| Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population B Wang, Z Miao, S Liu, J Wang, S Zhou, L Han, D Meng, Y Wang, C Li, ... Human genetics 127, 245-246, 2010 | 80 | 2010 |
| Femtosecond-laser-driven wire-guided helical undulator for intense terahertz radiation Y Tian, J Liu, Y Bai, S Zhou, H Sun, W Liu, J Zhao, R Li, Z Xu Nature Photonics 11 (4), 242-246, 2017 | 79 | 2017 |
| A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family B Wang, C Yu, YB Xi, HC Cai, J Wang, S Zhou, S Zhou, Y Wu, YB Yan, ... Human mutation 32 (1), E1939-E1947, 2011 | 61 | 2011 |
| Development and validation of a predictive model for chronic kidney disease progression in type 2 diabetes mellitus based on a 13-year study in Singapore S Low, SC Lim, X Zhang, S Zhou, LY Yeoh, YL Liu, S Tavintharan, ... Diabetes research and clinical practice 123, 49-54, 2017 | 47 | 2017 |
| A novel mutation impairing the tertiary structure and stability of γC‐crystallin (CRYGC) leads to cataract formation in humans and zebrafish lens XQ Li, HC Cai, SY Zhou, JH Yang, YB Xi, XB Gao, WJ Zhao, P Li, ... Human mutation 33 (2), 391-401, 2012 | 42 | 2012 |
| A novel GJA8 mutation (p. I31T) causing autosomal dominant congenital cataract in a Chinese family K Wang, B Wang, J Wang, S Zhou, B Yun, P Suo, J Cheng, X Ma, S Zhu Molecular Vision 15, 2813, 2009 | 37 | 2009 |
| The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe … H Liu, C Lu, Z Li, S Zhou, X Li, L Ji, Q Lu, R Lv, L Wu, X Ma Epilepsy research 95 (1-2), 94-99, 2011 | 34 | 2011 |
| Genetic variants in the receptor for advanced glycation end products (RAGE) gene were associated with circulating soluble RAGE level but not with renal function … SC Lim, R Dorajoo, X Zhang, L Wang, SF Ang, CSH Tan, LY Yeoh, ... Nephrology Dialysis Transplantation 32 (10), 1697-1704, 2017 | 33 | 2017 |
| Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3) Z Zhou, S Hu, B Wang, N Zhou, S Zhou, X Ma, Y Qi Molecular Vision 16, 713, 2010 | 29 | 2010 |
| Cloning and expression of a toxin gene from Pseudomonas fluorescens GcM5-1A L Kong, D Guo, S Zhou, X Yu, G Hou, R Li, B Zhao Archives of microbiology 192, 585-593, 2010 | 27 | 2010 |
| Self-organized kilotesla magnetic-tube array in an expanding spherical plasma irradiated by kHz femtosecond laser pulses S Zhou, Y Bai, Y Tian, H Sun, L Cao, J Liu Physical review letters 121 (25), 255002, 2018 | 26 | 2018 |
| Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect B Wang, J Yan, R Mi, SY Zhou, XD Xie, J Wang, X Ma International journal of cardiology 145 (1), 83-85, 2010 | 26 | 2010 |
| The study of copy number variations in the regions of NOTCH1 among Chinese VSD and TOF patients J Wang, XD Xie, S Zhou, G Huang, X Ma, P Suo, S Zhou, B Wang, X Ma International journal of cardiology 147 (3), 444-446, 2011 | 14 | 2011 |
| Knockdown of p66Shc by siRNA injection rescues arsenite-induced developmental retardation in mouse preimplantation embryos K Ren, X Li, J Yan, G Huang, S Zhou, B Yang, X Ma, C Lu Reproductive Toxicology 43, 8-18, 2014 | 13 | 2014 |
| Laser-driven fast electron ionization wave propagation in a dielectric target Y Bai, Y Tian, S Zhou, Y Zeng, H Sun, C Wang, J Liu Physics of Plasmas 24 (4), 2017 | 5 | 2017 |
| Hairy-related transcription factor 2 is not potentially related to congenital heart disease in Chinese patients B Wang, S Zhou, Q Chen, XD Xie, G Huang, J Wang, S Zhoua, X Ma International journal of cardiology 146 (3), 415-416, 2011 | 5 | 2011 |
| High-energy electron radiography of microstructures in a dense material R Qi, Y Tian, GQ Zhang, YF Bai, SY Zhou, YS Zeng, HY Sun, XT Wang, ... The European Physical Journal Applied Physics 75 (3), 30701, 2016 | 2 | 2016 |
| Metabolic Dysregulation in Patients with Diabetic Neuropathy S Tavintharan, JP Kovalik, SLT Pek, S Zhou, LY Yeoh, SC Lim, CF Sum DIABETES 65, A153-A153, 2016 | | 2016 |
| Hairy-related transcription factor 2 is not potentially related to Congenital Heart Disease in Chinese patients S Zhou, B Wang, Q Chen, XD Xie, J Wang, S Zhou, X Ma | | |
