Masayoshi Mishina

25.1k total citations · 8 hit papers
267 papers, 20.8k citations indexed

About

Masayoshi Mishina is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Masayoshi Mishina has authored 267 papers receiving a total of 20.8k indexed citations (citations by other indexed papers that have themselves been cited), including 205 papers in Cellular and Molecular Neuroscience, 161 papers in Molecular Biology and 44 papers in Cognitive Neuroscience. Recurrent topics in Masayoshi Mishina's work include Neuroscience and Neuropharmacology Research (177 papers), Ion channel regulation and function (73 papers) and Memory and Neural Mechanisms (37 papers). Masayoshi Mishina is often cited by papers focused on Neuroscience and Neuropharmacology Research (177 papers), Ion channel regulation and function (73 papers) and Memory and Neural Mechanisms (37 papers). Masayoshi Mishina collaborates with scholars based in Japan, United States and Germany. Masayoshi Mishina's co-authors include Kenji Sakimura, Hisashi Mori, Masahiko Watanabe, Shosaku Numa, Yoshiro Inoue, Keiji Imoto, Kazuaki Araki, Bert Sakmann, Kazuhiko Fukuda and Tomoyuki Takahashi and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Masayoshi Mishina

265 papers receiving 20.3k citations

Hit Papers

Molecular diversity of th... 1986 2026 1999 2012 1992 1986 1986 2004 1988 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masayoshi Mishina Japan 76 13.5k 12.9k 2.6k 2.4k 2.2k 267 20.8k
Stephen J. Moss United Kingdom 85 14.1k 1.0× 11.5k 0.9× 2.5k 1.0× 2.1k 0.9× 1.2k 0.5× 236 20.4k
Stephen F. Heinemann United States 78 16.7k 1.2× 15.2k 1.2× 3.0k 1.2× 2.6k 1.1× 1.4k 0.6× 147 23.4k
Kenji Sakimura Japan 72 11.7k 0.9× 9.6k 0.7× 3.4k 1.3× 2.4k 1.0× 2.1k 1.0× 387 19.2k
Jon Storm‐Mathisen Norway 76 16.8k 1.2× 9.2k 0.7× 3.8k 1.5× 2.3k 1.0× 2.1k 1.0× 204 21.8k
Erin M. Schuman Germany 69 9.7k 0.7× 11.2k 0.9× 3.2k 1.2× 1.3k 0.6× 2.2k 1.0× 145 19.9k
Gary L. Westbrook United States 72 17.8k 1.3× 12.5k 1.0× 4.5k 1.7× 2.0k 0.8× 2.1k 1.0× 129 22.2k
Ronald S. Petralia United States 63 11.5k 0.9× 9.2k 0.7× 3.1k 1.2× 1.8k 0.7× 1.1k 0.5× 176 16.1k
Werner Sieghart Austria 75 17.8k 1.3× 12.2k 0.9× 4.3k 1.7× 2.6k 1.1× 1.2k 0.6× 317 23.6k
Menahem Segal Israel 81 13.0k 1.0× 7.5k 0.6× 5.2k 2.0× 2.4k 1.0× 2.8k 1.3× 286 19.9k
Jean‐Marc Fritschy Switzerland 88 19.8k 1.5× 11.3k 0.9× 6.2k 2.4× 3.6k 1.5× 2.5k 1.2× 291 26.8k

Countries citing papers authored by Masayoshi Mishina

Since Specialization
Citations

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

Fields of papers citing papers by Masayoshi Mishina

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masayoshi Mishina

This figure shows the co-authorship network connecting the top 25 collaborators of Masayoshi Mishina. A scholar is included among the top collaborators of Masayoshi Mishina 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 Masayoshi Mishina. Masayoshi Mishina 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.
Vinnakota, Chitra, Matthew R. Hudson, Kazutaka Ikeda, et al.. (2025). Effects of NMDA receptor antagonists on working memory and gamma oscillations, and the mediating role of the GluN2D subunit. Neuropsychopharmacology. 50(13). 1938–1948.
2.
Suzuki, Nami, Masayuki Itoh, Maya Yamazaki, et al.. (2024). Limb-Clasping Response in NMDA Receptor Palmitoylation-Deficient Mice. Molecular Neurobiology. 61(11). 9125–9135. 2 indexed citations
3.
Vinnakota, Chitra, Anna Schroeder, Xin Du, et al.. (2023). Understanding the role of the NMDA receptor subunit, GluN2D , in mediating NMDA receptor antagonist‐induced behavioral disruptions in male and female mice. Journal of Neuroscience Research. 102(1). e25257–e25257. 5 indexed citations
4.
Jury, Nicholas J., Anna K. Radke, Dipanwita Pati, et al.. (2018). NMDA receptor GluN2A subunit deletion protects against dependence-like ethanol drinking. Behavioural Brain Research. 353. 124–128. 7 indexed citations
5.
Yamamoto, Hideko, Yoko Hagino, Yukio Takamatsu, et al.. (2016). Loss of GluN2D subunit results in social recognition deficit, social stress, 5-HT2C receptor dysfunction, and anhedonia in mice. Neuropharmacology. 112(Pt A). 188–197. 25 indexed citations
6.
Uemura, Takeshi, et al.. (2014). Striatal dopamine D1 receptor is essential for contextual fear conditioning. Scientific Reports. 4(1). 3976–3976. 28 indexed citations
7.
Yamamoto, Hideko, Toshifumi Yamamoto, Yoko Hagino, et al.. (2013). Involvement of the N-methyl-d-aspartate receptor GluN2D subunit in phencyclidine-induced motor impairment, gene expression, and increased Fos immunoreactivity. Molecular Brain. 6(1). 56–56. 25 indexed citations
8.
Yasumura, Misato, Tomoyuki Yoshida, Sung‐Jin Lee, et al.. (2011). Glutamate receptor δ1 induces preferentially inhibitory presynaptic differentiation of cortical neurons by interacting with neurexins through cerebellin precursor protein subtypes. Journal of Neurochemistry. 121(5). 705–716. 53 indexed citations
9.
Biase, Lindsay M. De, Shin Hyeok Kang, Emily G. Baxi, et al.. (2011). NMDA Receptor Signaling in Oligodendrocyte Progenitors Is Not Required for Oligodendrogenesis and Myelination. Journal of Neuroscience. 31(35). 12650–12662. 121 indexed citations
10.
Miyazaki, Taisuke, Miwako Yamasaki, Tomonori Takeuchi, et al.. (2010). Ablation of Glutamate Receptor GluRδ2 in Adult Purkinje Cells Causes Multiple Innervation of Climbing Fibers by Inducing Aberrant Invasion to Parallel Fiber Innervation Territory. Journal of Neuroscience. 30(45). 15196–15209. 39 indexed citations
11.
Xu, Li, Tamaki Mabuchi, Tayo Katano, et al.. (2007). Nitric oxide (NO) serves as a retrograde messenger to activate neuronal NO synthase in the spinal cord via NMDA receptors. Nitric Oxide. 17(1). 18–24. 33 indexed citations
12.
Taniguchi, Masahiko, Tomoyuki Masuda, Masahiro Fukaya, et al.. (2005). Identification and characterization of a novel member of murine semaphorin family. Genes to Cells. 10(8). 785–792. 54 indexed citations
13.
Weitlauf, Carl, Yumiko Honse, Yves P. Auberson, et al.. (2005). Activation of NR2A-Containing NMDA Receptors Is Not Obligatory for NMDA Receptor-Dependent Long-Term Potentiation. Journal of Neuroscience. 25(37). 8386–8390. 137 indexed citations
14.
Kawakami, Koichi, Hisashi Takeda, N. Kawakami, et al.. (2004). A Transposon-Mediated Gene Trap Approach Identifies Developmentally Regulated Genes in Zebrafish. Developmental Cell. 7(1). 133–144. 691 indexed citations breakdown →
15.
Takehara‐Nishiuchi, Kaori, Shigenori Kawahara, Hiromichi Kuriyama, et al.. (2004). The N-methyl-d-aspartate (NMDA)-type glutamate receptor GluRε2 is important for delay and trace eyeblink conditioning in mice. Neuroscience Letters. 364(1). 43–47. 16 indexed citations
16.
Nishimura, Wataru, Shinichi Tatsumi, Kenji Sakimura, et al.. (2004). Characterization of N-methyl-d-aspartate receptor subunits responsible for postoperative pain. European Journal of Pharmacology. 503(1-3). 71–75. 11 indexed citations
17.
Takatsuki, Kanako, et al.. (2003). The Hippocampus Plays an Important Role in Eyeblink Conditioning with a Short Trace Interval in Glutamate Receptor Subunit δ2 Mutant Mice. Journal of Neuroscience. 23(1). 17–22. 37 indexed citations
18.
Hattori, Satoshi, Kenji Okuda, Kenji Hamajima, et al.. (1994). Expression and characterization of the α2 subunit of the α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) -selective glutamate receptor channel in a baculovirus system. Brain Research. 666(1). 43–52. 9 indexed citations
19.
Morita, Takao, Kenji Sakimura, Etsuko Kushiya, et al.. (1992). Cloning and functional expression of a cDNA encoding the mouse β2 subunit of the kainate-selective glutamate receptor channel. Molecular Brain Research. 14(1-2). 143–146. 24 indexed citations
20.
Nakano, Ryoichi, Nobuya Fujita, Takashi Inuzuka, et al.. (1991). Structure of mouse myelin-associated glycoprotein gene. Biochemical and Biophysical Research Communications. 178(1). 282–290. 24 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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