Yanguang Cong

1.2k total citations · 1 hit paper
43 papers, 912 citations indexed

About

Yanguang Cong is a scholar working on Molecular Biology, Food Science and Infectious Diseases. According to data from OpenAlex, Yanguang Cong has authored 43 papers receiving a total of 912 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Food Science and 12 papers in Infectious Diseases. Recurrent topics in Yanguang Cong's work include Salmonella and Campylobacter epidemiology (11 papers), Bacteriophages and microbial interactions (10 papers) and Viral gastroenteritis research and epidemiology (7 papers). Yanguang Cong is often cited by papers focused on Salmonella and Campylobacter epidemiology (11 papers), Bacteriophages and microbial interactions (10 papers) and Viral gastroenteritis research and epidemiology (7 papers). Yanguang Cong collaborates with scholars based in China, United States and Pakistan. Yanguang Cong's co-authors include Xiancai Rao, Sijin Yang, Fuquan Hu, Kun Xiong, Zhijin Chen, Xiaomei Hu, Junmin Zhu, Jing Wang, Yinling Tan and Zheng Feng and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Scientific Reports.

In The Last Decade

Yanguang Cong

38 papers receiving 898 citations

Hit Papers

Vancomycin resistant Stap... 2019 2026 2021 2023 2019 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yanguang Cong China 16 416 295 185 154 108 43 912
Louis Bryden Canada 14 248 0.6× 257 0.9× 121 0.7× 135 0.9× 109 1.0× 17 718
Alexander Zipperer Germany 5 615 1.5× 303 1.0× 204 1.1× 217 1.4× 59 0.5× 9 1.1k
Emilie L. Fisher United States 10 609 1.5× 352 1.2× 237 1.3× 116 0.8× 79 0.7× 15 1.1k
Yoann Le Breton United States 23 591 1.4× 475 1.6× 224 1.2× 77 0.5× 164 1.5× 41 1.3k
Piera Anna Martino Italy 20 291 0.7× 200 0.7× 161 0.9× 114 0.7× 64 0.6× 81 1.2k
Irena Zdovc Slovenia 17 274 0.7× 301 1.0× 137 0.7× 97 0.6× 41 0.4× 75 781
Pipat Piewngam United States 13 472 1.1× 325 1.1× 216 1.2× 72 0.5× 77 0.7× 16 912
Mahmoud Mabrok Egypt 18 336 0.8× 169 0.6× 150 0.8× 123 0.8× 142 1.3× 46 1.2k
Justin S. Bae United States 8 550 1.3× 435 1.5× 125 0.7× 149 1.0× 61 0.6× 9 1.0k
Fernanda R. Buzzola Argentina 22 483 1.2× 522 1.8× 264 1.4× 168 1.1× 40 0.4× 46 1.1k

Countries citing papers authored by Yanguang Cong

Since Specialization
Citations

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

Fields of papers citing papers by Yanguang Cong

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yanguang Cong

This figure shows the co-authorship network connecting the top 25 collaborators of Yanguang Cong. A scholar is included among the top collaborators of Yanguang Cong 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 Yanguang Cong. Yanguang Cong 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.
Chen, Ying, et al.. (2025). Research progress on immunoprotective mechanisms of enteric fever and vaccine development. Journal of Advanced Research. 81. 583–592. 1 indexed citations
2.
Cui, Xiaojing & Yanguang Cong. (2025). Role of Gut Microbiota in the Development of Some Autoimmune Diseases. Journal of Inflammation Research. Volume 18. 4409–4419. 2 indexed citations
3.
Guo, X. H., Yichu Nie, Tingting He, et al.. (2025). Multimetallic intra-nanogap nanozyme-mediated lateral flow immunoassay for ultrasensitive and multimode detection of K. pneumonia in clinical samples. Chemical Engineering Journal. 520. 166410–166410.
5.
Ullah, Sadeeq, Chunyan Wu, Xiaohui Zou, et al.. (2025). Understanding microbiota-driven oncogenesis: The role of metabolites in tumorigenesis. iScience. 28(12). 113945–113945.
6.
Wang, Jingwei, Yu Yin, Lingzhi Chen, et al.. (2025). NIR-triggered and glucose-powered hollow mesoporous Mo-based single-atom nanozymes for cascade chemodynamic diabetic infection therapy. Materials Today Bio. 31. 101557–101557. 3 indexed citations
7.
Chen, Dong, Liping Hu, Hanlin Zhou, et al.. (2024). Dual‐Enhanced SERS Satellite Immuno‐Nanocomplex for Multiple PSA‐Mediated PHI Assay Toward Clinical Prostate Cancer Screening. Advanced Science. 12(5). e2411747–e2411747. 6 indexed citations
9.
Cong, Yanguang, et al.. (2019). Bacillus coagulans and its applications in medicine. Beneficial Microbes. 10(6). 679–688. 69 indexed citations
10.
Cong, Yanguang, Sijin Yang, & Xiancai Rao. (2019). Vancomycin resistant Staphylococcus aureus infections: A review of case updating and clinical features. Journal of Advanced Research. 21. 169–176. 368 indexed citations breakdown →
12.
Hu, Zhen, Weilong Shang, Qiwen Hu, et al.. (2016). Molecular and Phenotypic Characterization Revealed High Prevalence of Multidrug-Resistant Methicillin-Susceptible Staphylococcus aureus in Chongqing, Southwestern China. Microbial Drug Resistance. 23(2). 241–246. 27 indexed citations
13.
Xiong, Kun, Zhijin Chen, Xiaomei Hu, et al.. (2015). Construction of an attenuated Salmonella enterica serovar Paratyphi A vaccine strain harboring defined mutations in htrA and yncD. Microbiology and Immunology. 59(8). 443–451. 10 indexed citations
14.
Li, Jianhua, Kun Xiong, Zhijin Chen, et al.. (2015). Lytic Action of the Truncated yncE Gene in Escherichia coli. Current Microbiology. 72(4). 390–396. 3 indexed citations
15.
Li, Shu, Hui Huang, Wei Chen, et al.. (2013). Identification of in-vivo induced genes of Streptococcus suis serotype 2 specially expressed in infected human. Microbial Pathogenesis. 63. 8–15. 7 indexed citations
16.
Xiong, Kun, Zhijin Chen, Guiming Xiang, et al.. (2011). Deletion of yncD gene in Salmonella enterica ssp. enterica serovar Typhi leads to attenuation in mouse model. FEMS Microbiology Letters. 328(1). 70–77. 19 indexed citations
17.
Chen, Zhijin, Dongmei Wang, Yanguang Cong, et al.. (2010). Recombinant antimicrobial peptide hPAB-β expressed in Pichia pastoris, a potential agent active against methicillin-resistant Staphylococcus aureus. Applied Microbiology and Biotechnology. 89(2). 281–291. 22 indexed citations
18.
Hu, Yong, et al.. (2009). Identification of in vivo induced protein antigens of Salmonella enterica serovar Typhi during human infection. Science in China Series C Life Sciences. 52(10). 942–948. 11 indexed citations
19.
Liu, Lina, Gong Cheng, Changjun Wang, et al.. (2008). Identification and Experimental Verification of Protective Antigens Against Streptococcus suis Serotype 2 Based on Genome Sequence Analysis. Current Microbiology. 58(1). 11–17. 46 indexed citations
20.
Rao, Xiancai, Shu Li, Xiaolin Jin, et al.. (2005). Design and expression of peptide antibiotic hPAB-β as tandem multimers in Escherichia coli. Peptides. 26(5). 721–729. 41 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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