| Overexpressed SIRT6 attenuates cisplatin-induced acute kidney injury by inhibiting ERK1/2 signaling Z Li, K Xu, N Zhang, G Amador, Y Wang, S Zhao, L Li, Y Qiu, Z Wang Kidney international 93 (4), 881-892, 2018 | 94 | 2018 |
| ADAMTS5 in osteoarthritis: biological functions, regulatory network, and potential targeting therapies L Jiang, J Lin, S Zhao, J Wu, Y Jin, L Yu, N Wu, Z Wu, Y Wang, M Lin Frontiers in molecular biosciences 8, 703110, 2021 | 81 | 2021 |
| The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating … J Liu, Y Zhou, S Liu, X Song, XZ Yang, Y Fan, W Chen, ZC Akdemir, Z Yan, ... Human genetics 137, 553-567, 2018 | 72 | 2018 |
| TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene … J Liu, N Wu, ... Genetics in Medicine 21 (7), 1548-1558, 2019 | 70 | 2019 |
| Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM) K Wang, S Zhao, B Liu, Q Zhang, Y Li, J Liu, Y Shen, X Ding, J Lin, Y Wu, ... Journal of medical genetics 55 (10), 675-684, 2018 | 65 | 2018 |
| Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome N Chen, S Zhao, A Jolly, L Wang, H Pan, J Yuan, S Chen, A Koch, C Ma, ... The American Journal of Human Genetics 108 (2), 337-345, 2021 | 60 | 2021 |
| Genome-wide cell-free DNA methylation analyses improve accuracy of non-invasive diagnostic imaging for early-stage breast cancer J Liu, H Zhao, Y Huang, S Xu, Y Zhou, W Zhang, J Li, Y Ming, X Wang, ... Molecular cancer 20, 1-7, 2021 | 59 | 2021 |
| TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice N Yang, N Wu, L Zhang, Y Zhao, J Liu, X Liang, X Ren, W Li, W Chen, ... Human molecular genetics 28 (4), 539-547, 2019 | 57 | 2019 |
| Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS) S Zhao, Y Zhang, W Chen, W Li, S Wang, L Wang, Y Zhao, M Lin, Y Ye, ... Journal of medical genetics 58 (1), 41-47, 2021 | 48 | 2021 |
| Genetic polymorphism of LBX1 is associated with adolescent idiopathic scoliosis in Northern Chinese Han population S Liu, N Wu, Y Zuo, Y Zhou, J Liu, Z Liu, W Chen, G Liu, Y Chen, J Chen, ... Spine 42 (15), 1125-1129, 2017 | 47 | 2017 |
| Integrative genomics analysis reveals a 21q22. 11 locus contributing risk to COVID-19 Y Ma, Y Huang, S Zhao, Y Yao, Y Zhang, J Qu, N Wu, J Su Human molecular genetics 30 (13), 1247-1258, 2021 | 41 | 2021 |
| TBX6 missense variants expand the mutational spectrum in a non‐Mendelian inheritance disease W Chen, J Lin, L Wang, X Li, S Zhao, J Liu, ZC Akdemir, Y Zhao, R Du, ... Human mutation 41 (1), 182-195, 2020 | 36 | 2020 |
| Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature X Fan, S Zhao, C Yu, D Wu, Z Yan, L Fan, Y Song, Y Wang, C Li, Y Ming, ... Journal of Genetics and Genomics 48 (5), 396-402, 2021 | 32 | 2021 |
| Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11. 2 microdeletion syndrome N Yang, N Wu, S Dong, L Zhang, Y Zhao, W Chen, R Du, C Song, X Ren, ... Kidney international 98 (4), 1020-1030, 2020 | 29 | 2020 |
| Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population G Liu, S Liu, M Lin, X Li, W Chen, Y Zuo, J Liu, Y Niu, S Zhao, B Long, ... Journal of Cellular and Molecular Medicine 22 (3), 1964-1971, 2018 | 29 | 2018 |
| The progress of CRISPR/Cas9-mediated gene editing in generating mouse/zebrafish models of human skeletal diseases N Wu, B Liu, H Du, S Zhao, Y Li, X Cheng, S Wang, J Lin, J Zhou, G Qiu, ... Computational and Structural Biotechnology Journal 17, 954-962, 2019 | 28 | 2019 |
| Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice X Ren, N Yang, N Wu, X Xu, W Chen, L Zhang, Y Li, RQ Du, S Dong, ... Journal of medical genetics 57 (6), 371-379, 2020 | 27 | 2020 |
| Clinical characteristics of 1,055 Chinese patients with Mayer-Rokitansky-Küster-Hauser syndrome: a nationwide multicentric study N Chen, H Pan, G Luo, P Wang, Z Xie, K Hua, X Luo, X Huang, Q Liu, ... Fertility and Sterility 116 (2), 558-565, 2021 | 26 | 2021 |
| The mutational burden and oligogenic inheritance in Klippel-Feil syndrome Z Li, S Zhao, S Cai, Y Zhang, L Wang, Y Niu, X Li, J Hu, J Chen, S Wang, ... BMC Musculoskeletal Disorders 21, 1-9, 2020 | 26 | 2020 |
| Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral–basilar artery dissection (IVAD) K Wang, S Zhao, Q Zhang, J Yuan, J Liu, X Ding, X Song, J Lin, R Du, ... Journal of human genetics 63 (11), 1119-1128, 2018 | 26 | 2018 |
Nan WuOrthopaedic surgery Dept.,Peking Union Medical College Hospital, Chinese Academy of Medical SciencesVerified email at pumch.cn