Xiuli Zhao (X Zhao)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 8

Top Topics

Neuropathic Pain

Top Venues

BMC medical genetics

BMC medical genomics

Molecular genetics & genomic medicine

European journal of neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Yixuan Cao, Lulu Li, Xiuzhi Ren, Bin Mao, Yujiao Yang, Huan Mi, Yun Guan, Shan Li, Siji Zhou, Xin Guan, Tao Yang, Xiuli Zhao
Identifying the dominant variant of a cis-double-variant in COL1A1 from an osteogenesis imperfecta patient and developing gene therapies. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research (2023)
Yixuan Cao, Yi You, Qiong Wang, Xiuzhi Ren, Shan Li, Lulu Li, Weibo Xia, Xin Guan, Tao Yang, Shiro Ikegawa, Zheng Wang, Xiuli Zhao
Identification of six novel variants from nine Chinese families with hypophosphatemic rickets. BMC medical genomics 15 (1) (2022)
Yixuan Cao, Xin Guan, Shan Li, Nan Wu, Xiumin Chen, Tao Yang, Bo Yang, Xiuli Zhao
Identification of variants in ACAN and PAPSS2 leading to spondyloepi(meta)physeal dysplasias in four Chinese families. Molecular genetics & genomic medicine 10 (5) (2022)
Feiyue Zhao, Bin Mao, X Geng, X Ren, Y Wang, Y Guan, S Li, L Li, S Zhang, Y You, Y Cao, T Yang, Xiuli Zhao
Molecular genetic analysis in 21 Chinese families with congenital insensitivity to pain with or without anhidrosis. European journal of neurology 27 (8) (2020)
Shan Li, Jianfei Zhang, Yixuan Cao, Yi You, Xiuli Zhao
Novel mutations identified in Chinese families with autosomal dominant congenital cataracts by targeted next-generation sequencing. BMC medical genetics 20 (1) (2019)
Lulu Li, Bin Mao, Shan Li, Jifang Xiao, Han Wang, Jing Zhang, Xiuzhi Ren, Yanzhou Wang, Yiyang Wu, Yixuan Cao, Chaoxia Lu, Jinsong Gao, Yi You, Feiyue Zhao, Xingzhu Geng, Yaxiong Xiao, Chendan Jiang, Yuqian Ye, Tao Yang, Xiuli Zhao, Xue Zhang
Genotypic and phenotypic characterization of Chinese patients with osteogenesis imperfecta. Human mutation 40 (5) (2019)
Bin Mao, Siyu Chen, Xin Chen, Xiumei Yu, Xiaojia Zhai, Tao Yang, Lulu Li, Zheng Wang, Xiuli Zhao, Xue Zhang
Clinical characteristics and spectrum of NF1 mutations in 12 unrelated Chinese families with neurofibromatosis type 1. BMC medical genetics 19 (1) (2018)
Shan Li, Yi You, Jinsong Gao, Bin Mao, Yixuan Cao, Xiuli Zhao, Xue Zhang
Novel mutations in TPM2 and PIEZO2 are responsible for distal arthrogryposis (DA) 2B and mild DA in two Chinese families. BMC medical genetics 19 (1) (2018)