Gao Qingping

770 total citations
34 papers, 616 citations indexed

About

Gao Qingping is a scholar working on Oncology, Immunology and Molecular Biology. According to data from OpenAlex, Gao Qingping has authored 34 papers receiving a total of 616 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Oncology, 10 papers in Immunology and 9 papers in Molecular Biology. Recurrent topics in Gao Qingping's work include Chronic Lymphocytic Leukemia Research (5 papers), Mesenchymal stem cell research (4 papers) and Immune Cell Function and Interaction (4 papers). Gao Qingping is often cited by papers focused on Chronic Lymphocytic Leukemia Research (5 papers), Mesenchymal stem cell research (4 papers) and Immune Cell Function and Interaction (4 papers). Gao Qingping collaborates with scholars based in China, United States and Saudi Arabia. Gao Qingping's co-authors include Baixin Ye, Xiaoxing Xiong, Chunsheng Kang, Creed M. Stary, Xuping Sun, Xi–Shi Tai, Qiuping Zhang, Tan Jinquan, Kejian Zhang and Xuejun Li and has published in prestigious journals such as The Journal of Immunology, PLoS ONE and Cancer Research.

In The Last Decade

Gao Qingping

34 papers receiving 612 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gao Qingping China 12 209 185 168 168 127 34 616
J Engel United States 9 169 0.8× 147 0.8× 25 0.1× 105 0.6× 32 0.3× 14 557
Chaoying Liang United States 5 70 0.3× 512 2.8× 148 0.9× 93 0.6× 120 0.9× 7 774
Guancheng Li China 14 127 0.6× 60 0.3× 37 0.2× 367 2.2× 47 0.4× 40 645
Eva Oswald Germany 12 110 0.5× 187 1.0× 23 0.1× 74 0.4× 18 0.1× 39 493
Juan Tornín Spain 18 257 1.2× 70 0.4× 15 0.1× 436 2.6× 92 0.7× 26 1.0k
Guofen Chen China 13 66 0.3× 171 0.9× 50 0.3× 166 1.0× 67 0.5× 24 584
Ruixiang Xia China 13 30 0.1× 44 0.2× 106 0.6× 234 1.4× 221 1.7× 25 722
Chung Hee Sonn South Korea 13 165 0.8× 149 0.8× 29 0.2× 233 1.4× 12 0.1× 20 602
Xinzhong Wang China 10 258 1.2× 49 0.3× 56 0.3× 158 0.9× 83 0.7× 27 603
Guangjian Huang China 16 149 0.7× 243 1.3× 36 0.2× 466 2.8× 32 0.3× 25 998

Countries citing papers authored by Gao Qingping

Since Specialization
Citations

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

Fields of papers citing papers by Gao Qingping

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gao Qingping

This figure shows the co-authorship network connecting the top 25 collaborators of Gao Qingping. A scholar is included among the top collaborators of Gao Qingping 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 Gao Qingping. Gao Qingping 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.
Zou, Fang, Li Zhang, Gao Qingping, et al.. (2023). Polyoxometalate‐Incorporated CuI‐Resorcin[4]arene Metal‐Organic Complexes as Heterogeneous Catalysts for Catalytic Oxidation of Mustard Gas Simulant. European Journal of Inorganic Chemistry. 26(27). 5 indexed citations
2.
Wu, Qian, Gao Qingping, Yuping Qi, et al.. (2023). Boosting electrocatalytic performance via electronic structure regulation for acidic oxygen evolution. iScience. 27(1). 108738–108738. 29 indexed citations
3.
Wu, Qian, Gao Qingping, Bin Shan, et al.. (2023). Recent Advances in Self-Supported Transition-Metal-Based Electrocatalysts for Seawater Oxidation. Acta Physico-Chimica Sinica. 0(0). 2303012–2303012. 52 indexed citations
4.
5.
Qingping, Gao, Limei Sun, Xi–Shi Tai, et al.. (2020). Facilitating active species by decorating CeO2 on Ni3S2 nanosheets for efficient water oxidation electrocatalysis. CHINESE JOURNAL OF CATALYSIS (CHINESE VERSION). 42(3). 482–489. 95 indexed citations
6.
Ye, Baixin, Creed M. Stary, Xuejun Li, et al.. (2018). Engineering chimeric antigen receptor-T cells for cancer treatment. Molecular Cancer. 17(1). 32–32. 72 indexed citations
7.
Ye, Baixin, Daniel Smerin, Gao Qingping, Chunsheng Kang, & Xiaoxing Xiong. (2017). High-throughput sequencing of the immune repertoire in oncology: Applications for clinical diagnosis, monitoring, and immunotherapies. Cancer Letters. 416. 42–56. 29 indexed citations
8.
Chen, Zhanguo, Yan Li, Yongqing Tong, et al.. (2016). Stepwise discriminant function analysis for rapid identification of acute promyelocytic leukemia from acute myeloid leukemia with multiparameter flow cytometry. International Journal of Hematology. 103(3). 306–315. 14 indexed citations
9.
Li, Xianguo, et al.. (2016). Interaction mechanism exploration of HEA derivatives as BACE1 inhibitors by in silico analysis. Molecular BioSystems. 12(4). 1151–1165. 9 indexed citations
10.
11.
Ye, Baixin, Xiaoxing Xiong, Xu Deng, et al.. (2016). Meisoindigo, but not its core chemical structure indirubin, inhibits zebrafish interstitial leukocyte chemotactic migration. Pharmaceutical Biology. 55(1). 673–679. 11 indexed citations
12.
13.
Ruan, Xiaolan, et al.. (2015). The Role of TP53 Gene Codon 72 Polymorphism in Leukemia. Medicine. 94(38). e1588–e1588. 5 indexed citations
14.
Deng, Chaohua, et al.. (2013). Anaplastic myeloma and T-cell lymphoma in the same patient. Chinese Medical Journal. 126(5). 996–996. 1 indexed citations
15.
Qingping, Gao, Dan Li, Jinghui Wang, et al.. (2013). Inhibition mechanism exploration of quinoline derivatives as PDE10A inhibitors by in silico analysis. Molecular BioSystems. 9(3). 386–397. 6 indexed citations
16.
Guo, Feng, et al.. (2007). [Effect of astragalus polysaccharides on the proliferation and ultrastructure of dog bone marrow stem cells induced into osteoblasts in vitro].. PubMed. 25(5). 432–6. 5 indexed citations
17.
Chunsong, Hu, Yuling He, Wang Li, et al.. (2006). CXC Chemokine Ligand 13 and CC Chemokine Ligand 19 Cooperatively Render Resistance to Apoptosis in B Cell Lineage Acute and Chronic Lymphocytic Leukemia CD23+CD5+ B Cells. The Journal of Immunology. 177(10). 6713–6722. 54 indexed citations
18.
Hu, Chunsong, Baojun Huang, Qiuping Zhang, et al.. (2004). PEG10 activation by co-stimulation of CXCR5 and CCR7 essentially contributes to resistance to apoptosis in CD19+CD34+ B cells from patients with B cell lineage acute and chronic lymphocytic leukemia.. PubMed. 1(4). 280–94. 43 indexed citations
19.
Zhang, Qiuping, Qun Li, Hu Chunsong, et al.. (2003). Selectively increased expression and functions of chemokine receptor CCR9 on CD4+ T cells from patients with T-cell lineage acute lymphocytic leukemia.. PubMed. 63(19). 6469–77. 38 indexed citations
20.
Qingping, Gao. (2001). The expression of Fas protein and Fas-L protein in the lymphocytes and platelets from patients with idiopathic thrombocytopenic purpura. 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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