Xiao-Sheng Huang (Xiaosheng Huang)

Publication Activity (10 Years)

Years Active: 2018-2022
Publications (10 Years): 7

Top Topics

Top Venues

Journal of immunology research

Journal of ophthalmology

The British journal of ophthalmology

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

Publications

Wei Bai, Xiao-Sheng Huang, Xiaoli Shen, Ye Ye, Shiming Peng, Tianhui Zhu, Shaoyi Mei, Jiajie Kuang, Sejie Yu, Xiaochen Ma, Jun Zhao
HSP70 and TNF Loci Polymorphism Associated with the Posner-Schlossman Syndrome in a Southern Chinese Population. Journal of immunology research 2022 (2022)
Wei Bai, Xiao-Sheng Huang, Xiaoli Shen, Ye Ye, Shiming Peng, Tianhui Zhu, Shaoyi Mei, Jiajie Kuang, Sejie Yu, Xiaochen Ma, Jun Zhao
HSP70 and TNF Loci Polymorphism Associated with the Posner-Schlossman Syndrome in a Southern Chinese Population. Journal of immunology research 2022 (2022)
Wei Bai, Xiao-Sheng Huang, Xiaoli Shen, Ye Ye, Shiming Peng, Tianhui Zhu, Shaoyi Mei, Jiajie Kuang, Sejie Yu, Xiaochen Ma, Jun Zhao
HSP70 and TNF Loci Polymorphism Associated with the Posner-Schlossman Syndrome in a Southern Chinese Population. Journal of immunology research 2022 (2022)
Xiao-Sheng Huang, Guiqin Liu, Shaoyi Mei, Jiamin Cai, Jing Rao, Minzhong Tang, Tianhui Zhu, Wenchiew Chen, Shiming Peng, Yan Wang, Ye Ye, Tong Zhang, Zhi-Hui Deng, Jun Zhao
Human leucocyte antigen alleles confer susceptibility and progression to Graves' ophthalmopathy in a Southern Chinese population. The British journal of ophthalmology 105 (10) (2020)
Shaoyi Mei, Xiao-Sheng Huang, Lin Cheng, Shiming Peng, Tianhui Zhu, Liang Chen, Yan Wang, Jun Zhao
A Missense Mutation in OPA1 Causes Dominant Optic Atrophy in a Chinese Family. Journal of ophthalmology 2019 (2019)
Xiao-Sheng Huang, Jun Zhao, Siqi Cai, Zhi-Hui Deng
Characterization of the novel KIR3DL3*062 allele identified in a Southern Chinese Han individual. HLA 94 (1) (2019)
Shao-Yi Mei, Yan Wang, Xiao-Sheng Huang, Yun-Ping Xu, Jun Zhao
Genomic full-length sequence of the HLA-A*24:20:01:01 allele, identified by cloning and sequencing. HLA 93 (1) (2018)