Mengqian Chen

1.8k total citations
46 papers, 1.1k citations indexed

About

Mengqian Chen is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Oncology. According to data from OpenAlex, Mengqian Chen has authored 46 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 18 papers in Pulmonary and Respiratory Medicine and 13 papers in Oncology. Recurrent topics in Mengqian Chen's work include Advanced Breast Cancer Therapies (11 papers), Cancer-related Molecular Pathways (9 papers) and Prostate Cancer Treatment and Research (8 papers). Mengqian Chen is often cited by papers focused on Advanced Breast Cancer Therapies (11 papers), Cancer-related Molecular Pathways (9 papers) and Prostate Cancer Treatment and Research (8 papers). Mengqian Chen collaborates with scholars based in United States, China and Hungary. Mengqian Chen's co-authors include Ralph Buttyan, Li‐Mei Chen, Karl X. Chai, Michael Shtutman, Eugenia V. Broude, Igor B. Roninson, Matthew Tanner, Chen‐Yong Lin, Alexander A. Chumanevich and Jiaxin Liang and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Mengqian Chen

39 papers receiving 1.1k citations

Peers

Mengqian Chen
Susan Korenchuk United States
Yoko Ueno Japan
Michaela Medová Switzerland
Jinah Park South Korea
Sujatha Jagadeeswaran United States
Shuangbing Xu China
Georg Emons Germany
Changxian Shen United States
Vinod Vathipadiekal United States
Ani Arakelian Canada
Susan Korenchuk United States
Mengqian Chen
Citations per year, relative to Mengqian Chen Mengqian Chen (= 1×) peers Susan Korenchuk

Countries citing papers authored by Mengqian Chen

Since Specialization
Citations

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

Fields of papers citing papers by Mengqian Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mengqian Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Mengqian Chen. A scholar is included among the top collaborators of Mengqian Chen 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 Mengqian Chen. Mengqian Chen 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.
Cao, Hao, Hongye Pan, Hai Li, et al.. (2025). A rotational wind energy harvester based on the centrifugal mechanism for self-powered sensing. Sustainable materials and technologies. 46. e01718–e01718.
2.
Vorobyeva, Nadezhda E., Alexander Tyakht, Jing Li, et al.. (2025). CDK8/19 inhibition attenuates G1 arrest induced by BCR-ABL antagonists and accelerates death of chronic myelogenous leukemia cells. Cell Death Discovery. 11(1). 62–62.
3.
Pang, Shanqi, Mengqian Chen, & Rong Yan. (2024). Hamming distances of unsaturated orthogonal arrays. Communication in Statistics- Theory and Methods. 54(13). 3761–3789.
4.
5.
Chen, Mengqian, Zhijian Xu, Bo Liu, et al.. (2023). Loss of RACK1 promotes glutamine addiction via activating AKT/mTOR/ASCT2 axis to facilitate tumor growth in gastric cancer. Cellular Oncology. 47(1). 113–128. 5 indexed citations
6.
Chen, Mengqian, Lei Chang, Jianxin Gu, et al.. (2022). De novo pyrimidine synthesis fuels glycolysis and confers chemoresistance in gastric cancer. Cancer Letters. 549. 215837–215837. 29 indexed citations
7.
Wu, Hao, Bo Liu, Mengqian Chen, et al.. (2021). Up‐regulation of FUT8 inhibits TGF-β1-induced activation of hepatic stellate cells during liver fibrogenesis. Glycoconjugate Journal. 38(1). 77–87. 6 indexed citations
8.
Liang, Jiaxin, Mengqian Chen, Daniel Hughes, et al.. (2018). CDK8 Selectively Promotes the Growth of Colon Cancer Metastases in the Liver by Regulating Gene Expression of TIMP3 and Matrix Metalloproteinases. Cancer Research. 78(23). 6594–6606. 68 indexed citations
9.
Bi, Laixi, Bin Zhou, Haiying Li, et al.. (2018). A novel miR-375-HOXB3-CDCA3/DNMT3B regulatory circuitry contributes to leukemogenesis in acute myeloid leukemia. BMC Cancer. 18(1). 182–182. 53 indexed citations
10.
Oliver, David J., Hao Ji, Alexander V. Gasparian, et al.. (2017). Identification of novel cancer therapeutic targets using a designed and pooled shRNA library screen. Scientific Reports. 7(1). 43023–43023. 33 indexed citations
11.
Broude, Eugenia V., Balázs Győrffy, Alexander A. Chumanevich, et al.. (2015). Expression of CDK8 and CDK8-interacting Genes as Potential Biomarkers in Breast Cancer. Current Cancer Drug Targets. 15(8). 739–749. 62 indexed citations
12.
Levina, Elina, et al.. (2011). Paracrine hedgehog increases the steroidogenic potential of prostate stromal cells in a Gli‐dependent manner. The Prostate. 72(8). 817–824. 18 indexed citations
13.
Gao, Wenlong, et al.. (2010). Prostasin regulates human placental trophoblast cell proliferation via the epidermal growth factor receptor signaling pathway. Human Reproduction. 25(3). 623–632. 20 indexed citations
14.
Chen, Mengqian, Michael Feuerstein, Elina Levina, et al.. (2010). Hedgehog/Gli supports androgen signaling in androgen deprived and androgen independent prostate cancer cells. Molecular Cancer. 9(1). 89–89. 49 indexed citations
15.
Chen, Mengqian, Matthew Tanner, Alice C. Levine, et al.. (2009). Androgenic regulation of hedgehog signaling pathway components in prostate cancer cells. Cell Cycle. 8(1). 149–157. 61 indexed citations
16.
Chen, Mengqian, Li‐Mei Chen, Chen‐Yong Lin, & Karl X. Chai. (2009). Hepsin activates prostasin and cleaves the extracellular domain of the epidermal growth factor receptor. Molecular and Cellular Biochemistry. 337(1-2). 259–266. 30 indexed citations
17.
Chen, Mengqian, et al.. (2007). Prostasin induces protease-dependent and independent molecular changes in the human prostate carcinoma cell line PC-3. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1773(7). 1133–1140. 31 indexed citations
18.
Chen, Li‐Mei, Cindy Wang, Mengqian Chen, et al.. (2006). Prostasin attenuates inducible nitric oxide synthase expression in lipopolysaccharide-induced urinary bladder inflammation. American Journal of Physiology-Renal Physiology. 291(3). F567–F577. 31 indexed citations
19.
Chen, Mengqian, Li‐Mei Chen, & Karl X. Chai. (2006). Mechanisms of sterol regulatory element-binding protein-2 (SREBP-2) regulation of human prostasin gene expression. Biochemical and Biophysical Research Communications. 346(4). 1245–1253. 3 indexed citations
20.
Chen, Mengqian, Li‐Mei Chen, & Karl X. Chai. (2006). Androgen regulation of prostasin gene expression is mediated by sterol-regulatory element-binding proteins and SLUG. The Prostate. 66(9). 911–920. 26 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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