| Novel calmodulin mutations associated with congenital arrhythmia susceptibility N Makita, N Yagihara, L Crotti, CN Johnson, BM Beckmann, MS Roh, ... Circulation: Cardiovascular Genetics 7 (4), 466-474, 2014 | 221 | 2014 |
| 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 | 215 | 2011 |
| Dilated cardiomyopathy‐associated BAG3 mutations impair Z‐disc assembly and enhance sensitivity to apoptosis in cardiomyocytes T Arimura, T Ishikawa, S Nunoda, S Kawai, A Kimura Human mutation 32 (12), 1481-1491, 2011 | 182 | 2011 |
| A novel disease gene for brugada syndrome: sarcolemmal membrane–associated protein gene mutations impair intracellular trafficking of hnav1. 5 T Ishikawa, A Sato, CA Marcou, DJ Tester, MJ Ackerman, L Crotti, ... Circulation: Arrhythmia and Electrophysiology 5 (6), 1098-1107, 2012 | 135 | 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 | 128 | 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 | 111 | 2017 |
| Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1. 5 T Ishikawa, N Takahashi, S Ohno, H Sakurada, K Nakamura, YK On, ... Circulation Journal 77 (4), 959-967, 2013 | 93 | 2013 |
| Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls R Walsh, N Lahrouchi, R Tadros, F Kyndt, C Glinge, PG Postema, ... Genetics in medicine 23 (1), 47-58, 2021 | 82 | 2021 |
| Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers S Nishiuchi, T Makiyama, T Aiba, K Nakajima, S Hirose, H Kohjitani, ... Circulation: cardiovascular genetics 10 (6), e001603, 2017 | 78 | 2017 |
| The effect of pimobendan on left atrial pressure in dogs with mitral valve regurgitation S Suzuki, R Fukushima, T Ishikawa, L Hamabe, D Aytemiz, H Huai‐Che, ... Journal of Veterinary Internal Medicine 25 (6), 1328-1333, 2011 | 76 | 2011 |
| Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias A Koizumi, T Sasano, W Kimura, Y Miyamoto, T Aiba, T Ishikawa, ... European Heart Journal 37 (18), 1469-1475, 2016 | 73 | 2016 |
| Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome DT Harrell, T Ashihara, T Ishikawa, I Tominaga, A Mazzanti, K Takahashi, ... International journal of cardiology 190, 393-402, 2015 | 70 | 2015 |
| Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome T Ishikawa, H Kimoto, H Mishima, K Yamagata, S Ogata, Y Aizawa, ... European heart journal 42 (29), 2854-2863, 2021 | 68 | 2021 |
| Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction T Ishikawa, S Ohno, T Murakami, K Yoshida, H Mishima, T Fukuoka, ... Heart Rhythm 14 (5), 717-724, 2017 | 62 | 2017 |
| Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics K Abe, T Machida, N Sumitomo, H Yamamoto, K Ohkubo, I Watanabe, ... Circulation: Arrhythmia and Electrophysiology 7 (3), 511-517, 2014 | 62 | 2014 |
| Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations T Arimura, K Onoue, Y Takahashi-Tanaka, T Ishikawa, M Kuwahara, ... Cardiovascular research 99 (3), 382-394, 2013 | 61 | 2013 |
| SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families YD Wijeyeratne, MW Tanck, Y Mizusawa, V Batchvarov, J Barc, L Crotti, ... Circulation: Genomic and Precision Medicine 13 (6), e002911, 2020 | 60 | 2020 |
| Dilated cardiomyopathy-associated FHOD3 variant impairs the ability to induce activation of transcription factor serum response factor T Arimura, R Takeya, T Ishikawa, T Yamano, A Matsuo, T Tatsumi, ... Circulation Journal 77 (12), 2990-2996, 2013 | 59 | 2013 |
| 40th EASD Annual Meeting of the European Association for the Study of Diabetes: Munich, Germany, 5–9 September 2004 M Veitenhansl, K Stegner, FX Hierl, C Dieterle, H Feldmeier, B Gutt, ... Diabetologia 47, A1-A464, 2004 | 56 | 2004 |
| HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node Y Kozasa, N Nakashima, M Ito, T Ishikawa, H Kimoto, K Ushijima, ... The Journal of physiology 596 (5), 809-825, 2018 | 52 | 2018 |
