Xiang Sun

804 total citations
23 papers, 579 citations indexed

About

Xiang Sun is a scholar working on Infectious Diseases, Molecular Biology and Molecular Medicine. According to data from OpenAlex, Xiang Sun has authored 23 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Infectious Diseases, 13 papers in Molecular Biology and 8 papers in Molecular Medicine. Recurrent topics in Xiang Sun's work include Antimicrobial Resistance in Staphylococcus (14 papers), Bacterial biofilms and quorum sensing (11 papers) and Antibiotic Resistance in Bacteria (8 papers). Xiang Sun is often cited by papers focused on Antimicrobial Resistance in Staphylococcus (14 papers), Bacterial biofilms and quorum sensing (11 papers) and Antibiotic Resistance in Bacteria (8 papers). Xiang Sun collaborates with scholars based in China and United States. Xiang Sun's co-authors include Jinxin Zheng, Qiwen Deng, Di Qu, Zhiwei Lin, Zhijian Yu, Guangjian Xu, Zhijian Yu, Yang Wu, Junwen Chen and Bing Bai and has published in prestigious journals such as Gastroenterology, Antimicrobial Agents and Chemotherapy and Frontiers in Microbiology.

In The Last Decade

Xiang Sun

23 papers receiving 575 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xiang Sun China 16 279 256 217 92 85 23 579
Feng-Jui Chen Taiwan 16 228 0.8× 289 1.1× 284 1.3× 160 1.7× 131 1.5× 36 627
Henning Büttner Germany 14 143 0.5× 377 1.5× 344 1.6× 80 0.9× 69 0.8× 29 682
Rosslyn Maybank United States 13 250 0.9× 151 0.6× 112 0.5× 65 0.7× 85 1.0× 23 440
Xiangkuo Zheng China 15 278 1.0× 174 0.7× 109 0.5× 55 0.6× 55 0.6× 27 486
Ryan P. Lamers Canada 12 240 0.9× 371 1.4× 217 1.0× 57 0.6× 72 0.8× 14 674
Emily K. Crispell United States 13 193 0.7× 313 1.2× 294 1.4× 171 1.9× 185 2.2× 17 774
Anthony J. Yeh United States 15 380 1.4× 373 1.5× 234 1.1× 131 1.4× 96 1.1× 17 870
Rafael Ríos Colombia 15 279 1.0× 142 0.6× 274 1.3× 157 1.7× 110 1.3× 37 594
Matthias Steglich Germany 13 181 0.6× 259 1.0× 221 1.0× 71 0.8× 79 0.9× 22 546
Akio Kuga Japan 6 245 0.9× 191 0.7× 192 0.9× 101 1.1× 95 1.1× 10 456

Countries citing papers authored by Xiang Sun

Since Specialization
Citations

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

Fields of papers citing papers by Xiang Sun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiang Sun

This figure shows the co-authorship network connecting the top 25 collaborators of Xiang Sun. A scholar is included among the top collaborators of Xiang 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 Xiang Sun. Xiang 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.
Fu, Jiaxin, Xiang Sun, Xi Zhou, et al.. (2024). Bioluminescence Resonance Energy Transfer Sensor with Tunable Conjugation Efficiency for Highly Sensitive Detection of Superoxide Anion in Tumors. ACS Applied Bio Materials. 7(12). 8709–8717. 4 indexed citations
2.
Zheng, Jinxin, Yongpeng Shang, Yang Wu, et al.. (2022). Loratadine inhibits Staphylococcus aureus virulence and biofilm formation. iScience. 25(2). 103731–103731. 26 indexed citations
3.
Mao, Hengxu, Yongyi Ye, Xiang Sun, et al.. (2022). Quiescent Elongation of α-Synuclein Pre-form Fibrils Under Different Solution Conditions. Frontiers in Neuroscience. 16. 902077–902077. 3 indexed citations
4.
Chen, Baili, Jie Zhong, Xiuling Li, et al.. (2022). Efficacy and Safety of Ivarmacitinib in Patients With Moderate-to-Severe, Active, Ulcerative Colitis: A Phase II Study. Gastroenterology. 163(6). 1555–1568. 30 indexed citations
5.
6.
Chen, Junwen, Xiang Sun, Guangjian Xu, et al.. (2021). The Antibacterial and Antibiofilm Activity of Telithromycin Against Enterococcus spp. Isolated From Patients in China. Frontiers in Microbiology. 11. 11 indexed citations
7.
Zheng, Jinxin, Yongpeng Shang, Yang Wu, et al.. (2021). Diclazuril Inhibits Biofilm Formation and Hemolysis of Staphylococcus aureus. ACS Infectious Diseases. 7(6). 1690–1701. 30 indexed citations
8.
Sun, Xiang, Guangjian Xu, Junwen Chen, et al.. (2020). In Vitro Activity of the Novel Tetracyclines, Tigecycline, Eravacycline, and Omadacycline, Against Moraxella catarrhalis. Annals of Laboratory Medicine. 41(3). 293–301. 6 indexed citations
9.
Zheng, Jinxin, Yang Wu, Zhiwei Lin, et al.. (2020). ClpP participates in stress tolerance, biofilm formation, antimicrobial tolerance, and virulence of Enterococcus faecalis. BMC Microbiology. 20(1). 30–30. 36 indexed citations
10.
Lin, Zhiwei, Jinxin Zheng, Bing Bai, et al.. (2020). Characteristics of Hypervirulent Klebsiella pneumoniae: Does Low Expression of rmpA Contribute to the Absence of Hypervirulence?. Frontiers in Microbiology. 11. 436–436. 59 indexed citations
11.
Zheng, Jinxin, Zhong Chen, Zhiwei Lin, et al.. (2020). Radezolid Is More Effective Than Linezolid Against Planktonic Cells and Inhibits Enterococcus faecalis Biofilm Formation. Frontiers in Microbiology. 11. 196–196. 18 indexed citations
12.
Zheng, Jinxin, Xiang Sun, Guangjian Xu, et al.. (2020). In vitro activities of telithromycin against Staphylococcus aureus biofilms compared with azithromycin, clindamycin, vancomycin and daptomycin. Journal of Medical Microbiology. 69(1). 120–131. 19 indexed citations
13.
Zheng, Jinxin, Zhong Chen, Junwen Chen, et al.. (2019). In vitro evaluation of the antibacterial activities of radezolid and linezolid for Streptococcus agalactiae. Microbial Pathogenesis. 139. 103866–103866. 13 indexed citations
14.
Yao, Weiming, Guangjian Xu, Duoyun Li, et al.. (2019). Staphylococcus aureus with an erm-mediated constitutive macrolide-lincosamide-streptogramin B resistance phenotype has reduced susceptibility to the new ketolide, solithromycin. BMC Infectious Diseases. 19(1). 175–175. 28 indexed citations
16.
Zheng, Jinxin, Zhiwei Lin, Chen Chen, et al.. (2018). Biofilm Formation in Klebsiella pneumoniae Bacteremia Strains Was Found to be Associated with CC23 and the Presence of wcaG. Frontiers in Cellular and Infection Microbiology. 8. 21–21. 86 indexed citations
17.
Zhang, Fan, Bing Bai, Guangjian Xu, et al.. (2018). Eravacycline activity against clinical S. aureus isolates from China: in vitro activity, MLST profiles and heteroresistance. BMC Microbiology. 18(1). 211–211. 25 indexed citations
18.
Sun, Xiang, Zhiwei Lin, Weiming Yao, et al.. (2018). Biofilm formation in erythromycin-resistant Staphylococcus aureus and the relationship with antimicrobial susceptibility and molecular characteristics. Microbial Pathogenesis. 124. 47–53. 25 indexed citations
19.
Zheng, Jinxin, Zhiwei Lin, Xiang Sun, et al.. (2018). Overexpression of OqxAB and MacAB efflux pumps contributes to eravacycline resistance and heteroresistance in clinical isolates of Klebsiella pneumoniae. Emerging Microbes & Infections. 7(1). 1–11. 75 indexed citations
20.
Sun, Xiang, et al.. (1997). Studies on the drought resistance of four specis of plant in the stage of seed germination and seedlings. Xibei zhiwu xuebao. 17(3). 410–415. 1 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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