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Xueying Zhou
Researcher at Peking Union Medical College Hospital
Publications - 12
Citations - 232
Xueying Zhou is an academic researcher from Peking Union Medical College Hospital. The author has contributed to research in topics: Hypophosphatemia & Fibroblast growth factor 23. The author has an hindex of 10, co-authored 12 publications receiving 196 citations.
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Journal ArticleDOI
Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia
Cong Zhang,Zhen Zhao,Yue Sun,Lijun Xu,Ruizhi Jiajue,Lijia Cui,Qianqian Pang,Yan Jiang,Mei Li,Ou Wang,Xiaodong He,Shuli He,Min Nie,Xiaoping Xing,Xunwu Meng,Xueying Zhou,Lina Yan,Jared Kaplan,Karl L. Insogna,Weibo Xia +19 more
TL;DR: A retrospective analysis of the most recent 261 Chinese patients with XLH evaluated at Peking Union Medical College Hospital provided a comprehensive characterization of the largest cohort of patients reported to date from China, which will help in evaluating the applicability of emerging therapies for this disease in this ethnic group.
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Three Novel Mutations of the PHEX Gene in Three Chinese Families with X-linked Dominant Hypophosphatemic Rickets
Weibo Xia,Xunwu Meng,Yan Jiang,Mei Li,Xiaoping Xing,Li Pang,Ou Wang,Yu Pei,Li-Yun Yu,Yue Sun,Yingying Hu,Xueying Zhou +11 more
TL;DR: The results suggest that PHEX gene mutations were responsible for XLH in these patients and these mutations may contribute to a higher serum FGF23 level.
Journal ArticleDOI
Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia.
Jing Sun,Weibo Xia,Shuli He,Zhen Zhao,Min Nie,Mei Li,Yan Jiang,Xiaoping Xing,Ou Wang,Xunwu Meng,Xueying Zhou +10 more
TL;DR: The results of this study expand the spectrum of WISP3 mutations that are associated with PPD and further elucidate the function of W ISP3.
Journal ArticleDOI
Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients.
Ningyi Cui,Weibo Xia,Hua Su,Li Pang,Yan Jiang,Yue Sun,Min Nie,Xiaoping Xing,Mei Li,Ou Wang,Tao Yuan,Yue Chi,Yingying Hu,Huaicheng Liu,Xunwu Meng,Xueying Zhou +15 more
TL;DR: Nine novel mutations in addition to 37 known mutations of CYP27B1 gene are described and the correlation between these mutations and the clinical findings of 1α-hydroxylase deficiency is shown.
Journal Article
Polymorphisms of vitamin D receptor gene and its association with bone mineral density and osteocalcin in Chinese.
TL;DR: Allele frequencies of VDR gene in Chinese are different from those in Caucasians, but in a different pattern from other reports, and no relationship were found between VDR genotypes and the serum osteocalcin level in Chinese women.