Wenjuan Zhuang

发表

Peripapillary retinal nerve fiber layer thickness distribution in Chinese with myopia measured by 3D-optical coherence tomography.

W. Xiang, Jing-jing Zhao, Wenjuan Zhuang, 2013, International journal of ophthalmology.

GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity

B. Yan, Wenjuan Zhuang, Qingshun Zhao, 2017, Genetics in Medicine.

Development and Evaluation of Diagnostic Criteria for Vogt-Koyanagi-Harada Disease

A. Kijlstra, Yuqin Wang, Zhengxuan Jiang, 2018, JAMA ophthalmology.

A peptide derived from type 1 thrombospondin repeat-containing protein WISP-1 inhibits corneal and choroidal neovascularization.

A. Popel, E. Karagiannis, M. Cano, 2009, Investigative ophthalmology & visual science.

Variants of RP1 gene in Chinese patients with autosomal dominant retinitis pigmentosa.

Wenjuan Zhuang, X. Sheng, W. Rong, 2008, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Expanding the Phenotypic and Genotypic Landscape of Nonsyndromic High Myopia: A Cross-Sectional Study in 731 Chinese Patients.

L. Xia, J. Qu, F. Lu, 2019, Investigative ophthalmology & visual science.

Lacrimal gland inflammatory cytokine gene expression in the botulinum toxin B-induced murine dry eye model.

C. Zhang, R. Chuck, Woo-Seok Lee, 2007, Molecular vision.

Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3

Lulin Huang, B. Gong, Zhenglin Yang, 2014, Nature Genetics.

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia

Meixiao Shen, Ting Xie, Fan Lu, 2017, Proceedings of the National Academy of Sciences.

Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China

Wenjuan Zhuang, Zi-Bing Jin, Ren-Juan Shen, 2021, Frontiers in Cell and Developmental Biology.

Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract

Yuk Fai Leung, Wenjuan Zhuang, Lue Xiang, 2018, Experimental & Molecular Medicine.

Evaluating correlation between the ocular biometry and genetic variants of MYOC and ABCA1 with primary angle-closure glaucoma in a cohort from northern China.

Wenjuan Zhuang, Shao-ping Ha, Shunyu Piao, 2019, International journal of ophthalmology.

A novel mutation in retinitis pigmentosa GTPase regulator gene with a distinctive retinitis pigmentosa phenotype in a Chinese family

Wenjuan Zhuang, X. Sheng, Zi-li Li, 2010, Molecular vision.

Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis

Changqing Zeng, M. He, Lulin Huang, 2020, EBioMedicine.

Causes of Visual Impairment and Blindness in the 2006 and 2014 Nine-Province Surveys in Rural China.

M. He, L. Ellwein, Peizeng Yang, 2019, American journal of ophthalmology.

Cataract Surgical Coverage and Visual Acuity Outcomes in Rural China in 2014 and Comparisons With the 2006 China Nine-Province Survey.

M. He, L. Ellwein, Peizeng Yang, 2018, American journal of ophthalmology.

Prevalence of Vision Impairment in Older Adults in Rural China in 2014 and Comparisons With the 2006 China Nine-Province Survey.

M. He, L. Ellwein, Peizeng Yang, 2018, American journal of ophthalmology.

Association of insulin-like growth factor-1 polymorphisms with high myopia in the Chinese population

W. Xiang, Peizeng Yang, Jing-jing Zhao, 2012, Molecular vision.

Association of Specific Genetic Polymorphisms with Age-related Macular Degeneration in a Northern Chinese Population

W. Xiang, Ying Han, Jing-jing Zhao, 2014, Ophthalmic genetics.

Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China

Wenjuan Zhuang, Yang Liu, Bo Cai, 2023, Molecular Genetics and Genomics.

FGFR2 mutation in a Chinese family with unusual Crouzon syndrome.

Wenjuan Zhuang, Wei Zhao, Xue Chen, 2016, International journal of ophthalmology.

Association of Single-Nucleotide Polymorphisms in ABCC5 Gene with Primary Angle Closure Glaucoma and the Ocular Biometric Parameters in a Northern Chinese Population

Wenjuan Zhuang, Shao-ping Ha, Shunyu Piao, 2020, Ophthalmic Research.

Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract

Yuk Fai Leung, Wenjuan Zhuang, Lue Xiang, 2018, Experimental & Molecular Medicine.

Genotype-ocular biometry correlation analysis of eight primary angle closure glaucoma susceptibility loci in a cohort from Northern China

Wenjuan Zhuang, Shao-ping Ha, Shunyu Piao, 2018, PloS one.

Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population

Wenjuan Zhuang, Shao-ping Ha, Shunyu Piao, 2018, BMC Ophthalmology.

Mutational screening of AGRN, SLC39A5, SCO2, P4HA2, BSG, ZNF644, and CPSF1 in a Chinese cohort of 103 patients with nonsyndromic high myopia

Xue-Bi Cai, Wenjuan Zhuang, Xin-Ran Wen, 2021, Molecular vision.

Identification of Novel Risk Loci for Behçet's Disease–Related Uveitis in a Chinese Population in a Genome‐Wide Association Study

X. Zuo, S. Ohno, A. Meguro, 2022 .

Genetic detection of two novel LRP5 pathogenic variants in patients with familial exudative vitreoretinopathy

Wenjuan Zhuang, Xiaolong Qi, Shaochi Zhang, 2023, BMC Ophthalmology.

Identification of Novel Risk Loci for Behçet's Disease–Related Uveitis in a Chinese Population in a Genome‐Wide Association Study

X. Zuo, Xiaoli Liu, S. Ohno, 2021, Arthritis & rheumatology.