Kaiqun Ren

1.3k total citations
36 papers, 760 citations indexed

About

Kaiqun Ren is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Kaiqun Ren has authored 36 papers receiving a total of 760 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 11 papers in Oncology and 7 papers in Cancer Research. Recurrent topics in Kaiqun Ren's work include Cancer Cells and Metastasis (7 papers), FOXO transcription factor regulation (7 papers) and Genomics and Chromatin Dynamics (6 papers). Kaiqun Ren is often cited by papers focused on Cancer Cells and Metastasis (7 papers), FOXO transcription factor regulation (7 papers) and Genomics and Chromatin Dynamics (6 papers). Kaiqun Ren collaborates with scholars based in China, United States and Hong Kong. Kaiqun Ren's co-authors include Jianguo Cao, Meifang Quan, Jianlin Zhou, Xiaocheng Cao, Xiang Hu, Xiwen Xiong, Xiaozheng Cao, Yingxia Ning, Fei Liu and Yingli Zhong and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Kaiqun Ren

35 papers receiving 755 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kaiqun Ren China 20 561 164 152 106 90 36 760
Seunghwan Lim United States 15 600 1.1× 229 1.4× 151 1.0× 122 1.2× 38 0.4× 21 874
Hongpeng He China 20 682 1.2× 139 0.8× 312 2.1× 98 0.9× 46 0.5× 54 974
Aparna Maiti United States 16 494 0.9× 135 0.8× 136 0.9× 87 0.8× 39 0.4× 25 759
Kyeong Ah Park South Korea 17 578 1.0× 122 0.7× 207 1.4× 218 2.1× 66 0.7× 28 951
Wen-Chun Hung Taiwan 25 809 1.4× 366 2.2× 369 2.4× 119 1.1× 62 0.7× 30 1.3k
Xin Ge China 18 512 0.9× 163 1.0× 341 2.2× 118 1.1× 69 0.8× 31 804
Lei Gong China 15 378 0.7× 158 1.0× 129 0.8× 73 0.7× 24 0.3× 45 700
Mudan Lu China 17 564 1.0× 136 0.8× 199 1.3× 108 1.0× 24 0.3× 36 856

Countries citing papers authored by Kaiqun Ren

Since Specialization
Citations

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

Fields of papers citing papers by Kaiqun Ren

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kaiqun Ren

This figure shows the co-authorship network connecting the top 25 collaborators of Kaiqun Ren. A scholar is included among the top collaborators of Kaiqun Ren 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 Kaiqun Ren. Kaiqun Ren 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.
Hu, Jihong, et al.. (2025). The multifaceted impact of a high-salt environment on the immune system and its contribution to salt-sensitive hypertension. Biochemistry and Biophysics Reports. 44. 102244–102244.
2.
Liu, Yuanyuan, Qing Li, Hao Chen, et al.. (2023). Adenine base editor–mediated splicing remodeling activates noncanonical splice sites. Journal of Biological Chemistry. 299(12). 105442–105442. 5 indexed citations
3.
Ma, Tao, Daoyuan Wang, Jiajun Wu, et al.. (2023). KCTD10 functions as a tumor suppressor in hepatocellular carcinoma by triggering the Notch signaling pathway. PubMed Central. 5 indexed citations
4.
Wang, Xueli, Xiaozheng Cao, Daoyuan Wang, et al.. (2022). Casticin Attenuates Stemness in Cervical Cancer Stem-Like Cells by Regulating Activity and Expression of DNMT1. Chinese Journal of Integrative Medicine. 29(3). 224–232. 6 indexed citations
5.
Ren, Kaiqun, Xiwen Xiong, Meng Cheng, et al.. (2020). Protein O-GlcNAc Modification Links Dietary and Gut Microbial Cues to the Differentiation of Enteroendocrine L Cells. Cell Reports. 32(6). 108013–108013. 32 indexed citations
6.
Zou, Hui, Xiaozheng Cao, Qiao Xiao, et al.. (2016). Synergistic inhibition of characteristics of liver cancer stem-like cells with a combination of sorafenib and 8-bromo-7-methoxychrysin in SMMC-7721 cell line. Oncology Reports. 36(3). 1731–1738. 13 indexed citations
7.
Cui, Yinghong, Shuwen Sun, Kaiqun Ren, et al.. (2016). Reversal of liver cancer-associated stellate cell-induced stem-like characteristics in SMMC-7721 cells by 8-bromo-7-methoxychrysin via inhibiting STAT3 activation. Oncology Reports. 35(5). 2952–2962. 16 indexed citations
8.
Cui, Yinghong, et al.. (2016). 8-bromo-7-methoxychrysin Reversed M2 Polarization of Tumor-associated Macrophages Induced by Liver Cancer Stem-like Cells. Anti-Cancer Agents in Medicinal Chemistry. 17(2). 286–293. 23 indexed citations
9.
10.
Ren, Kaiqun, Jing Yuan, Manjun Yang, et al.. (2014). KCTD10 Is Involved in the Cardiovascular System and Notch Signaling during Early Embryonic Development. PLoS ONE. 9(11). e112275–e112275. 27 indexed citations
11.
Ning, Yingxia, Qingxiu Li, Kaiqun Ren, Meifang Quan, & Jianguo Cao. (2014). 7-difluoromethoxyl-5,4′-di-n-octyl genistein inhibits ovarian cancer stem cell characteristics through the downregulation of FOXM1. Oncology Letters. 8(1). 295–300. 24 indexed citations
12.
Qu, Lin, et al.. (2014). Activation of the apoptosis signal-regulating kinase 1/c-Jun N-terminal kinase pathway is involved in the casticin-induced apoptosis of colon cancer cells. Experimental and Therapeutic Medicine. 8(5). 1494–1500. 27 indexed citations
13.
Jiang, Ling, Xiaocheng Cao, Jianguo Cao, et al.. (2013). Casticin induces ovarian cancer cell apoptosis by repressing FoxM1 through the activation of FOXO3a. Oncology Letters. 5(5). 1605–1610. 38 indexed citations
14.
Zhao, Xiaochun, Xiaocheng Cao, Fei Liu, et al.. (2012). Regulation of the FOXO3a/Bim signaling pathway by 5,7-dihydroxy-8-nitrochrysin in MDA-MB-453 breast cancer cells. Oncology Letters. 5(3). 929–934. 11 indexed citations
15.
Ren, Kaiqun, Shuanglin Xiang, Wenfeng Zhang, et al.. (2011). CK2 phosphorylates AP-2α and increases its transcriptional activity. BMB Reports. 44(7). 490–495. 6 indexed citations
16.
Ding, Xiaofeng, Chang Luo, Jianlin Zhou, et al.. (2008). The interaction of KCTD1 with transcription factor AP‐2α inhibits its transactivation. Journal of Cellular Biochemistry. 106(2). 285–295. 49 indexed citations
17.
Zhong, Yingli, Yan Wang, Jianlin Zhou, et al.. (2008). LIM domain protein TES changes its conformational states in different cellular compartments. Molecular and Cellular Biochemistry. 320(1-2). 85–92. 14 indexed citations
18.
Luo, Chang, Kaiqun Ren, Jing Zhang, et al.. (2008). Characterization and Expression of a Human KCTD1 Gene Containing the BTB Domain, Which Mediates Transcriptional Repression and Homomeric Interactions. DNA and Cell Biology. 27(5). 257–265. 25 indexed citations
19.
Zhou, Jianlin, Xiaoxiao Hu, Xiwen Xiong, et al.. (2005). Cloning of two rat PDIP1 related genes and their interactions with proliferating cell nuclear antigen. Journal of Experimental Zoology Part A Comparative Experimental Biology. 303A(3). 227–240. 38 indexed citations
20.
Gu, Jianxin, Kaiqun Ren, Ronald Dubner, & Michael J. Iadarola. (1994). Cloning of a DNA binding protein that is a tyrosine kinase substrate and recognizes an upstream initiator-like sequence in the promoter of the preprodynorphin gene. Molecular Brain Research. 24(1-4). 77–88. 22 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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