| Retrospective analysis of associated anomalies in 636 patients with operatively treated congenital scoliosis N Wu, L Liu, Y Zhang, L Wang, S Wang, S Zhao, G Li, Y Yang, G Lin, ... JBJS 105 (7), 537-548, 2023 | 6 | 2023 |
| TBX6 as a cause of a combined skeletal‐kidney dysplasia syndrome G Li, A Strong, H Wang, JS Kim, D Watson, S Zhao, C Vaccaro, E Hartung, ... American Journal of Medical Genetics Part A 188 (12), 3469-3481, 2022 | 3 | 2022 |
| SIGMA leverages protein structural information to predict the pathogenicity of missense variants H Zhao, H Du, S Zhao, Z Chen, Y Li, K Xu, B Liu, X Cheng, W Wen, G Li, ... Cell Reports Methods 4 (1), 2024 | 2 | 2024 |
| COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis D Rebello, E Wohler, V Erfani, G Li, AN Aguilera, A Santiago-Cornier, ... Human molecular genetics 32 (19), 2913-2928, 2023 | 2 | 2023 |
| Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment F Liu, C Liang, Z Li, S Zhao, H Yuan, R Yao, Z Qin, S Shangguan, ... Brain 146 (8), 3347-3363, 2023 | 2 | 2023 |
| Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine S Zhao, H Zhao, L Zhao, X Cheng, Z Zheng, M Wu, W Wen, S Wang, ... Nature Communications 15 (1), 1125, 2024 | 1 | 2024 |
| Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations X Feng, Y Ye, J Zhang, Y Zhang, S Zhao, JCW Mak, N Otomo, Z Zhao, ... Proceedings of the National Academy of Sciences 121 (18), e2310283121, 2024 | | 2024 |
| Suggested searches Y Wang, J Li, W Wang, Y Wang, S Schmitt, P Heuret, V Troispoux, ... Perspective, 2024 | | 2024 |
