Ling‐Wen Ding

6.2k total citations · 1 hit paper
65 papers, 2.4k citations indexed

About

Ling‐Wen Ding is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Ling‐Wen Ding has authored 65 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 15 papers in Cancer Research and 12 papers in Oncology. Recurrent topics in Ling‐Wen Ding's work include Cancer-related gene regulation (8 papers), Ubiquitin and proteasome pathways (7 papers) and Cancer-related molecular mechanisms research (7 papers). Ling‐Wen Ding is often cited by papers focused on Cancer-related gene regulation (8 papers), Ubiquitin and proteasome pathways (7 papers) and Cancer-related molecular mechanisms research (7 papers). Ling‐Wen Ding collaborates with scholars based in Singapore, China and United States. Ling‐Wen Ding's co-authors include H. Phillip Koeffler, De‐Chen Lin, Boon Cher Goh, Anand Mayakonda, Qiao‐Yang Sun, Lingzhi Wang, Xiaoqiang Xiang, Paul C. Ho, Wenwen Chien and Pei Shi Ong and has published in prestigious journals such as Nucleic Acids Research, Advanced Materials and Angewandte Chemie International Edition.

In The Last Decade

Ling‐Wen Ding

60 papers receiving 2.4k citations

Hit Papers

Resveratrol for cancer therapy: Challenges and future per... 2021 2026 2022 2024 2021 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
Ling‐Wen Ding Singapore 29 1.6k 541 506 318 260 65 2.4k
Chern Ein Oon Malaysia 23 1.6k 1.0× 682 1.3× 533 1.1× 220 0.7× 225 0.9× 71 2.8k
In‐Chul Park South Korea 32 1.8k 1.1× 589 1.1× 543 1.1× 256 0.8× 228 0.9× 116 2.8k
Yanping Xu China 22 1.7k 1.0× 552 1.0× 587 1.2× 299 0.9× 337 1.3× 46 2.7k
Zhenyi Su China 16 1.4k 0.9× 714 1.3× 408 0.8× 327 1.0× 291 1.1× 31 2.2k
Mohamed Ali‐Seyed Saudi Arabia 20 1.6k 1.0× 400 0.7× 891 1.8× 429 1.3× 197 0.8× 44 2.7k
Miao Yin China 27 1.3k 0.8× 603 1.1× 330 0.7× 159 0.5× 263 1.0× 83 2.4k
Ernesto Yagüe United Kingdom 30 1.6k 1.0× 632 1.2× 830 1.6× 147 0.5× 110 0.4× 60 2.5k
Jingxuan Pan China 38 2.7k 1.7× 795 1.5× 1.0k 2.0× 284 0.9× 409 1.6× 90 4.1k
Helena Pópulo Portugal 13 1.2k 0.7× 344 0.6× 518 1.0× 188 0.6× 250 1.0× 21 1.9k

Countries citing papers authored by Ling‐Wen Ding

Since Specialization
Citations

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

Fields of papers citing papers by Ling‐Wen Ding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ling‐Wen 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 Ling‐Wen Ding. The network helps show where Ling‐Wen Ding may publish in the future.

Co-authorship network of co-authors of Ling‐Wen Ding

This figure shows the co-authorship network connecting the top 25 collaborators of Ling‐Wen Ding. A scholar is included among the top collaborators of Ling‐Wen 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 Ling‐Wen Ding. Ling‐Wen 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.
Chen, Ying, Ou Xu, Yibin Liu, et al.. (2025). Feedback-Amplified Drug Delivery of αPD-L1-Modified Lipoplatin for Chronological Synergy in NSCLC through PD-L1 Upregulation. ACS Applied Materials & Interfaces. 17(40). 55861–55875.
2.
Li, Zheng, Guodong Ren, Xuewei Wang, et al.. (2025). Tumor microenvironment responsive nano-PROTAC for BRD4 degradation enhanced cancer photo-immunotherapy. Biomaterials. 322. 123387–123387. 9 indexed citations
3.
Zhang, Miao, Yongling Wang, Benhao Li, et al.. (2025). STING‐Activating Polymers Boost Lymphatic Delivery of mRNA Vaccine to Potentiate Cancer Immunotherapy (Adv. Mater. 10/2025). Advanced Materials. 37(10). 1 indexed citations
4.
Ding, Ling‐Wen, Jia Li, Benedict Yan, et al.. (2024). A Pre-Leukemic DNA Methylation Signature in Healthy Individuals at Higher Risk for Developing Myeloid Malignancy. Clinical Cancer Research. 30(10). 2170–2180. 1 indexed citations
5.
Liu, Jianping, Ye Zhang, Yingbo Jia, et al.. (2024). Synergistic Glutathione Depletion and STING Activation to Potentiate Dendritic Cell Maturation and Cancer Vaccine Efficacy. Angewandte Chemie. 136(10). 5 indexed citations
6.
Wang, Rong, Lan Zhang, Jun Wang, et al.. (2024). Prebiotic stachyose inhibits PRDX5 activity and castration-resistant prostate cancer development. International Journal of Biological Macromolecules. 278(Pt 3). 134844–134844. 2 indexed citations
7.
Ding, Ling‐Wen, Henry Yang, Jonathan W. Said, et al.. (2023). Targeting RNA Exonuclease XRN1 Potentiates Efficacy of Cancer Immunotherapy. Cancer Research. 83(6). 922–938. 12 indexed citations
8.
Ma, Sai, Bo Zhou, Qian Yang, et al.. (2021). A Transcriptional Regulatory Loop of Master Regulator Transcription Factors, PPARG, and Fatty Acid Synthesis Promotes Esophageal Adenocarcinoma. Cancer Research. 81(5). 1216–1229. 60 indexed citations
9.
Ke, Xinyu, Ye Chen, Ruby Yu‐Tong Lin, et al.. (2021). MNK1 and MNK2 enforce expression of E2F1, FOXM1, and WEE1 to drive soft tissue sarcoma. Oncogene. 40(10). 1851–1867. 16 indexed citations
10.
Shi, Xianping, Yueyuan Zheng, Bo Zhou, et al.. (2020). EWS-FLI1 regulates and cooperates with core regulatory circuitry in Ewing sarcoma. Nucleic Acids Research. 48(20). 11434–11451. 26 indexed citations
11.
Pan, Jian, Tiago C. Silva, Nicole Gull, et al.. (2020). Lineage-Specific Epigenomic and Genomic Activation of Oncogene HNF4A Promotes Gastrointestinal Adenocarcinomas. Cancer Research. 80(13). 2722–2736. 38 indexed citations
12.
Ding, Ling‐Wen, Qiao‐Yang Sun, Jarem Edwards, et al.. (2019). LNK suppresses interferon signaling in melanoma. Nature Communications. 10(1). 2230–2230. 20 indexed citations
13.
Zhang, Yin, Anand Mayakonda, Vikas Madan, et al.. (2018). ARID1A and CEBPα cooperatively inhibit UCA1 transcription in breast cancer. Oncogene. 37(45). 5939–5951. 23 indexed citations
14.
Chien, Wenwen, Makoto Sudo, Ling‐Wen Ding, et al.. (2018). Functional Genome-wide Screening Identifies Targets and Pathways Sensitizing Pancreatic Cancer Cells to Dasatinib. Journal of Cancer. 9(24). 4762–4773. 28 indexed citations
15.
Lin, De‐Chen, Anand Mayakonda, Huy Q. Dinh, et al.. (2017). Genomic and Epigenomic Heterogeneity of Hepatocellular Carcinoma. Cancer Research. 77(9). 2255–2265. 148 indexed citations
16.
Jiang, Yuan, Anand Mayakonda, Moli Huang, et al.. (2017). Super-Enhancers Promote Transcriptional Dysregulation in Nasopharyngeal Carcinoma. Cancer Research. 77(23). 6614–6626. 77 indexed citations
17.
Takao, Sumiko, Wenwen Chien, Vikas Madan, et al.. (2017). Targeting the vulnerability to NAD+ depletion in B-cell acute lymphoblastic leukemia. Leukemia. 32(3). 616–625. 30 indexed citations
18.
Lin, De‐Chen, Liang Xu, Ye Chen, et al.. (2015). Genomic and Functional Analysis of the E3 Ligase PARK2 in Glioma. Cancer Research. 75(9). 1815–1827. 51 indexed citations
19.
Ding, Ling‐Wen, Qiao‐Yang Sun, Wenwen Chien, et al.. (2014). LNK (SH2B3): paradoxical effects in ovarian cancer. Oncogene. 34(11). 1463–1474. 20 indexed citations
20.
Hayano, Takahide, Manoj Garg, Dong Yin, et al.. (2013). SOX7 is down-regulated in lung cancer. Journal of Experimental & Clinical Cancer Research. 32(1). 17–17. 61 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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