Works by Wenmin Sun

Results: 35

Retinopathy as an initial sign of hereditary immunological diseases: report of six families and challenges in eye clinic.

Published in:

Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1239886

By:

Yingwei Wang;
Yi Jiang;
Junwen Wang;
Shiqiang Li;
Xiaoyun Jia;
Xueshan Xiao;
Wenmin Sun;
Panfeng Wang;
Qingjiong Zhang

Publication type:

Article

Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasia.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49376-w

By:

Sun, Wenmin;
Xiong, Dan;
Ouyang, Jiamin;
Xiao, Xueshan;
Jiang, Yi;
Wang, Yingwei;
Li, Shiqiang;
Xie, Ziying;
Wang, Junwen;
Tang, Zhonghui;
Zhang, Qingjiong

Publication type:

Article

Heterozygous GJA1 variants with ocular phenotype: Missense in domain but truncation out of domain.

Published in:

Molecular Vision, 2021, v. 27, p. 309

By:

Xueqing Li;
Xueshan Xiao;
Shiqiang Li;
Jiamin Ouyang;
Wenmin Sun;
Xing Liu;
Qingjiong Zhang

Publication type:

Article

Confirming and expanding the phenotypes of FZD5 variants: Coloboma, inferior chorioretinal hypoplasia, and high myopia.

Published in:

Molecular Vision, 2021, v. 27, p. 50

By:

Yi Jiang;
Jiamin Ouyang;
Shiqiang Li;
Xueshan Xiao;
Wenmin Sun;
Qingjiong Zhang

Publication type:

Article

Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testing.

Published in:

Molecular Vision, 2020, v. 26, p. 588

By:

Wenmin Sun;
Shiqiang Li;
Xueshan Xiao;
Panfeng Wang;
Qingjiong Zhang

Publication type:

Article

Spectrum, frequency, and genotype--phenotype of mutations in SPATA7.

Published in:

Molecular Vision, 2019, v. 25, p. 821

By:

Xueshan Xiao;
Wenmin Sun;
Shiqiang Li;
Xiaoyun Jia;
Qingjiong Zhang

Publication type:

Article

Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia.

Published in:

Molecular Vision, 2016, v. 22, p. 1

By:

Jiali Li;
Bei Gao;
Xueshan Xiao;
Shiqiang Li;
Xiaoyun Jia;
Wenmin Sun;
Xiangming Guo;
Qingjiong Zhang

Publication type:

Article

Does the Association Between TMEM98 and Nanophthalmos Require Further Confirmation?

Published in:

JAMA Ophthalmology, 2015, v. 133, n. 3, p. 358, doi. 10.1001/jamaophthalmol.2014.4915

By:

Wenmin Sun;
Qingjiong Zhang;
Awadalla, Mona S.;
Burdon, Kathryn P.;
Craig, Jamie E.

Publication type:

Article

Variants in HNRNPH1 are associated with high myopia in humans and ocular coloboma in zebrafish.

Published in:

Clinical Genetics, 2022, v. 102, n. 5, p. 424, doi. 10.1111/cge.14213

By:

Ouyang, Jiamin;
Li, Shiqiang;
Sun, Wenmin;
Xiao, Xueshan;
Wang, Yingwei;
Jiang, Yi;
Zhang, Qingjiong

Publication type:

Article

Landscape of pathogenic variants in six pre‐mRNA processing factor genes for retinitis pigmentosa based on large in‐house data sets and database comparisons.

Published in:

Acta Ophthalmologica (1755375X), 2022, v. 100, n. 7, p. e1412, doi. 10.1111/aos.15104

By:

Wang, Junwen;
Xiao, Xueshan;
Li, Shiqiang;
Jiang, Hongmei;
Sun, Wenmin;
Wang, Panfeng;
Zhang, Qingjiong

Publication type:

Article

RPE65 mutation frequency and phenotypic variation according to exome sequencing in a tertiary centre for genetic eye diseases in China.

Published in:

Acta Ophthalmologica (1755375X), 2020, v. 98, n. 2, p. e181, doi. 10.1111/aos.14181

By:

Li, Shiqiang;
Xiao, Xueshan;
Yi, Zhen;
Sun, Wenmin;
Wang, Panfeng;
Zhang, Qingjiong

Publication type:

Article

Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia.

Published in:

Journal of Translational Medicine, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12967-024-04886-5

By:

Jiang, Yi;
Xiao, Xueshan;
Sun, Wenmin;
Wang, Yingwei;
Li, Shiqiang;
Jia, Xiaoyun;
Wang, Panfeng;
Hejtmancik, J. Fielding;
Zhang, Qingjiong

Publication type:

Article

A novel deep intronic COL2A1 mutation in a family with early‐onset high myopia/ocular‐only Stickler syndrome.

Published in:

Ophthalmic & Physiological Optics, 2020, v. 40, n. 3, p. 281, doi. 10.1111/opo.12682

By:

Sun, Wenmin;
Xiao, Xueshan;
Li, Shiqiang;
Jia, Xiaoyun;
Zhang, Qingjiong

Publication type:

Article

Clinical and Genetic Features of NR2E3 -Associated Retinopathy: A Report of Eight Families with a Longitudinal Study and Literature Review.

Published in:

Genes, 2023, v. 14, n. 8, p. 1525, doi. 10.3390/genes14081525

By:

Xiao, Sainan;
Yi, Zhen;
Xiao, Xueshan;
Li, Shiqiang;
Jia, Xiaoyun;
Lian, Ping;
Sun, Wenmin;
Wang, Panfeng;
Lu, Lin;
Zhang, Qingjiong

Publication type:

Article

FDXR -Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population.

Published in:

Genes, 2023, v. 14, n. 4, p. 952, doi. 10.3390/genes14040952

By:

Yi, Shutong;
Zheng, Yuxi;
Yi, Zhen;
Wang, Yingwei;
Jiang, Yi;
Ouyang, Jiamin;
Li, Shiqiang;
Xiao, Xueshan;
Sun, Wenmin;
Wang, Panfeng;
Zhang, Qingjiong

Publication type:

Article

New Insight into the Genotype-Phenotype Correlation of PRPH2 -Related Diseases Based on a Large Chinese Cohort and Literature Review.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 7, p. 6728, doi. 10.3390/ijms24076728

By:

Wang, Yingwei;
Wang, Junwen;
Jiang, Yi;
Zhu, Di;
Ouyang, Jiamin;
Yi, Zhen;
Li, Shiqiang;
Jia, Xiaoyun;
Xiao, Xueshan;
Sun, Wenmin;
Wang, Panfeng;
Zhang, Qingjiong

Publication type:

Article

Awareness, Attitudes, and Willingness of Young Adults in Mainland China Regarding Advance Care Planning: A Cross-Sectional Study.

Published in:

Malaysian Journal of Nursing (MJN), 2022, v. 14, n. 1, p. 10, doi. 10.31674/mjn.2022.v14i01.002

By:

Min Liu;
Dela Rosa, Ronnell D.;
Wenmin Sun;
Gaoqiao Liu;
Dandan Li

Publication type:

Article

Genotype–Phenotype Analysis of RPGR Variations: Reporting of 62 Chinese Families and a Literature Review.

Published in:

Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.600210

By:

Yang, Junxing;
Zhou, Lin;
Ouyang, Jiamin;
Xiao, Xueshan;
Sun, Wenmin;
Li, Shiqiang;
Zhang, Qingjiong

Publication type:

Article

A novel variant in IDH3A identified in a case with Leber congenital amaurosis accompanied by macular pseudocoloboma.

Published in:

Ophthalmic Genetics, 2018, v. 39, n. 5, p. 662, doi. 10.1080/13816810.2018.1502788

By:

Sun, Wenmin;
Zhang, Qingjiong

Publication type:

Article

Pathogenicity evaluation and the genotype–phenotype analysis of OPA1 variants.

Published in:

Molecular Genetics & Genomics, 2021, v. 296, n. 4, p. 845, doi. 10.1007/s00438-021-01783-0

By:

Xu, Xingyu;
Wang, Panfeng;
Jia, Xiaoyun;
Sun, Wenmin;
Li, Shiqiang;
Xiao, Xueshan;
Hejtmancik, J. Fielding;
Zhang, Qingjiong

Publication type:

Article

Truncation mutations in MYRF underlie primary angle closure glaucoma.

Published in:

Human Genetics, 2023, v. 142, n. 1, p. 103, doi. 10.1007/s00439-022-02487-0

By:

Ouyang, Jiamin;
Sun, Wenmin;
Shen, Huangxuan;
Liu, Xing;
Wu, Yingchen;
Jiang, Hongmei;
Li, Xueqing;
Wang, Yingwei;
Jiang, Yi;
Li, Shiqiang;
Xiao, Xueshan;
Hejtmancik, J. Fielding;
Tan, Zhiqun;
Zhang, Qingjiong

Publication type:

Article

Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families.

Published in:

Human Genetics, 2020, v. 139, n. 8, p. 1057, doi. 10.1007/s00439-020-02156-0

By:

Sun, Wenmin;
Li, Shiqiang;
Jia, Xiaoyun;
Wang, Panfeng;
Hejtmancik, J. Fielding;
Xiao, Xueshan;
Zhang, Qingjiong

Publication type:

Article

Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3.

Published in:

Human Genetics, 2019, v. 138, n. 10, p. 1077, doi. 10.1007/s00439-019-02039-z

By:

Xiao, Xueshan;
Sun, Wenmin;
Ouyang, Jiamin;
Li, Shiqiang;
Jia, Xiaoyun;
Tan, Zhiqun;
Hejtmancik, J. Fielding;
Zhang, Qingjiong

Publication type:

Article

Datasets-Based IMPDH1 Revisited: Heterozygous Missense Variants for Dominant Retinitis Pigmentosa While Truncation Variants Are Likely Non-Pathogenic.

Published in:

Current Eye Research, 2024, v. 49, n. 8, p. 853, doi. 10.1080/02713683.2024.2336158

By:

Wang, Junwen;
Wang, Yingwei;
Jiang, Yi;
Li, Shiqiang;
Jia, Xiaoyun;
Xiao, Xueshan;
Sun, Wenmin;
Wang, Panfeng;
Zhang, Qingjiong

Publication type:

Article

Start and End with Genetics: RCBTB1 and Beyond.

Published in:

Current Eye Research, 2021, v. 46, n. 12, p. 1932, doi. 10.1080/02713683.2021.1933060

By:

Yang, Junxing;
Sun, Wenmin;
Zhang, Qingjiong

Publication type:

Article

Variants in RCBTB1 are Associated with Autosomal Recessive Retinitis Pigmentosa but Not Autosomal Dominant FEVR.

Published in:

Current Eye Research, 2021, v. 46, n. 6, p. 839, doi. 10.1080/02713683.2020.1842457

By:

Yang, Junxing;
Xiao, Xueshan;
Sun, Wenmin;
Li, Shiqiang;
Jia, Xiaoyun;
Zhang, Qingjiong

Publication type:

Article

Correspondence to Rossetti et al.'s review of the phenotypic spectrum associated with haploinsufficiency of MYRF.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 11, p. 2315, doi. 10.1002/ajmg.a.61326

By:

Sun, Wenmin;
Xiao, Xueshan;
Zhang, Qingjiong

Publication type:

Article

Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes.

Published in:

Brain: A Journal of Neurology, 2025, v. 148, n. 5, p. 1604, doi. 10.1093/brain/awae324

By:

Zheng, Yuxi;
Wang, Panfeng;
Li, Shiqiang;
Long, Yuxi;
Jiang, Yi;
Guo, Dongwei;
Jia, Xiaoyun;
Liu, Mengchu;
Zeng, Yiyan;
Xiao, Xueshan;
Hejtmancik, J Fielding;
Zhang, Qingjiong;
Sun, Wenmin

Publication type:

Article

Exome Sequencing of 18 Chinese Families with Congenital Cataracts: A New Sight of the <i>NHS</i> Gene.

Published in:

PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0100455

By:

Sun, Wenmin;
Xiao, Xueshan;
Li, Shiqiang;
Guo, Xiangming;
Zhang, Qingjiong

Publication type:

Article

Exome Sequencing of 47 Chinese Families with Cone-Rod Dystrophy: Mutations in 25 Known Causative Genes.

Published in:

PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065546

By:

Huang, Li;
Zhang, Qingyan;
Li, Shiqiang;
Guan, Liping;
Xiao, Xueshan;
Zhang, Jianguo;
Jia, Xiaoyun;
Sun, Wenmin;
Zhu, Zhihong;
Gao, Yang;
Yin, Ye;
Wang, Panfeng;
Guo, Xiangming;
Wang, Jun;
Zhang, Qingjiong

Publication type:

Article

Clinical and Genetic Characteristics of 18 Patients from Southeast China with ABCA4-Associated Stargardt Disease.

Published in:

International Journal of Molecular Sciences, 2025, v. 26, n. 7, p. 3354, doi. 10.3390/ijms26073354

By:

Liu, Xinyu;
Liu, Zehao;
Cui, Jinli;
Tan, Chen;
Sun, Wenmin;
Lin, Ying

Publication type:

Article

Pathogenic variants and associated phenotypic spectrum of TSPAN12 based on data from a large cohort.

Published in:

Graefe's Archive of Clinical & Experimental Ophthalmology, 2021, v. 259, n. 10, p. 2929, doi. 10.1007/s00417-021-05196-y

By:

Sun, Wenmin;
Xiao, Xueshan;
Li, Shiqiang;
Jia, Xiaoyun;
Wang, Panfeng;
Zhang, Qingjiong

Publication type:

Article

Influence of Dyadic Coping Model on Anxiety and Depression Level and Treatment Compliance in Glaucoma Patients.

Published in:

Alternative Therapies in Health & Medicine, 2024, v. 30, n. 12, p. 362

By:

Jinming Cheng;
Wenmin Sun;
Chaoxia Yu;
Wenhong Zhang;
Ling Qin

Publication type:

Article

Clinical manifestation and genetic analysis in Chinese early onset X‐linked retinoschisis.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1421

By:

Huang, Li;
Sun, Limei;
Wang, Zhirong;
Chen, Chonglin;
Wang, Panfeng;
Sun, Wenmin;
Luo, Xiaoling;
Ding, Xiaoyan

Publication type:

Article

CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection.

Published in:

Human Molecular Genetics, 2019, v. 28, n. 12, p. 1959, doi. 10.1093/hmg/ddz029

By:

Ouyang, Jiamin;
Sun, Wenmin;
Xiao, Xueshan;
Li, Shiqiang;
Jia, Xiaoyun;
Zhou, Lin;
Wang, Panfeng;
Zhang, Qingjiong

Publication type:

Article