Chenghua Zhou

1.7k total citations
59 papers, 1.3k citations indexed

About

Chenghua Zhou is a scholar working on Physiology, Molecular Biology and Oncology. According to data from OpenAlex, Chenghua Zhou has authored 59 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Physiology, 12 papers in Molecular Biology and 12 papers in Oncology. Recurrent topics in Chenghua Zhou's work include Anesthesia and Neurotoxicity Research (11 papers), Pain Mechanisms and Treatments (11 papers) and Sirtuins and Resveratrol in Medicine (11 papers). Chenghua Zhou is often cited by papers focused on Anesthesia and Neurotoxicity Research (11 papers), Pain Mechanisms and Treatments (11 papers) and Sirtuins and Resveratrol in Medicine (11 papers). Chenghua Zhou collaborates with scholars based in China, United States and Canada. Chenghua Zhou's co-authors include Yuqing Wu, Zhiyu Qian, Min Xiang, Shengnan Li, Jin Tao, Yangzi Zhu, Yuqing Wu, HE Shu-ying, Guanglin Xu and Xiaoxing Yin and has published in prestigious journals such as Journal of Neuroscience, The Journal of Immunology and PLoS ONE.

In The Last Decade

Chenghua Zhou

56 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chenghua Zhou China 23 404 327 240 218 153 59 1.3k
Abedin Vakili Iran 18 347 0.9× 211 0.6× 113 0.5× 165 0.8× 156 1.0× 50 1.1k
Marwa M. Safar Egypt 25 502 1.2× 277 0.8× 128 0.5× 147 0.7× 280 1.8× 57 1.7k
Haifeng Zhao China 20 334 0.8× 363 1.1× 68 0.3× 126 0.6× 120 0.8× 42 1.2k
Aparna Areti India 16 378 0.9× 515 1.6× 347 1.4× 167 0.8× 155 1.0× 22 1.3k
Jie Qi China 26 502 1.2× 273 0.8× 84 0.3× 150 0.7× 174 1.1× 67 1.6k
Eyüp Altınöz Türkiye 19 268 0.7× 165 0.5× 231 1.0× 111 0.5× 67 0.4× 55 1.2k
Tahir Muhammad Pakistan 17 488 1.2× 293 0.9× 111 0.5× 136 0.6× 81 0.5× 58 1.3k
Hong Jiang China 27 660 1.6× 302 0.9× 62 0.3× 87 0.4× 170 1.1× 72 1.9k

Countries citing papers authored by Chenghua Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Chenghua Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chenghua Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Chenghua Zhou. A scholar is included among the top collaborators of Chenghua 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 Chenghua Zhou. Chenghua 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.
2.
Liu, Qiang, Yanping Liu, Tianzuo Li, et al.. (2025). Role of brain-derived neurotrophic factor in dysfunction of short-term to long-term memory transformation after surgery and anaesthesia in older mice. British Journal of Anaesthesia. 134(4). 1134–1145. 3 indexed citations
3.
Chen, Chen, Qiang Liu, Yongkang Qiu, et al.. (2024). Impaired synaptic plasticity and decreased glutamatergic neuron excitability induced by SIRT1/BDNF downregulation in the hippocampal CA1 region are involved in postoperative cognitive dysfunction. Cellular & Molecular Biology Letters. 29(1). 79–79. 26 indexed citations
4.
Chen, Chen, et al.. (2023). DNMT1 Mediates Chronic Pain–Related Depression by Inhibiting GABAergic Neuronal Activation in the Central Amygdala. Biological Psychiatry. 94(8). 672–684. 20 indexed citations
5.
Liu, Qiang, et al.. (2022). LncRNA XR_351665 Contributes to Chronic Pain-Induced Depression by Upregulating DNMT1 via Sponging miR-152-3p. Journal of Pain. 24(3). 449–462. 5 indexed citations
6.
Miao, Huihui, Qiang Liu, Ning Wang, et al.. (2022). The Effect of SIRT3/Ac-SOD2 Mediated Oxidative Stress and HCN1 Channel Activity on Anesthesia/Surgery Induced Anxiety-Like Behavior in Mice. Frontiers in Medicine. 9. 783931–783931. 3 indexed citations
7.
8.
Zhou, Chenghua, et al.. (2020). SIRT1 Decreases Emotional Pain Vulnerability with Associated CaMKIIα Deacetylation in Central Amygdala. Journal of Neuroscience. 40(11). 2332–2342. 26 indexed citations
9.
Wang, Ruiyao, Guizhi Wang, Qian Hu, et al.. (2020). Quercetin attenuates diabetic neuropathic pain by inhibiting mTOR/p70S6K pathway-mediated changes of synaptic morphology and synaptic protein levels in spinal dorsal horn of db/db mice. European Journal of Pharmacology. 882. 173266–173266. 34 indexed citations
10.
Zhou, Chenghua, et al.. (2020). Flow Cytometric Analysis of Lymphocyte Infiltration in Central Nervous System during Experimental Autoimmune Encephalomyelitis. Journal of Visualized Experiments. 1 indexed citations
11.
Zhang, Zongqin, Zhiwei Zhou, Shasha Zhou, et al.. (2019). Sirtuin 1 alleviates diabetic neuropathic pain by regulating synaptic plasticity of spinal dorsal horn neurons. Pain. 160(5). 1082–1092. 54 indexed citations
12.
Zhou, Chenghua, Jin Pan, He Huang, et al.. (2014). Salusin-β, but Not Salusin-α, Promotes Human Umbilical Vein Endothelial Cell Inflammation via the p38 MAPK/JNK-NF-κB Pathway. PLoS ONE. 9(9). e107555–e107555. 29 indexed citations
13.
Zhou, Chenghua, Xiaotian Shi, He Huang, Yangzi Zhu, & Yuqing Wu. (2014). Montelukast Attenuates Neuropathic Pain Through Inhibiting p38 Mitogen-Activated Protein Kinase and Nuclear Factor-Kappa B in a Rat Model of Chronic Constriction Injury. Anesthesia & Analgesia. 118(5). 1090–1096. 43 indexed citations
14.
Zhou, Chenghua, Min Xiang, HE Shu-ying, & Zhiyu Qian. (2010). Protein kinase C pathway is involved in the inhibition by crocetin of vascular smooth muscle cells proliferation. Phytotherapy Research. 24(11). 1680–1686. 16 indexed citations
15.
Zhou, Chenghua. (2008). Crocetin reduces expression of receptor for advanced glycation end products (RAGE) on endothelial cells induced by AGE. Zhongguo linchuang yaolixue yu zhiliaoxue. 1 indexed citations
16.
Liu, Xiaodong, et al.. (2007). Crocetin attenuates palmitate‐induced insulin insensitivity and disordered tumor necrosis factor‐α and adiponectin expression in rat adipocytes. British Journal of Pharmacology. 151(5). 610–617. 48 indexed citations
17.
Zhou, Chenghua. (2006). Effects of crocetin on formation of advanced glycation end products and expression of releptor for advanced glycation and prodmts protein in diabetic rats. Zhongguo linchuang yaolixue yu zhiliaoxue. 1 indexed citations
18.
Xiang, Min, et al.. (2006). Crocetin inhibits leukocyte adherence to vascular endothelial cells induced by AGEs. Journal of Ethnopharmacology. 107(1). 25–31. 61 indexed citations
19.
Zhou, Chenghua, Zhiyu Qian, Shuguo Zheng, & Min Xiang. (2006). ERK1/2 pathway is involved in the inhibitory effect of crocetin on angiotensin II-induced vascular smooth muscle cell proliferation. European Journal of Pharmacology. 535(1-3). 61–68. 18 indexed citations
20.
Wu, Yuqing, Chenghua Zhou, Jin Tao, & Shengnan Li. (2005). Antagonistic effects of nobiletin, a polymethoxyflavonoid, on eosinophilic airway inflammation of asthmatic rats and relevant mechanisms. Life Sciences. 78(23). 2689–2696. 92 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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