メディカルゲノムセンター
研究業績
  1. Kato K, Higo Y, Aizawa T, Fukuyama M, Sonoda K, Hisamatsu T, Fujii Y, Itoh H, Makiyama T, Ohno S, Nakagawa Y, Horie M. Long-Term Arrhythmic Outcomes of KCNJ2 Variant Carriers in Japan. Circulation: Genomic and Precision Medicine. e005188, 2025, 18.
  2. Nomura Y, Ishikawa T, Ohno S, Makita N, Horie M, Naruse H, Koshikawa M, Nishimura A, Motoike Y, Harada M, Sobue Y, Watanabe E, Izawa H. Atypical Holt-Oram syndrome: Early-onset sick sinus syndrome in a Japanese family with a novel TBX5 mutation, Q469. Journal of Cardiology Cases. 10-14, 2025, 32.
  3. Ohno S, Kato K, Fukuyama M, Hirono K, Nishida K, Horie M. Long-term follow-up of patients with catecholaminergic polymorphic ventricular tachycardia related to a novel CALM2 variant. Journal of Cardiology Cases. 6-8, 2025, 33.
  4. Ohya H, Inaba O, Inamura Y, Kato K, Ohno S, Sasano T. Episodic long-lasting atrial standstill associated with an SCN5A variant resulting in atrial pacing failure: Is an atrial lead necessary for familial atrial standstill? Heart Rhythm Case Reports. 56-60, 2025, 11.
  5. Takeda Y, Fujita S, Yachi Y, Honda M, Iwata M, Sakumura N, Ueno K, Miyashita K, Futatani T, Usuda K, Chikata A, Usuda K, Nishida K, Araki R, Kato K, Ohno S. SCN5A mutation-associated sick sinus syndrome revealed by atrial flutter in a pediatric patient. Journal of Cardiology Cases. 5-9, 2025, 32.