| Direct differentiation of atrial and ventricular myocytes from human embryonic stem cells by alternating retinoid signals Q Zhang, J Jiang, P Han, Q Yuan, J Zhang, X Zhang, Y Xu, H Cao, ... Cell research 21 (4), 579-587, 2011 | 405 | 2011 |
| Structural Basis for Gating and Activation of RyR1 JF Amédée des Georges, Oliver B Clarke, Ran Zalk, Qi Yuan, Kendall J Condon ... Cell 167 (1), 145-157. e17, 2016 | 378 | 2016 |
| Mitochondrial oxidative stress promotes atrial fibrillation W Xie, G Santulli, SR Reiken, Q Yuan, BW Osborne, BX Chen, AR Marks Scientific reports 5, 2015 | 287 | 2015 |
| Intracellular calcium release channels: an update G Santulli, R Nakashima, Q Yuan, AR Marks The Journal of Physiology 595 (10), 3041-3051, 2017 | 219 | 2017 |
| Intracellular calcium leak in heart failure and atrial fibrillation: a unifying mechanism and therapeutic target ARM Haikel Dridi, Alexander Kushnir, Ran Zalk, Qi Yuan, Zephan Melville Nature Reviews Cardiology, 2020 | 141 | 2020 |
| Functional role of Calstabin2 in age-related cardiac alterations Q Yuan, Z Chen, G Santulli, L Gu, ZG Yang, ZQ Yuan, YT Zhao, HB Xin, ... Scientific reports 4, 7425, 2014 | 72 | 2014 |
| Maintenance of normal blood pressure is dependent on IP3R1-mediated regulation of eNOS Q Yuan, J Yang, G Santulli, SR Reiken, A Wronska, MM Kim, BW Osborne, ... Proceedings of the National Academy of Sciences 113 (30), 8532-8537, 2016 | 70 | 2016 |
| Intracellular calcium leak as a therapeutic target for RYR1-related myopathies. A Kushnir, JJ Todd, JW Witherspoon, Q Yuan, S Reiken, H Lin, RH Munce, ... Acta neuropathologica, 2020 | 37 | 2020 |
| Role of defective calcium regulation in cardiorespiratory dysfunction in Huntington’s disease H Dridi, X Liu, Q Yuan, S Reiken, M Yehya, L Sittenfeld, P Apostolou, ... JCI insight, 2020 | 34 | 2020 |
| ERP44 inhibits human lung cancer cell migration mainly via IP3R2 X Huang, M Jin, YX Chen, J Wang, K Zhai, Y Chang, Q Yuan, KT Yao, G Ji Aging (Albany NY) 8 (6), 1276, 2016 | 28 | 2016 |
| A drug and ATP binding site in type 1 ryanodine receptor Z Melville, H Dridi, Q Yuan, S Reiken, A Wronska, Y Liu, OB Clarke, ... Structure, 2022 | 26 | 2022 |
| Structural analyses of human ryanodine receptor type 2 channels reveal the mechanisms for sudden cardiac death and treatment MC Miotto, G Weninger, H Dridi, Q Yuan, Y Liu, A Wronska, Z Melville, ... Science Advances 8 (29), eabo1272, 2022 | 25 | 2022 |
| Sensitized signalling between L-type Ca2+ channels and ryanodine receptors in the absence or inhibition of FKBP12.6 in cardiomyocytes YT Zhao, YB Guo, L Gu, XX Fan, HQ Yang, Z Chen, P Zhou, Q Yuan, GJ Ji, ... Cardiovascular research 113 (3), 332-342, 2017 | 24 | 2017 |
| Calstabin 2: An important regulator for learning and memory in mice Q Yuan, KY Deng, L Sun, S Chi, Z Yang, J Wang, HB Xin, X Wang, G Ji Scientific reports 6, 2016 | 24 | 2016 |
| CUG-BP1 regulates RyR1 ASI alternative splicing in skeletal muscle atrophy Y Tang, H Wang, B Wei, Y Guo, L Gu, Z Yang, Q Zhang, Y Wu, Q Yuan, ... Scientific reports 5, 2015 | 24 | 2015 |
| Attenuating persistent sodium current–induced atrial myopathy and fibrillation by preventing mitochondrial oxidative stress UMR Avula, H Dridi, B Chen, Q Yuan, AN Katchman, SR Reiken, ... JCI insight 6 (23), 2021 | 23 | 2021 |
| NFAT5-mediated CACNA1C expression is critical for cardiac electrophysiological development and maturation W Li, NZ Zheng, Q Yuan, K Xu, F Yang, L Gu, GY Zheng, GJ Luo, C Fan, ... Journal of Molecular Medicine 94 (9), 993-1002, 2016 | 22 | 2016 |
| Erratum to: NFAT5-mediated CACNA1C expression is critical for cardiac electrophysiological development and maturation. W Li, NZ Zheng, Q Yuan, K Xu, F Yang, L Gu, GY Zheng, GJ Luo, C Fan, ... Journal of molecular medicine (Berlin, Germany) 94 (9), 1003, 2016 | 22* | 2016 |
| NFAT5-mediated CACNA1C expression is critical for cardiac electrophysiological development and maturation W Li, NZ Zheng, Q Yuan, K Xu, F Yang, L Gu, GY Zheng, GJ Luo, C Fan, ... Journal of Molecular Medicine 94 (9), 993-1002, 2016 | 22 | 2016 |
| Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation H Dridi, W Wu, SR Reiken, RM Ofer, Y Liu, Q Yuan, L Sittenfeld, ... Human molecular genetics 29 (24), 3919-3934, 2020 | 18 | 2020 |
