Long Zhou

1.0k total citations
42 papers, 786 citations indexed

About

Long Zhou is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Long Zhou has authored 42 papers receiving a total of 786 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 19 papers in Cancer Research and 6 papers in Oncology. Recurrent topics in Long Zhou's work include MicroRNA in disease regulation (13 papers), Cancer-related molecular mechanisms research (9 papers) and Circular RNAs in diseases (9 papers). Long Zhou is often cited by papers focused on MicroRNA in disease regulation (13 papers), Cancer-related molecular mechanisms research (9 papers) and Circular RNAs in diseases (9 papers). Long Zhou collaborates with scholars based in China, Sweden and Germany. Long Zhou's co-authors include Shuai Mu, Xiaoyue Chen, Qin Fu, Xiaoping Wan, Yinyan He, Yameng Fan, Xiaodan Zhao, Yuxuan Yang, Yan Yu and Liyu Yang and has published in prestigious journals such as Biomaterials, Biochemical and Biophysical Research Communications and Experimental Cell Research.

In The Last Decade

Long Zhou

41 papers receiving 779 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Long Zhou China 16 510 352 97 91 76 42 786
Meng Ye China 19 651 1.3× 246 0.7× 68 0.7× 94 1.0× 51 0.7× 47 876
Maria Mesuraca Italy 20 631 1.2× 181 0.5× 109 1.1× 129 1.4× 69 0.9× 41 966
Ernesto Soto‐Reyes Mexico 17 623 1.2× 220 0.6× 91 0.9× 123 1.4× 53 0.7× 41 915
Xiaoping Wan China 19 836 1.6× 661 1.9× 137 1.4× 173 1.9× 87 1.1× 30 1.2k
Huojun Cao United States 22 691 1.4× 329 0.9× 146 1.5× 84 0.9× 34 0.4× 43 1.0k
I–Shou Chang Taiwan 12 427 0.8× 225 0.6× 60 0.6× 111 1.2× 56 0.7× 13 668
Chian‐Feng Chen Taiwan 18 533 1.0× 240 0.7× 54 0.6× 150 1.6× 56 0.7× 32 830
Zhimin Liu China 15 357 0.7× 213 0.6× 93 1.0× 241 2.6× 100 1.3× 32 741
Yu Hou China 20 680 1.3× 287 0.8× 81 0.8× 103 1.1× 103 1.4× 55 1.0k

Countries citing papers authored by Long Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Long Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Long Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Long Zhou. A scholar is included among the top collaborators of Long Zhou 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 Long Zhou. Long Zhou 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.
Zhang, Yiqi, et al.. (2025). FOXG1 promotes osteogenesis of bone marrow-derived mesenchymal stem cells by activating autophagy through regulating USP14. Communications Biology. 8(1). 59–59. 2 indexed citations
3.
Li, Nan, Yuying Fan, Zhan Zhang, et al.. (2025). WDR3 undergoes phase separation to mediate the therapeutic mechanism of Nilotinib against osteosarcoma. Journal of Experimental & Clinical Cancer Research. 44(1). 201–201. 1 indexed citations
4.
Wang, Qiang, Tao Wang, Siyuan Liang, & Long Zhou. (2023). Ox-LDL-Induced Vascular Smooth Muscle Cell Dysfunction Partly Depends on the Circ_0044073/miR-377-3p/AURKA Axis in Atherosclerosis. International Heart Journal. 64(2). 252–262. 6 indexed citations
5.
Zhang, Jie, Long Zhou, Jiangdong Xiang, et al.. (2021). Artesunate-induced ATG5-related autophagy enhances the cytotoxicity of NK92 cells on endometrial cancer cells via interactions between CD155 and CD226/TIGIT. International Immunopharmacology. 97. 107705–107705. 26 indexed citations
6.
He, Li, Jianjun Wang, Long Zhou, & Xiaobing Li. (2021). LncRNA PCAT18 Promotes Non-Small Cell Lung Cancer Progression by Sponging miR-4319. Cancer Management and Research. Volume 13. 3761–3774. 6 indexed citations
7.
Zhou, Long, Xueyuan Yu, Yuan Guo, & Xiangyu Liu. (2021). LncRNA RMRP knockdown promotes proliferation and migration of Schwann cells by mediating the miR-766-5p/CAND1 axis. Neuroscience Letters. 770. 136440–136440. 5 indexed citations
8.
Zhou, Long, et al.. (2020). Polyphyllin VII attenuated RANKL-induced osteoclast differentiation via inhibiting of TRAF6/c-Src/PI3K pathway and ROS production. BMC Musculoskeletal Disorders. 21(1). 112–112. 22 indexed citations
9.
Zhou, Long, Min Qiu, Lei Yang, et al.. (2020). MicroRNA-1-3p enhances osteoblast differentiation of MC3T3-E1 cells by interacting with hypoxia-inducible factor 1 α inhibitor (HIF1AN). Mechanisms of Development. 162. 103613–103613. 10 indexed citations
10.
Shi, Bo, et al.. (2019). The role of copper and zinc accumulation in defense against bacterial pathogen in the fujian oyster (Crassostrea angulata). Fish & Shellfish Immunology. 92. 72–82. 28 indexed citations
11.
Feng, Yang, Yuxuan Yang, Xiaodan Zhao, et al.. (2019). Circular RNA circ0005276 promotes the proliferation and migration of prostate cancer cells by interacting with FUS to transcriptionally activate XIAP. Cell Death and Disease. 10(11). 792–792. 111 indexed citations
12.
Yang, Liyu, Shengye Liu, Shuai Mu, et al.. (2018). Leonurine hydrochloride promotes osteogenic differentiation and increases osteoblastic bone formation in ovariectomized mice by Wnt/β-catenin pathway. Biochemical and Biophysical Research Communications. 504(4). 941–948. 12 indexed citations
13.
Zhou, Xueyan, Changwei Lei, Rong Xiang, et al.. (2018). Co-occurrence of biofilm formation and quinolone resistance in Salmonella enterica serotype typhimurium carrying an IncHI2-type oqxAB-positive plasmid. Microbial Pathogenesis. 123. 68–73. 12 indexed citations
15.
Shi, Bo, et al.. (2015). Abcb1 gene expression pattern and function of copper detoxification in Fujian oyster, Crassostrea angulata. Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 190. 8–15. 16 indexed citations
16.
Zhou, Long, et al.. (2015). Knockdown of Aurora-B inhibits the growth of non-small cell lung cancer A549 cells. Oncology Letters. 10(3). 1642–1648. 8 indexed citations
18.
Feng, Xue, Qingjie Meng, Kejia Wang, et al.. (2013). Yeast-Incorporated Gallium Attenuates Glucocorticoid-Induced Bone Loss in Rats by Inhibition of Bone Resorption. Biological Trace Element Research. 152(3). 396–402. 4 indexed citations
19.
Wang, Lilin, Wei Tang, Long Zhou, et al.. (2013). Efficient delivery of miR-122 to regulate cholesterol metabolism using a non-covalent peptide-based strategy. Molecular Medicine Reports. 8(5). 1472–1478. 13 indexed citations
20.
Chen, Xiaoyue, Yan Qin, Shuangdi Li, et al.. (2011). Expression of the tumor suppressor miR-206 is associated with cellular proliferative inhibition and impairs invasion in ERα-positive endometrioid adenocarcinoma. Cancer Letters. 314(1). 41–53. 80 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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