Renping Zhou

5.1k total citations
101 papers, 4.2k citations indexed

About

Renping Zhou is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Renping Zhou has authored 101 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Cellular and Molecular Neuroscience, 50 papers in Molecular Biology and 30 papers in Cell Biology. Recurrent topics in Renping Zhou's work include Axon Guidance and Neuronal Signaling (56 papers), Neurogenesis and neuroplasticity mechanisms (25 papers) and Zebrafish Biomedical Research Applications (19 papers). Renping Zhou is often cited by papers focused on Axon Guidance and Neuronal Signaling (56 papers), Neurogenesis and neuroplasticity mechanisms (25 papers) and Zebrafish Biomedical Research Applications (19 papers). Renping Zhou collaborates with scholars based in United States, China and Canada. Renping Zhou's co-authors include Douglas Pat Cerretti, Yong Yue, Margaret A. Cooper, Cheryl F. Dreyfus, Alexander I. Son, Baisong Liao, Harold L. Newmark, Jian‐Hua Zhang, Gary M. Fox and Shuqian Jing and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Renping Zhou

100 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Renping Zhou United States	36	2.2k	2.0k	1.1k	958	246	101	4.2k
Kazutoshi Kiuchi Japan	33	1.6k 0.7×	1.8k 0.9×	293 0.3×	446 0.5×	53 0.2×	127	3.8k
Freesia L. Huang United States	38	1.3k 0.6×	3.3k 1.7×	295 0.3×	824 0.9×	54 0.2×	79	4.6k
Giambattista Bonanno Italy	45	3.4k 1.5×	3.1k 1.6×	337 0.3×	330 0.3×	125 0.5×	204	6.8k
Sheng‐Tao Hou Canada	32	960 0.4×	1.4k 0.7×	262 0.2×	448 0.5×	73 0.3×	93	2.9k
Giuseppa Mudò Italy	35	1.8k 0.8×	2.5k 1.2×	563 0.5×	317 0.3×	33 0.1×	110	4.1k
Minh Dang Nguyen Canada	32	1.1k 0.5×	2.5k 1.3×	365 0.3×	557 0.6×	86 0.3×	70	5.7k
Shoei Furukawa Japan	39	1.9k 0.8×	1.8k 0.9×	850 0.8×	239 0.2×	66 0.3×	168	5.0k
Arabinda Das United States	35	737 0.3×	1.6k 0.8×	208 0.2×	378 0.4×	191 0.8×	81	4.0k
Flávia Carvalho Alcântara Gomes Brazil	41	1.1k 0.5×	1.6k 0.8×	769 0.7×	197 0.2×	172 0.7×	92	4.3k
Mark P. Mattson United States	35	1.5k 0.7×	2.1k 1.1×	495 0.5×	500 0.5×	61 0.2×	39	4.9k

Countries citing papers authored by Renping Zhou

Since Specialization

Citations

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

Fields of papers citing papers by Renping Zhou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renping Zhou

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

All Works

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20 of 20 papers shown

Liu, Gongjie, et al.. (2025). AAV-mediated BDNF and GAS6 muscle delivery delays disease onset in SOD1G93A ALS mice. Gene Therapy.

Jia, Ziqi, Heng Cao, Jiayi Li, et al.. (2025). Advanced strategy for cancer detection based on volatile organic compounds in breath. Journal of Nanobiotechnology. 23(1). 468–468. 2 indexed citations

Xu, Xue-Tao, Jie Chen, Kun Zhang, et al.. (2019). Synthesis and biological evaluation of coumarin derivatives as α-glucosidase inhibitors. European Journal of Medicinal Chemistry. 189. 112013–112013. 107 indexed citations

Chen, Min, Hang Ma, Xi Zheng, et al.. (2019). Downregulating NF-κB signaling pathway with triterpenoids for attenuating inflammation:in vitroandin vivostudies. Food & Function. 10(8). 5080–5090. 27 indexed citations

Biswas, Sondip K., et al.. (2015). Breakdown of interlocking domains may contribute to formation of membranous globules and lens opacity in ephrin-A5−/− mice. Experimental Eye Research. 145. 130–139. 18 indexed citations

Cooper, Margaret A. & Renping Zhou. (2013). β-Galactosidase Staining of LacZ Fusion Proteins in Whole Tissue Preparations. Methods in molecular biology. 1018. 189–197. 6 indexed citations

Yue, Xin, Alexander I. Son, & Renping Zhou. (2013). Growth Cone Collapse Assay. Methods in molecular biology. 1018. 221–227. 5 indexed citations

Reuhl, Kenneth R., et al.. (2013). The Golgi–Cox Method. Methods in molecular biology. 1018. 313–321. 44 indexed citations

Park, Jeong Eun, Alexander I. Son, Rui Hua, et al.. (2012). Human Cataract Mutations in EPHA2 SAM Domain Alter Receptor Stability and Function. PLoS ONE. 7(5). e36564–e36564. 51 indexed citations

10.

Son, Alexander I., et al.. (2011). Ephrin-A5 as a Regulator Of Angiogenesis During Development As Well As Oxygen-induced Retinopathy. Investigative Ophthalmology & Visual Science. 52(14). 3121–3121. 1 indexed citations

11.

DeCastro, Andrew, Amanda K. Smolarek, Jae Young So, et al.. (2010). Dietary intake of pterostilbene, a constituent of blueberries, inhibits the -catenin/p65 downstream signaling pathway and colon carcinogenesis in rats. Carcinogenesis. 31(7). 1272–1278. 114 indexed citations

12.

Cooper, Margaret A., David P. Crockett, Richard S. Nowakowski, Nicholas W. Gale, & Renping Zhou. (2009). Distribution of EphA5 receptor protein in the developing and adult mouse nervous system. The Journal of Comparative Neurology. 514(4). 310–328. 39 indexed citations

13.

Cooper, Margaret A., Kazuto Kobayashi, & Renping Zhou. (2008). Ephrin‐A5 regulates the formation of the ascending midbrain dopaminergic pathways. Developmental Neurobiology. 69(1). 36–46. 36 indexed citations

14.

Zhou, Ding-biao, Lihong Wang, Yan Gao, et al.. (2006). Increased neuroglobin levels in the cerebral cortex and serum after ischemia–reperfusion insults. Brain Research. 1078(1). 219–226. 60 indexed citations

15.

Cooper, Margaret A., et al.. (2004). Differentiation of the midbrain dopaminergic pathways during mouse development. The Journal of Comparative Neurology. 476(3). 301–311. 58 indexed citations

16.

Zhou, Xiaofeng, Junghyup Suh, Douglas Pat Cerretti, Renping Zhou, & Emanuel DiCicco‐Bloom. (2001). Ephrins stimulate neurite outgrowth during early cortical neurogenesis. Journal of Neuroscience Research. 66(6). 1054–1063. 35 indexed citations

17.

Jing, Shuqian, Yanbin Yu, Mei Fang, et al.. (1997). GFRα-2 and GFRα-3 Are Two New Receptors for Ligands of the GDNF Family. Journal of Biological Chemistry. 272(52). 33111–33117. 195 indexed citations

18.

Zhou, Renping, et al.. (1996). Receptor tyrosine kinase gene Tyro3 maps to mouse Chromosome 2, closely linked to Ltk. Mammalian Genome. 7(5). 395–396. 3 indexed citations

19.

Zhou, Renping, et al.. (1992). pp39 ^mos Is Associated with p34 ^cdc2 Kinase in c- mos ^xe -Transformed NIH 3T3 Cells. Molecular and Cellular Biology. 12(8). 3583–3589. 17 indexed citations

20.

Duesberg, Peter, David W. Goodrich, & Renping Zhou. (1991). Cancer Genes by Non-Homologous Recombination. PubMed. 57. 197–211. 2 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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