研究者
J-GLOBAL ID：202001011328503067   更新日: 2022年04月14日

園田 桂子

Sonoda Keiko
論文 (22件)：
  • Keisuke Suzuki, Keiko Sonoda, Hisaaki Aoki, Yuko Nakamura, Seiichi Watanabe, Yoko Yoshida, Kenji Hoshino, Junichi Ozawa, Tomohiko Imamura, Takeshi Aiba, et al. Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome. JACC. Clinical electrophysiology. 2022. 8. 3. 297-305
  • Keiko Shimamoto, Seiko Ohno, Koichi Kato, Koichiro Takayama, Keiko Sonoda, Megumi Fukuyama, Takeru Makiyama, Satomi Okamura, Koko Asakura, Noriaki Imanishi, et al. Impact of cascade screening for catecholaminergic polymorphic ventricular tachycardia type 1. Heart (British Cardiac Society). 2022
  • Keiko Sonoda, Haruko Ishihara, Hisanori Sakazaki, Tsugutoshi Suzuki, Minoru Horie, Seiko Ohno. Long-Read Sequence Confirmed a Large Deletion Including MYH6 and MYH7 in an Infant of Atrial Septal Defect and Atrial Arrhythmias. Circulation. Genomic and precision medicine. 2021. 14. 4. e003223
  • Koichi Kato, Seiko Ohno, Keiko Sonoda, Megumi Fukuyama, Takeru Makiyama, Tomoya Ozawa, Minoru Horie. LMNA Missense Mutation Causes Nonsense-Mediated mRNA Decay and Severe Dilated Cardiomyopathy. Circulation. Genomic and precision medicine. 2020. 13. 5. 435-443
  • Keiko Sonoda, Seiko Ohno, Yukiko Shimizu, Kazuaki Kaitani, Takeru Makiyama, Yoshihisa Nakagawa, Minoru Horie. SCN5A mutation identified in a patient with short-coupled variant of torsades de pointes. Pacing and clinical electrophysiology : PACE. 2020. 43. 5. 456-461
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MISC (7件)：
  • 園田 桂子, 大野 聖子, 牧山 武, 堀江 稔. 短連結性異型トルサードドポアント患者で同定されたSCN5A遺伝子変異の機能変化(Functional Change of SCN5A Mutations Identified in the Patients with Short-Coupled Variant of Torsades de Pointes). 日本循環器学会学術集会抄録集. 2018. 82回. PJ016-4
  • 園田 桂子, 大野 聖子, 牧山 武, 堀江 稔. Functional Change of SCN5A Mutations Identified in the Patients with Short-Coupled Variant of Torsades de Pointes(和訳中). 日本循環器学会学術集会抄録集. 2018. 82回. PJ016-4
  • 園田 桂子, 大野 聖子, 市川 麻理, 服部 哲久, 伊藤 英樹, 牧山 武, 堀江 稔. 心臓突然死の遺伝的背景 ブルガダ症候群におけるSCN5Aコピー数の多様性(Copy Number Variations of SCN5A in Brugada Syndrome). 日本循環器学会学術集会抄録集. 2017. 81回. SY09-3
  • K. Sonoda, S. Ohno, J. Ozawa, M. Hayano, H. Ito, T. Makiyama, M. Horie. Copy number variations in SCN5A associated with Brugada syndrome. EUROPEAN HEART JOURNAL. 2016. 37. 841-842
  • S. Ohno, J. Wu, Y. Mizusawa, K. Sonoda, H. Itoh, T. Makiyama, M. Horie. Triple mutations in three major genes for long QT syndrome are very rare and cause complicated phenotypes with ventricular arrhythmia. EUROPEAN HEART JOURNAL. 2016. 37. 683-683
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