Guo-Zhang Jin

2.2k total citations
101 papers, 1.9k citations indexed

About

Guo-Zhang Jin is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Pharmacology. According to data from OpenAlex, Guo-Zhang Jin has authored 101 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Cellular and Molecular Neuroscience, 54 papers in Molecular Biology and 14 papers in Pharmacology. Recurrent topics in Guo-Zhang Jin's work include Neuroscience and Neuropharmacology Research (40 papers), Receptor Mechanisms and Signaling (34 papers) and Neurotransmitter Receptor Influence on Behavior (29 papers). Guo-Zhang Jin is often cited by papers focused on Neuroscience and Neuropharmacology Research (40 papers), Receptor Mechanisms and Signaling (34 papers) and Neurotransmitter Receptor Influence on Behavior (29 papers). Guo-Zhang Jin collaborates with scholars based in China, United States and France. Guo-Zhang Jin's co-authors include Xuechu Zhen, Kechun Yang, Yang Shen, Bao-Cun Sun, Jie Wu, Yu Fu, Eitan Friedman, Hong‐Yuan Chu, Wei‐Xing Shi and Jiang‐Yuan Hu and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Guo-Zhang Jin

101 papers receiving 1.9k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Guo-Zhang Jin 1.1k 933 370 241 198 101 1.9k
Krystyna Gołembiowska 1.8k 1.7× 954 1.0× 440 1.2× 185 0.8× 306 1.5× 130 3.0k
Claudia Fracasso 927 0.9× 575 0.6× 366 1.0× 78 0.3× 166 0.8× 55 2.0k
Philippe Protais 1.4k 1.3× 946 1.0× 202 0.5× 121 0.5× 152 0.8× 63 2.3k
Timothy T. Soncrant 525 0.5× 436 0.5× 408 1.1× 96 0.4× 183 0.9× 52 1.5k
Eric A. Muth 713 0.7× 519 0.6× 380 1.0× 77 0.3× 154 0.8× 24 1.4k
Marina Perfumi 697 0.6× 859 0.9× 336 0.9× 264 1.1× 85 0.4× 82 1.8k
Young Hoon Kim 530 0.5× 749 0.8× 201 0.5× 107 0.4× 148 0.7× 65 1.8k
Dean R. Haubrich 927 0.9× 678 0.7× 231 0.6× 60 0.2× 159 0.8× 48 1.8k
Steven M. Bromidge 1.5k 1.4× 1.2k 1.3× 274 0.7× 67 0.3× 278 1.4× 41 2.3k
You‐Zhi Zhang 542 0.5× 626 0.7× 339 0.9× 131 0.5× 130 0.7× 118 2.0k

Countries citing papers authored by Guo-Zhang Jin

Since Specialization
Citations

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

Fields of papers citing papers by Guo-Zhang Jin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Guo-Zhang Jin. 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 Guo-Zhang Jin. The network helps show where Guo-Zhang Jin may publish in the future.

Co-authorship network of co-authors of Guo-Zhang Jin

This figure shows the co-authorship network connecting the top 25 collaborators of Guo-Zhang Jin. A scholar is included among the top collaborators of Guo-Zhang Jin 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 Guo-Zhang Jin. Guo-Zhang Jin 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.
Liu, Changliang, et al.. (2018). Cocaine-induced locomotor sensitization associates with slow oscillatory firing of neurons in the ventral tegmental area. Scientific Reports. 8(1). 3274–3274. 4 indexed citations
2.
Zhang, Bing, Fei Guo, Rong Lin, et al.. (2017). Activation of D1R/PKA/mTOR signaling cascade in medial prefrontal cortex underlying the antidepressant effects of l-SPD. Scientific Reports. 7(1). 3809–3809. 27 indexed citations
3.
Yue, Kai, et al.. (2015). Study on Determination of Synephrine and Artemisinin in <em>Phellinus vaninii</em> by High Performance Capillary Electrophoresis. Advance Journal of Food Science and Technology. 7(1). 7–10. 1 indexed citations
4.
Fang, Xing, Lin Guo, Jia Jia, et al.. (2013). SKF83959 is a novel triple reuptake inhibitor that elicits anti-depressant activity. Acta Pharmacologica Sinica. 34(9). 1149–1155. 17 indexed citations
5.
Ma, Baomiao, Kai Yue, Lin Chen, et al.. (2013). l-Stepholidine, a natural dopamine receptor D1 agonist and D2 antagonist, inhibits heroin-induced reinstatement. Neuroscience Letters. 559. 67–71. 25 indexed citations
7.
Yue, Kai, Baomiao Ma, Qin Ru, et al.. (2012). The dopamine receptor antagonist levo-tetrahydropalmatine attenuates heroin self-administration and heroin-induced reinstatement in rats. Pharmacology Biochemistry and Behavior. 102(1). 1–5. 36 indexed citations
8.
Xiao, Cheng, Kechun Yang, Chunyi Zhou, et al.. (2009). Nicotine modulates GABAergic transmission to dopaminergic neurons in substantia nigra pars compacta. Acta Pharmacologica Sinica. 30(6). 851–858. 8 indexed citations
9.
Mo, Jiao, et al.. (2008). l-Stepholidine reduced l-DOPA-induced dyskinesia in 6-OHDA-lesioned rat model of Parkinson's disease. Neurobiology of Aging. 31(6). 926–936. 37 indexed citations
10.
Yang, Kechun, Jun Hu, Linda Lucero, et al.. (2008). Distinctive nicotinic acetylcholine receptor functional phenotypes of rat ventral tegmental area dopaminergic neurons. The Journal of Physiology. 587(2). 345–361. 64 indexed citations
11.
Fu, Wei, Jianhua Shen, Xiaomin Luo, et al.. (2007). Dopamine D1 Receptor Agonist and D2 Receptor Antagonist Effects of the Natural Product (−)–Stepholidine: Molecular Modeling and Dynamics Simulations. Biophysical Journal. 93(5). 1431–1441. 34 indexed citations
12.
Mo, Jiao, et al.. (2007). Recent Developments in Studies of l-Stepholidine and its Analogs: Chemistry, Pharmacology and Clinical Implications. Current Medicinal Chemistry. 14(28). 2996–3002. 46 indexed citations
13.
Yang, Kechun, et al.. (2007). The Neuropharmacology of (-)-Stepholidine and its Potential Applications. Current Neuropharmacology. 5(4). 289–294. 27 indexed citations
14.
Chen, Youting, et al.. (2004). Effects of l-Stepholidine on Forebrain Fos Expression: Comparison with Clozapine and Haloperidol. Neuropsychopharmacology. 30(2). 261–267. 25 indexed citations
15.
Zhang, Xuexiang, et al.. (1998). Comparison of (−)-stepholidine and D1 or D2 agonists on unit firing of globus pallidus in 6-hydroxydopamine-lesioned rats. Life Sciences. 63(7). 537–544. 8 indexed citations
16.
Zou, Linglong, Jian Liu, & Guo-Zhang Jin. (1997). Involvement of receptor reserve in D1 agonistic action of (−)-stepholidine in lesioned rats. Biochemical Pharmacology. 54(2). 233–240. 23 indexed citations
17.
Zhang, Xuexiang, Bao-Cun Sun, & Guo-Zhang Jin. (1997). Atypical neuroleptic properties ofl-stepholidine. Science in China Series C Life Sciences. 40(5). 531–538. 8 indexed citations
19.
Jin, Guo-Zhang, Kaixing Huang, & Bao-Cun Sun. (1992). Dual actions of (−)-stepholidine on dopamine receptor subtypes after substantia nigra lesion. Neurochemistry International. 20. 175–178. 25 indexed citations
20.
Jin, Guo-Zhang, et al.. (1984). [Effect of l-stepholidine on rotational behavior in rats].. PubMed. 5(4). 222–5. 10 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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