Xiangming Guo

3.6k total citations
100 papers, 2.8k citations indexed

About

Xiangming Guo is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Xiangming Guo has authored 100 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 50 papers in Ophthalmology and 27 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Xiangming Guo's work include Retinal Development and Disorders (37 papers), Retinal Diseases and Treatments (26 papers) and Glaucoma and retinal disorders (26 papers). Xiangming Guo is often cited by papers focused on Retinal Development and Disorders (37 papers), Retinal Diseases and Treatments (26 papers) and Glaucoma and retinal disorders (26 papers). Xiangming Guo collaborates with scholars based in China, United States and Spain. Xiangming Guo's co-authors include Qingjiong Zhang, Shiqiang Li, Xueshan Xiao, Xiaoyun Jia, Panfeng Wang, Wenmin Sun, J. Fielding Hejtmancik, Li Huang, Yong‐Gang Yao and Liping Guan and has published in prestigious journals such as PLoS ONE, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

In The Last Decade

Xiangming Guo

99 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xiangming Guo China 32 2.0k 1.4k 661 612 528 100 2.8k
Xiaoyun Jia China 31 1.9k 1.0× 1.2k 0.9× 650 1.0× 578 0.9× 492 0.9× 115 2.7k
Xueshan Xiao China 34 2.6k 1.3× 1.8k 1.3× 845 1.3× 754 1.2× 595 1.1× 147 3.6k
Mary J. van Schooneveld Netherlands 27 1.9k 0.9× 1.3k 0.9× 453 0.7× 347 0.6× 119 0.2× 69 2.4k
Bernhard Jurklies Germany 21 1.8k 0.9× 1.6k 1.1× 608 0.9× 243 0.4× 166 0.3× 49 2.6k
Panagiotis I. Sergouniotis United Kingdom 30 1.8k 0.9× 1.1k 0.8× 325 0.5× 579 0.9× 103 0.2× 83 2.3k
Motokazu Tsujikawa Japan 35 1.3k 0.6× 1.8k 1.3× 1.8k 2.7× 395 0.6× 123 0.2× 102 3.6k
Isabelle Perrault France 30 2.7k 1.3× 1.5k 1.1× 329 0.5× 628 1.0× 76 0.1× 71 3.0k
Arif O. Khan Saudi Arabia 24 845 0.4× 669 0.5× 396 0.6× 610 1.0× 161 0.3× 131 1.8k
Gavin Arno United Kingdom 29 1.7k 0.8× 818 0.6× 306 0.5× 714 1.2× 114 0.2× 113 2.3k
B. Jeroen Klevering Netherlands 38 3.3k 1.6× 3.4k 2.4× 1.5k 2.3× 435 0.7× 147 0.3× 102 4.9k

Countries citing papers authored by Xiangming Guo

Since Specialization
Citations

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

Fields of papers citing papers by Xiangming Guo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiangming Guo

This figure shows the co-authorship network connecting the top 25 collaborators of Xiangming Guo. A scholar is included among the top collaborators of Xiangming Guo 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 Xiangming Guo. Xiangming Guo 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.
Li, Jiali, Xueshan Xiao, Shiqiang Li, et al.. (2016). RGR variants in different forms of retinal diseases: The undetermined role of truncation mutations. Molecular Medicine Reports. 14(5). 4811–4815. 7 indexed citations
2.
Xu, Yan, Liping Guan, Xueshan Xiao, et al.. (2015). Mutation analysis in 129 genes associated with other forms of retinal dystrophy in 157 families with retinitis pigmentosa based on exome sequencing.. PubMed. 21. 477–86. 31 indexed citations
3.
Hu, Huan, Xueshan Xiao, Shiqiang Li, et al.. (2015). KIF11mutations are a common cause of autosomal dominant familial exudative vitreoretinopathy. British Journal of Ophthalmology. 100(2). 278–283. 57 indexed citations
4.
Li, Jie, Xiaoyun Jia, Shiqiang Li, Shaohua Fang, & Xiangming Guo. (2014). Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis.. PubMed. 20. 1017–24. 14 indexed citations
5.
Li, Shiqiang, Tao Shen, Xueshan Xiao, Xiangming Guo, & Qingjiong Zhang. (2014). Detection of CRB1 mutations in families with retinal dystrophy through phenotype-oriented mutational screening. International Journal of Molecular Medicine. 33(4). 913–918. 13 indexed citations
6.
Jiang, Dan, Jiali Li, Xueshan Xiao, et al.. (2014). Detection of Mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 Families With Early-Onset High Myopia by Exome Sequencing. Investigative Ophthalmology & Visual Science. 56(1). 339–345. 87 indexed citations
7.
Huang, Li, Qingyan Zhang, Shiqiang Li, et al.. (2013). Exome Sequencing of 47 Chinese Families with Cone-Rod Dystrophy: Mutations in 25 Known Causative Genes. PLoS ONE. 8(6). e65546–e65546. 53 indexed citations
8.
Huang, Li, Shiqiang Li, Xueshan Xiao, et al.. (2013). Screening for variants in 20 genes in 130 unrelated patients with cone-rod dystrophy. Molecular Medicine Reports. 7(6). 1779–1785. 15 indexed citations
9.
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
10.
Li, Shiqiang, et al.. (2012). Screening forNDPMutations in 44 Unrelated Patients with Familial Exudative Vitreoretinopathy or Norrie Disease. Current Eye Research. 37(8). 726–729. 12 indexed citations
11.
Li, Lin, Xueshan Xiao, Xiaodong Jiao, et al.. (2012). Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3–q32.1. Journal of Human Genetics. 57(12). 756–759. 3 indexed citations
12.
Wang, Qin, Yang Gao, Shiqiang Li, Xiangming Guo, & Qingjiong Zhang. (2012). Mutation screening of TRPM1, GRM6, NYX and CACNA1F genes in patients with congenital stationary night blindness. International Journal of Molecular Medicine. 30(3). 521–526. 13 indexed citations
13.
Li, Shiqiang, Xiaoyun Jia, Xueshan Xiao, et al.. (2012). Evaluation of the ELOVL4, PRPH2 and ABCA4 genes in patients with Stargardt macular degeneration. Molecular Medicine Reports. 6(5). 1045–1049. 20 indexed citations
14.
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
15.
Jia, Xiaoyun, Shiqiang Li, Panfeng Wang, Xiangming Guo, & Qingjiong Zhang. (2010). mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population. Biochemical and Biophysical Research Communications. 403(2). 237–241. 13 indexed citations
16.
Wang, Panfeng, Zhikuan Yang, Shiqiang Li, et al.. (2009). Evaluation of MFRP as a candidate gene for high hyperopia.. PubMed. 15. 181–6. 12 indexed citations
17.
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
18.
Xiao, Xueshan, Xiaoyun Jia, Xiangming Guo, et al.. (2006). CSNB1 in Chinese families associated with novel mutations in NYX. Journal of Human Genetics. 51(7). 634–640. 18 indexed citations
19.
Zhang, Qingjiong, Shifu Li, Xin Xiao, Xiangming Guo, & Xinzheng Jia. (2002). An A112V mutation in the CRX gene identified in 3 Chinese family with retinal degeneration other than LCA. Investigative Ophthalmology & Visual Science. 43(13). 812–812. 2 indexed citations
20.
Zhang, Qingjiong, Shiqiang Li, Xiangming Guo, et al.. (2001). Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype. Ophthalmic Genetics. 22(2). 89–96. 25 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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