Zhe Zhou

1.6k total citations
19 papers, 1.0k citations indexed

About

Zhe Zhou is a scholar working on Molecular Biology, Organic Chemistry and Cancer Research. According to data from OpenAlex, Zhe Zhou has authored 19 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 3 papers in Organic Chemistry and 3 papers in Cancer Research. Recurrent topics in Zhe Zhou's work include Click Chemistry and Applications (3 papers), Extracellular vesicles in disease (3 papers) and MicroRNA in disease regulation (3 papers). Zhe Zhou is often cited by papers focused on Click Chemistry and Applications (3 papers), Extracellular vesicles in disease (3 papers) and MicroRNA in disease regulation (3 papers). Zhe Zhou collaborates with scholars based in China, United States and Switzerland. Zhe Zhou's co-authors include Christopher T. Walsh, Jun Yin, Alison J. Lin, David E. Golan, Yu Wang, Andrew P. McMahon, Roberto Kolter, Shaun M. McLoughlin, Neil L. Kelleher and Paul D. Straight and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and PLoS ONE.

In The Last Decade

Zhe Zhou

19 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Zhe Zhou China 12 761 200 146 132 125 19 1.0k
Sonia Di Gaetano Italy 24 974 1.3× 177 0.9× 69 0.5× 77 0.6× 131 1.0× 72 1.3k
Margot G. Paulick United States 12 784 1.0× 275 1.4× 138 0.9× 95 0.7× 122 1.0× 14 1.1k
Nicolas Floquet France 23 890 1.2× 109 0.5× 87 0.6× 87 0.7× 89 0.7× 45 1.4k
E. Salah United Kingdom 19 1.0k 1.4× 172 0.9× 139 1.0× 54 0.4× 239 1.9× 47 1.4k
Uyen Nguyen United States 17 1.2k 1.5× 169 0.8× 164 1.1× 164 1.2× 115 0.9× 29 1.4k
Yangqing Xu United States 10 718 0.9× 116 0.6× 112 0.8× 88 0.7× 73 0.6× 10 909
Johan Schultz Sweden 17 873 1.1× 69 0.3× 171 1.2× 52 0.4× 188 1.5× 37 1.1k
Anuradha S. Raghavan United States 12 1.0k 1.3× 293 1.5× 209 1.4× 73 0.6× 234 1.9× 15 1.4k
Nobumasa Hino Japan 17 1.0k 1.4× 209 1.0× 71 0.5× 123 0.9× 64 0.5× 32 1.2k
Kimberly M. Bonger Netherlands 19 843 1.1× 495 2.5× 68 0.5× 190 1.4× 123 1.0× 45 1.2k

Countries citing papers authored by Zhe Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Zhe Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zhe Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Zhe Zhou. A scholar is included among the top collaborators of Zhe 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 Zhe Zhou. Zhe Zhou is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Zhou, Zhe, et al.. (2025). Crizotinib: A Novel Strategy to Reverse Immunosuppression in Melanoma by Targeting Lactate Transport. MedComm. 6(8). e70286–e70286. 2 indexed citations
2.
Liu, Peng, et al.. (2024). Mitochondrial targeted modification and anticancer mechanism of natural product ergosterol peroxide. Bioorganic Chemistry. 151. 107688–107688. 4 indexed citations
3.
Dong, Bing, Yumin Qiu, Jinsheng Huang, et al.. (2023). Manipulating bioactivities of endothelial progenitor cell-derived exosomes for promoting angiogenesis in ischemic vascular diseases. Nano Today. 48. 101758–101758. 1 indexed citations
4.
Zhou, Zhe, Wei Zheng, Zheng Xiang, et al.. (2022). Clinical implications of exosome-derived noncoding RNAs in liver. Laboratory Investigation. 102(5). 464–473. 10 indexed citations
5.
Zhou, Zhe, Rongfang Qiu, Wei Liu, et al.. (2021). BCAS3 exhibits oncogenic properties by promoting CRL4A‐mediated ubiquitination of p53 in breast cancer. Cell Proliferation. 54(8). 11 indexed citations
6.
Guo, Yeye, Xu Zhang, Min Li, et al.. (2021). The plasma exosomal miR-1180-3p serves as a novel potential diagnostic marker for cutaneous melanoma. Cancer Cell International. 21(1). 487–487. 38 indexed citations
8.
Tang, Ling, et al.. (2020). Tre2-Bub2-Cdc16 Family Proteins Based Nomogram Serve as a Promising Prognosis Predicting Model for Melanoma. Frontiers in Oncology. 10. 579625–579625. 8 indexed citations
9.
Zhou, Zhe, Jing Long, Yuan Wang, et al.. (2020). Targeted degradation of CD147 proteins in melanoma. Bioorganic Chemistry. 105. 104453–104453. 17 indexed citations
10.
Gu, Youquan, Tianhong Wang, Jun Chen, et al.. (2020). The Chinese Herb Codonopsis pilosula Isolate Isorhapontigenin protects against oxidative stress injury by inhibiting the activation of PI3K/Akt signaling pathway. Journal of Integrative Neuroscience. 19(2). 333–340. 11 indexed citations
11.
Wang, Tianlin, Jingjing Zou, Zhe Zhou, et al.. (2018). Highly chemoselective fluorescent probe for the detection of tyrosinase in living cells and zebrafish model. Sensors and Actuators B Chemical. 283. 873–880. 44 indexed citations
12.
Zhou, Zhe, Feiyi Wang, Guichun Yang, et al.. (2017). A Ratiometric Fluorescent Probe for Monitoring Leucine Aminopeptidase in Living Cells and Zebrafish Model. Analytical Chemistry. 89(21). 11576–11582. 92 indexed citations
14.
Hector, Andreas, Michael Kormann, Ines Mack, et al.. (2011). The Chitinase-Like Protein YKL-40 Modulates Cystic Fibrosis Lung Disease. PLoS ONE. 6(9). e24399–e24399. 46 indexed citations
15.
Wang, Yu, Zhe Zhou, Christopher T. Walsh, & Andrew P. McMahon. (2009). Selective translocation of intracellular Smoothened to the primary cilium in response to Hedgehog pathway modulation. Proceedings of the National Academy of Sciences. 106(8). 2623–2628. 159 indexed citations
16.
Zhou, Zhe, Alexander Koglin, Yu Wang, Andrew P. McMahon, & Christopher T. Walsh. (2008). An Eight Residue Fragment of an Acyl Carrier Protein Suffices for Post-Translational Introduction of Fluorescent Pantetheinyl Arms in Protein Modification in vitro and in vivo. Journal of the American Chemical Society. 130(30). 9925–9930. 42 indexed citations
17.
Zhou, Zhe, Jonathan R. Lai, & Christopher T. Walsh. (2007). Directed evolution of aryl carrier proteins in the enterobactin synthetase. Proceedings of the National Academy of Sciences. 104(28). 11621–11626. 39 indexed citations
18.
Zhou, Zhe, Pablo Cironi, Alison J. Lin, et al.. (2007). Genetically Encoded Short Peptide Tags for Orthogonal Protein Labeling by Sfp and AcpS Phosphopantetheinyl Transferases. ACS Chemical Biology. 2(5). 337–346. 179 indexed citations
19.
Yin, Jun, Paul D. Straight, Shaun M. McLoughlin, et al.. (2005). Genetically encoded short peptide tag for versatile protein labeling by Sfp phosphopantetheinyl transferase. Proceedings of the National Academy of Sciences. 102(44). 15815–15820. 306 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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