Ayumu Tashiro

4.5k total citations
49 papers, 3.6k citations indexed

About

Ayumu Tashiro is a scholar working on Cellular and Molecular Neuroscience, Developmental Neuroscience and Molecular Biology. According to data from OpenAlex, Ayumu Tashiro has authored 49 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Cellular and Molecular Neuroscience, 16 papers in Developmental Neuroscience and 13 papers in Molecular Biology. Recurrent topics in Ayumu Tashiro's work include Neuroscience and Neuropharmacology Research (21 papers), Neurogenesis and neuroplasticity mechanisms (16 papers) and Pain Mechanisms and Treatments (12 papers). Ayumu Tashiro is often cited by papers focused on Neuroscience and Neuropharmacology Research (21 papers), Neurogenesis and neuroplasticity mechanisms (16 papers) and Pain Mechanisms and Treatments (12 papers). Ayumu Tashiro collaborates with scholars based in United States, Singapore and Norway. Ayumu Tashiro's co-authors include Rafael Yuste, Fred H. Gage, Hiroshi Makino, Chunmei Zhao, Ania K. Majewska, Anna Dunaevsky, Carol A. Mason, Nicolas Toni, Vladislav M. Sandler and David A. Bereiter and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Ayumu Tashiro

48 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ayumu Tashiro United States 24 2.3k 1.3k 1.1k 769 442 49 3.6k
Inma Cobos United States 26 2.1k 0.9× 1.4k 1.0× 1.9k 1.7× 811 1.1× 609 1.4× 40 4.1k
Cynthia R. Keller-Peck United States 13 2.2k 1.0× 839 0.6× 1.9k 1.6× 372 0.5× 290 0.7× 18 4.2k
Nancy O’Rourke United States 20 2.0k 0.9× 1.2k 0.9× 2.8k 2.4× 491 0.6× 366 0.8× 32 4.7k
Jozsef Z. Kiss Switzerland 36 1.9k 0.9× 1.4k 1.1× 1.2k 1.1× 490 0.6× 181 0.4× 72 4.0k
María E. Rubio United States 36 2.9k 1.3× 1.3k 1.0× 2.9k 2.5× 853 1.1× 295 0.7× 73 5.5k
J. Tiago Gonçalves United States 16 1.3k 0.6× 1.0k 0.8× 1.7k 1.5× 845 1.1× 265 0.6× 21 3.6k
Petti T. Pang United States 10 3.3k 1.4× 1.3k 1.0× 1.1k 1.0× 1.2k 1.6× 470 1.1× 11 4.6k
Geneviève Chazal France 22 1.6k 0.7× 1.0k 0.8× 1.3k 1.2× 517 0.7× 181 0.4× 37 3.2k
Patrick Carroll France 31 4.0k 1.8× 2.3k 1.8× 2.2k 1.9× 569 0.7× 607 1.4× 66 5.9k
Matthew S. Grubb United Kingdom 24 2.6k 1.2× 1.2k 0.9× 1.2k 1.0× 1.4k 1.8× 240 0.5× 37 4.2k

Countries citing papers authored by Ayumu Tashiro

Since Specialization
Citations

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

Fields of papers citing papers by Ayumu Tashiro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ayumu Tashiro

This figure shows the co-authorship network connecting the top 25 collaborators of Ayumu Tashiro. A scholar is included among the top collaborators of Ayumu Tashiro 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 Ayumu Tashiro. Ayumu Tashiro 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.
Lee, Bernett T. K., Lee Wei Lim, Jingtao Zhang, et al.. (2025). Choline intake during pregnancy influences maternal cognitive function and hippocampal gene expression in late adulthood. Nutritional Neuroscience. 29(2). 139–164. 1 indexed citations
2.
Nair, Rajeevkumar Raveendran, et al.. (2021). Role of NMDA Receptors in Adult Neurogenesis and Normal Development of the Dentate Gyrus. eNeuro. 8(4). ENEURO.0566–20.2021. 14 indexed citations
3.
Uemura, Masato, et al.. (2021). A neurogenic microenvironment defined by excitatory-inhibitory neuronal circuits in adult dentate gyrus. Cell Reports. 36(1). 109324–109324. 8 indexed citations
4.
5.
Weitemier, Adam Z., Kotaro Mizuta, Masaaki Sato, et al.. (2020). Two Functionally Distinct Serotonergic Projections into Hippocampus. Journal of Neuroscience. 40(25). 4936–4944. 35 indexed citations
6.
Sundaram, Suresh, et al.. (2017). A critical period for antidepressant-induced acceleration of neuronal maturation in adult dentate gyrus. Translational Psychiatry. 7(9). e1235–e1235. 18 indexed citations
7.
Tashiro, Ayumu, et al.. (2016). Place cells and long-term potentiation in the hippocampus. Neurobiology of Learning and Memory. 138. 206–214. 23 indexed citations
8.
Kitanishi, Takuma, et al.. (2015). Novelty-Induced Phase-Locked Firing to Slow Gamma Oscillations in the Hippocampus: Requirement of Synaptic Plasticity. Neuron. 86(5). 1265–1276. 43 indexed citations
9.
Tashiro, Ayumu, et al.. (2011). Critical maturational period of new neurons in adult dentate gyrus for their involvement in memory formation. European Journal of Neuroscience. 33(6). 1094–1100. 37 indexed citations
10.
Chang, Zhengshi, Keiichiro Okamoto, Ayumu Tashiro, & David A. Bereiter. (2010). Ultraviolet irradiation of the eye and Fos-positive neurons induced in trigeminal brainstem after intravitreal or ocular surface transient receptor potential vanilloid 1 activation. Neuroscience. 170(2). 678–685. 10 indexed citations
11.
Tashiro, Ayumu, Keiichiro Okamoto, & David A. Bereiter. (2009). NMDA receptor blockade reduces temporomandibular joint-evoked activity of trigeminal subnucleus caudalis neurons in an estrogen-dependent manner. Neuroscience. 164(4). 1805–1812. 11 indexed citations
12.
Marumoto, Tomotoshi, Ayumu Tashiro, Dinorah Friedmann‐Morvinski, et al.. (2009). Development of a novel mouse glioma model using lentiviral vectors. Nature Medicine. 15(1). 110–116. 253 indexed citations
13.
Tashiro, Ayumu, Keiichiro Okamoto, & David A. Bereiter. (2008). Morphine modulation of temporomandibular joint‐responsive units in superficial laminae at the spinomedullary junction in female rats depends on estrogen status. European Journal of Neuroscience. 28(10). 2065–2074. 25 indexed citations
14.
Tashiro, Ayumu, Chunmei Zhao, & Fred H. Gage. (2006). Retrovirus-mediated single-cell gene knockout technique in adult newborn neurons in vivo. Nature Protocols. 1(6). 3049–3055. 108 indexed citations
15.
Imbe, Hiroki, Ayumu Tashiro, Akihisa Kimura, et al.. (2004). The role of peripheral 5HT2A and 5HT1A receptors on the orofacial formalin test in rats with persistent temporomandibular joint inflammation. Neuroscience. 130(2). 465–474. 27 indexed citations
16.
Tashiro, Ayumu & Rafael Yuste. (2004). Regulation of dendritic spine motility and stability by Rac1 and Rho kinase: evidence for two forms of spine motility. Molecular and Cellular Neuroscience. 26(3). 429–440. 216 indexed citations
17.
Tashiro, Ayumu, Anna Dunaevsky, Richard Blazeski, Carol A. Mason, & Rafael Yuste. (2003). Bidirectional Regulation of Hippocampal Mossy Fiber Filopodial Motility by Kainate Receptors. Neuron. 38(5). 773–784. 138 indexed citations
18.
Ogaẃa, Atsuhiro, Toshifumi Morimoto, Jim Hu, et al.. (2003). Hard-food mastication suppresses complete FREUND's adjuvant-induced nociception. Neuroscience. 120(4). 1081–1092. 17 indexed citations
19.
Tashiro, Ayumu, Jesse H. Goldberg, & Rafael Yuste. (2001). Calcium oscillations in neocortical astrocytes under epileptiform conditions. Journal of Neurobiology. 50(1). 45–55. 80 indexed citations
20.
Tashiro, Ayumu. (2000). Regulation of Dendritic Spine Morphology by the Rho Family of Small GTPases: Antagonistic Roles of Rac and Rho. Cerebral Cortex. 10(10). 927–938. 357 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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