Qian‐Ping Shi

470 total citations
24 papers, 401 citations indexed

About

Qian‐Ping Shi is a scholar working on Molecular Biology, Pharmacology and Oncology. According to data from OpenAlex, Qian‐Ping Shi has authored 24 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Pharmacology and 8 papers in Oncology. Recurrent topics in Qian‐Ping Shi's work include Flavonoids in Medical Research (10 papers), Neurological Disease Mechanisms and Treatments (6 papers) and Natural product bioactivities and synthesis (6 papers). Qian‐Ping Shi is often cited by papers focused on Flavonoids in Medical Research (10 papers), Neurological Disease Mechanisms and Treatments (6 papers) and Natural product bioactivities and synthesis (6 papers). Qian‐Ping Shi collaborates with scholars based in China, United States and Taiwan. Qian‐Ping Shi's co-authors include Yuping Tang, Hao Tang, Nian‐Guang Li, Jin‐Ao Duan, Zhi‐Hao Shi, Yifan Fu, Nian‐Guang Li, Jianming Guo, Erxin Shang and Jianping Yang and has published in prestigious journals such as PLoS ONE, Molecules and Bioorganic & Medicinal Chemistry.

In The Last Decade

Qian‐Ping Shi

24 papers receiving 397 citations

Peers

Qian‐Ping Shi
Terry C. T. Or Hong Kong
Ho Won Seo South Korea
Li-Kang Ho Taiwan
Wang-Fun Fong Hong Kong
Belnaser A. Busnena United States
Terry C. T. Or Hong Kong
Qian‐Ping Shi
Citations per year, relative to Qian‐Ping Shi Qian‐Ping Shi (= 1×) peers Terry C. T. Or

Countries citing papers authored by Qian‐Ping Shi

Since Specialization
Citations

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

Fields of papers citing papers by Qian‐Ping Shi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Qian‐Ping Shi. 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 Qian‐Ping Shi. The network helps show where Qian‐Ping Shi may publish in the future.

Co-authorship network of co-authors of Qian‐Ping Shi

This figure shows the co-authorship network connecting the top 25 collaborators of Qian‐Ping Shi. A scholar is included among the top collaborators of Qian‐Ping Shi 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 Qian‐Ping Shi. Qian‐Ping Shi 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.
Shi, Qian‐Ping, Xuan Wang, Zhi-Xi Liu, Jianjun Zhang, & Zhaoyang Wang. (2021). Autoantibody Signatures as a Biomarker Panel for the Detection of Nasopharyngeal Carcinoma. Archives of Medical Research. 52(6). 620–626. 2 indexed citations
2.
Xu, Shan, Qian‐Ping Shi, Bo Li, et al.. (2020). High MTHFR promoter methylation levels in men confer protection against ischemic stroke. Bosnian Journal of Basic Medical Sciences. 20(4). 477–486. 9 indexed citations
4.
Tang, Hao, Zhi‐Hao Shi, Nian‐Guang Li, et al.. (2015). Investigation on the interactions of scutellarin and scutellarein with bovine serum albumin using spectroscopic and molecular docking techniques. Archives of Pharmacal Research. 38(10). 1789–1801. 14 indexed citations
5.
Shi, Zhi‐Hao, Nian‐Guang Li, Qian‐Ping Shi, et al.. (2015). Synthesis of scutellarein derivatives to increase biological activity and water solubility. Bioorganic & Medicinal Chemistry. 23(21). 6875–6884. 17 indexed citations
6.
Tang, Hao, Yuping Tang, Nian‐Guang Li, et al.. (2014). Neuroprotective effects of scutellarin and scutellarein on repeatedly cerebral ischemia–reperfusion in rats. Pharmacology Biochemistry and Behavior. 118. 51–59. 67 indexed citations
7.
Tang, Hao, Nian‐Guang Li, Yuping Tang, et al.. (2014). Identification of scutellarein metabolites in rat using ultra performance liquid chromatography/quadrupole-time-of-flight mass spectrometry. Analytical Methods. 6(13). 4667–4667. 7 indexed citations
8.
Shi, Zhi‐Hao, Nian‐Guang Li, Yuping Tang, et al.. (2014). Synthesis, biological evaluation and SAR analysis of O-alkylated analogs of quercetin for anticancer. Bioorganic & Medicinal Chemistry Letters. 24(18). 4424–4427. 26 indexed citations
9.
Shi, Zhi‐Hao, Nian‐Guang Li, Qian‐Ping Shi, et al.. (2014). Immobilization of Chiral Manganese(III)-salen Complexes for Enantioselective Epoxidation of Unfunctionalised Olefins. Current Organic Synthesis. 11(2). 204–243. 7 indexed citations
10.
Shi, Qian‐Ping, Nian‐Guang Li, Wei Li, et al.. (2014). ChemInform Abstract: Asymmetric Epoxidation of Olefins with Homogeneous Chiral (Salen) Manganese(III) Complexes. ChemInform. 45(33). 1 indexed citations
11.
Shi, Qian‐Ping, Zhi‐Hao Shi, Nian‐Guang Li, et al.. (2014). Efficient Chemical Synthesis of a Scutellarein Derivative Containing Morpholine Ring. Letters in Organic Chemistry. 11(8). 590–595. 3 indexed citations
12.
Shi, Zhi‐Hao, Nian‐Guang Li, Qian‐Ping Shi, et al.. (2013). Synthesis and structure–activity relationship analysis of caffeic acid amides as selective matrix metalloproteinase inhibitors. Bioorganic & Medicinal Chemistry Letters. 23(5). 1206–1211. 26 indexed citations
13.
Shi, Zhi‐Hao, Nian‐Guang Li, Qian‐Ping Shi, et al.. (2013). Design, Synthesis and Biological Evaluation of Ferulic Acid Amides as Selective Matrix Metalloproteinase Inhibitors. Medicinal Chemistry. 9(7). 947–954. 8 indexed citations
14.
Shi, Zhi‐Hao, Nian‐Guang Li, Hao Tang, et al.. (2013). Efficient Synthesis of 6-O-methyl-scutellarein from Scutellarin via Selective Methylation. Letters in Organic Chemistry. 10(10). 733–737. 11 indexed citations
15.
Shi, Qian‐Ping, Nian‐Guang Li, Yuping Tang, et al.. (2013). Asymmetric Epoxidation of Olefins with Homogeneous Chiral (Salen) Manganese (III) Complex. Current Organic Chemistry. 17(23). 2936–2970. 15 indexed citations
16.
Shi, Zhi‐Hao, Nian‐Guang Li, Qian‐Ping Shi, et al.. (2012). Design, Synthesis and Biological Evaluation of Caffeic Acid Amides as Selective MMP‐2 and MMP‐9 Inhibitors. Drug Development Research. 73(6). 343–351. 9 indexed citations
17.
Li, Nian‐Guang, Shulin Song, Yuping Tang, et al.. (2012). Mannich bases of scutellarein as thrombin-inhibitors: Design, synthesis, biological activity and solubility. Bioorganic & Medicinal Chemistry. 20(24). 6919–6923. 46 indexed citations
18.
Li, Nian‐Guang, Yuping Tang, Zhi‐Hao Shi, et al.. (2012). Design, synthesis and biological evaluation of glucose-containing scutellarein derivatives as neuroprotective agents based on metabolic mechanism of scutellarin in vivo. Bioorganic & Medicinal Chemistry Letters. 23(1). 102–106. 26 indexed citations
19.
Shi, Zhi‐Hao, et al.. (2012). Design, Synthesis, and Preliminary Evaluation of Substituted Cinnamic Acid Esters as Selective Matrix Metalloproteinase Inhibitors. Drug Development Research. 73(6). 317–324. 11 indexed citations
20.
Tang, Hao, Yuping Tang, Zhang Li, et al.. (2012). Synthesis and Protective Effect of Scutellarein on Focal Cerebral Ischemia/Reperfusion in Rats. Molecules. 17(9). 10667–10674. 50 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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