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Ultrastructural maturation of human-induced pluripotent stem cell-derived cardiomyocytes in a long-term culture T Kamakura, T Makiyama, K Sasaki, Y Yoshida, Y Wuriyanghai, J Chen, ... Circulation Journal 77 (5), 1307-1314, 2013 | 340 | 2013 |
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome N Makita, E Behr, W Shimizu, M Horie, A Sunami, L Crotti, E Schulze-Bahr, ... The Journal of clinical investigation 118 (6), 2219-2229, 2008 | 269 | 2008 |
A Novel SCN5A Gain-of-Function Mutation M1875T Associated With Familial Atrial Fibrillation T Makiyama, M Akao, S Shizuta, T Doi, K Nishiyama, Y Oka, S Ohno, ... Journal of the American College of Cardiology 52 (16), 1326-1334, 2008 | 250 | 2008 |
High prevalence of early repolarization in short QT syndrome H Watanabe, T Makiyama, T Koyama, PJ Kannankeril, S Seto, K Okamura, ... Heart rhythm 7 (5), 647-652, 2010 | 211 | 2010 |
Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization H Watanabe, A Nogami, K Ohkubo, H Kawata, Y Hayashi, T Ishikawa, ... Circulation: Arrhythmia and Electrophysiology 4 (6), 874-881, 2011 | 209 | 2011 |
The genetics underlying acquired long QT syndrome: impact for genetic screening H Itoh, L Crotti, T Aiba, C Spazzolini, I Denjoy, V Fressart, K Hayashi, ... European heart journal 37 (18), 1456-1464, 2016 | 196 | 2016 |
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome Y Nishio, T Makiyama, H Itoh, T Sakaguchi, S Ohno, YZ Gong, ... Journal of the American College of Cardiology 54 (9), 812-819, 2009 | 179 | 2009 |
High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations T Makiyama, M Akao, K Tsuji, T Doi, S Ohno, K Takenaka, A Kobori, ... Journal of the American College of Cardiology 46 (11), 2100-2106, 2005 | 171 | 2005 |
Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese … K Yamagata, M Horie, T Aiba, S Ogawa, Y Aizawa, T Ohe, M Yamagishi, ... Circulation 135 (23), 2255-2270, 2017 | 170 | 2017 |
KCNE5 (KCNE1L) Variants Are Novel Modulators of Brugada Syndrome and Idiopathic Ventricular Fibrillation S Ohno, DP Zankov, WG Ding, H Itoh, T Makiyama, T Doi, S Shizuta, ... Circulation: Arrhythmia and Electrophysiology 4 (3), 352-361, 2011 | 153 | 2011 |
Anticoagulation therapy for venous thromboembolism in the real world―From the COMMAND VTE Registry― Y Yamashita, T Morimoto, H Amano, T Takase, S Hiramori, K Kim, ... Circulation Journal 82 (5), 1262-1270, 2018 | 137 | 2018 |
Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome H Itoh, T Sakaguchi, WG Ding, E Watanabe, I Watanabe, Y Nishio, ... Circulation: Arrhythmia and Electrophysiology 2 (5), 511-523, 2009 | 126 | 2009 |
Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study H Itoh, W Shimizu, K Hayashi, K Yamagata, T Sakaguchi, S Ohno, ... Heart Rhythm 7 (10), 1411-1418, 2010 | 119 | 2010 |
Impact of CYP2C19 polymorphisms on the antiplatelet effect of clopidogrel in an actual clinical setting in Japan T Jinnai, H Horiuchi, T Makiyama, J Tazaki, T Tada, M Akao, K Ono, ... Circulation Journal 73 (8), 1498-1503, 2009 | 116 | 2009 |
Phenotype Variability in Patients Carrying KCNJ2 Mutations H Kimura, J Zhou, M Kawamura, H Itoh, Y Mizusawa, WG Ding, J Wu, ... Circulation: Cardiovascular Genetics 5 (3), 344-353, 2012 | 112 | 2012 |
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome N Lahrouchi, R Tadros, L Crotti, Y Mizusawa, PG Postema, L Beekman, ... Circulation 142 (4), 324-338, 2020 | 111 | 2020 |
Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation Y Yamamoto, T Makiyama, T Harita, K Sasaki, Y Wuriyanghai, M Hayano, ... Human Molecular Genetics 26 (9), 1670-1677, 2017 | 108 | 2017 |
Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction S Ohno, M Omura, M Kawamura, H Kimura, H Itoh, T Makiyama, ... Europace 16 (11), 1646-1654, 2014 | 103 | 2014 |
Long-term follow-up of a pediatric cohort with short QT syndrome J Villafañe, J Atallah, MH Gollob, P Maury, C Wolpert, R Gebauer, ... Journal of the American College of Cardiology 61 (11), 1183-1191, 2013 | 103 | 2013 |