Fukuyama Megumi 福山恵

… Alternative Names

FUKUYAMA MEGUMI 福山恵

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Researcher Number	60625771
Other IDs
Affiliation (Current)	2025: 滋賀医科大学, 医学部, 助教
Affiliation (based on the past Project Information) *help	2015 – 2025: 滋賀医科大学, 医学部, 助教
Review Section/Research Field	Principal Investigator Basic Section 53020:Cardiology-related / Cardiovascular medicine Except Principal Investigator Basic Section 53020:Cardiology-related / Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator リアノジン受容体遺伝子 / カテコラミン誘発性多型性心室頻拍 / カテコラミン誘発多型性心室頻拍 / QT延長症候群 / 家族性不整脈症候群 / 循環器 / 遺伝子 / 遺伝性不整脈 / 遺伝性心疾患 / リアノジン受容体 … More / リアノジン受容体遺伝子異常 / CACNA1C遺伝子変異 / CACNA1C遺伝子 / QT延長症候群8型 / SCN10A遺伝子 / ブルガダ症候群 / Nav1.8 / SCN10A / 心筋ナトリウムチャネル / 遺伝性不整脈症候群 … More Except Principal Investigator 家族性心房細動 / 若年性心房細動 / 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 / 遺伝性不整脈 Less

原因が同定されていない遺伝性特発性心室細動の発症メカニズム解明と最適化治療の探索Principal Investigator
- Principal Investigator
  
  福山恵
- Project Period (FY)
  2025 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  Shiga University of Medical Science
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
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
- 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 etiology
- 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
Elucidation of pathology of inherited cardiac disease caused by mutations in ryanodine receptor genePrincipal Investigator
- 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
Elucidation of mechanism of cardiac calcium channel (CaV1.2) abnormality in long QT syndromePrincipal Investigator
- Principal Investigator
  
  Fukuyama Megumi
- Project Period (FY)
  2017 – 2018
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Shiga University of Medical Science
Mechanism of Inherited Arrhythmia Syndrome with SCN10A mutationPrincipal Investigator
- Principal Investigator
  
  FUKUYAMA MEGUMI
- Project Period (FY)
  2015 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Shiga University of Medical Science

All 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015

All Journal Article Presentation Book

[Book] 『循環器内科』第77巻4号345~352頁「特殊なQT延長：Andersen症候群・Timothy症候群」2015
- Author(s)
  福山　恵
- Total Pages
  8
- Publisher
  科学評論社
- Data Source
  KAKENHI-PROJECT-15K19375
[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] 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] Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry2023
- Author(s)
  Crotti L, Spazzolini C, Nyegaard M, Fukuyama M, Horie M, Wilde AAM, Wolf CM, Ackerman MJ, Schwartz PJ. et al
- Journal Title
  
  European Heart Journal
  
  Volume: 44 Issue: 35 Pages: 3357-3370
- DOI
  10.1093/eurheartj/ehad418
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-21H02920
[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] 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] Clopidogrel Use in CYP2C19 Loss-of-Function Carriers With High Bleeding Risk After Percutaneous Coronary Intervention2023
- Author(s)
 Yuichi Sawayama, Yukinori Tomita, Soji Kohyama, Yosuke Higo, Kenji Kodama, Kohei Asada, Noriaki Yagi, Megumi Fukuyama, Atsushi Hayashi, Wataru Shioyama, Hiroshi Sakai, Tomoya Ozawa, Tetsuichiro Isono, Daiki Hira, Takashi Yamamoto, Shin-Ya Morita, Yoshihisa Nakagawa
- Journal Title
 
 Circ J
 
 Volume: 87 Issue: 6 Pages: 755-763
- DOI
 10.1253/circj.CJ-22-0826
- ISSN
 1346-9843, 1347-4820
- Year and Date
 2023-05-25
- Language
 English
- Peer Reviewed
- Data Source
 KAKENHI-PROJECT-22K08179
[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] 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] Impact of statin therapy on late target lesion revascularization after everolimus-eluting stent implantation according to pre-interventional vessel remodeling and vessel size of treated lesion2022
- Author(s)
  Kohei Asada, Teruki Takeda, Yosuke Higo, Yuichi Sawayama, Noriaki Yagi, Megumi Fukuyama, Masayuki Yamaji, Hiroshi Sakai, Hiroshi Mabuchi, Takashi Yamamoto, Yoshihisa Nakagawa
- Journal Title
  
  Heart Vessels
  
  Volume: 37 Issue: 11 Pages: 1817-1828
- DOI
  10.1007/s00380-022-02104-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K08179
[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] 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] 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] 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] Comparison Between Clopidogrel and Prasugrel Associated With CYP2C19 Genotypes in Patients Receiving Percutaneous Coronary Intervention in a Japanese Population2020
- Author(s)
 Yuichi Sawayama, Takashi Yamamoto, Yukinori Tomita, Kohei Asada, Noriaki Yagi, Megumi Fukuyama, Akashi Miyamoto, Hiroshi Sakai, Tomoya Ozawa, Tetsuichiro Isono, Daiki Hira, Tomohiro Terada, Minoru Horie, Yoshihisa Nakagawa
- Journal Title
 
 Circ J
 
 Volume: 84 Issue: 9 Pages: 1575-1581
- DOI
 10.1253/circj.CJ-20-0254
- NAID
 130007890783
- ISSN
 1346-9843, 1347-4820
- Year and Date
 2020-08-25
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-19K08555, KAKENHI-PROJECT-19K17520, KAKENHI-PROJECT-18K06782
[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] 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] Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes2016
- Author(s)
 Ichikawa M, Horie M, et al.
- Journal Title
 
 Circ J
 
 Volume: 80 Issue: 12 Pages: 2435-2442
- DOI
 10.1253/circj.CJ-16-0486
- NAID
 130005284992
- ISSN
 1346-9843, 1347-4820
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25460406, KAKENHI-PROJECT-15K19375, KAKENHI-PROJECT-15K09150
[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] 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
[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] 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] 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] 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] 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] 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] 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] 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] 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] Association between CYP2C19 Polymorphism and High Bleeding Risk in Patients Received Percutaneous Coronary Intervention2021
- Author(s)
  Yuichi Sawayama, Takashi Yamamoto, Yousuke Higo, Kohei Asada, Noriaki Yagi, Megumi Fukuyama, Akashi Miyamoto, 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] 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] 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] 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] Usefulness of Genetic Screening for Long QT syndrome in the School-Based Electrocardiographic Screening Programs2019
- Author(s)
  福山　恵, 大野聖子, 小澤淳一, 髙山幸一郎, 加藤浩一, 伊藤英樹, 青木寿明, 牧山武, 堀江稔
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-17K15999
[Presentation] 常染色体優性多発性嚢胞腎に合併した重症心不全の 1 例2019
- Author(s)
  植村裕樹, 福山恵, 酒井宏, 山本孝, 中川義久
- Organizer
  日本内科学会第 226 回近畿地方会
- Data Source
  KAKENHI-PROJECT-19K08555
[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] Ebstein病に左室緻密化障害を合併した心室頻拍の一例2019
- Author(s)
  西川拓磨, 小澤友哉, 奥谷雄介, 藤居祐介, 加藤浩一, 福山恵, 芦原貴司, 山本孝
- Organizer
  第126回日本循環器学会近畿地方会
- Data Source
  KAKENHI-PROJECT-17K15999
[Presentation] A case of successful recanalization of thrombotic occlusion of the external iliac artery2019
- Author(s)
  澤山裕一浅田紘平, 八木典章, 福山恵, 宮本証, 酒井宏, 山本孝, 中川義久
- Organizer
  CCT2019
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] An NGS-based genotyping in LQTS; minor genes are no longer minor2019
- Author(s)
  Seiko Ohno, Junichi Ozawa, Megumi Fukuyama, Takeru Makiyama, Minoru Horie
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-17K15999
[Presentation] A severely calcified coronary lesion that a burr cannot penetrate2019
- Author(s)
  Asada K, Sawayama Y, Yagi N, Fukuyama M, Sakai H, Yamamoto T, Nakagawa Y.
- Organizer
  CCT2019
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] Excessive Ca2+ Release from Ryanodine Receptors Underlying a RyR2 Mutation Associated with Catecholaminergic Polymorphic Ventricular Tachycardia2019
- Author(s)
  伊藤英樹, 村山尚, 呉林なごみ, 大野聖子, 藤居祐介, 加藤浩一, 福山恵, 髙山幸一郎, 渡邉昌也, 安斉俊久, 堀江稔
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-17K15999
[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] DCB versus DES in STEMI.2019
- Author(s)
  浅田紘平, 澤山裕一, 八木典章, 福山恵, 宮本証, 酒井宏, 山本孝, 中川義久
- Organizer
  PAC19
- Data Source
  KAKENHI-PROJECT-19K08555
[Presentation] How to Confirm the Pathogenicity of Gene Variants in Inherited Primary Arrhythmia Syndrome.2018
- Author(s)
  Fukuyama M, Ohno S, Takayama K, Ichikawa M, Fukumoto D, Horie M.
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-17K15999
[Presentation] Consideration of CACNA1C variants in Long QT Syndrome2018
- Author(s)
  Megumi Fukuyama, Seiko Ohno, Minoru Horie
- Organizer
  第65回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-17K15999
[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-17K15999
[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-17K15999
[Presentation] Rare Single Nucleotide Polymorphism of SCN10A in Patients with Inherited Primary Arrhythmia Syndromes2017
- Author(s)
  Megumi Fukuyama, Seiko Ohno, Mari Ichikawa, Takeru Makiyama, Minoru Horie
- Organizer
  第81回日本循環器学会学術集会
- Place of Presentation
  金沢、石川
- Year and Date
  2017-03-17
- Data Source
  KAKENHI-PROJECT-15K19375
[Presentation] Novel intracellular transport-refractory mutations in KCNH2 identified in symptomatic long QT syndrome patients2017
- Author(s)
  Fukumoto D, Ohno S, Wada Y, Fujii Y, Ichikawa M, Takayama K, Fukuyama M, Makiyama T, Itoh H, Ding WG, Matsuura H, Horie M.
- Organizer
  ESC Congress 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K15999
[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-17K15999
[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-17K15999
[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-17K15999
[Presentation] Double mutations in RYR2 cause severe phenotype of catecholaminergic polymorphic ventricular tachycardia2017
- Author(s)
  Takayama K, Ohno S, Fukumoto D, Wada Y, Ichikawa M, Fukuyama M, Itoh H, Horie M.
- Organizer
  ESC Congress 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K15999
[Presentation] A Novel Transport Refractory Mutation in KCNH2 Identified in Symptomatic Long QT Syndrome Patients.2017
- Author(s)
  Fukumoto D, Ohno S, Wada Y, Fujii Y, Ichikawa M, Fukuyama M, Itoh H, Matsuura H, Horie M
- Organizer
  第81回日本循環器学会学術集会
- Place of Presentation
  金沢、石川
- Year and Date
  2017-03-17
- Data Source
  KAKENHI-PROJECT-15K19375
[Presentation] High frequency of CACNA1C mutations among 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-17K15999
[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-17K15999
[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
  Seoul, Korea
- Year and Date
  2016-10-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19375
[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
  2016-08-27
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19375
[Presentation] Rare Single Nucleotide Polymorphism of SCN10A in Patients with Inherited Primary Arrhythmia Syndromes2016
- Author(s)
  Megumi Fukuyama, Seiko Ohno, Mari Ichikawa, Takeru Makiyama, Minoru Horie
- Organizer
  ESC CONGRESS 2016
- Place of Presentation
  Rome, Italy
- Year and Date
  2016-08-27
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19375
[Presentation] High prevalence of late onset T in patients with long QT syndrome type 8.2016
- Author(s)
  Ohno S, Junichi Ozawa, Megumi Fukuyama, Takeru Makiyama, Minoru Horie
- Organizer
  American Heart Association
- Place of Presentation
  New Orleans, USA
- Year and Date
  2016-11-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19375
[Presentation] Arrhythmogenic ventricular cardiomyopathy with peculiar ventricular aneurysm and TMEM43 mutations.2015
- Author(s)
  Ichikawa M, Ohno S, Fujii Y, Ozawa J, Sonoda K, Fukuyama M, Kato K, Itoh H,Horie M
- Organizer
  Europace
- Place of Presentation
  Milan, Italy
- Year and Date
  2015-06-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19375
[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
  Heart Rhythm
- Place of Presentation
  Boston, USA
- Year and Date
  2015-05-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19375
[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
- Place of Presentation
  Milan, Italy
- Year and Date
  2015-06-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19375
[Presentation] AKAP9 mutations identified in young patientswith idiopathic ventricular fibrillation or polymorphic ventricular tachycardia.2015
- 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
  London, England
- Year and Date
  2015-08-29
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19375

1. 大野聖子 (20610025)

# of Collaborated Projects: 6 results

# of Collaborated Products: 42 results
2. 堀江稔 (90183938)

# of Collaborated Projects: 4 results

# of Collaborated Products: 39 results
3. 加藤浩一 (70736983)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
4. 園田桂子 (90824417)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
5. ZANKOV DimitarP (20631295)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 牧山武 (30528302)

# of Collaborated Projects: 1 results

# of Collaborated Products: 7 results
7. 相庭武司 (40574348)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
8. 高山幸一郎 (20816988)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. Wang Qi (70756767)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. 小澤友哉 (20584395)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. KOBAYASHI Takuya

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
12. 藍智彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
13. 松浦博

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
14. 丁維光

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
15. 国広なごみ

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Fukuyama Megumi 福山 恵

FUKUYAMA MEGUMI 福山 恵

Research Projects

Research Products

Co-Researchers

原因が同定されていない遺伝性特発性心室細動の発症メカニズム解明と最適化治療の探索Principal Investigator

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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

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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

Principal Investigator

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Research Institution

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

Principal Investigator

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Elucidation of pathology of inherited cardiac disease caused by mutations in ryanodine receptor genePrincipal Investigator

Principal Investigator

Project Period (FY)

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Review Section

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Elucidation of mechanism of cardiac calcium channel (CaV1.2) abnormality in long QT syndromePrincipal Investigator

Principal Investigator

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Research Institution

Mechanism of Inherited Arrhythmia Syndrome with SCN10A mutationPrincipal Investigator

Principal Investigator

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Research Institution

[Book] 『循環器内科』第77巻4号345~352頁「特殊なQT延長：Andersen症候群・Timothy症候群」2015

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[Journal Article] Holter Electrocardiographic Approach to Predicting Outcomes of Pediatric Patients With Long QT Syndrome2024

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[Journal Article] Clinical characterization of type 1 long QT syndrome caused by C-terminus Kv7.1 variants2024

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[Journal Article] Non-missense variants of <i>KCNH2</i> show better outcomes in type 2 long QT syndrome2023

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[Journal Article] Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry2023

Author(s)

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[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

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Fukuyama Megumi 福山恵

FUKUYAMA MEGUMI 福山恵

[Journal Article] Calmodulinopathy in Japanese Children　― Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy ―2023