Guoping Zheng

8.6k total citations · 1 hit paper
112 papers, 4.7k citations indexed

About

Guoping Zheng is a scholar working on Immunology, Molecular Biology and Nephrology. According to data from OpenAlex, Guoping Zheng has authored 112 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Immunology, 35 papers in Molecular Biology and 24 papers in Nephrology. Recurrent topics in Guoping Zheng's work include Immune Cell Function and Interaction (19 papers), Renal Diseases and Glomerulopathies (16 papers) and T-cell and B-cell Immunology (12 papers). Guoping Zheng is often cited by papers focused on Immune Cell Function and Interaction (19 papers), Renal Diseases and Glomerulopathies (16 papers) and T-cell and B-cell Immunology (12 papers). Guoping Zheng collaborates with scholars based in Australia, China and Brazil. Guoping Zheng's co-authors include David C.H. Harris, Stephen I. Alexander, Thian Kui Tan, Vincent Lee, Qiang Shu, Jianguo Xu, Menghua Ge, Qi Cao, Guanguan Qiu and Jiangmei Wang and has published in prestigious journals such as PLoS ONE, Journal of Cell Science and International Journal of Molecular Sciences.

In The Last Decade

Guoping Zheng

103 papers receiving 4.6k citations

Hit Papers

Treatment of acute respiratory distress syndrome with all... 2014 2026 2018 2022 2014 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
Guoping Zheng Australia 33 1.7k 1.6k 843 714 704 112 4.7k
Jeremy S. Duffield United States 31 1.8k 1.1× 1.7k 1.1× 1.7k 2.0× 782 1.1× 334 0.5× 47 5.3k
Laurent Daniel France 34 1.5k 0.9× 909 0.6× 575 0.7× 645 0.9× 321 0.5× 161 4.1k
Lloyd G. Cantley United States 30 1.7k 1.0× 918 0.6× 1.7k 2.0× 953 1.3× 593 0.8× 61 4.4k
Benedetta Mazzinghi Italy 30 2.6k 1.5× 2.9k 1.8× 1.0k 1.2× 1.3k 1.8× 1.5k 2.2× 55 7.4k
Ralph Kettritz Germany 37 1.3k 0.7× 2.2k 1.4× 602 0.7× 313 0.4× 504 0.7× 135 4.5k
Naotake Tsuboi Japan 28 951 0.6× 1.3k 0.8× 585 0.7× 378 0.5× 237 0.3× 114 3.3k
Laura Lasagni Italy 38 2.8k 1.6× 1.9k 1.2× 1.5k 1.8× 1.0k 1.4× 436 0.6× 78 6.5k
Yoshiaki Tomiyama Japan 49 2.0k 1.1× 2.0k 1.3× 318 0.4× 912 1.3× 828 1.2× 275 8.3k
Carl Atkinson United States 38 1.1k 0.6× 1.3k 0.8× 192 0.2× 1.1k 1.5× 483 0.7× 141 4.9k
Anil K. Chauhan United States 41 1.7k 1.0× 1.5k 0.9× 183 0.2× 441 0.6× 319 0.5× 129 5.3k

Countries citing papers authored by Guoping Zheng

Since Specialization
Citations

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

Fields of papers citing papers by Guoping Zheng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guoping Zheng

This figure shows the co-authorship network connecting the top 25 collaborators of Guoping Zheng. A scholar is included among the top collaborators of Guoping Zheng 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 Guoping Zheng. Guoping Zheng 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.
Thallas‐Bonke, Vicki, Matthew Snelson, Karly C. Sourris, et al.. (2025). Proximal tubular deletion of superoxide dismutase-2 reveals disparate effects on kidney function in diabetes. Redox Biology. 82. 103601–103601. 1 indexed citations
2.
3.
Wang, Heng, Yaling Li, Keyang Xu, et al.. (2025). Global Epidemiology of Early-Onset Aortic Aneurysm: Temporal Trends, Risk Factors, and Future Burden Projections. Journal of Epidemiology and Global Health. 15(1). 25–25. 4 indexed citations
4.
Xu, Xiaoxue, Hien Duong, Ping Ye, et al.. (2025). Renal clearable sucrose carbon dots for doxorubicin delivery to treat renal carcinoma. Nanoscale Advances. 7(9). 2751–2760. 1 indexed citations
5.
6.
Cao, Qi, Yiping Wang, Jianwei Chen, et al.. (2025). Targeting inflammation with chimeric antigen receptor macrophages using a signal switch. Nature Biomedical Engineering. 9(9). 1502–1516. 11 indexed citations
7.
Cheng, Xing, Yaling Li, Heng Wang, et al.. (2024). Mesenchymal stem cell therapy in atherosclerosis: A bibliometric and visual analysis. World Journal of Stem Cells. 16(12). 1062–1085.
8.
Zhao, Yuanfei, Qian Yi, Wayne J. Hawthorne, et al.. (2024). Intragraft memory-like CD127hiCD4+Foxp3+ Tregs maintain transplant tolerance. JCI Insight. 9(6). 1 indexed citations
11.
Rao, Padmashree, Xi Qiao, Min Hu, et al.. (2021). Promotion of β-Catenin/Forkhead Box Protein O Signaling Mediates Epithelial Repair in Kidney Injury. American Journal Of Pathology. 191(6). 993–1009. 7 indexed citations
12.
Tian, Xinli, et al.. (2021). Targeted inhibition of β-catenin alleviates airway inflammation and remodeling in asthma via modulating the profibrotic and anti-inflammatory actions of transforming growth factor-β 1. Therapeutic Advances in Respiratory Disease. 15. 3272716898–3272716898. 28 indexed citations
13.
Zheng, Guoping, et al.. (2021). Microwave ablation for the management of pulmonary inflammatory myofibroblastic tumor: a case report and literature review. Translational Cancer Research. 10(10). 4582–4590. 3 indexed citations
14.
Li, Qing, Qi Cao, Chengshi Wang, et al.. (2019). Dendritic cell-targeted CD40 DNA vaccine suppresses Th17 and ameliorates progression of experimental autoimmune glomerulonephritis. Journal of Leukocyte Biology. 105(4). 809–819. 5 indexed citations
15.
Zheng, Guoping, Ruoqiong Huang, Guanguan Qiu, et al.. (2018). Mesenchymal stromal cell-derived extracellular vesicles: regenerative and immunomodulatory effects and potential applications in sepsis. Cell and Tissue Research. 374(1). 1–15. 113 indexed citations
16.
Tian, Xinrui, Xinli Tian, Qin Chang, et al.. (2017). Bacillus Calmette-Guerin alleviates airway inflammation and remodeling by preventing TGF-β1induced epithelial–mesenchymal transition. Human Vaccines & Immunotherapeutics. 13(8). 1758–1764. 15 indexed citations
17.
Hu, Min, Yuan Min Wang, Yiping Wang, et al.. (2016). Regulatory T cells in kidney disease and transplantation. Kidney International. 90(3). 502–514. 53 indexed citations
18.
Zheng, Guoping, Menghua Ge, Guanguan Qiu, Qiang Shu, & Jianguo Xu. (2015). Mesenchymal Stromal Cells Affect Disease Outcomes via Macrophage Polarization. Stem Cells International. 2015. 1–11. 73 indexed citations
19.
Cao, Qi, Yi‐Ping Wang, Zheng Dong, et al.. (2013). Failed renoprotection by alternatively activated bone marrow macrophages is due to a proliferation-dependent phenotype switch in vivo. Kidney International. 85(4). 794–806. 66 indexed citations
20.
Wang, Ying, Yiping Wang, Qi Cai, et al.. (2008). By Homing to the Kidney, Activated Macrophages Potently Exacerbate Renal Injury. American Journal Of Pathology. 172(6). 1491–1499. 62 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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