Wei-Qun Ding

2.6k total citations
38 papers, 2.2k citations indexed

About

Wei-Qun Ding is a scholar working on Molecular Biology, Cancer Research and Nutrition and Dietetics. According to data from OpenAlex, Wei-Qun Ding has authored 38 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 12 papers in Cancer Research and 9 papers in Nutrition and Dietetics. Recurrent topics in Wei-Qun Ding's work include MicroRNA in disease regulation (7 papers), Fatty Acid Research and Health (4 papers) and Heme Oxygenase-1 and Carbon Monoxide (4 papers). Wei-Qun Ding is often cited by papers focused on MicroRNA in disease regulation (7 papers), Fatty Acid Research and Health (4 papers) and Heme Oxygenase-1 and Carbon Monoxide (4 papers). Wei-Qun Ding collaborates with scholars based in United States, China and France. Wei-Qun Ding's co-authors include Bethany N. Hannafon, Stuart E. Lind, Haijun Yu, Xiaoxi Zhang, William L. Berry, Jundong Zhou, Ralf Janknecht, William C. Dooley, Doris M. Benbrook and Yan D. Zhao and has published in prestigious journals such as Journal of Biological Chemistry, Blood and Gastroenterology.

In The Last Decade

Wei-Qun Ding

38 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wei-Qun Ding United States 24 1.5k 989 379 264 152 38 2.2k
Wei‐Qun Ding United States 20 1.3k 0.9× 841 0.9× 345 0.9× 244 0.9× 93 0.6× 62 1.9k
Andras G. Lacko United States 29 1.3k 0.9× 855 0.9× 360 0.9× 133 0.5× 158 1.0× 122 3.1k
Amanda F. Baker United States 32 1.6k 1.1× 453 0.5× 606 1.6× 149 0.6× 417 2.7× 56 2.7k
Bethany N. Hannafon United States 19 1.8k 1.3× 1.4k 1.4× 252 0.7× 143 0.5× 89 0.6× 40 2.3k
Saroj P. Mathupala United States 24 2.6k 1.8× 2.1k 2.1× 479 1.3× 139 0.5× 177 1.2× 32 3.6k
Martina Raudenská Czechia 22 862 0.6× 438 0.4× 477 1.3× 213 0.8× 209 1.4× 69 1.9k
D. Lynn Kirkpatrick United States 18 1.4k 0.9× 436 0.4× 282 0.7× 84 0.3× 189 1.2× 34 1.8k
Saverio Tardito Italy 24 1.6k 1.1× 1.0k 1.0× 916 2.4× 163 0.6× 161 1.1× 37 3.1k
Angel L. Armesilla United Kingdom 30 1.6k 1.1× 416 0.4× 507 1.3× 170 0.6× 118 0.8× 50 2.8k
Ladislav Anděra Czechia 29 1.9k 1.3× 435 0.4× 778 2.1× 165 0.6× 134 0.9× 79 2.7k

Countries citing papers authored by Wei-Qun Ding

Since Specialization
Citations

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

Fields of papers citing papers by Wei-Qun Ding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wei-Qun Ding. 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 Wei-Qun Ding. The network helps show where Wei-Qun Ding may publish in the future.

Co-authorship network of co-authors of Wei-Qun Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Wei-Qun Ding. A scholar is included among the top collaborators of Wei-Qun Ding 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 Wei-Qun Ding. Wei-Qun Ding 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, Shitao, Jianlong Yang, Jiaming Guo, et al.. (2018). RAD18 promotes the migration and invasion of esophageal squamous cell cancer via the JNK-MMPs pathway. Cancer Letters. 417. 65–74. 43 indexed citations
2.
Li, Ming, Shanhu Li, Biao Liu, et al.. (2017). PIG3 promotes NSCLC cell mitotic progression and is associated with poor prognosis of NSCLC patients. Journal of Experimental & Clinical Cancer Research. 36(1). 39–39. 18 indexed citations
3.
Xue, Jiao, Chenxiao Yu, Wei Zhu, et al.. (2017). The Nrf2/GCH1/BH4 Axis Ameliorates Radiation-Induced Skin Injury by Modulating the ROS Cascade. Journal of Investigative Dermatology. 137(10). 2059–2068. 81 indexed citations
4.
Hannafon, Bethany N., et al.. (2017). microRNA regulation of human pancreatic cancer stem cells. PubMed. 4. 5–5. 31 indexed citations
5.
Hannafon, Bethany N., et al.. (2016). Disulfiram';s Anticancer Activity: Evidence and Mechanisms. Anti-Cancer Agents in Medicinal Chemistry. 16(11). 1378–1384. 95 indexed citations
6.
Zou, Shitao, Jundong Zhou, Hongsheng Zhu, et al.. (2016). REV3L, the catalytic subunit of DNA polymerase ζ, is involved in the progression and chemoresistance of esophageal squamous cell carcinoma. Oncology Reports. 35(3). 1664–1670. 18 indexed citations
7.
Wang, Shuai, Bethany N. Hannafon, Roman F. Wolf, et al.. (2014). Characterization of docosahexaenoic acid (DHA)-induced heme oxygenase-1 (HO-1) expression in human cancer cells: the importance of enhanced BTB and CNC homology 1 (Bach1) degradation. The Journal of Nutritional Biochemistry. 25(5). 515–525. 18 indexed citations
8.
Wang, Shuai, Bethany N. Hannafon, Jundong Zhou, & Wei-Qun Ding. (2013). Clofibrate Induces Heme Oxygenase 1 Expression through a PPARa-Independent Mechanism in Human Cancer Cells. Cellular Physiology and Biochemistry. 32(5). 1255–1264. 14 indexed citations
10.
Zhang, Shuyu, Chuanjun Song, Jundong Zhou, et al.. (2012). Amelioration of radiation-induced skin injury by adenovirus-mediated heme oxygenase-1 (HO-1) overexpression in rats. Radiation Oncology. 7(1). 4–4. 26 indexed citations
11.
Dong, Jia-Yi, et al.. (2012). Dietary intake of n-3 fatty acids and colorectal cancer risk: a meta-analysis of data from 489 000 individuals. British Journal Of Nutrition. 108(9). 1550–1556. 31 indexed citations
12.
Zheng, Jie, et al.. (2012). Zinc at Cytotoxic Concentrations Affects Posttranscriptional Events of Gene Expression in Cancer Cells. Cellular Physiology and Biochemistry. 29(1-2). 181–188. 16 indexed citations
13.
Jiang, Hongchao, et al.. (2011). Nitroxoline (8-hydroxy-5-nitroquinoline) is more a potent anti-cancer agent than clioquinol (5-chloro-7-iodo-8-quinoline). Cancer Letters. 312(1). 11–17. 134 indexed citations
14.
Zhang, Xiaoxi, Haijun Yu, Jie Zheng, et al.. (2010). MicroRNA-19 (miR-19) Regulates Tissue Factor Expression in Breast Cancer Cells. Journal of Biological Chemistry. 286(2). 1429–1435. 116 indexed citations
15.
Tuller, Erin, et al.. (2009). PPARα signaling mediates the synergistic cytotoxicity of clioquinol and docosahexaenoic acid in human cancer cells. Biochemical Pharmacology. 77(9). 1480–1486. 33 indexed citations
16.
Ding, Wei-Qun, Haijun Yu, & Stuart E. Lind. (2008). Zinc-binding compounds induce cancer cell death via distinct modes of action. Cancer Letters. 271(2). 251–259. 57 indexed citations
18.
Ding, Wei-Qun, Maoqing Dong, Dora Ninova, et al.. (2003). Forskolin suppresses insulin gene transcription in islet β-cells through a protein kinase A-independent pathway. Cellular Signalling. 15(1). 27–35. 18 indexed citations
19.
Ding, Wei-Qun, Susan M. Kuntz, Michael Böhmig, Bertram Wiedenmann, & Laurence J. Miller. (2002). Dominant negative action of an abnormal secretin receptor arising from mRNA missplicing in a gastrinoma. Gastroenterology. 122(2). 500–511. 31 indexed citations
20.
Ding, Wei-Qun & Laurence J. Miller. (2002). Signaling from Novel Splice Variants of Hormone Receptors in Cancer. International Journal of Gastrointestinal Cancer. 31(1-3). 31–40. 4 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026