Xiaosheng Huang

Chinese Academy of Medical Sciences & Peking Union Medical College — China

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index308citations39works4.92yr avg
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Research Topics

Connexins and lens biology(5), Glaucoma and retinal disorders(4), Retinal Development and Disorders(4), Retinal Diseases and Treatments(3), Corneal surgery and disorders(3)

Publications39 total

Genetic determinants of gene expression noise and its role in complex trait variation
Cell Reports·2025Open Access
Inhibiting Fear Memory Recall-induced Oligodendrogenesis Rescues PTSD-like Behaviors
2025Open Access
Revealing age-related changes in the intraocular microenvironment and senescence modulators using aqueous humor proteomics and machine learning
Frontiers in Cell and Developmental Biology·2025Open Access
Polysaccharides from hawthorn fruit alleviate high-fat diet-induced NAFLD in mice by improving gut microbiota dysbiosis and hepatic metabolic disorder
Phytomedicine·2025· 29 cited
PIKFYVE deficiency induces vacuole-like cataract via perturbing late endosome homeostasis
Biochemical and Biophysical Research Communications·2024
Enhanced spinal cord repair using bioengineered induced pluripotent stem cell-derived exosomes loaded with miRNA
Molecular Medicine·2024· 11 citedOpen Access
Novel MIP gene mutation causes autosomal-dominant congenital cataract
International Journal of Ophthalmology·2024· 2 citedOpen Access
A novel frameshift mutation in the NHS gene causes Nance-Horan syndrome in a Chinese family
Gene·2024· 2 cited
Gut Microbiota Related Metabolites Changes - New Break through Point for Treating Diabetes
Journal of Bacteriology and Mycology·2024Open Access
HSP70 and TNF Loci Polymorphism Associated with the Posner-Schlossman Syndrome in a Southern Chinese Population
Journal of Immunology Research·2022· 1 citedOpen Access
Ultrasound Targeted Microbubble Destruction Promotes the Therapeutic Effect of HUMSC Transplantation on Glaucoma-Caused Optic Nerve Injury in Rabbits
Translational Vision Science & Technology·2022· 10 citedOpen Access
Paeoniflorin inhibits epithelial mesenchymal transformation and oxidative damage of lens epithelial cells in diabetic cataract via sirtuin 1 upregulation
Bioengineered·2022· 12 citedOpen Access
The effect of QiangGuYin on osteoporosis through the AKT/mTOR/autophagy signaling pathway mediated by CKIP-1
Aging·2022· 18 citedOpen Access
Disruption of PIKFYVE causes congenital cataract in human and zebrafish
eLife·2022· 29 citedOpen Access
Author response: Disruption of PIKFYVE causes congenital cataract in human and zebrafish
2021Open Access
A Novel Frameshift Mutation in The NHS Gene Causes Nance-Horan Syndrome in a Chinese Family
Research Square (Research Square)·2021Open Access
Incorporating Differential Gene Expression Analysis with Predictive Biomarkers to Identify Novel Therapeutic Drugs for Fuchs Endothelial Corneal Dystrophy
Journal of Ophthalmology·2021· 11 citedOpen Access
Mutations in <i>PIKFYVE</i> cause autosomal dominant congenital cataract
2021Open Access
Polymorphisms and Circulating Plasma Protein Levels of Immune Checkpoints (CTLA-4 and PD-1) Are Associated With Posner-Schlossman Syndrome in Southern Chinese
Frontiers in Immunology·2021· 13 citedOpen Access
Human leucocyte antigen alleles confer susceptibility and progression to Graves’ ophthalmopathy in a Southern Chinese population
British Journal of Ophthalmology·2020· 10 citedOpen Access
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Frequent Co-authors

Shaoyi Mei(15), Jun Zhao(15), Tianhui Zhu(9), Shiming Peng(6), Yan Wang(4), Sejie Yu(4), Jiamin Cai(4), Linkai Huang(3), Haidong Yan(3), Yi Wu(3), Yubo Cui(3), Tao Yu(3), WenChieh Chen(3), Shiming Peng(3), Zhihui Deng(3), Baojian Fan(3), Ye Ye(3), Tong Zhang(3), Kun Zeng(3), Wenqun Xi(3)