Transplantation of Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells Improves Cartilage Repair in a Rabbit Model

by Guihua Yang, Jiashen Shao, Jiachen Lin, Haixia Yang, Jing Jin, Chenxi Yu, Bo Shen, Xiaorui Hu, Huijie Si, Xiaoxin Li, Yuchen Niu, Zhihong Wu
Published 2021-01-01

Novel <i>FGFR1</i> Variants Are Associated with Congenital Scoliosis

by Shengru Wang, Xiran Chai, Zihui Yan, Sen Zhao, Yang Yang, Xiaoxin Li, Yuchen Niu, Guanfeng Lin, Zhe Su, Zhihong Wu, Terry Jianguo Zhang, Nan Wu
Published 2021-07-01

Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis

by Gang Liu, Hengqiang Zhao, Zihui Yan, Sen Zhao, Yuchen Niu, Xiaoxin Li, Shengru Wang, Yang Yang, Sen Liu, Terry Jianguo Zhang, Zhihong Wu, Nan Wu
Published 2021-03-01

Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function Mechanism

by Bowen Liu, Bowen Liu, Sen Zhao, Sen Zhao, Zihui Yan, Zihui Yan, Zihui Yan, Lina Zhao, Lina Zhao, Jiachen Lin, Jiachen Lin, Jiachen Lin, Shengru Wang, Shengru Wang, Yuchen Niu, Yuchen Niu, Xiaoxin Li, Xiaoxin Li, Guixing Qiu, Guixing Qiu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Terry Jianguo Zhang, Terry Jianguo Zhang, Zhihong Wu, Zhihong Wu, Nan Wu, Nan Wu
Published 2021-03-01

A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia

by Jiashen Shao, Sen Zhao, Zihui Yan, Lianlei Wang, Yuanqiang Zhang, Mao Lin, Chenxi Yu, Shengru Wang, Yuchen Niu, Xiaoxin Li, Guixing Qiu, Jianguo Zhang, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Zhihong Wu, Nan Wu
Published 2020-05-01

Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosi...

by Gang Liu, Gang Liu, Lianlei Wang, Lianlei Wang, Xinyu Wang, Zihui Yan, Zihui Yan, Xinzhuang Yang, Xinzhuang Yang, Mao Lin, Mao Lin, Sen Liu, Sen Liu, Yuzhi Zuo, Yuzhi Zuo, Yuchen Niu, Yuchen Niu, Sen Zhao, Sen Zhao, Yanxue Zhao, Yanxue Zhao, Jianguo Zhang, Jianguo Zhang, Jianguo Zhang, Jianxiong Shen, Jianxiong Shen, Jianxiong Shen, Yipeng Wang, Yipeng Wang, Yipeng Wang, Guixing Qiu, Guixing Qiu, Guixing Qiu, Zhihong Wu, Zhihong Wu, Zhihong Wu, Nan Wu, Nan Wu, Nan Wu
Published 2019-12-01

Mutational burden and potential oligogenic model of TBX6‐mediated genes in congenital scoliosis

by Yang Yang, Sen Zhao, Yuanqiang Zhang, Shengru Wang, Jiashen Shao, Bowen Liu, Yaqi Li, Zihui Yan, Yuchen Niu, Xiaoxin Li, Lianlei Wang, Yongyu Ye, Xisheng Weng, Zhihong Wu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Jianguo Zhang, Nan Wu
Published 2020-10-01

The mutational burden and oligogenic inheritance in Klippel-Feil syndrome

by Ziquan Li, Sen Zhao, Siyi Cai, Yuanqiang Zhang, Lianlei Wang, Yuchen Niu, Xiaoxin Li, Jianhua Hu, Jingdan Chen, Shengru Wang, Huizi Wang, Gang Liu, Ye Tian, Zhihong Wu, Terry Jianguo Zhang, DISCO (Deciphering Disorders Involving Scoliosis and COmorbidities) study, Yipeng Wang, Nan Wu
Published 2020-04-01

Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis

by Zefu Chen, Zihui Yan, Chenxi Yu, Jiaqi Liu, Yanbin Zhang, Sen Zhao, Jiachen Lin, Yuanqiang Zhang, Lianlei Wang, Mao Lin, Yingzhao Huang, Xiaoxin Li, Yuchen Niu, Shengru Wang, Zhihong Wu, DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) study group, Guixing Qiu, Terry Jianguo Zhang, Nan Wu
Published 2020-09-01

Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients

by Chenxi Yu, Chenxi Yu, Chenxi Yu, Bobo Xie, Bobo Xie, Bobo Xie, Zhengye Zhao, Zhengye Zhao, Sen Zhao, Sen Zhao, Lian Liu, Lian Liu, Xi Cheng, Xi Cheng, Xiaoxin Li, Xiaoxin Li, Bingyan Cao, Jiashen Shao, Jiashen Shao, Jiajia Chen, Hengqiang Zhao, Hengqiang Zhao, Zihui Yan, Zihui Yan, Chang Su, Yuchen Niu, Yuchen Niu, Yanning Song, Liya Wei, Yi Wang, Xiaoya Ren, Lijun Fan, Beibei Zhang, Chuan Li, Chuan Li, Chuan Li, Baoheng Gui, Baoheng Gui, Baoheng Gui, Yuanqiang Zhang, Lianlei Wang, Shaoke Chen, Shaoke Chen, Shaoke Chen, Jianguo Zhang, Jianguo Zhang, Jianguo Zhang, Zhihong Wu, Zhihong Wu, Zhihong Wu, Zhihong Wu, Chunxiu Gong, Xin Fan, Xin Fan, Xin Fan, Nan Wu, Nan Wu, Nan Wu, Nan Wu
Published 2021-09-01

Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

by Mao Lin, Zhenlei Liu, Gang Liu, Sen Zhao, Chao Li, Weisheng Chen, Zeynep Coban Akdemir, Jiachen Lin, Xiaofei Song, Shengru Wang, Qiming Xu, Yanxue Zhao, Lianlei Wang, Yuanqiang Zhang, Zihui Yan, Sen Liu, Jiaqi Liu, Yixin Chen, Yuzhi Zuo, Xu Yang, Tianshu Sun, Xin‐Zhuang Yang, Yuchen Niu, Xiaoxin Li, Wesley You, Bintao Qiu, Chen Ding, Pengfei Liu, Shuyang Zhang, Claudia M. B. Carvalho, Jennifer E. Posey, Guixing Qiu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, James R. Lupski, Zhihong Wu, Jianguo Zhang, Nan Wu
Published 2020-01-01

Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature

by Baoheng Gui, Baoheng Gui, Baoheng Gui, Chenxi Yu, Chenxi Yu, Xiaoxin Li, Sen Zhao, Sen Zhao, Hengqiang Zhao, Hengqiang Zhao, Zihui Yan, Zihui Yan, Xi Cheng, Xi Cheng, Jiachen Lin, Jiachen Lin, Haiyang Zheng, Haiyang Zheng, Haiyang Zheng, Jiashen Shao, Jiashen Shao, Zhengye Zhao, Zhengye Zhao, Lina Zhao, Yuchen Niu, Zhi Zhao, Huizi Wang, Bobo Xie, Bobo Xie, Bobo Xie, Xianda Wei, Xianda Wei, Chunrong Gui, Chunrong Gui, Chuan Li, Chuan Li, Chuan Li, Shaoke Chen, Shaoke Chen, Shaoke Chen, Yi Wang, Yanning Song, Chunxiu Gong, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang
Published 2021-04-01