Wenmin Sun

1.7k total citations
76 papers, 1.1k citations indexed

About

Wenmin Sun is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Wenmin Sun has authored 76 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 45 papers in Ophthalmology and 28 papers in Genetics. Recurrent topics in Wenmin Sun's work include Retinal Development and Disorders (37 papers), Retinal Diseases and Treatments (32 papers) and Ocular Disorders and Treatments (12 papers). Wenmin Sun is often cited by papers focused on Retinal Development and Disorders (37 papers), Retinal Diseases and Treatments (32 papers) and Ocular Disorders and Treatments (12 papers). Wenmin Sun collaborates with scholars based in China, United States and Pakistan. Wenmin Sun's co-authors include Qingjiong Zhang, Shiqiang Li, Xueshan Xiao, Xiaoyun Jia, Panfeng Wang, Xiangming Guo, Yi Zhen, Li Huang, Yan Xu and Jiali Li and has published in prestigious journals such as PLoS ONE, Brain and International Journal of Molecular Sciences.

In The Last Decade

Wenmin Sun

73 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Wenmin Sun China 20 796 514 332 284 200 76 1.1k
Christine N. Kay United States 13 871 1.1× 504 1.0× 372 1.1× 212 0.7× 111 0.6× 45 1.2k
Arif O. Khan Saudi Arabia 19 721 0.9× 343 0.7× 299 0.9× 146 0.5× 40 0.2× 74 960
Günther Rudolph Germany 19 809 1.0× 646 1.3× 204 0.6× 187 0.7× 41 0.2× 64 1.1k
Xunlun Sheng China 14 386 0.5× 249 0.5× 118 0.4× 121 0.4× 66 0.3× 48 598
S. Scott Whitmore United States 18 953 1.2× 821 1.6× 149 0.4× 421 1.5× 54 0.3× 32 1.4k
Frank C. Schlichtenbrede Germany 20 720 0.9× 910 1.8× 265 0.8× 618 2.2× 101 0.5× 50 1.5k
Zhangyong Wei United States 12 791 1.0× 257 0.5× 436 1.3× 91 0.3× 54 0.3× 13 1.0k
Gezhi Xu China 21 773 1.0× 962 1.9× 83 0.3× 535 1.9× 116 0.6× 112 1.6k
Nizar Smaoui United States 17 739 0.9× 256 0.5× 380 1.1× 151 0.5× 30 0.1× 29 938
Kinga M. Bujakowska United States 19 1.1k 1.4× 507 1.0× 340 1.0× 130 0.5× 27 0.1× 46 1.3k

Countries citing papers authored by Wenmin Sun

Since Specialization
Citations

This map shows the geographic impact of Wenmin Sun's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Wenmin Sun with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wenmin Sun more than expected).

Fields of papers citing papers by Wenmin Sun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wenmin Sun. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Wenmin Sun. The network helps show where Wenmin Sun may publish in the future.

Co-authorship network of co-authors of Wenmin Sun

This figure shows the co-authorship network connecting the top 25 collaborators of Wenmin Sun. A scholar is included among the top collaborators of Wenmin Sun based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Wenmin Sun. Wenmin Sun is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Xiao, Xueshan, Wenmin Sun, Shiqiang Li, et al.. (2024). Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of Translational Medicine. 22(1). 75–75. 7 indexed citations
2.
Wang, Panfeng, Shiqiang Li, Yi Jiang, et al.. (2024). Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes. Brain. 148(5). 1604–1620. 2 indexed citations
3.
Zhen, Yi, Xueshan Xiao, Shiqiang Li, et al.. (2023). Clinical and Genetic Features of NR2E3-Associated Retinopathy: A Report of Eight Families with a Longitudinal Study and Literature Review. Genes. 14(8). 1525–1525. 3 indexed citations
4.
Zhen, Yi, Yingwei Wang, Yi Jiang, et al.. (2023). FDXR-Associated Oculopathy: Congenital Amaurosis and Early-Onset Severe Retinal Dystrophy as Common Presenting Features in a Chinese Population. Genes. 14(4). 952–952. 8 indexed citations
5.
Wang, Yingwei, Yi Jiang, Yi Zhen, et al.. (2023). 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). 6728–6728. 6 indexed citations
6.
Li, Shiqiang, Yi Jiang, Zhen Yi, et al.. (2023). Pathogenic Variants in CEP290 or IQCB1 Cause Earlier-Onset Retinopathy in Senior-Loken Syndrome Compared to Those in INVS, NPHP3, or NPHP4. American Journal of Ophthalmology. 252. 188–204. 8 indexed citations
7.
Wang, Yingwei, Yi Jiang, Xueqing Li, et al.. (2022). Genetic and clinical features of BEST1-associated retinopathy based on 59 Chinese families and database comparisons. Experimental Eye Research. 223. 109217–109217. 2 indexed citations
8.
9.
Wang, Yingwei, Xueshan Xiao, Xueqing Li, et al.. (2022). Genetic and clinical landscape ofARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance. British Journal of Ophthalmology. 107(10). 1545–1553. 19 indexed citations
10.
Sun, Wenmin, Huangxuan Shen, Xing Liu, et al.. (2022). Truncation mutations in MYRF underlie primary angle closure glaucoma. Human Genetics. 142(1). 103–123. 5 indexed citations
11.
Li, Shiqiang, Wenmin Sun, Xueshan Xiao, et al.. (2022). Variants in HNRNPH1 are associated with high myopia in humans and ocular coloboma in zebrafish. Clinical Genetics. 102(5). 424–433. 4 indexed citations
12.
Sun, Wenmin, Xueshan Xiao, Shiqiang Li, et al.. (2021). Clinical and genetic features of retinoschisis in 120 families withRS1mutations. British Journal of Ophthalmology. 107(3). 367–372. 11 indexed citations
13.
Wang, Panfeng, Xiaoyun Jia, Wenmin Sun, et al.. (2021). Pathogenicity evaluation and the genotype–phenotype analysis of OPA1 variants. Molecular Genetics and Genomics. 296(4). 845–862. 5 indexed citations
14.
Li, Xueqing, Wenmin Sun, Xueshan Xiao, et al.. (2021). Biallelic variants inCPAMD8are associated with primary open-angle glaucoma and primary angle-closure glaucoma. British Journal of Ophthalmology. 106(12). 1710–1715. 8 indexed citations
15.
Chen, Liling, Xueqing Li, Wenmin Sun, et al.. (2021). DNAH17 is essential for rat spermatogenesis and fertility. Journal of Genetics. 100(1). 15 indexed citations
16.
Xiao, Xueshan, Shiqiang Li, Xiaoyun Jia, et al.. (2021). Severe Exudative Vitreoretinopathy as a Common Feature for CTNNB1, KIF11 and NDP Variants Plus Sector Degeneration for KIF11. American Journal of Ophthalmology. 235. 178–187. 5 indexed citations
17.
Sun, Wenmin, Shiqiang Li, Xiaoyun Jia, et al.. (2020). Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families. Human Genetics. 139(8). 1057–1064. 4 indexed citations
18.
Sun, Wenmin, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, & Qingjiong Zhang. (2020). A novel deep intronic COL2A1 mutation in a family with early‐onset high myopia/ocular‐only Stickler syndrome. Ophthalmic and Physiological Optics. 40(3). 281–288. 13 indexed citations
19.
Huang, Li, Limei Sun, Zhirong Wang, et al.. (2020). Clinical manifestation and genetic analysis in Chinese early onset X‐linked retinoschisis. Molecular Genetics & Genomic Medicine. 8(10). e1421–e1421. 14 indexed citations
20.
Sun, Wenmin, Xueshan Xiao, Shiqiang Li, Xiangming Guo, & Qingjiong Zhang. (2011). Mutational screening of six genes in Chinese patients with congenital cataract and microcornea.. PubMed. 17. 1508–13. 29 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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