yamamoto Y, Doi T, Shizuta S, Onoue K, Yagihara N, Ishikawa T, Watanabe I, Kawakami H, Oginosawa Y, Murakoshi N, Nogami A, Aonuma K, Saito Y, Kimura T, Yasuda S, Makita N, Shimizu W, Horie M, Kusano K.
- Journal Title
 
 Circ J
 
 Volume: 82 Issue: 11 Pages: 2707-2714
- DOI
 10.1253/circj.CJ-18-0339
- NAID
 40021697176
- ISSN
 1346-9843, 1347-4820
- Year and Date
 2018-10-25
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18K15847, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894
[Journal Article] Prediagnostic electrocardiographic and echocardiographic findings of biopsy‐proven hypertrophic cardiomyopathy2018
- Author(s)
  Seki Shunji、Yamashita Erika、Tanoue Kazuyuki、Nuruki Norihito、Sonoda Masahiro、Ohno Seiko、Ishibashi‐Ueda Hatsue、Tanaka Yuji、Yoshinaga Masao
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: 34 Issue: 6 Pages: 643-646
- DOI
  10.1002/joa3.12110
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07875
[Journal Article] Electrical storm in an infant with short-coupled variant of torsade de pointes2018
- Author(s)
  Kise Hiroaki、Ohno Seiko、Kono Yosuke、Yoshizawa Masashi、Harama Daisuke、Okafuji Asami、Toda Takako、Koizumi Keiichi、Hoshiai Minako、Sugita Kanji、Horie Minoru
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: 34 Issue: 3 Pages: 315-318
- DOI
  10.1002/joa3.12071
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875
[Journal Article] Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome2018
- Author(s)
  Fukumoto Daisuke、Ding Wei-Guang、Wada Yuko、Fujii Yusuke、Ichikawa Mari、Takayama Koichiro、Fukuyama Megumi、Kato Koichi、Itoh Hideki、Makiyama Takeru、Omatsu-Kanbe Mariko、Matsuura Hiroshi、Horie Minoru、Ohno Seiko
- Journal Title
  
  Journal of Cardiology
  
  Volume: 71 Issue: 4 Pages: 401-408
- DOI
  10.1016/j.jjcc.2017.10.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-17K15999
[Journal Article] Bradycardia Is a Specific Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Induced by RYR2 Mutations2018
- Author(s)
 Miyata Kazuaki、Ohno Seiko、Itoh Hideki、Horie Minoru
- Journal Title
 
 Intern. Med.
 
 Volume: 57 Issue: 13 Pages: 1813-1817
- DOI
 10.2169/internalmedicine.9843-17
- NAID
 130007387124
- ISSN
 0918-2918, 1349-7235
- Year and Date
 2018-07-01
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-18K07875
[Journal Article] Three cases of catecholaminergic polymorphic ventricular tachycardia with prolonged QT intervals including two cases of compound mutations2018
- Author(s)
  Saito Aki、Ohno Seiko、Nuruki Norihito、Nomura Yuichi、Horie Minoru、Yoshinaga Masao
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: 34 Issue: 3 Pages: 291-293
- DOI
  10.1002/joa3.12053
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875
[Journal Article] Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.2017
- Author(s)
  Seki A, Ishikawa T, Daumy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau AE, Thollet A, Fouchard S, Bonnaud S, Parent P, Shibata Y, Perrin JP, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura KI, Redon R, Schott JJ, Makita N.
- Journal Title
  
  J Am Coll Cardiol.
  
  Volume: 70 Issue: 3 Pages: 358-370
- DOI
  10.1016/j.jacc.2017.05.039
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15K15311
[Journal Article] Macro-pro-B-type natriuretic peptide (proBNP) and hidden macro-N-terminal proBNP:Case report.2017
- Author(s)
  Nakagawa Y, Nishikimi T, Sakai H, Ohno S, Kinoshita H, Inazumi H, Moriuchi K, Kuwahara K, Horie M, Kimura T.
- Journal Title
  
  Clinical Biochemistry
  
  Volume: 52 Pages: 148-152
- DOI
  10.1016/j.clinbiochem.2017.10.019
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K09498, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-17H04174, KAKENHI-PROJECT-15K09138, KAKENHI-PROJECT-16K15442, KAKENHI-PROJECT-18K08103
[Journal Article] Genotype-phenotype correlation of SCN5A mutation for clinical and electrocardiographic characteristics of probands with Brugada syndrome: Japanese Multicenter Registry.2017
- Author(s)
  Yamagata K, Horie M, et al.
- Journal Title
  
  Circulation
  
  Volume: 印刷中 Issue: 23 Pages: 0-0
- DOI
  10.1161/circulationaha.117.027983
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26461130, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15KK0302, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K09082, KAKENHI-PROJECT-15K09689
[Journal Article] Refractory ventricular fibrillations after surgical repair of atrial septal defects in a patient with CACNA1C gene mutation - case report2017
- Author(s)
  Kojima Ai、Shikata Fumiaki、Okamura Toru、Higaki Takashi、Ohno Seiko、Horie Minoru、Uchita Shunji、Kawanishi Yujiro、Namiguchi Kenji、Yasugi Takumi、Izutani Hironori
- Journal Title
  
  J Cardiothorac Surg.
  
  Volume: 12 Issue: 1 Pages: 118-118
- DOI
  10.1186/s13019-017-0683-4
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04818
[Journal Article] Elimination of ventricular arrhythmia in catecholaminergic polymorphic ventricular tachycardia by targeting “catecholamine-sensitive area”: a dominant-subordinate relationship between origin sites of bidirectional ventricular premature contractions.2017
- Author(s)
  Shirai Y, Horie M, et al.
- Journal Title
  
  PACE
  
  Volume: 印刷中 Issue: 5 Pages: 600-604
- DOI
  10.1111/pace.13006
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09689
[Journal Article] Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygote.2017
- Author(s)
  Fujii Y, Horie M, et al.
- Journal Title
  
  J Cardiol
  
  Volume: 印刷中 Issue: 1 Pages: 74-79
- DOI
  10.1016/j.jjcc.2016.09.010
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-17K09495
[Journal Article] Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.2017
- Author(s)
  Ishikawa T, Horie M, et al.
- Journal Title
  
  Heart Rhythm
  
  Volume: 印刷中 Issue: 5 Pages: 717-724
- DOI
  10.1016/j.hrthm.2017.01.020
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09680, KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-15K15311
[Journal Article] Allele-specific Ablation Rescues Electrophysiological Abnormalities in a Human iPS Cell Model of Long-QT Syndrome with a CALM2 Mutation.2017
- Author(s)
  Yamamoto Y, Horie M, et al.
- Journal Title
  
  Human Molecular Genetics
  
  Volume: 印刷中 Issue: 9 Pages: 1670-1677
- DOI
  10.1093/hmg/ddx073
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05297
[Journal Article] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.2017
- Author(s)
  Nishiuchi S, Makiyama T, Aiba T, Nakajima K, Hirose S, Kohjitani H, Yamamoto Y, Harita T, Hayano M, Wuriyanghai Y, Chen J, Sasaki K, Yagihara N, Ishikawa T, Onoue K, Murakoshi N, Watanabe I, Ohkubo K, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, et.al
- Journal Title
  
  Circ Cardiovasc Genet.
  
  Volume: 6 Issue: 6
- DOI
  10.1161/circgenetics.116.001603
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09421, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PLANNED-26115008, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-17H06806, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15K15311
[Journal Article] Cardiac conduction defects and brugada syndrome: A Family with overlap syndrome carrying a nonsense SCN5A mutation.2017
- Author(s)
  Aoki H, Nakamura T, Horie M, Ohno S, Makiyama T, Takemura T
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: 33 Issue: 1 Pages: 35-39
- DOI
  10.1016/j.joa.2016.05.007
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Journal Article] Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy2017
- Author(s)
  Wada Yuko、Ohno Seiko、Aiba Takeshi、Horie Minoru
- Journal Title
  
  Mol Genet Genomic Med.
  
  Volume: 5 Issue: 6 Pages: 639-651
- DOI
  10.1002/mgg3.311
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09689
[Journal Article] Development of a Patient-Derived Induced Pluripotent Stem Cell Model for the Investigation of SCN5A-D1275N-Related Cardiac Sodium Channelopathy2017
- Author(s)
 Hayano M, Makiyama T
- Journal Title
 
 Circ J
 
 Volume: 81 Issue: 12 Pages: 1783-1791
- DOI
 10.1253/circj.CJ-17-0064
- NAID
 130006219109
- ISSN
 1346-9843, 1347-4820
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-17K09860, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-17H04177, KAKENHI-PROJECT-17H06806
[Journal Article] Inherited catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation.2016
- Author(s)
  Watanabe T, Ohno S, Shirai M, Endoh A, Hongo T, Ueta I, Yoshimoto J
- Journal Title
  
  Pediatr Int
  
  Volume: 58 Issue: 6 Pages: 512-515
- DOI
  10.1111/ped.12910
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15H04818
[Journal Article] Cardiac Sodium Channel Mutation Associated with Epinephrine-Induced QT Prolongation and Sinus Node Dysfunction.2016
- Author(s)
  Chen J, Makiyama T, Wuriyanghai Y, Ohno S, Sasaki K, Hayano M, Harita T, Nishiuchi S, Yamamoto Y, Ueyama T, Shimizu A, Horie M, Kimura T.
- Journal Title
  
  Heart Rhythm.
  
  Volume: 13 Pages: 289-298
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Journal Article] Quantitative Analysis of PKP2 and Neighboring Genes in a Patient with Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Heterozygous PKP2 Deletion.2016
- Author(s)
  Sonoda K, Ohno S, Horie M, et al.
- Journal Title
  
  Europace
  
  Volume: 未定 Pages: 644-650
- DOI
  10.1093/europace/euw038
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15K15306, KAKENHI-PROJECT-16K09421, KAKENHI-PLANNED-26115008
[Journal Article] Patient-Specific Human Induced Pluripotent Stem Cell Model Assessed with Electrical Pacing Validates S107 as a Potential Therapeutic Agent for Catecholaminergic Polymorphic Ventricular Tachycardia2016
- Author(s)
  Sasaki K, Makiyama T, Yoshida Y, Wuriyanghai Y, Kamakura T, Nishiuchi S, Hayano M, Harita T, Yamamoto Y, Kohjitani H, Hirose S, Chen J, Kawamura M, Ohno S, Itoh H, Takeuchi A, Matsuoka S, Miura M, Sumitomo N, Horie M, Yamanaka S, Kimura T
- Journal Title
  
  PLoS One
  
  Volume: 11 Issue: 10 Pages: e0164795-e0164795
- DOI
  10.1371/journal.pone.0164795
- NAID
  120005860036
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04674, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26291019, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-16K09499
[Journal Article] Multigenerational Inheritance of Long QT Syndrome Type 2 in a Japanese Family2016
- Author(s)
  Ichikawa M, Ohno S, Fujii Y, Ozawa J, Sonoda K, Fukuyama M, Kato K, Kimura H, Itoh H, Hayashi H, Horie M.
- Journal Title
  
  Intern. Med.
  
  Volume: 55 Issue: 3 Pages: 259-262
- DOI
  10.2169/internalmedicine.55.6014
- NAID
  130005122603
- ISSN
  0918-2918, 1349-7235
- Language
  English
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15K19375, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406
[Journal Article] A type 2 ryanodine receptor variant associated with reduced Ca2+ release and short-coupled torsade de pointe ventricular arrhythmia.2016
- Author(s)
  Fujii Y, Horie M, et al.
- Journal Title
  
  Heart Rhythm
  
  Volume: 14 Issue: 1 Pages: 98-107
- DOI
  10.1016/j.hrthm.2016.10.015
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K08243, KAKENHI-PROJECT-16K08507, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15K09689
[Journal Article] Pediatric Cohort With Long QT Syndrome　– KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms –2016
- Author(s)
 Ozawa, J. Ohno, S. Horie M, et al.
- Journal Title
 
 Circ J
 
 Volume: 80 Issue: 3 Pages: 696-702
- DOI
 10.1253/circj.CJ-15-0933
- NAID
 130005128459
- ISSN
 1346-9843, 1347-4820
- Language
 English
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
 KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406
[Journal Article] LMNA cardiomyopathy detected in Japanese arrhythmogenic right ventricular cardiomyopathy cohort.2016
- Author(s)
  Kato K, Takahashi N, Fujii Y, Umehara A, Nishiuchi S, Makiyama T, Ohno S, Horie M
- Journal Title
  
  J Cardiol
  
  Volume: 印刷中 Issue: 4 Pages: 346-51
- DOI
  10.1016/j.jjcc.2015.10.013
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-16K09499
[Journal Article] Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction.2016
- Author(s)
  Chen J, Makiyama T, Wuriyanghai Y, Ohno S, Sasaki K, Hayano M, Harita T, Nishiuchi S, Yamamoto Y, Ueyama T, Shimizu A, Horie M, Kimura T.
- Journal Title
  
  Heart Rhythm
  
  Volume: 13(1) Issue: 1 Pages: 289-298
- DOI
  10.1016/j.hrthm.2015.08.021
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-15H04818
[Journal Article] Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Associated With Ryanodine Receptor (RyR2) Gene Mutations　– Long-Term Prognosis After Initiation of Medical Treatment –2016
- Author(s)
  Kawata H, Horie M, et al.
- Journal Title
  
  Circ J
  
  Volume: 80 Issue: 9 Pages: 1907-1915
- DOI
  10.1253/circj.CJ-16-0250
- NAID
  130005406854
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09689
[Journal Article] The genetic background of arrhythmogenic right ventricular cardiomyopathy2016
- Author(s)
  Seiko Ohno
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: 未定 Issue: 5 Pages: 398-403
- DOI
  10.1016/j.joa.2016.01.006
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15H04818
[Journal Article] Quantitative Analysis of PKP2 and Neighboring Genes in a Patient with Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Heterozygous PKP2 Deletion.2016
- Author(s)
  Sonoda K, Ohno S, Otsuki S, Kato K, Fukuyama M, Yagihara N, Watanabe H, Hayashi H, Minamino T, Horie M.
- Journal Title
  
  Europace. Mar
  
  Volume: 22
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Journal Article] The genetics underlying acquired long QT syndrome: impact for genetic screening.2016
- Author(s)
  Itoh H, Crotti L, Aiba T, Spazzolini C, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M.
- Journal Title
  
  European Heart Journal
  
  Volume: 37 (18) Issue: 18 Pages: 1456-1464
- DOI
  10.1093/eurheartj/ehv695
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K15311, KAKENHI-PUBLICLY-25136727, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26461056, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15KK0302
[Journal Article] A Common Mutation of Long QT Syndrome Type 1 in Japan2015
- Author(s)
  Itoh H, Dochi K, Shimizu W, Denjoy I, Ohno S, Aiba T, Kimura H, Kato K, Fukuyama M, Hasagawa K, Schulze-Bahr E, Guicheney P, Horie M.
- Journal Title
  
  Circ J
  
  Volume: 79 Issue: 9 Pages: 2026-2030
- DOI
  10.1253/circj.CJ-15-0342
- NAID
  130005095315
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15K19375, KAKENHI-PROJECT-15H04818
[Journal Article] Efficacy and safety of flecainide for ventricular arrhythmias in patients with Andersen-Tawil syndrome with KCNJ2 mutations.2015
- Author(s)
  Miyamoto K, Aiba T, Kimura H, Hayashi H, Ohno S, Yasuoka C, Tanioka Y, Tsuchiya T, Yoshida Y, Hayashi H, Tsuboi I, Nakajima I, Ishibashi K, Okamura H, Noda T, Ishihara M, Anzai T, Yasuda S, Miyamoto Y, Kamakura S, Kusano K, Ogawa H, Horie M, Shimizu W.
- Journal Title
  
  Heart Rhythm
  
  Volume: 12 Issue: 3 Pages: 596-603
- DOI
  10.1016/j.hrthm.2014.12.009
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591083, KAKENHI-PROJECT-24591086, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15H04818
[Journal Article] Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients.2015
- Author(s)
  Seiko Ohno, Kanae Hasegawa, Minoru Horie
- Journal Title
  
  PlosOne
  
  Volume: 10 Issue: 6 Pages: 6-6
- DOI
  10.1371/journal.pone.0131517
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15H04818
[Journal Article] Mosaic KCNJ2 mutation in Andersen-Tawil syndrome: targeted deep sequencing is useful for the detection of mosaicism.2015
- Author(s)
  Hasegawa K, Ohno S, Kimura H, Itoh H, Makiyama T, Yoshida Y, Horie M.
- Journal Title
  
  Clin Genet
  
  Volume: 87 Issue: 3 Pages: 279-83
- DOI
  10.1111/cge.12357
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-26461068, KAKENHI-PROJECT-15H04818
[Journal Article] The Genetics Underlying Acquired Long QT Syndrome. Impact on Management.2015
- Author(s)
  Itoh H, Crotti L, Aiba T, Spazzplini C, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M.
- Journal Title
  
  European Heart Journal
  
  Volume: 28
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Journal Article] Novel SCN10A Variants Associated with Brugada Syndrome.2015
- Author(s)
  Fukuyama M, Ohno S, Makiyama T, Horie M.
- Journal Title
  
  Europace
  
  Volume: 4
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Journal Article] Novel SCN10A variants associated with Brugada syndrome2015
- Author(s)
  Fukuyama M, Ohno S, Makiyama T, Horie M.
- Journal Title
  
  Europace
  
  Volume: 0 Issue: 6 Pages: 0-0
- DOI
  10.1093/europace/euv078
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24591575, KAKENHI-PROJECT-15K19375, KAKENHI-PROJECT-15H04818
[Journal Article] Gain-of-function KCNH2 mutations in patients with Brugada syndrome.2014
- Author(s)
  Wang Q, Ohno S, Ding WG, Fukuyama M, Miyamoto A, Itoh H, Makiyama T, Wu J, Bai J, Hasegawa K, Shinohara T, Takahashi N, Shimizu A, Matsuura H, Horie M.
- Journal Title
  
  J Cardiovasc Electrophysiol.
  
  Volume: 25 Issue: 5 Pages: 522533-522533
- DOI
  10.1111/jce.12361
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460287, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25461054
[Journal Article] A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.2014
- Author(s)
  Hasegawa K, Ohno S, Ashihara T, Itoh H, Ding WG, Toyoda F, Makiyama T, Aoki H, Nakamura Y, Delisle BP, Matsuura H, Horie M.
- Journal Title
  
  Heart Rhythm
  
  Volume: 11 Issue: 1 Pages: 67-75
- DOI
  10.1016/j.hrthm.2013.09.073
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23590258, KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460287, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-25461106
[Journal Article] A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation.2014
- Author(s)
  Bartos DC, Giudicessi JR, Tester DJ, Ackerman MJ, Ohno S, Horie M, Gollob MH, Burgess DE, Delisle BP.
- Journal Title
  
  Heart Rhythm.
  
  Volume: 11 Issue: 3 Pages: 459-468
- DOI
  10.1016/j.hrthm.2013.11.021
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591575
[Journal Article] Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction2014
- Author(s)
  Ohno S, Omura M, Kawamura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M
- Journal Title
  
  Europace
  
  Volume: in press Issue: 11 Pages: 1646-1654
- DOI
  10.1093/europace/eut382
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460406
[Journal Article] Long QT Syndrome Type8: Novel CACNA1C Mutations Causing QT Prolongation and Variant Phenotypes.2014
- Author(s)
  Fukuyama M, Wang Q, Kato K, Ohno S, Ding WG, Toyoda F, Itoh H, Kimura H, Makiyama T, Ito M, Matsuura H, Horie M.
- Journal Title
  
  Europace.
  
  Volume: in press Issue: 12 Pages: 1828-37
- DOI
  10.1093/europace/euu063
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460287, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-26460295
[Journal Article] A Molecular Mechanism for Adrenergic-Induced Long QT Syndrome.2014
- Author(s)
  Wu J, Naiki N, Ding WG, Ohno S, Kato K, Zang WJ, Delisle BP, Matsuura H, Horie M.
- Journal Title
  
  J Am Coll Cardiol
  
  Volume: 63 Issue: 8 Pages: 819827-819827
- DOI
  10.1016/j.jacc.2013.08.1648
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24591575, KAKENHI-PROJECT-25460287
[Journal Article] Age-Dependent Clinical and Genetic Characteristics in Japanese Patients With Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia2013
- Author(s)
  Itoh H, Horie M
- Journal Title
  
  Circ J
  
  Volume: 77 Issue: 6 Pages: 1534-1542
- DOI
  10.1253/circj.CJ-12-1446
- NAID
  10031158884
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575
[Journal Article] Novel SCN3B Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.52013
- Author(s)
 Ishikawa T
- Journal Title
 
 Circ J
 
 Volume: 77 Issue: 4 Pages: 959-967
- DOI
 10.1253/circj.CJ-12-0995
- NAID
 10031138998
- ISSN
 1346-9843, 1347-4820
- Language
 English
- Peer Reviewed
- Data Source
 KAKENHI-PROJECT-22390157, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-23659414, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591575
[Journal Article] Flecainide reduces ventricular arrhythmias via a mechanism that differs from that of β-blockers in catecholaminergic polymorphic ventricular tachycardia2013
- Author(s)
  DochiK,　WatanabeH,　KawamuraM,　MiyamotoA,　OzawaT,　NakazawaY,　AshiharaT, OhnoS,　HayashiH,　ItoM, SakazakiH, KawataH, UsinohamaH, KaszynskiRH, MinaminoT, SumitomoN, ShimizuW, HorieM
- Journal Title
  
  Journal of arrhythmia
  
  Volume: - Issue: 5 Pages: 255-260
- DOI
  10.1016/j.joa.2013.01.011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591575, KAKENHI-PROJECT-25461053
[Journal Article] A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillation2013
- Author(s)
  Nakano Y, Makita N, (32人中31番目) et al
- Journal Title
  
  PLOS Genet
  
  Volume: 9 Issue: 4 Pages: e1003364-e1003364
- DOI
  10.1371/journal.pgen.1003364
- NAID
  120006985866
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591086, KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136727, KAKENHI-PROJECT-25640066, KAKENHI-PROJECT-25670369
[Journal Article] Ultrastructural Maturation of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes in a Long-Term Culture2013
- Author(s)
  Kamakura T, Makiyama T, Horie M. et al.
- Journal Title
  
  Circ J
  
  Volume: 77 Issue: 5 Pages: 1307-1314
- DOI
  10.1253/circj.CJ-12-0987
- NAID
  10031151395
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575, KAKENHI-PROJECT-24790277
[Journal Article] L-Type Calcium Channel Mutations in Japanese Patients With Inherited Arrhythmias2013
- Author(s)
  Fukuyama M, Ohno S, Wang Q, Horie M. et al.
- Journal Title
  
  Circ J
  
  Volume: 77 Issue: 7 Pages: 1799-1806
- DOI
  10.1253/circj.CJ-12-1457
- NAID
  10031173762
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575
[Journal Article] Genetic Screening of KCNJ8 in Japanese Patients with J-wave Syndromes or Idiopathic Ventricular Fibrillation.2013
- Author(s)
  Wang Q, Ohno S, Kato K, Horie M. et al.
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: 29 Issue: 5 Pages: 261-264
- DOI
  10.1016/j.joa.2013.01.013
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575
[Journal Article] Genetic Background of Catecholaminergic Polymorphic Ventricular Tachycardia in Japan2013
- Author(s)
  Kawamura M, Ohno S, Naiki N, Horie M. et al.
- Journal Title
  
  Circ J
  
  Volume: 77 Issue: 7 Pages: 1705-1713
- DOI
  10.1253/circj.CJ-12-1460
- NAID
  10031173750
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575, KAKENHI-PROJECT-25461053
[Journal Article] KCNE3 T4A as the Genetic Basis of Brugada-Pattern Electrocardiogram2012
- Author(s)
  Nakajima T, Ashihara T, et al.
- Journal Title
  
  Circ J
  
  Volume: 76 Issue: 12 Pages: 2763-2772
- DOI
  10.1253/circj.CJ-12-0551
- NAID
  10031126046
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790717, KAKENHI-PROJECT-22590205, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-23591030, KAKENHI-PROJECT-24591575
[Journal Article] Phenotype variability in patients carrying KCNJ2 mutations.2012
- Author(s)
  Kimura H, Zhou J, Kawamura M, Itoh H, Mizusawa Y, Ding W-G, Wu J, Ohno S, Makiyama T, Miyamoto A, Naiki N, Wang Q, Xie Y, Suzuki T, Tateno S, Nakamura Y, Zang W-J, Ito M, Matsuura H, Horie M
- Journal Title
  
  Circ Cardiovasc Genet
  
  Volume: 5 Issue: 3 Pages: 344-353
- DOI
  10.1161/circgenetics.111.962316
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590205, KAKENHI-PROJECT-22590206, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575
[Journal Article] A novel gain-of-function KCNJ2 mutation associated with short QT syndrome impairs inward rectification of Kir2.1 currents.2012
- Author(s)
  Hattori T
- Journal Title
  
  Cardiovasculer Research
  
  Volume: 93 Issue: 4 Pages: 666-673
- DOI
  10.1093/cvr/cvr329
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575
[Journal Article] High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation.2012
- Author(s)
  Burgess DE
- Journal Title
  
  Biochemistry.
  
  Volume: 51 Issue: 45 Pages: 9076-9085
- DOI
  10.1021/bi3009449
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24591575
[Presentation] Improving the Clinical Diagnosis of Lethal Arrhythmic Syndrome by Genetic Testing for the Prediction and Prevention of Sudden Cardiac Death2024
- Author(s)
  福山恵, 大野聖子, 牧山武, 堀江稔, 他
- Organizer
  第88回日本循環器学会学術集会シンポジウム
- Data Source
  KAKENHI-PROJECT-22K08179
[Presentation] Non-cording deletions disrupt CTCF-mediated DNA loops flanking PITX2, causing a sinus node dysfunction: Novel molecular mechanism of inherited arrhythmias2023
- Author(s)
  村田広茂, Jean-Jacques Schott, 蒔田直昌, 牧山武, 大野　聖子, 清水渉
- Organizer
  第69回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-22K08168
[Presentation] Homozygous or compound heterozygous variants in DSG2 are mainly causative of Japanese arrhythmogenic right ventricular cardiomyopathy.2023
- Author(s)
  K. Sonoda , S. Nagase , T. Aiba , K. Kato , M. Fukuyama , N. Kikuchi , T. Shiga , M. Horie , S. Ohno
- Organizer
  ESC Congress 2023
- Data Source
  KAKENHI-PROJECT-22K08179
[Presentation] Clinically Diversity of Long QT syndrome type8; Timothy syndrome is no longer poor outcome2023
- Author(s)
  福山恵, 大野聖子, 牧山武, 堀江稔, 他
- Organizer
  第69回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-22K08179
[Presentation] Gain-of-Function KCND3 Variants Identified in Young Patients with Refractory Epilepsy might be a Cause of Sudden Unexpected Death in Epilepsy.2023
- Author(s)
  Byambajav Tserenlkham, Koichiro Takayama, Dimitar Zankov, Minoru Horie, Seiko Ohno
- Organizer
  Heart Rhythm Soceity Meeting 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K08119
[Presentation] 先天性QT延長症候群が疑われた症例に同定されたTBX5_TBX3 欠損2022
- Author(s)
  Seiko Ohno, Masao Yoshinaga
- Organizer
  日本人類遺伝学会第67回大会
- Data Source
  KAKENHI-PROJECT-21H02888
[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] 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] ARVC2022
- Author(s)
  Seiko Ohno
- Organizer
  KHRS2022
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[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] Global Expert Consensus Statement on State of Genetic Testing for Inherited Cardiac Diseases2022
- Author(s)
  Seiko Ohno
- Organizer
  HeartRhythm2022
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] Fetal and Infant Lethal Ventricular Arrhythmias are Common in Cardiac Calmodulinopathy2022
- Author(s)
  Megumi Fukuyama, Minoru Horie, Koichi Kato, Tomoya Ozawa, Yusuke Fujii, Yusuke Okuyama, Takeru Makiyama, Seiko Ohno, Yoshihisa Nakagawa
- Organizer
  日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-22K08179
[Presentation] Desmoglein 2 mutant mice reproduce arrhythmogenic right ventricular2022
- Author(s)
  Zankov D, Ohno S.
- Organizer
  ESC Congress 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] Calmodulinopathy is a common cause of critical cardiac phenotypes in fetus and infancy2022
- Author(s)
  Megumi Fukuyama, Koichi Kato, Minoru Horie, Seiko Ohno, et al
- Organizer
  ESC Congress 2022
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K08179
[Presentation] Genomic autopsy to determine the preventable cause of sudden cardiac arrest and save relatives2022
- Author(s)
  Ohno S
- Organizer
  ReSS2022
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] How to stratify the risk of ventricular arrhythmia and heart failure in arrhythmogenic right ventricular2022
- Author(s)
  Ohno S
- Organizer
  第68回日本不整脈心電学会学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] Calmodulinopathy is a Common Cause of Critical Cardiac Phenotypes in Fetus and Infancy2022
- Author(s)
  Megumi Fukuyama, Minoru Horie, Koichi Kato1, Takeru Makiyama, Seiko Ohno, Yoshihisa Nakagawa
- Organizer
  第85回日本循環器学会学術集会.
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] Arrhythmogenic Right Ventricular Cardiomyopathy2021
- Author(s)
  Ohno S
- Organizer
  European Heart Rhythm Association Meeting 2021
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[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] Contribution of Genetic Screening for Arrhythmogenic Cardiomyopathy2021
- Author(s)
  Fukuyama M, Ohno S, Kato K, Ozawa T, Makiyama T, Nakagawa Y, Horie M.
- Organizer
  第67回日本不整脈心電学会学術集会.
- Data Source
  KAKENHI-PROJECT-19K08555
[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
[Presentation] How to Utilize the Genetic Information in Arrhythmogenic Right Ventricular Cardiomyopathy2021
- Author(s)
  Ohno S
- Organizer
  第85回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] 小児不整脈原性右室心筋症患者をいかに早期に診断するか2021
- Author(s)
  大野聖子、園田桂子
- Organizer
  第25回小児心電学会
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] 特発性心筋症の遺伝学的検査に基づいた治療戦略2021
- Author(s)
  大野聖子
- Organizer
  第25回日本心不全学会
- Invited
- Data Source
  KAKENHI-PROJECT-21H02888
[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
  ESC Congress 2021
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] An Update on the Diagnosis and Management of Catecholaminergic Polymorphic Ventricular Tachycardia2021
- Author(s)
  Ohno S
- Organizer
  Korean Heart Rhythm Society Meeting 2021
- Invited / 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総会 with WCC2021
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] Human-specific desmoglein 2 mutations in mice models of arrythmogenic right ventricular cardiomyopathy reproduce patients' phenotype2021
- Author(s)
  Zankov DP, Ohno S
- Organizer
  European Heart Rhythm Association Meeting 2021
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02888
[Presentation] Contribution of Genetic Screening for Arrhythmogenic Cardiomyopathy2021
- Author(s)
  Megumi Fukuyama, Seiko Ohno, Koichi Kato, Tomoya Ozawa, Yuichi Sawayama, Yosuke Higo, Yusuke Okuyama, Kohei Asada, Yusuke Fujii, Noriaki Yagi, Akashi Miyamoto, Hiroshi Sakai, Takashi Yamamoto, Takeru Makiyama, Minoru Horie, Yoshihisa Nakagawa
- Organizer
  第85回日本循環器学会学術集会総会 with WCC2021
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] カテコラミン誘発性多形性心室頻拍におけるICD治療の実態2020
- Author(s)
  大野聖子、高山幸一郎、園田桂子、福山恵、加藤浩一、堀江稔
- Organizer
  第12回植込みデバイス関連冬季大会
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Arrhythmogenic Right Ventricular Cardiomyopathy2020
- Author(s)
  Ohno S
- Organizer
  APHRS Virtual Congress 2020
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Variable Electrophysiological Characteristics of CACNA1C Mutations Identified in Patients with Long QT Syndrome Type 82020
- Author(s)
  Wang Q , Sonoda K, Makiyama T, Ozawa J, Takayama K, Dimitar P, Horie M, Ohno S
- Organizer
  第85回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] An Update on the Diagnosis and Management of Catecholaminergic Polymorphic Ventricular Tachycardia2020
- Author(s)
  Ohno S
- Organizer
  The 12th Annual Scientific Sessions of the Korean Heart Rhythm Society
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] 遺伝子検査とその解釈2020
- Author(s)
  大野聖子
- Organizer
  第56回日本小児循環器学会総会・学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Long-read sequence confirmed a large deletion of MYH6 and MYH7 in a family with atrial septal defect2020
- Author(s)
  K. Sonoda, S. Ohno, M. Horie
- Organizer
  ESC CONGRESS 2020 - The Digital Experience
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Dynamic change in electrocardiogram in a neonate with HCN4 insertion mutation2020
- Author(s)
  Ohno S, Kan N, Kato K, Ushinohama H, Horie M
- Organizer
  Heart Rhythm Society Meeting 2020
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Genomic Research in Arrhythmia2020
- Author(s)
  Seiko Ohno
- Organizer
  第84回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] How to Utilize the Genetic Information in Arrhythmogenic Right Ventricular Cardiomyopathy2020
- Author(s)
  大野聖子
- Organizer
  第85回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Genetics in Brugada Syndrome2019
- Author(s)
  Ohno S
- Organizer
  Annual Scientific Session of the KHRS
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Genetic Background of ARVC2019
- Author(s)
  Ohno S,, Sonoda K, Horie M.
- Organizer
  第83回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Lower Frequency of Classical Triad in Andersen-Tawil Syndrome Probands with De Novo KCNJ2 Mutations than Those with Familial Mutations2019
- Author(s)
  Hattori T, Sonoda K, Horie M, Ohno S
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] Sodium channel cardiomyopathy: genetic and clinical spectrum.2019
- Author(s)
  Ohno S
- Organizer
  Asian Pacific Heart Rhythm Society
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Calmodulin Mutations in Japanese Children with Long QT Syndrome2019
- Author(s)
  Fukuyama M, Ohno S,Ozawa J, Horie M
- Organizer
  第 66 回日本不整脈心電学会学術集会
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] High Prevalence of Late Appearance T Wave in Patients with Long QT Syndrome Type 82019
- Author(s)
  Fukuyama M, Ohno S,Ozawa J,Kato K, Takayama K, Makiyama T, Horie M
- Organizer
  第 66 回日本不整脈心電学会学術集会
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] Ventricular septum defect can be a key for the early diagnosis of Brugada syndrome in young patients with SCN5A mutations.2019
- Author(s)
  Ohno S, Ozawa J, Sonoda K, Makiyama T, Horie M.
- Organizer
  American Society of Human Genetics
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] De novo RYR2 mutations are associated with severe phenotype of CPVT more strongly than inherited ones2019
- Author(s)
  Keiko Sonoda, Tetsuhisa Hattori, Minoru Horie, Seiko Ohno
- Organizer
  The American Society of Human Genetics 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] Clinical use of genetic analysis for the inherited primary arrhythmia syndromes2019
- Author(s)
  Ohno S
- Organizer
  第83回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Lower Frequency of Classical Triad in Andersen-Tawil Syndrome Probands with De Novo KCNJ2 Mutations than Those with Familial Mutations2019
- Author(s)
  Tetsuhisa Hattori, Keiko Sonoda, Minoru Horie, Seiko Ohno
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] An NGS-based genotyping in LQTS; minor genes are no longer minor2019
- Author(s)
  Ohno S,, Ozawa J, Fukuyama M, Makiyama T, Horie M
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Mutation specific clinical characteristics in long QT syndrome type 8; severe phenotype in Timothy syndrome patients.2019
- Author(s)
  Ohno S, Yoshinaga M, Ozawa J, Fukuyama M, Sato S, Kashiwa A, Yasuda K, Kaneko S, Nakau K, Inukai S, Makiyama T, Aiba T, Suzuki H, Horie M.
- Organizer
  European Society of Cardiology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Pathophysiological substrate & Risk Stratification2019
- Author(s)
  Ohno S
- Organizer
  Asian Pacific Heart Rhythm Society
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] LQTS, Ventricular Arrhythmias and SCD Pathophysiology and Mechanisms Ion Channel Disorders2018
- Author(s)
  Seiko Ohno
- Organizer
  EHRA2018
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Functional Analysis of Mutant Nav1.5 Channels Clarified Severe Phenotype of a Female Patient with Compound SCN5A Mutations.2018
- Author(s)
  Fukumoto D, Ohno S,, Makiyama T, Kubo T, Kitaoka H, Matsuura H, Horie M.
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Usefulness of genetic screening for long QT syndrome in the school-based electrocardiographic screening programs2018
- Author(s)
  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
- Organizer
  The 83rd Annual Scientific Meeting of the Japanese Circulation Society
- Data Source
  KAKENHI-PROJECT-17K09494
[Presentation] Functional Change of an SCN5A Mutation Identified in the Patient with Short-Coupled Variant of Torsades de Pointes.2018
- Author(s)
  Sonoda K, Ohno S,, Hattori T, Horie M,
- Organizer
  Asian Pacific Heart Rhythm Society Meeting 2018 in Taiwan
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Genetic background in patients with idiopathic ventricular fibrillation: known gene screening from whole exome analysis data2018
- Author(s)
  Aiba T, Cha PC, Takahashi A, Ohno S, Kamakura T, Ishikawa T, Ishibashi-Ueda H, Shiba-Harada M, Minamino N, Hayashi K, Yagihara N, Nakano Y, Itoh H, Miyamoto Y, Tanaka T, Makita N, Horie M, Shimizu W, Kusano K, Yasuda S.
- Organizer
  The 83rd Annual Scientific Meeting of the Japanese Circulation Society
- Data Source
  KAKENHI-PROJECT-17K09494
[Presentation] LQTS, Ventricular Arrhythmias and SCD Pathophysiology and Mechanisms Ion Channel Disorders2018
- Author(s)
  Ohno S
- Organizer
  European Heart Rhythm Society Meeting 2018 in Barcelona
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] What is New in the Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy?2018
- Author(s)
  Ohno S
- Organizer
  Asian Pacific Heart Rhythm Society Meeting 2018 in Taiwan
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] 不整脈を呈するCALM2変異キャリアの特徴2018
- Author(s)
  大野聖子、中右弘一、真鍋博美、吉田葉子、青木寿明、藤田修平、牧山武、堀江稔
- Organizer
  第23回日本小児心電学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Functional Change of an SCN5A Mutation Identified in the Patient with Short-Coupled Variant of Torsades de Pointes2018
- Author(s)
  Keiko Sonoda, Seiko Ohno, Tetsuhisa Hattori, Minoru Horie
- Organizer
  APHRS2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] High Frequency of De Novo KCNJ2 Mutations in Andersen-Tawil Syndrome Patients2018
- Author(s)
  Tetsuhisa Hattori, Keiko Sonoda, Minoru Horie, Seiko Ohno
- Organizer
  APHRS2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08102
[Presentation] 不整脈原性右室心筋症に特異的な遺伝子変異の病原性を考える2018
- Author(s)
  大野聖子、和田悠子、堀江稔
- Organizer
  第4回日本心筋症研究会
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] VT/VF: Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC): From Bench to Bedside2018
- Author(s)
  Ohno S
- Organizer
  Asian Pacific Heart Rhythm Society Meeting 2018 in Taiwan
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] 20.Detection of Copy Number Variations by Next Generation Sequencer, a Missing Genetic Defect.2018
- Author(s)
  Seiko Ohno
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Detection of Copy Number Variations by Next Generation Sequencer,a Missing Genetic Defect2018
- Author(s)
  Ohno S,, Sonoda K, Ichikawa M, Yoshinaga M, Horie M.
- Organizer
  第82回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] ゲノム医療を活用した不整脈診療2018
- Author(s)
  大野聖子
- Organizer
  第66回日本心臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] 遺伝性不整脈の遺伝子診断2018
- Author(s)
  大野聖子
- Organizer
  第22回日本心不全学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Genetic and clinical aspects of congenital long-QT syndrome: results from the Japanese multicenter registry2018
- Author(s)
  清水渉、山形研一郎、野田崇、草野研吾、宮崎文、牧山武、伊藤英樹、大野聖子、渡部裕、林研至、森田宏、吉永正夫、福田恵一、宮本恵宏、鎌倉史郎、田中敏博、住友直方、萩原誠久、蒔田直昌、堀江稔、相庭武司
- Organizer
  The 83rd Annual Scientific Meeting of the Japanese Circulation Society
- Data Source
  KAKENHI-PROJECT-17K09494
[Presentation] High Frequency of De Novo KCNJ2 Mutations in Andersen-Tawil Syndrome Patients2018
- Author(s)
  Hattori T, Sonoda K, Horie M, Ohno S
- Organizer
  Asian Pacific Heart Rhythm Society Meeting 2018 in Taiwan
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Early Repolarization Syndrome Caused by a de novo KCND3 Gain-of-Function Mutation2018
- Author(s)
  Takayama K, Ohno S,, Ding WG, Ashihara T, Kise H, Hoshiai M, Matsuura H, Horie M..
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07875
[Presentation] Exercise Inducible Polymorphic Ventricular Tachycardia Depending on the Different RYR2 Mutation Spectrum2017
- Author(s)
  Wada Y, Ohno S, Wuriyanghai Y, Makiyama T, Horie M
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Next-Generation Sequencing Is One of the Promising Ways for Identifying Copy Number Variations in Patients with Inherited Primary Arrhythmia Syndromes.2017
- Author(s)
  Ichikawa M, Ohno S, Fukumoto D, Takayama K, Wada Y, Fukuyama M, Makiyama T, Itoh H, Horie M
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Novel N-Terminal KCNH2 Mutations Identified in Symptomatic Long QT Syndrome Patients.2017
- Author(s)
  Fukumoto D, Ohno S, Wada Y, Fujii Y, Ichikawa M, Takayama K, Fukuyama M, Itoh H, Ding WG, Matsuura H, Horie M
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] ex Dependent Risk of Sudden Death or Sick Sinus Syndrome in a Family with Brugada Syndrome.2017
- Author(s)
  Aizawa Y, Fujisawa T, Katsumata Y, Ohno S, Sonoda K, Hayashi H, Hojo R, Fukamizu S, Nakajima K, Kunitomi A, Nishiyama T, Kimura T, Nishiyama N, Kurita Y, Takatsuki S, Ogwa S, Kosaki K, Nakazato Y, Horie M, Fukuda K
- Organizer
  APHRS2017.
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Propranolol Inhibits Late Sodium Current in Long-QT Syndrome Type 3 Human Induced Pluripotent Stem Cell-drived Myocyte Model.2017
- Author(s)
  irose S, Makiyama T, Melgari D, Wu J, Yokoi F, Wuriyanghai Y, Yamamoto Y, Kohjitani H, Nishiguchi S, Harita T, Hayano M, Yoshimoto J, Ohno S, Yoshida Y, Horie M, Kimura T.
- Organizer
  AHA2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Novel RYR2 mutations causative for long QT syndromes.2017
- Author(s)
  Fukuyama M, Ohno S, Takayama K, Ichikawa M, Horie M
- Organizer
  ESC Congress 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Identification of novel long QT syndrome-associated mutations by targeted sequencing analyses.2017
- Author(s)
  Watanabe R, Ohno S, Aiba T et al.
- Organizer
  European Society of Human Genetics Conference.
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Can We Detect and Know All the Pathogenic Mutations by Next Generation Sequencer in Patients with Inherited Cardiovascular Diseases?2017
- Author(s)
  Ohno S
- Organizer
  日本循環器病学会
- Place of Presentation
  金沢
- Year and Date
  2017-03-17
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] CALM2-D134H Mutation Associated with Long-QT Syndrome Prevents Inactivation of L-type Ca2+ Currents in Human iPS Cell Derived Cardiomyocytes.2017
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Yokoi F, Ishikawa T, Ohno S, Chinabayashi K, Suda K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Ankyrin-B mutation identified in a patient with chronic atrial fibrillation, atrioventricular conduction disturbance and left ventricular dysfunction2017
- Author(s)
  Imai Y, Higashi Y, Yoshino T, Tarutani Y, Ichikawa M, Ohno S, Horie M.
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Early Repolarization Syndrome Caused by a de novo KCND3 Gain-of-Function Mutation.2017
- Author(s)
  Takayama K, Ohno S, Ding W-G, Kise H, Hoshiai M, Matsuura H, Horie M.
- Organizer
  AHA2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Score System for Diagnosis of Syncope after Alcohol Intake in Brugada Syndrome.2017
- Author(s)
  Wu Q, Hira D, Hayashi H, Sonoda K, Ohno S, Makiyama T, Terada T, Horie M.
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Is Cardiac Resynchronization Therapy Able to Improve Mortality of Heart Failure in Patients with Laminopathy?2017
- Author(s)
  Nakajima K, Aiba T, Nishiuchi S, Makiyama T, Onoue K, Kamakura T, Wada M, Ishibashi K, Inoue Y, Miyamoto K, Okamura H, Nagase S, Noda T, Ohno S, Miyamoto Y, Saito Y, Horie M, Kimura T, Shimizu W, Kusano K.
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] KCNJ3 N496H A Rare Variant in Japanese as a Cause of Susceptible Gene for Ventricular Fibrillation in Overlap Syndromes between LQT and CPVT.2017
- Author(s)
  Aiba T, Ohno S, Ono M, Shigemizu D, Toyoda F, Miake J, Hagiwara A, Shinohara T, Okumura S, Toda T, Satake W, Tsunoda T, Shimamoto K, Sekine A, Takahashi A, Miyamoto Y, Tanaka T, Kusano K, Horie M, Shimizu W.
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.2017
- Author(s)
  Nishiuchi S, Makiyama T, Aiba T, Nakajima K, Ishikawa T, Murakoshi N, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, Saito Y, Oginosawa Y, Nogami A, Aonuma K, Kusano K, Makita N, Shimizu W, Horie M, Kimura T
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Human iPSC-Derived Myocyte Mmodel of SCN5A-D1275N-Related Cardiac Sodium Channelopathy Reveals Diminished Sodium Currents Resulting From Enhanced Protein Degradation.2017
- Author(s)
  Hayano M,Makiyama T, Kamakura T, Watanabe H, Sasaki K, Funakoshi S, Wuriyanghai Y, Nishiguchi S, Harita T, Yamamoto Y,.Kohjitani H, Hirose S, Yokoi F, Chen J, Baba O, Horie T, Chonabayahi K, Ohno S, Toyoda F, Yoshida Y, Ohno K, Horie M, Kimura T.
- Organizer
  AHA2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Inherited Primary Arrhythmia Syndrome Presenting with Phenotypic Features of Catecholaminergic Polymorphic Ventricular Tachycardia Plus Prominent U-Waves.2017
- Author(s)
  Dharmawan T, Nakajima T, Ohno S, Iizuka T, Irie T, Kaneko Y, Horie M, Kurabayashi M.
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Drug-Induced Long QT Syndrome in a Patient with an ANK2 Mutation.2017
- Author(s)
  Kyodo A, Sakatani T, Shimoo S, Takamatsu K, Tsuji Y, Mera K, Koide M, Isodono K, Tsubakimoto Y, Matsuo A, Inoue K, Fujita H, Ichikawa M, Ohno S, Horie M
- Organizer
  APHRS2017.
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Novel RYR2 Mutations Causative for Long QT Syndromes.2017
- Author(s)
  Fukuyama M, Ohno S, Takayama K, Ichikawa M, Fukumoto D, Horie M.
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Early Repolarization Syndrome Caused by a de novo KCND3 Gain-of-Function Mutation.2017
- Author(s)
  Takayama K, Ohno S, Ding W-G, Kise H, Hoshiai M, Matsuura H, Horie M.
- Organizer
  AHA2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] High frequency of CACNA1C mutation carriers in genotyped LQTS patients2017
- Author(s)
  Ohno S, Ozawa J, Fukuyama M, Horie M.
- Organizer
  ESC Congress 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] RYR2 Mutations in LQTS2017
- Author(s)
  Seiko Ohno
- Organizer
  APHRS 2017
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Severe Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia Caused by Double RYR2 Mutations.2017
- Author(s)
  Takayama K, Ohno S, Horie M
- Organizer
  APHRS2017.
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] CALM2-D134H Mutation Associated with Long-QT Syndrome Delayed Inactivation of L-type Ca2+ Currents in Human iPS Cells Derived Cardiomyocytes.2017
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Hayano M, Suguru N, Wuriyanghai Y, Kohjitani H, Hirose S, Yokoi F, Ishikawa T, Ohno S, Chonabayashi K, Suda K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  AHA2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] SCN10A Mutations Related with Bradycardia and Conduction Block in Young Patients.2017
- Author(s)
  Aoki H, Ohno S, Fukuyama M, Yoshinaga M, Horie M.
- Organizer
  ESC Congress 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Identification of copy number variations by next generation sequencer in patients with inherited primary arrhythmia syndromes.2017
- Author(s)
  Ichikawa M, Ohno S, Fukumoto D, Takayama K, Wada Y, Fukuyama M, Makiyama T, Itoh H, Horie M
- Organizer
  ESC Congress 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Modelling Long-QT Syndrome Type 3 Associated　with Near-Miss Sudden Infant Death Syndrome Using Human-Induced Pluripotent Stem Cells.2017
- Author(s)
  Hirose S, Makiyama T, Melgari D, Wu J, Yokoi F, Wuriyanghai Y, Kohjitani H, Yamamoto Y, Nishiuchi S, Hayano M, Harita T, Yoshimoto J, Ohno S, Yoshida Y, Horie M, Kimura T
- Organizer
  APHRS2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] l-cis diltiazem rescues impaired calcium channel inactivation in a patient-specific stem cell model of long QT syndrome with a CACNA1C mutation.2016
- Author(s)
  Harita T, Makiyama T, Toyoda F, Nishiuchi S, Hayano M, Yamamoto Y, Wuriyanghai Y, Kohjitani H, Ohno S, Yoshida Y, Ueyama T, Yamanaka S, Shimizu A, Horie M, Kimura T
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Triple mutations in three major genes for long QT syndrome are very rare and cause complicated phenotypes with ventricular arrhythmia.2016
- Author(s)
  Ohno S, Wu J, Mizusawa Y, Sonoda K, Itoh H, Makiyama T, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Triple mutations in three major genes for long QT syndrome are very rare but produce severe phenotypes.2016
- Author(s)
  Ohno S, Wu J, Sonoda K, Itoh H, Makiyama T, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] KCNH2 mutation in patients with long QT syndrome type 2.2016
- Author(s)
  Fukumoto D, Ohno S, Wada Y, Fujii Y, Ichikawa M, Ito H, Ding WG, Matsuura H, Horie M
- Organizer
  9th APHRS Scientific Session.
- Place of Presentation
  Korea
- Year and Date
  2016-10-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Specific Phenotypes Caused by RYR2 Mutations Relate with Bradycardia but not with Mutation Locations in RYR2.2016
- Author(s)
  Ohno S, Ozawa J, Fujii Y, Itoh H, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] The RYR2 Mutations Identified Not Only in CPVT But Also Short Coupled Variant of Torsade De Pointes and LQTS.2016
- Author(s)
  Ohno S
- Organizer
  APHRS2016
- Place of Presentation
  Korea
- Year and Date
  2016-10-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Allele-specific Disruption Rescues Electrophysiological Abnormalities in Human iPS Cell Model of Long-QT Syndrome With a CALM2 Mutation2016
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Sasaki K, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Chen J, Ishikawa T, Motomura H, Ohno S, Chonabayashi K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  AHA2016,
- Place of Presentation
  New Orleans, USA
- Year and Date
  2016-11-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] The RYR2 Mutations Identified Not Only in CPVT But Also Short Coupled Variant of Torsade De Pointes and LQTS.2016
- Author(s)
  Ohno S
- Organizer
  Asian Pacific Heart Rhythm Society Meeting
- Place of Presentation
  Seoul, Korea
- Year and Date
  2016-10-12
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Various ANK2 Mutations in Japanese Patients with Inherited Primary Arrhythmia Syndromes2016
- Author(s)
  Ichikawa M, Ohno S, Fujii Y, Ozwa J, Sonoda K, Fukuyama M, Kato K, Kimura H, Hayashi H, Horie M
- Organizer
  第80回日本循環器学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2016-03-18
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Specific phenotypes caused by RYR2 mutations relate with bradycardia but not with mutation locations in RYR2.2016
- Author(s)
  Ohno S, Ozawa J, Fujii Y, Itoh H, Horie M
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Non desmosomal mutations detected in japanese patients with arrhythmogenic right ventricular cardiomyopathy.2016
- Author(s)
  Takayama K, Ohno S, Wada Y, Horie M
- Organizer
  9th APHRS Scientific Session
- Place of Presentation
  Korea
- Year and Date
  2016-10-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Copy number variations in SCN5A associated with Brugada syndrome.2016
- Author(s)
  Sonoda K, Ohno S, Ozawa J, Hayano M, Ito H, Makiyama T, Horie M
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] High prevalence of late onset T in patients with long QT syndrome type 8.2016
- Author(s)
  Ohno S, Ozawa J, Fukuyama M, Makiyama T, Horie M.
- Organizer
  AHA2016
- Place of Presentation
  New Orleans, USA
- Year and Date
  2016-11-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Generation of lmna knock out human induced pluripotent stem cells using the crispr-cas9 nickase system.2016
- Author(s)
  Wuriyanghai Y, Makiyama T, Nishiuchi S, Yokoi F, Hayano M, Yamamoto Y, Harita T, Kohjitani H, Hirose A, Ohno S, Yoshida Y, Horie M, Kimura T
- Organizer
  9th APHRS Scientific Session
- Place of Presentation
  Korea
- Year and Date
  2016-10-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Copy Number Variations in SCN5A associated with Brugada Syndrome.2016
- Author(s)
  Sonoda K, Ohno S, Ozawa J, Hayano M, Ichikawa M, Ito H, Makiyama T, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] A Unique Genetic Background and Prognostic Impact on Non-Caucasian ARVD/C Probands2016
- Author(s)
  Wada Y, Ohno S, Aiba T, Horie M
- Organizer
  AHA2016
- Place of Presentation
  New Orleans, USA
- Year and Date
  2016-11-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] RYR2 mutations underlying in patients with short-coupled variant of torsade de pointes.2016
- Author(s)
  Fujii Y, Itoh H, Ohno S, Blancard M, Aoki H, Nakagawa Y, Yamamoto S, Matsui Y, Ichikawa M, sonoda K, Ozawa T, Ohkubo K, Watanabe I, Guicheney P, Horie M.
- Organizer
  第80回日本循環器学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2016-03-18
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Various ANK2 mutations in patients with inherited primary arrhythmia syndromes.2016
- Author(s)
  Ichikawa M, Aiba T, Ohno S, Shigemizu D, Ozawa J, Sonoda K, Fukuyama M, Itoh H, Miyamoto Y, Tsunoda T, Makiyama T, Tanaka T, Shimizu W, Horie M
- Organizer
  9th APHRS Scientific Session
- Place of Presentation
  Korea
- Year and Date
  2016-10-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Rare single nucleotide polymorphism of scn10a in patients with inherited primary arrhythmia syndromes.2016
- Author(s)
  Fukuyama M, Ohno S, Ichikawa M, Makiyama T, Horie M
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] High prevalence of late onset T in patients with long QT syndrome type 82016
- Author(s)
  Ohno S, Ozawa J, Fukuyama M, Makiyama T, Horie M
- Organizer
  American Heart Association meeting 2016
- Place of Presentation
  New Orleans, USA
- Year and Date
  2016-11-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Specific Phenotypes Caused by RYR2 Mutations Relate with Bradycardia but not with Mutation Locations in RYR2.2016
- Author(s)
  Ohno S, Ozawa J, Fujii Y, Itoh H, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Triple mutations in three major genes for long QT syndrome are very rare and cause complicated phenotypes with ventricular arrhythmia.2016
- Author(s)
  Ohno S, Wu J, Mizusawa Y, Sonoda K, Itoh H, Makiyama T, Horie M
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] RYR2 mutations underlying in patients with short-coupled variant of torsade de pointes.2016
- Author(s)
  Fujii Y, Itoh H, Ohno S, Blancard M, Aoki H, Nakagawa Y, Yamamoto S, Matsui Y, Ichikawa M, Sonoda K, Ozawa T, Ohkubo K, Watanabe I, Guicheney P, Horie M
- Organizer
  ESC2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] AKAP9 mutations identified in young patients with idiopathic ventricular fibrillation or polymorphic ventricular tachycardia2016
- Author(s)
  Sonoda K, Ohno S, Wada Y, Ichikawa M, Fujii Y, Ozawa J, Itoh H, Ashihara T, Hayashi H, Horie M:
- Organizer
  第80回日本循環器学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2016-03-18
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Rare Single Nucleotide Polymorphism of SCN10A in Patients with Inherited Primary Arrhythmia Syndromes.2016
- Author(s)
  Fukuyama M, Ohno S, Ichikawa M, Makiyama T, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] ECG Screening of 1-Month-Old Infants May Prevent Out-of-Hospital Cardiac Arrest in Infancy2016
- Author(s)
  Yoshinaga M, Ohno S, Ushinohama H, Sato S, Miyamoto T, Tauchi N, Horigome H, Sumitomo N, Shiraishi H, Ichida F, Hata T, Nomura Y, Horie M, Makita N, Nagashima M
- Organizer
  AHA2016
- Place of Presentation
  New Orleans
- Year and Date
  2016-11-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] A novel CACNA1C mutation identified in a patient with atypical Timothy syndrome exerts both loss- and gain-of-function effects on Cav1.2.2016
- Author(s)
  Ozawa J, Ohno S, Toyoda F, Itoh H, Fukuyama M, Harita T, Makiyama T, Hiroshi Suzuki, Akihiko Saitoh, Matsuura H, Horie M
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Quantitative Analysisof PKP2 and Neighboring Genesin a Patient with Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Heterozygous PKP2 Deletion2015
- Author(s)
  Sonoda K,Ohno S,Otsuki S,Yagihara N,Watanabe H,Horie M
- Organizer
  The Heart Rhythm Society's 36th Annual Scientific Sessions
- Place of Presentation
  アメリカ合衆国
- Year and Date
  2015-05-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Nonsense-Mediated mRNA Decay due to a CACNA1C Splicing Mutation in a Patient with Brugada Syndrome2015
- Author(s)
  Fukuyama M, Ohno S, Wang Q, ShirayamaT，Itoh H, Horie M:
- Organizer
  第30回日本不整脈学会学術大会
- Place of Presentation
  京都
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Modelling Long-QT Syndrome Associated With a Calmodulin Mutation Using Human Induced Pluripotent Stem Cells2015
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Sasaki K, Hayano H, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Chen J, Ishikawa T, Ohno S, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  AHA Scientific Sessions 2015
- Place of Presentation
  アメリカ合衆国
- Year and Date
  2015-11-07
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Lamin A/C-related cardiomyopthy―From Bench to Bedside―2015
- Author(s)
  Makiyama T, Nishiuchi S, Kohjitani H, Ohno S, Horie M, Kimura T
- Organizer
  第30回日本不整脈学会学術大会
- Place of Presentation
  京都
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] SY11-6 What is Needed for Cardiologists Who Engage Themselves in Childcar2015
- Author(s)
  Ohno S, Horie M
- Organizer
  第79回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] desmosome gene mutations cause or modify the Brugada syndrome?2015
- Author(s)
  Ohno S, Aizawa Y,Fukuyama M,Makiyama T,Kosaki K,Fukuda K,Horie M
- Organizer
  The Heart Rhythm Society's 36th Annual Scientific Sessions
- Place of Presentation
  アメリカ合衆国
- Year and Date
  2015-05-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Differential Diagnosis of Catecholaminergic Polymorphic Ventricular Tachycardia vs. Long QT Syndrome Type 1: A Modified Schwartz Scoring2015
- Author(s)
  Ozawa J, Ohno S, Fujii Y, Makiyama T, Suzuki H, Saitoh A, Horie M.
- Organizer
  AHA Scientific Sessions 2015
- Place of Presentation
  アメリカ合衆国
- Year and Date
  2015-11-07
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] CPVT:Challenging inherited arrhythmia syndromes: the latest.2015
- Author(s)
  Seiko Ohno
- Organizer
  Asian Pacific Heart Rhythm Society 2015
- Place of Presentation
  Melbourne, Australia
- Year and Date
  2015-11-19
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Abnormal expression of cardiac ion channels-associated genes in lamin A/C-related cardiomyopathy-specific induced pluripotent stem cell derived cardiomyocytes2015
- Author(s)
  Nishiuchi S, Makiyama T, Sasaki K, Kohjitani Y, Ohno S, Yoshida Y, Doi T, Shizuta S, Horie.M, Kimura T
- Organizer
  ESC CONGRESS 2015
- Place of Presentation
  イギリス
- Year and Date
  2015-08-29
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction.2015
- Author(s)
  Chen J, Makiyama T, Wuriyanghai Y, Ohno S, Ueyama T, Shimizu A, Horie M, Kimur T.
- Organizer
  ESC CONGRESS 2015
- Place of Presentation
  イギリス
- Year and Date
  2015-08-29
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] High Frequency of J Wave in Hypercalcemia2015
- Author(s)
  Sonoda K,Watanabe H,Ohno S, Horie M, Minamino T.
- Organizer
  第79回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Identification of Novel SCN10A Mutations in Brugada Syndrome Patients.2015
- Author(s)
  Fukuyama M,Ohno S,Makiyama T,Horie M
- Organizer
  第79回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] SCN10A polymorphisms are associated with the clinical severity of probands with sodium channelopathies.2015
- Author(s)
  Fukuyama M, Ohno S, Ichikawa M, Makiyama T, Horie M.
- Organizer
  Europace 2015
- Place of Presentation
  Milan, Italy
- Year and Date
  2015-06-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Drug challenge test and genetic test for the diagnosis and management ofinherited primary arrhythmia syndromes2015
- Author(s)
  Ueyama T, Shimizu A, Yoshiga Y, Ono M,Kato T, Fumimoto T, Ishiguchi H, Ohno S, Makiyama T, Horie M, Yano M
- Organizer
  第30回日本不整脈学会学術大会
- Place of Presentation
  京都
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Arrhythmogenic Right Ventricular Cardiomyopathy from the Genetic Basis to the Clinical Symptoms2015
- Author(s)
  Ohno S, Wada Y, Sonoda K, Horie M
- Organizer
  第30回日本不整脈学会学術大会
- Place of Presentation
  京都
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] SCN10A polymorphisms are associated with the clinical severity of probands with sodium channelopathies.2015
- Author(s)
  Fukuyama M, Ohno S, Ichikawa M, Makiyama T, Horie M
- Organizer
  EUROPACE- CARDIOSTIM 2015
- Place of Presentation
  イタリア
- Year and Date
  2015-06-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Differential diagnosis of catecholaminergic polymorphic ventricular tachycardia vs. long QT syndrome type 1: a modified Schwartz scoring2015
- Author(s)
  Junichi Ozawa, Seiko Ohno, Minoru Horie, et al,
- Organizer
  American Heart Association meeting 2015
- Place of Presentation
  Orlando, FL, USA
- Year and Date
  2015-11-07
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] ML277 shortens prolonged action potential durations in a patientspecific induced pluripotent stem cell-based model of long-QT syndrome　type 12015
- Author(s)
  Wuriyanghai Y, Makiyama T, Sasaki K, Kamakura T, Chen J, Hayano M, Yamamoto Y, Harita T, Nishiuchi S, Kohjitani H, Ohno S, Watanabe K, Kimura T, Horie M
- Organizer
  第30回日本不整脈学会学術大会
- Place of Presentation
  京都
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] The Screening of Calmodulin Genes in Genotype-negative Long QT Syndrome Patients2015
- Author(s)
  Ichikawa M,Ohno S,Fujii Y,Ozawa J,Sonoda K,Fukuyama M,Kato K,Kimura H, Horie M
- Organizer
  第79回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Brady and Atrial Arrhythmias in CPVT Patients with RYR2 Mutations2015
- Author(s)
  Seiko Ohno
- Organizer
  Asian Pacific Heart Rhythm Society 2015
- Place of Presentation
  Melbourne, Australia
- Year and Date
  2015-11-19
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Quantitative Analysis of PKP2 and Neighboring Genes in a Patient with Arrhythmogenic Right Ventricular Cardiomyopathy Caused by Heterozygous PKP2 Deletion.2015
- Author(s)
  Sonoda K,Ohno S,Ohtsuki S, Yagihara N,Watanabe H,Horie M
- Organizer
  第79回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Usefulness of Benchtop Next Generation Sequencer in Research of Inherited Primary Arrhythmia Syndromes2015
- Author(s)
  Ohno S,Fukuyama M,Itoh H,Makiyama T,Horie M
- Organizer
  第79回日本循環器学会総会・学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] AKAP9 mutations identified in young patientswith idiopathic ventricular fibrillation or polymorphic ventricular tachycardia2015
- Author(s)
  Sonoda K, Ohno S, Ichikawa M, Fujii Y, Wang Q, Kato K, Fukuyama M, Ito H, Hayashi H, Horie M:
- Organizer
  ESC CONGRESS 2015
- Place of Presentation
  イギリス
- Year and Date
  2015-08-29
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] The genetics underlying the acquired long QT syndrome. Impact on management.2015
- Author(s)
  Itoh H, Spazzolini C, Crotti L, Aiba T, Denjoy I, Fressart V, Hayashi K, Nakajima T, Ohno S, Makiyama T, Wu J, Hasegawa K, Mastantuono E, Dagradi F, Pedrazzini M, Yamagishi M, Berthet M, Murakami Y, Shimizu W, Guicheney P, Schwartz PJ, Horie M.
- Organizer
  The Heart Rhythm Society's 36th Annual Scientific Sessions
- Place of Presentation
  アメリカ合衆国
- Year and Date
  2015-05-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Do desmosome gene mutations cause or modify the Brugada syndrome?2015
- Author(s)
  Ohno S, Aizawa Y,Horie M. et,al.
- Organizer
  Heart Rhythm 2015
- Place of Presentation
  Boston, USA
- Year and Date
  2015-05-14
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09689
[Presentation] Arrhythmogenic ventricular cardiomyopathy with peculiar ventricular aneurysm and TMEM43 mutations2015
- Author(s)
  Ichikawa M, Ohno S, Fujii Y, Ozawa J, Sonoda K, Fukuyama M, Kato K, Itoh H,Horie M
- Organizer
  EUROPACE- CARDIOSTIM 2015
- Place of Presentation
  イタリア
- Year and Date
  2015-06-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818
[Presentation] Exon-3 deletion of RyR2 encoding cardiac ryanodine receptor related to left ventricular non-compaction (LVNC) with ventricular arrhythmia and bradycardia.2013
- Author(s)
  S. Ohno, M. Omura, M. Kawamura, H. Kimua, H. Itoh, T. Makiyama, H. Ushinohama, N. Makita, M. Horie
- Organizer
  European Heart Rhythm Society Meeting
- Place of Presentation
  Athene、ギリシャ共和国
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Different regulation of IKs channels by two KCNE1 C-terminal variants predicts the QTc response to the exercise stress.2013
- Author(s)
  Ohno S, Hasegawa K, Makiyama T, Doi S, Horie M
- Organizer
  Heart Rhythm 2013
- Place of Presentation
  Denver, CO, USA
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Exon-3 Deletion of RYR2 Leads to Left Ventricular Non-compaction with Catecholaminergic Polymorphic Ventricular Tachycardia and Severe Bradycardia2013
- Author(s)
  Ohno S, Kawamura M, Omura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M
- Organizer
  Japanese Circulation Cociety meeting 2013
- Place of Presentation
  横浜、神奈川
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Exon-3 Deletion of RyR2 Encoding Cardiac Ryanodine Receptor Related to Left Ventricular Non-Compaction (LVNC) with Ventricular Arrhythmia and Bradycardia.2013
- Author(s)
  Ohno S, Omura M, Kawamura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M
- Organizer
  EHRA Europace 2013
- Place of Presentation
  Athens, Greece
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Age dependent clinical and genetic characteristics in Japanese patients with Arrhythmogenic right ventricular cardiomyopathy/dysplasia2012
- Author(s)
  Ohno S, Nishio Y, Nagaoka I, Fukuyama M, Kimura H, Itoh H, Makiyama T, Shimiu A, Horie M
- Organizer
  APHRS2012
- Place of Presentation
  Taipei, Taiwan
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] 不整脈源性右室心筋症/異型性 (ARVC/D) における年齢依存性の臨床および遺伝的特徴2012
- Author(s)
  大野聖子、西尾由貴子、長岡伊織、福山恵、木村紘美、伊藤英樹、牧山武、清水昭彦、堀江稔
- Organizer
  第60回心臓病学会
- Place of Presentation
  金沢、石川
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] QT延長症候群合併Down症候群症例におけるSNaP shot法を用いたKCNE1-D85Nアレル頻度の同定2012
- Author(s)
  大野聖子、高橋実穂、福山　恵、王　琦、木村紘美、伊藤英樹、牧山　武、堀米仁志、堀江　稔
- Organizer
  第30回日本心電学会
- Place of Presentation
  幕張、千葉
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] High frequency of ANK2 mutations in patients with non-genotyped primary inherited arrhythmia syndromes.
- Author(s)
  S Ohno, M Fukuyama, H Itoh, T Makiyama, M Horie
- Organizer
  European Society of Cardiology Meeting 2015
- Place of Presentation
  Barceｌona, Spain
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Do desmosome gene mutations cause or modify the Brugada syndrome?
- Author(s)
  S Ohno, Y Aizawa, M Fukuyama, T Makiyama, K Kosaki, K Fukuda, M Horie
- Organizer
  Heart Rhythm Society Meeting 2015
- Place of Presentation
  Boston, USA
- Year and Date
  2015-05-13 – 2015-05-16
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Mosaic KCNJ2 Mutation in Andersen–Tawil syndrome: Targeted Deep Sequencing is Useful for the Detection of Mosaicism
- Author(s)
  K Hasegawa, S Ohno, H Kimura, H Itoh, T Makiyama, Y Yoshida, M Horie
- Organizer
  Heart Rhythm Society Meeting 2014
- Place of Presentation
  San Francisco, USA
- Year and Date
  2014-05-07 – 2014-05-10
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Identification of latent mutations in primary inherited arrhythmia syndromes using benchtop next generation sequencer. Benchtop Next Generation Sequencer Has Facilitated the Genetic Analysis for Inherited Arrhythmias
- Author(s)
  S Ohno, M Fukuyama, H Itoh, T Makiyama, M Horie
- Organizer
  European Society of Cardiology Meeting 2015
- Place of Presentation
  Barceｌona, Spain
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Copy number variations in KCNQ1 gene were frequently identified in the pediatric patients of long QT syndrome and caused exercise related QT prolongation
- Author(s)
  S. Ohno, M. Fukuyama, H. Itoh, T. Makiyama, M. Horie
- Organizer
  European Society of Cardiology Meeting
- Place of Presentation
  Amsterdam、オランダ王国
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Benchtop Next Generation Sequencer Has Facilitated the Genetic Analysis for Inherited Arrhythmias
- Author(s)
  S Ohno, K Hasegawa, M Fukuyama, T Makiyama, M Horie
- Organizer
  日本循環器病学会
- Place of Presentation
  東京国際フォーラム
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Phenotypic characterization of two patients with lethal arrhythmia related to KCNH2-R148W variant
- Author(s)
  S Ohno, W Qi, K Hasegwas, H Itoh, T Makiyama, M Horie
- Organizer
  Asian Pacific Heart Rhythm Society
- Place of Presentation
  香港、中華人民共和国
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Usefulness of benchtop next generation sequencer in research of inherited primary arrhythmia syndromes
- Author(s)
  S Ohno, M Fukuyama, H Itoh, T Makiyama, M Horie
- Organizer
  第79回日本循環器病学会
- Place of Presentation
  大阪、日本
- Year and Date
  2015-04-24 – 2015-04-26
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Young long QT syndrome patients with KCNH2 mutations have late onset but severe symptoms
- Author(s)
  J Ozawa, S Ohno, H Itoh, T Makiyama, M Horie
- Organizer
  American Heart Association Meeting 2015
- Place of Presentation
  Chicago, USA
- Year and Date
  2014-11-10 – 2014-11-19
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] ARRHYTHMOGENICRIGHTVENTRICULARCARDIOMYOPATHY
- Author(s)
  S Ohno
- Organizer
  Asia Pacific Heart Rhythm Society Meeting 2014
- Place of Presentation
  Delhi, India
- Year and Date
  2014-10-29 – 2014-11-01
- Invited
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] Gender differences in the inheritance mode of RYR2 mutations in catecholaminergic polymorphic ventricular tachycardia patients
- Author(s)
  S. Ohno, M. Kawamura, K. Hasegawa, M. Horie
- Organizer
  European Society of Cardiology Meeting 2015
- Place of Presentation
  Barceｌona, Spain
- Year and Date
  2014-08-30 – 2014-09-03
- Data Source
  KAKENHI-PROJECT-24591575
[Presentation] WHICH GENETIC TESTS:SINGLE GENES, PANELS OR GENOMES?
- Author(s)
  S Ohno
- Organizer
  Asia Pacific Heart Rhythm Society Meeting 2014
- Place of Presentation
  Delhi, India
- Year and Date
  2014-10-29 – 2014-11-01
- Invited
- Data Source
  KAKENHI-PROJECT-24591575

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Ohno Seiko 大野 聖子

OHNO Seiko 大野 聖子

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

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Elucidation of pathogenesis and clinical characteristics, establishment of the therapy in patients with LQTS caused by calcium related gene variantsPrincipal Investigator

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Effective diagnosis and establishment of the therapy for catecholaminergic polymorphic ventricular tachycardiaPrincipal Investigator

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Ohno Seiko 大野聖子

OHNO Seiko 大野聖子

[Book] 循環器診療コンプリート　心筋症　「不整脈原性右室心筋症」2021

[Book] 最新ガイドラインに基づく循環器疾患診療指針2021-'22　その他の遺伝性不整脈（CPVT, QT短縮症候群, PCCD, ARVC）2020

[Book] 循環器ジャーナル　心電図診断スキルアップ2017