| Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ... Nature genetics 45 (9), 1044-1049, 2013 | 540 | 2013 |
| 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 | 334 | 2013 |
| 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 |
| European heart rhythm association (EHRA)/heart rhythm society (HRS)/Asia pacific heart rhythm society (APHRS)/latin American heart rhythm society (LAHRS) expert consensus … AAM Wilde, C Semsarian, MF Márquez, AS Shamloo, MJ Ackerman, ... Europace 24 (8), 1307-1367, 2022 | 209* | 2022 |
| 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 | 198 | 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 | 176 | 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 | 170 | 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 | 163 | 2017 |
| Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan W Shimizu, M Horie, S Ohno, K Takenaka, M Yamaguchi, M Shimizu, ... Journal of the American College of Cardiology 44 (1), 117-125, 2004 | 159 | 2004 |
| 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 | 152 | 2011 |
| Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry L Crotti, C Spazzolini, DJ Tester, A Ghidoni, AE Baruteau, BM Beckmann, ... European heart journal 40 (35), 2964-2975, 2019 | 138 | 2019 |
| 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 | 124 | 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 | 117 | 2010 |
| 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 | 114 | 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 | 107 | 2020 |
| Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest C Van Der Werf, KV Lieve, JM Bos, CM Lane, I Denjoy, F Roses-Noguer, ... European heart journal 40 (35), 2953-2961, 2019 | 107 | 2019 |
| 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 | 104 | 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 |
| A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents T Hattori, T Makiyama, M Akao, E Ehara, S Ohno, M Iguchi, Y Nishio, ... Cardiovascular research 93 (4), 666-673, 2012 | 101 | 2012 |
| Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes M Fukuyama, Q Wang, K Kato, S Ohno, WG Ding, F Toyoda, H Itoh, ... Europace 16 (12), 1828-1837, 2014 | 95 | 2014 |
