Qingjiong Zhang

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 34

Top Venues

Genes

The British journal of ophthalmology

International journal of molecular sciences

Journal of translational medicine

Sun Yat-Sen University

Sun Yat-Sen University of Medical Sciences (PHD)

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

Affiliation History

Sun Yat-Sen University

China

Professor and Vice President :: Zhongshan Ophthalmic Center

Sun Yat-Sen University

China

Professor and Deputy Director of Eye Research Institute :: Zhongshan Ophthalmic Center

National Eye Institute

United States

Research Fellow :: Ophthalmic Molecular Genetics, OGVFB

Medical College of Wisconsin

United States

Visiting Scientist :: Department of Cell Biology, Neurobiology & Anatomy

Sun Yat-sen University of Medical Sciences

China

Professor of Ophthalmology and Principal Investigator :: Zhongshan Ophthalmic Center

Sun Yat-sen University of Medical Sciences

China

Associate Professor :: Zhongshan Ophthalmic Center

Teikyo University Ichihara Hospital

Japan

Postdoctoral Fellow :: Department of Ophthalmology

Sun Yat-sen University of Medical Sciences

China

Assistant and Asscociate Professor :: Zhongshan Ophthalmic Center

Education History

Sun Yat-Sen University of Medical Sciences

China

PHD :: Department of Ophthalmology

Tongji Medical University Sep 01 1980 - Jun 30 1985

China

BSC :: Faculty of Clinical Medicine

Publications

Wenmin Sun, Dan Xiong, Jiamin Ouyang, Xueshan Xiao, Yi Jiang, Yingwei Wang, Shiqiang Li, Ziying Xie, Junwen Wang, Zhonghui Tang, Qingjiong Zhang
Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasia. Nature communications 15 (1) (2024)
Yi Jiang, Xueshan Xiao, Wenmin Sun, Yingwei Wang, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J Fielding Hejtmancik, Qingjiong Zhang
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of translational medicine 22 (1) (2024)
Wenmin Sun, Dan Xiong, Jiamin Ouyang, Xueshan Xiao, Yi Jiang, Yingwei Wang, Shiqiang Li, Ziying Xie, Junwen Wang, Zhonghui Tang, Qingjiong Zhang
Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasia. Nature communications 15 (1) (2024)
Wenmin Sun, Dan Xiong, Jiamin Ouyang, Xueshan Xiao, Yi Jiang, Yingwei Wang, Shiqiang Li, Ziying Xie, Junwen Wang, Zhonghui Tang, Qingjiong Zhang
Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasia. Nature communications 15 (1) (2024)
Xueqing Li, Hui Xiao, Yihua Su, Xueshan Xiao, Shiqiang Li, Shufen Lin, Lei Fang, Wenmin Sun, Panfeng Wang, James Fielding Hejtmancik, Min Bin Yu, Liming Chen, Qingjiong Zhang, Xing Liu
Clinical features of patients with mutations in genes for nanophthalmos. The British journal of ophthalmology (2024)
Yi Jiang, Xueshan Xiao, Wenmin Sun, Yingwei Wang, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J Fielding Hejtmancik, Qingjiong Zhang
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of translational medicine 22 (1) (2024)
Yi Jiang, Xueshan Xiao, Wenmin Sun, Yingwei Wang, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J Fielding Hejtmancik, Qingjiong Zhang
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of translational medicine 22 (1) (2024)
Yuxi Zheng, Yingwei Wang, Yi Jiang, Junwen Wang, Shiqiang Li, Xueshan Xiao, Wenmin Sun, Panfeng Wang, Qingjiong Zhang, Xiaoyun Jia
Variant and clinical landscape of Leber hereditary optic neuropathy based on 1516 families with mtDNA variants in a tertiary centre. The British journal of ophthalmology 108 (9) (2024)
Yuxi Zheng, Yingwei Wang, Yi Jiang, Junwen Wang, Shiqiang Li, Xueshan Xiao, Wenmin Sun, Panfeng Wang, Qingjiong Zhang, Xiaoyun Jia
Variant and clinical landscape of Leber hereditary optic neuropathy based on 1516 families with mtDNA variants in a tertiary centre. The British journal of ophthalmology (2024)
Di Zhu, Junwen Wang, Yingwei Wang, Yi Jiang, Shiqiang Li, Xueshan Xiao, Panfeng Wang, Qingjiong Zhang
Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature. International journal of molecular sciences 24 (5) (2023)
Shutong Yi, Yuxi Zheng, Zhen Yi, Yingwei Wang, Yi Jiang, Jiamin Ouyang, Shiqiang Li, Xueshan Xiao, Wenmin Sun, Panfeng Wang, Qingjiong Zhang
FDXR -Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. Genes 14 (4) (2023)
Shutong Yi, Yuxi Zheng, Zhen Yi, Yingwei Wang, Yi Jiang, Jiamin Ouyang, Shiqiang Li, Xueshan Xiao, Wenmin Sun, Panfeng Wang, Qingjiong Zhang
FDXR -Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. Genes 14 (4) (2023)
Yuxi Zheng, Xiaoyun Jia, Shiqiang Li, Xueshan Xiao, Qingjiong Zhang, Panfeng Wang
Non-Pharmaceutical Interventions against COVID-19 Causing a Lower Trend in Age of LHON Onset. Genes 14 (6) (2023)
Sainan Xiao, Zhen Yi, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Ping Lian, Wenmin Sun, Panfeng Wang, Lin Lu, Qingjiong Zhang
Clinical and Genetic Features of NR2E3 -Associated Retinopathy: A Report of Eight Families with a Longitudinal Study and Literature Review. Genes 14 (8) (2023)
Dongwei Guo, Qingjiong Zhang
A case of LSS-associated congenital nuclear cataract with hypotrichosis and literature review. American journal of medical genetics. Part A (2023)
Di Zhu, Junwen Wang, Yingwei Wang, Yi Jiang, Shiqiang Li, Xueshan Xiao, Panfeng Wang, Qingjiong Zhang
Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature. International journal of molecular sciences 24 (5) (2023)
Shutong Yi, Yuxi Zheng, Zhen Yi, Yingwei Wang, Yi Jiang, Jiamin Ouyang, Shiqiang Li, Xueshan Xiao, Wenmin Sun, Panfeng Wang, Qingjiong Zhang
FDXR -Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. Genes 14 (4) (2023)
Wenhui Zhou, Zixuan Jiang, Zhen Yi, Jiamin Ouyang, Xueqing Li, Qingjiong Zhang, Panfeng Wang
Defect of TIMP4 Is Associated with High Myopia and Participates in Rat Ocular Development in a Dose-Dependent Manner. International journal of molecular sciences 24 (23) (2023)
Yuxi Zheng, Xiaoyun Jia, Shiqiang Li, Xueshan Xiao, Qingjiong Zhang, Panfeng Wang
Non-Pharmaceutical Interventions against COVID-19 Causing a Lower Trend in Age of LHON Onset. Genes 14 (6) (2023)
Di Zhu, Junwen Wang, Yingwei Wang, Yi Jiang, Shiqiang Li, Xueshan Xiao, Panfeng Wang, Qingjiong Zhang
Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature. International journal of molecular sciences 24 (5) (2023)
Shutong Yi, Yuxi Zheng, Zhen Yi, Yingwei Wang, Yi Jiang, Jiamin Ouyang, Shiqiang Li, Xueshan Xiao, Wenmin Sun, Panfeng Wang, Qingjiong Zhang
FDXR -Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. Genes 14 (4) (2023)
Yingwei Wang, Junwen Wang, Yi Jiang, Di Zhu, Jiamin Ouyang, Zhen Yi, Shiqiang Li, Xiaoyun Jia, Xueshan Xiao, Wenmin Sun, Panfeng Wang, Qingjiong Zhang
New Insight into the Genotype-Phenotype Correlation of PRPH2 -Related Diseases Based on a Large Chinese Cohort and Literature Review. International journal of molecular sciences 24 (7) (2023)
Shutong Yi, Yuxi Zheng, Zhen Yi, Yingwei Wang, Yi Jiang, Jiamin Ouyang, Shiqiang Li, Xueshan Xiao, Wenmin Sun, Panfeng Wang, Qingjiong Zhang
FDXR -Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. Genes 14 (4) (2023)
Yuxi Zheng, Xiaoyun Jia, Shiqiang Li, Xueshan Xiao, Qingjiong Zhang, Panfeng Wang
Non-Pharmaceutical Interventions against COVID-19 Causing a Lower Trend in Age of LHON Onset. Genes 14 (6) (2023)
Jiamin Ouyang, Wenmin Sun, Huangxuan Shen, Xing Liu, Yingchen Wu, Hongmei Jiang, Xueqing Li, Yingwei Wang, Yi Jiang, Shiqiang Li, Xueshan Xiao, J Fielding Hejtmancik, Zhiqun Tan, Qingjiong Zhang
Truncation mutations in MYRF underlie primary angle closure glaucoma. Human genetics (2022)
Junwen Wang, Xueshan Xiao, Shiqiang Li, Hongmei Jiang, Wenmin Sun, Panfeng Wang, Qingjiong Zhang
Landscape of pathogenic variants in six pre-mRNA processing factor genes for retinitis pigmentosa based on large in-house data sets and database comparisons. Acta ophthalmologica 100 (7) (2022)
Yingwei Wang, Xueshan Xiao, Xueqing Li, Zhen Yi, Yi Jiang, Fengsheng Zhang, Lin Zhou, Shiqiang Li, Xiaoyun Jia, Wenmin Sun, Panfeng Wang, Qingjiong Zhang
Genetic and clinical landscape of ARR3 -associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance. The British journal of ophthalmology (2022)
Jiamin Ouyang, Shiqiang Li, Wenmin Sun, Xueshan Xiao, Yingwei Wang, Yi Jiang, Qingjiong Zhang
Variants in HNRNPH1 are associated with high myopia in humans and ocular coloboma in zebrafish. Clinical genetics 102 (5) (2022)
Xueqing Li, Wenmin Sun, Xueshan Xiao, Lei Fang, Shiqiang Li, Xing Liu, Qingjiong Zhang
Biallelic variants in CPAMD8 are associated with primary open-angle glaucoma and primary angle-closure glaucoma. The British journal of ophthalmology (2021)
Sainan Xiao, Wenmin Sun, Xueshan Xiao, Shiqiang Li, Hualei Luo, Xiaoyun Jia, Jiamin Ouyang, Xueqing Li, Yingwei Wang, Yi Jiang, Panfeng Wang, Qingjiong Zhang
Clinical and genetic features of retinoschisis in 120 families with RS1 mutations. The British journal of ophthalmology (2021)
Xingyu Xu, Panfeng Wang, Xiaoyun Jia, Wenmin Sun, Shiqiang Li, Xueshan Xiao, J Fielding Hejtmancik, Qingjiong Zhang
Pathogenicity evaluation and the genotype-phenotype analysis of OPA1 variants. Molecular genetics and genomics : MGG 296 (4) (2021)
Wenmin Sun, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J Fielding Hejtmancik, Xueshan Xiao, Qingjiong Zhang
Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families. Human genetics 139 (8) (2020)
Wenmin Sun, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Qingjiong Zhang
A novel deep intronic COL2A1 mutation in a family with early-onset high myopia/ocular-only Stickler syndrome. Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) 40 (3) (2020)
Wenmin Sun, Xueshan Xiao, Qingjiong Zhang
Correspondence to Rossetti et al.'s review of the phenotypic spectrum associated with haploinsufficiency of MYRF. American journal of medical genetics. Part A 179 (11) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Qingjiong Zhang