Seiko Ohno
- Director, Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute
- 1. Genomic epidemiology in cardiovascular disease
2. Study of inherited cardiovascular disease
CV
1997 Graduate Tohoku University of Medical Science
2006 Graduate Kyoto University Graduate School of Mryakedicine
2011 Assistant professor, cardiovascular and respiratory department in Shiga University of Medicine
2014 Assistant professor (Lecturer), center for epidemiologic research in Asia
2018 Director, Department of Bioscience and Genetics, National Cerebral and Cardiovascular Center Research Institute
Message
Publication
1. Ohno S, Hasegawa K, Horie M. Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients. PLoS ONE. 2015;10(6):e0131517.
2. Ohno S, Omura M, Kawamura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M. Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction. Europace. 2014;16(11):1646-1654.
3. Bezzina CR, Barc J, Mizusawa Y, Remme CA, Gourraud JB, Simonet F, Verkerk AO, Schwartz PJ, Crotti L, Dagradi F, Guicheney P, Fressart V, Leenhardt A, Antzelevitch C, Bartkowiak S, Borggrefe M, Schimpf R, Schulze-Bahr E, Zumhagen S, Behr ER, Bastiaenen R, Tfelt-Hansen J, Olesen MS, Kaab S, Beckmann BM, Weeke P, Watanabe H, Endo N, Minamino T, Horie M, Ohno S, Hasegawa K, Makita N, Nogami A, Shimizu W, Aiba T, Froguel P, Balkau B, Lantieri O, Torchio M, Wiese C, Weber D, Wolswinkel R, Coronel R, Boukens BJ, Bezieau S, Charpentier E, Chatel S, Despres A, Gros F, Kyndt F, Lecointe S, Lindenbaum P, Portero V, Violleau J, Gessler M, Tan HL, Roden DM, Christoffels VM, Le Marec H, Wilde AA, Probst V, Schott JJ, Dina C, Redon R. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nat Genet. 2013;45(9):1044-1049.