Shanting Zhao

3.3k total citations
83 papers, 2.6k citations indexed

About

Shanting Zhao is a scholar working on Cellular and Molecular Neuroscience, Developmental Neuroscience and Molecular Biology. According to data from OpenAlex, Shanting Zhao has authored 83 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Cellular and Molecular Neuroscience, 41 papers in Developmental Neuroscience and 25 papers in Molecular Biology. Recurrent topics in Shanting Zhao's work include Neurogenesis and neuroplasticity mechanisms (41 papers), Axon Guidance and Neuronal Signaling (26 papers) and Neuroscience and Neuropharmacology Research (18 papers). Shanting Zhao is often cited by papers focused on Neurogenesis and neuroplasticity mechanisms (41 papers), Axon Guidance and Neuronal Signaling (26 papers) and Neuroscience and Neuropharmacology Research (18 papers). Shanting Zhao collaborates with scholars based in China, Germany and United States. Shanting Zhao's co-authors include Michael Frotscher, Eckart Förster, Xuejun Chai, Hans H. Bock, Bianka Brunne, Joachim Herz, Bernd Heimrich, Carola A. Haas, Lingzhen Song and Dirk Junghans and has published in prestigious journals such as Journal of Neuroscience, Nature reviews. Neuroscience and Development.

In The Last Decade

Shanting Zhao

83 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shanting Zhao China 29 1.3k 1.1k 997 333 289 83 2.6k
Masayuki Sakamoto Japan 22 885 0.7× 1.3k 1.1× 1.1k 1.1× 201 0.6× 204 0.7× 68 3.0k
Mathias De Roo Switzerland 22 1.3k 1.0× 694 0.6× 748 0.8× 183 0.5× 172 0.6× 30 2.3k
Steven Poser United States 16 1.5k 1.2× 553 0.5× 1.8k 1.8× 194 0.6× 196 0.7× 33 3.0k
Ravi Jagasia Switzerland 25 674 0.5× 767 0.7× 2.0k 2.0× 415 1.2× 273 0.9× 42 3.3k
Toby Behar United States 27 1.5k 1.1× 1.2k 1.1× 1.1k 1.1× 232 0.7× 183 0.6× 33 2.7k
Daniela M. Vogt Weisenhorn Germany 34 1.5k 1.2× 507 0.5× 1.9k 1.9× 401 1.2× 297 1.0× 64 3.6k
Shernaz X. Bamji Canada 32 1.9k 1.5× 604 0.5× 2.0k 2.0× 609 1.8× 355 1.2× 47 3.8k
Tomohisa Toda United States 17 529 0.4× 766 0.7× 1.3k 1.3× 141 0.4× 211 0.7× 27 2.3k
Martin L. Doughty United States 16 1.7k 1.4× 577 0.5× 2.0k 2.0× 231 0.7× 452 1.6× 31 3.6k
Kazunori Toida Japan 30 970 0.8× 481 0.4× 911 0.9× 400 1.2× 165 0.6× 64 2.9k

Countries citing papers authored by Shanting Zhao

Since Specialization
Citations

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

Fields of papers citing papers by Shanting Zhao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shanting Zhao

This figure shows the co-authorship network connecting the top 25 collaborators of Shanting Zhao. A scholar is included among the top collaborators of Shanting Zhao 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 Shanting Zhao. Shanting Zhao 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.
Zhu, Xiaoyan, et al.. (2021). Effect of Heat Stress on Hippocampal Neurogenesis: Insights into the Cellular and Molecular Basis of Neuroinflammation-Induced Deficits. Cellular and Molecular Neurobiology. 43(1). 1–13. 13 indexed citations
2.
Wang, Shuzhong, Xuejun Chai, Yi Wang, et al.. (2019). Nyap1 Regulates Multipolar–Bipolar Transition and Morphology of Migrating Neurons by Fyn Phosphorylation during Corticogenesis. Cerebral Cortex. 30(3). 929–941. 4 indexed citations
3.
Cheng, Xinran, et al.. (2018). The effect of P85 on neuronal proliferation and differentiation during development of mouse cerebral cortex. Developmental Biology. 441(1). 95–103. 6 indexed citations
4.
Brunne, Bianka, Shanting Zhao, Xuejun Chai, et al.. (2017). Trajectory Analysis Unveils Reelin's Role in the Directed Migration of Granule Cells in the Dentate Gyrus. Journal of Neuroscience. 38(1). 137–148. 22 indexed citations
5.
Tang, Jianli, et al.. (2017). High level of CTP synthase induces formation of cytoophidia in cortical neurons and impairs corticogenesis. Histochemistry and Cell Biology. 149(1). 61–73. 12 indexed citations
6.
Wu, Haibo, Jiamin Zhao, Beibei Fu, et al.. (2017). Retinoic acid-induced upregulation of miR-219 promotes the differentiation of embryonic stem cells into neural cells. Cell Death and Disease. 8(7). e2953–e2953. 31 indexed citations
7.
Frotscher, Michael, Shanting Zhao, Shaobo Wang, & Xuejun Chai. (2017). Reelin Signaling Inactivates Cofilin to Stabilize the Cytoskeleton of Migrating Cortical Neurons. Frontiers in Cellular Neuroscience. 11. 148–148. 23 indexed citations
8.
Cheng, Xinran, et al.. (2016). The function of sperm-associated antigen 6 in neuronal proliferation and differentiation. Journal of Molecular Histology. 47(6). 531–540. 16 indexed citations
9.
Song, Lingzhen, et al.. (2015). The SH2 domain is crucial for function of Fyn in neuronal migration and cortical lamination. BMB Reports. 48(2). 97–102. 8 indexed citations
10.
An, Lei, et al.. (2014). The aspartic acid of Fyn at 390 is critical for neuronal migration during corticogenesis. Experimental Cell Research. 328(2). 419–428. 6 indexed citations
11.
Chai, Xuejun, Li Fan, Wei Zhang, et al.. (2014). Reelin Induces Branching of Neurons and Radial Glial Cells during Corticogenesis. Cerebral Cortex. 25(10). 3640–3653. 47 indexed citations
12.
Panther, Patricia, et al.. (2014). Alterations in the hippocampal and striatal catecholaminergic fiber densities of heterozygous reeler mice. Neuroscience. 275. 404–419. 6 indexed citations
13.
Chai, Xuejun, et al.. (2013). Epilepsy-Induced Motility of Differentiated Neurons. Cerebral Cortex. 24(8). 2130–2140. 35 indexed citations
14.
Zhao, Shanting, Daniel Studer, Werner Graber, Sigrun Nestel, & Michael Frotscher. (2012). Fine structure of hippocampal mossy fiber synapses following rapid high‐pressure freezing. Epilepsia. 53(s1). 4–8. 11 indexed citations
15.
Frotscher, Michael, Shanting Zhao, Werner Graber, Alexander Drakew, & Daniel Studer. (2007). New ways of looking at synapses. Histochemistry and Cell Biology. 128(2). 91–96. 17 indexed citations
16.
Zhao, Shanting, Xuejun Chai, Hans H. Bock, et al.. (2006). Rescue of the reeler phenotype in the dentate gyrus by wild-type coculture is mediated by lipoprotein receptors for reelin and disabled 1. The Journal of Comparative Neurology. 495(1). 1–9. 30 indexed citations
17.
Förster, Eckart, Shanting Zhao, & Michael Frotscher. (2006). Laminating the hippocampus. Nature reviews. Neuroscience. 7(4). 259–268. 185 indexed citations
18.
Schwab, Markus H., Bernd Heimrich, Dirk Feldmeyer, et al.. (2000). Neuronal Basic Helix-Loop-Helix Proteins (NEX and BETA2/Neuro D) Regulate Terminal Granule Cell Differentiation in the Hippocampus. Journal of Neuroscience. 20(10). 3714–3724. 206 indexed citations
19.
Zhao, Shanting, et al.. (2000). Development of the Entorhino‐Hippocampal Projection: Guidance by Cajal‐Retzius Cell Axons. Annals of the New York Academy of Sciences. 911(1). 43–54. 25 indexed citations
20.
Deng, Jinbo, Bernd Heimrich, Joachim Lübke, et al.. (1999). Hippocampal Cajal–Retzius cells project to the entorhinal cortex: retrograde tracing and intracellular labelling studies. European Journal of Neuroscience. 11(12). 4278–4290. 49 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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