Xueshan Xiao

5.0k total citations
147 papers, 3.6k citations indexed

About

Xueshan Xiao is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Xueshan Xiao has authored 147 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 110 papers in Molecular Biology, 84 papers in Ophthalmology and 43 papers in Genetics. Recurrent topics in Xueshan Xiao's work include Retinal Development and Disorders (66 papers), Retinal Diseases and Treatments (52 papers) and Glaucoma and retinal disorders (35 papers). Xueshan Xiao is often cited by papers focused on Retinal Development and Disorders (66 papers), Retinal Diseases and Treatments (52 papers) and Glaucoma and retinal disorders (35 papers). Xueshan Xiao collaborates with scholars based in China, United States and Pakistan. Xueshan Xiao's co-authors include Qingjiong Zhang, Shiqiang Li, Xiangming Guo, Xiaoyun Jia, Panfeng Wang, Wenmin Sun, J. Fielding Hejtmancik, Li Huang, Yan Xu and Jianguo Zhang and has published in prestigious journals such as Nature Communications, PLoS ONE and Brain.

In The Last Decade

Xueshan Xiao

145 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xueshan Xiao China 34 2.6k 1.8k 845 754 595 147 3.6k
Xiangming Guo China 32 2.0k 0.8× 1.4k 0.8× 661 0.8× 612 0.8× 528 0.9× 100 2.8k
Xiaoyun Jia China 31 1.9k 0.7× 1.2k 0.7× 650 0.8× 578 0.8× 492 0.8× 115 2.7k
Mary J. van Schooneveld Netherlands 27 1.9k 0.7× 1.3k 0.7× 453 0.5× 347 0.5× 119 0.2× 69 2.4k
Bernhard Jurklies Germany 21 1.8k 0.7× 1.6k 0.9× 608 0.7× 243 0.3× 166 0.3× 49 2.6k
Motokazu Tsujikawa Japan 35 1.3k 0.5× 1.8k 1.0× 1.8k 2.1× 395 0.5× 123 0.2× 102 3.6k
Enrico Maria Surace Italy 33 2.1k 0.8× 653 0.4× 242 0.3× 686 0.9× 177 0.3× 55 2.6k
B. Jeroen Klevering Netherlands 38 3.3k 1.3× 3.4k 1.9× 1.5k 1.8× 435 0.6× 147 0.2× 102 4.9k
Panagiotis I. Sergouniotis United Kingdom 30 1.8k 0.7× 1.1k 0.6× 325 0.4× 579 0.8× 103 0.2× 83 2.3k
Maher Noureddine United States 15 1.3k 0.5× 1.4k 0.8× 827 1.0× 372 0.5× 124 0.2× 19 3.0k
Gavin Arno United Kingdom 29 1.7k 0.6× 818 0.5× 306 0.4× 714 0.9× 114 0.2× 113 2.3k

Countries citing papers authored by Xueshan Xiao

Since Specialization
Citations

This map shows the geographic impact of Xueshan Xiao'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 Xueshan Xiao with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Xueshan Xiao more than expected).

Fields of papers citing papers by Xueshan Xiao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Xueshan Xiao. 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 Xueshan Xiao. The network helps show where Xueshan Xiao may publish in the future.

Co-authorship network of co-authors of Xueshan Xiao

This figure shows the co-authorship network connecting the top 25 collaborators of Xueshan Xiao. A scholar is included among the top collaborators of Xueshan Xiao 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 Xueshan Xiao. Xueshan Xiao 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.
Wang, Yingwei, Yi Zhen, Shiqiang Li, et al.. (2025). ABCA4 Deep Intronic Variants Contributed to Nearly Half of Unsolved Stargardt Cases With a Milder Phenotype. Investigative Ophthalmology & Visual Science. 66(1). 65–65. 1 indexed citations
2.
Li, Xueqing, Hui Xiao, Xueshan Xiao, et al.. (2024). Clinical features of patients with mutations in genes for nanophthalmos. British Journal of Ophthalmology. 108(12). 1679–1687. 1 indexed citations
3.
Wang, Yingwei, Yi Jiang, Shiqiang Li, et al.. (2024). Variant and clinical landscape of Leber hereditary optic neuropathy based on 1516 families with mtDNA variants in a tertiary centre. British Journal of Ophthalmology. 108(9). 1318–1327. 2 indexed citations
4.
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
5.
Xiong, Dan, Xueshan Xiao, Yi Jiang, et al.. (2024). Altered chromatin topologies caused by balanced chromosomal translocation lead to central iris hypoplasia. Nature Communications. 15(1). 5048–5048. 1 indexed citations
6.
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
7.
Wang, Yingwei, Yi Jiang, Shiqiang Li, et al.. (2023). 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). 5012–5012.
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.
Zhen, Yi, Wenmin Sun, Xueshan Xiao, et al.. (2021). Novel variants in GUCY2D causing retinopathy and the genotype-phenotype correlation. Experimental Eye Research. 208. 108637–108637. 7 indexed citations
13.
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
14.
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
15.
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
16.
Liu, Xing, Jiali Li, Xueshan Xiao, et al.. (2020). Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa. Experimental Eye Research. 197. 108118–108118. 8 indexed citations
17.
Zhen, Yi, et al.. (2020). Comparative exome sequencing reveals novel candidate genes for retinitis pigmentosa. EBioMedicine. 56. 102792–102792. 10 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.
Li, Shiqiang, et al.. (2012). Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy.. PubMed Central. 36 indexed citations
20.
Zhang, Qingjiong, Shiqiang Li, Xueshan Xiao, Xiaoyun Jia, & Xiangming Guo. (2007). The 208delG Mutation inFSCN2Does Not Associate with Retinal Degeneration in Chinese Individuals. Investigative Ophthalmology & Visual Science. 48(2). 530–530. 34 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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