Hongsheng Wang

2.3k total citations
49 papers, 1.6k citations indexed

About

Hongsheng Wang is a scholar working on Molecular Biology, Oncology and Surgery. According to data from OpenAlex, Hongsheng Wang has authored 49 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 20 papers in Oncology and 8 papers in Surgery. Recurrent topics in Hongsheng Wang's work include Cancer Cells and Metastasis (9 papers), Cytokine Signaling Pathways and Interactions (4 papers) and Peptidase Inhibition and Analysis (3 papers). Hongsheng Wang is often cited by papers focused on Cancer Cells and Metastasis (9 papers), Cytokine Signaling Pathways and Interactions (4 papers) and Peptidase Inhibition and Analysis (3 papers). Hongsheng Wang collaborates with scholars based in China, United States and United Kingdom. Hongsheng Wang's co-authors include Zhengdong Cai, Yingqi Hua, Shaohui Cai, Jun Du, Dongqing Zuo, Wei Sun, Hao Wang, Binhua P. Zhou, Fan Zhang and Fei Yin and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Hongsheng Wang

49 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hongsheng Wang China 21 845 575 337 204 195 49 1.6k
Yan Fan China 20 695 0.8× 453 0.8× 304 0.9× 209 1.0× 353 1.8× 67 1.5k
Xiaochun Peng China 23 807 1.0× 490 0.9× 226 0.7× 181 0.9× 321 1.6× 74 1.8k
Yihui Shi United States 21 841 1.0× 493 0.9× 386 1.1× 138 0.7× 276 1.4× 50 1.8k
Xiaoyan Xin China 25 998 1.2× 426 0.7× 365 1.1× 195 1.0× 338 1.7× 115 1.9k
Jie Gao China 24 910 1.1× 251 0.4× 296 0.9× 128 0.6× 170 0.9× 90 1.7k
Dariusz Grzanka Poland 20 805 1.0× 350 0.6× 236 0.7× 179 0.9× 121 0.6× 132 1.8k
Chia‐Hung Hsieh Taiwan 22 588 0.7× 450 0.8× 268 0.8× 114 0.6× 241 1.2× 33 1.4k
Katiuscia Dallaglio Italy 21 1.0k 1.2× 644 1.1× 395 1.2× 132 0.6× 300 1.5× 31 1.8k
Haiyan Yang China 23 604 0.7× 498 0.9× 347 1.0× 404 2.0× 108 0.6× 84 1.6k

Countries citing papers authored by Hongsheng Wang

Since Specialization
Citations

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

Fields of papers citing papers by Hongsheng Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hongsheng Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Hongsheng Wang. A scholar is included among the top collaborators of Hongsheng Wang 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 Hongsheng Wang. Hongsheng Wang 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, Yanqing, et al.. (2025). Immunophenotypic characteristics of Langhans giant cells and the role of CCR7 in their formation. Immunobiology. 230(4). 153086–153086. 1 indexed citations
2.
Liu, Kaiyuan, Pengfei Zan, Zihua Li, et al.. (2024). Engineering Bimetallic Polyphenol for Mild Photothermal Osteosarcoma Therapy and Immune Microenvironment Remodeling by Activating Pyroptosis and cGAS‐STING Pathway. Advanced Healthcare Materials. 13(22). e2400623–e2400623. 10 indexed citations
3.
Jiang, Ming, Zhongjun Jia, Hongsheng Wang, et al.. (2024). Safeguarding the “Black Soil Granary”: Innovations in Soil Conservation and Sustainable Agriculture. 38. 2024018–2024018. 2 indexed citations
4.
Li, Ruotong, Kaiyuan Liu, Jiakang Shen, et al.. (2024). NIR‐II AIEgens nanosystem for fluorescence and chemiluminescence synergistic imaging‐guided precise resection in osteosarcoma surgery. SHILAP Revista de lepidopterología. 6(1). 6 indexed citations
5.
Lv, Yu, et al.. (2023). Applications and Future Prospects of Micro/Nanorobots Utilizing Diverse Biological Carriers. Micromachines. 14(5). 983–983. 14 indexed citations
6.
7.
Wang, Gangyang, Lingling Cao, Yafei Jiang, et al.. (2022). Anlotinib Reverses Multidrug Resistance (MDR) in Osteosarcoma by Inhibiting P-Glycoprotein (PGP1) Function In Vitro and In Vivo. Frontiers in Pharmacology. 12. 798837–798837. 20 indexed citations
8.
Zan, Pengfei, Xiaojun Ma, Hongsheng Wang, et al.. (2022). Feasibility and preliminary efficacy of tantalum components in the management of acetabular reconstruction following periacetabular oncologic resection in primary malignancies. European journal of medical research. 27(1). 151–151. 2 indexed citations
9.
10.
Han, Jing, Jing Xu, Tao Zhang, et al.. (2020). Her4 promotes cancer metabolic reprogramming via the c-Myc-dependent signaling axis. Cancer Letters. 496. 57–71. 28 indexed citations
11.
Wang, Zhuoying, Chongren Wang, Dongqing Zuo, et al.. (2019). Attenuation of STAT3 Phosphorylation Promotes Apoptosis and Chemosensitivity in Human Osteosarcoma Induced by Raddeanin A. International Journal of Biological Sciences. 15(3). 668–679. 30 indexed citations
12.
Li, Ziqian, Junjie Zhang, Jiawang Zhou, et al.. (2019). Nodal Facilitates Differentiation of Fibroblasts to Cancer-Associated Fibroblasts that Support Tumor Growth in Melanoma and Colorectal Cancer. Cells. 8(6). 538–538. 35 indexed citations
13.
Wang, Hongsheng, Wei Sun, Mengxiong Sun, et al.. (2018). HER4 promotes cell survival and chemoresistance in osteosarcoma via interaction with NDRG1. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(5). 1839–1849. 22 indexed citations
14.
Wang, Gangyang, Tao Zhang, Wei Sun, et al.. (2017). Arsenic sulfide induces apoptosis and autophagy through the activation of ROS/JNK and suppression of Akt/mTOR signaling pathways in osteosarcoma. Free Radical Biology and Medicine. 106. 24–37. 131 indexed citations
15.
Chen, Xiaohong, Zongcai Liu, Ge Zhang, et al.. (2015). TGF-β and EGF induced HLA-I downregulation is associated with epithelial-mesenchymal transition (EMT) through upregulation of snail in prostate cancer cells. Molecular Immunology. 65(1). 34–42. 68 indexed citations
16.
Wang, Hao, Rui Fang, Xianfeng Wang, et al.. (2013). Stabilization of Snail through AKT/GSK-3β signaling pathway is required for TNF-α-induced epithelial–mesenchymal transition in prostate cancer PC3 cells. European Journal of Pharmacology. 714(1-3). 48–55. 66 indexed citations
17.
Du, Jing, Yifeng Xu, Shiwei Duan, et al.. (2009). A case–control association study between the CYP3A4 and CYP3A5 genes and schizophrenia in the Chinese Han population. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 33(7). 1200–1204. 11 indexed citations
18.
Wang, Hongsheng. (2006). Study on Change Regulation of Environment Factors at Cordyceps sinensis Growth Area. 4 indexed citations
19.
Duan, Shiwei, Rui Gao, Qinghe Xing, et al.. (2005). A family-based association study of schizophrenia with polymorphisms at three candidate genes. Neuroscience Letters. 379(1). 32–36. 41 indexed citations
20.
Liu, Jixia, Yongyong Shi, Wei Tang, et al.. (2005). Positive association of the human GABA-A-receptor beta 2 subunit gene haplotype with schizophrenia in the Chinese Han population. Biochemical and Biophysical Research Communications. 334(3). 817–823. 22 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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