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Circulation Journal : Official Journal of the Japanese Circulation Society|February 5, 2014
A novel HCN4 mutation, G1097W, is associated with atrioventricular blockJun Zhou, Wei-Guang Ding, Takeru Makiyama, et al.Circulation Journal : Official Journal of the Japanese Circulation Society|July 28, 2020
Comparison Between Clopidogrel and Prasugrel Associated With CYP2C19 Genotypes in Patients Receiving Percutaneous Coronary Intervention in a Japanese PopulationYuichi Sawayama, Takashi Yamamoto, Yukinori Tomita, et al.Circulation. Arrhythmia and Electrophysiology|April 16, 2011
KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idiopathic ventricular fibrillationSeiko Ohno, Dimitar P Zankov, Wei-Guang Ding, et al.Journal of Cardiovascular Electrophysiology|January 10, 2014
Gain-of-function KCNH2 mutations in patients with Brugada syndromeQ I Wang, Seiko Ohno, Wei-Guang Ding, et al.Circulation. Cardiovascular Genetics|May 17, 2012
Phenotype variability in patients carrying KCNJ2 mutationsHiromi Kimura, Jun Zhou, Mihoko Kawamura, et al.Circulation Journal : Official Journal of the Japanese Circulation Society|April 19, 2013
Genetic background of catecholaminergic polymorphic ventricular tachycardia in JapanMihoko Kawamura, Seiko Ohno, Nobu Naiki, et al.Circulation. Arrhythmia and Electrophysiology|October 22, 2009
Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndromeHideki Itoh, Tomoko Sakaguchi, Wei-Guang Ding, et al.Pageof 2