T. Moriizumi

913 total citations
38 papers, 747 citations indexed

About

T. Moriizumi is a scholar working on Cellular and Molecular Neuroscience, Neurology and Sensory Systems. According to data from OpenAlex, T. Moriizumi has authored 38 papers receiving a total of 747 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cellular and Molecular Neuroscience, 12 papers in Neurology and 10 papers in Sensory Systems. Recurrent topics in T. Moriizumi's work include Neuroscience and Neuropharmacology Research (14 papers), Nerve injury and regeneration (12 papers) and Neurogenesis and neuroplasticity mechanisms (10 papers). T. Moriizumi is often cited by papers focused on Neuroscience and Neuropharmacology Research (14 papers), Nerve injury and regeneration (12 papers) and Neurogenesis and neuroplasticity mechanisms (10 papers). T. Moriizumi collaborates with scholars based in Japan, Canada and United States. T. Moriizumi's co-authors include T. Hattori, Nanae Fukushima, Kumiko Yokouchi, Masahiko Takada, Kyutaro Kawagishi, Derek van der Kooy, Yasuko Kitao, Yasukazu Nakamura, Takaki Miwa and Hironobu Tokuno and has published in prestigious journals such as The Journal of Comparative Neurology, Neuroscience and Experimental Brain Research.

In The Last Decade

T. Moriizumi

37 papers receiving 737 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T. Moriizumi Japan 18 505 199 172 155 122 38 747
Bengt T. Fundín Sweden 20 752 1.5× 119 0.6× 82 0.5× 148 1.0× 292 2.4× 26 1.2k
L.E. Westrum United States 20 678 1.3× 120 0.6× 84 0.5× 160 1.0× 282 2.3× 45 1.0k
Russell L. McBride United States 15 698 1.4× 451 2.3× 144 0.8× 195 1.3× 203 1.7× 24 1.2k
Michel Roger France 15 656 1.3× 349 1.8× 89 0.5× 106 0.7× 200 1.6× 30 969
Robert W. Rhoades United States 15 556 1.1× 283 1.4× 51 0.3× 83 0.5× 188 1.5× 18 771
Nobuo Katakura Japan 10 513 1.0× 278 1.4× 87 0.5× 58 0.4× 234 1.9× 16 978
Syosuke Kawamura Japan 15 384 0.8× 337 1.7× 68 0.4× 83 0.5× 220 1.8× 23 730
Bertrand Bearzatto Belgium 11 430 0.9× 142 0.7× 69 0.4× 74 0.5× 291 2.4× 13 692
M Roger France 13 311 0.6× 158 0.8× 72 0.4× 49 0.3× 79 0.6× 22 518
Laurence C. Schmued United States 9 712 1.4× 291 1.5× 131 0.8× 56 0.4× 263 2.2× 9 1.2k

Countries citing papers authored by T. Moriizumi

Since Specialization
Citations

This map shows the geographic impact of T. Moriizumi'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 T. Moriizumi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Moriizumi more than expected).

Fields of papers citing papers by T. Moriizumi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Moriizumi

This figure shows the co-authorship network connecting the top 25 collaborators of T. Moriizumi. A scholar is included among the top collaborators of T. Moriizumi 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 T. Moriizumi. T. Moriizumi 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.
Hayashida, Kentaro, T. Moriizumi, Hikaru Tsuruta, et al.. (2025). Long‐Term Impact of Early Subclinical Leaflet Thrombosis After Transcatheter Aortic Valve Implantation. Catheterization and Cardiovascular Interventions. 105(5). 1161–1170.
2.
Moriizumi, T., Takahiro Hiraide, Yoshikazu Kishino, et al.. (2024). Rapid Reversal of Pulmonary Hypertension by High-Dose Thiamine Supplementation: A Case Report. CJC Open. 6(12). 1534–1537. 1 indexed citations
3.
Kawagishi, Kyutaro, et al.. (2013). Regenerative Capacity of Bulbar Projection Neurons During Development: A Quantitative Neuronal Analysis With Functional Correlation. Chemical Senses. 39(1). 47–56. 7 indexed citations
4.
Maruyama, Yūji, et al.. (2009). Effectiveness of wearing protective devices (gas masks and eye protectors) against exposure to formaldehyde during an anatomy lab course.. 85(3). 120–131. 1 indexed citations
5.
Tanaka, Yuichiro, et al.. (2007). A transverse ligament located anterosuperiorly in the lower orbital fat space restricts lower eyelid retraction in the Mongoloid eye. Journal of Plastic Reconstructive & Aesthetic Surgery. 61(6). 603–609. 4 indexed citations
6.
Yokouchi, Kumiko, et al.. (2003). Neurotrophic effect of hepatocyte growth factor on neonatal facial motor neurons. Neurological Research. 25(7). 701–707. 18 indexed citations
7.
Kamijo, Yuji, Jun-ichi Koyama, Susumu Oikawa, et al.. (2003). Regenerative process of the facial nerve: rate of regeneration of fibers and their bifurcations. Neuroscience Research. 46(2). 135–143. 18 indexed citations
8.
Fukushima, Nanae, et al.. (2003). Effects of bilateral resection of facial nerves on suckling in developing rats. Brain Research Bulletin. 62(5). 385–389. 6 indexed citations
9.
Koyama, Jun-ichi, Kumiko Yokouchi, Nanae Fukushima, Kyutaro Kawagishi, & T. Moriizumi. (2003). Great potentiality of neonatal facial motor neurons for neural plasticity as determined by functionally essential neuronal population. Neuroscience Research. 46(1). 85–93. 12 indexed citations
10.
Kobayashi, Shigeaki, Jun-ichi Koyama, Kumiko Yokouchi, et al.. (2003). Functionally essential neuronal population of the facial motor nucleus. Neuroscience Research. 45(3). 357–361. 25 indexed citations
11.
Fukushima, Nanae, Kumiko Yokouchi, Kyutaro Kawagishi, & T. Moriizumi. (2002). Differential neurogenesis and gliogenesis by local and migrating neural stem cells in the olfactory bulb. Neuroscience Research. 44(4). 467–473. 34 indexed citations
12.
Moriizumi, T. & T. Hattori. (1992). Anatomical and functional compartmentalization of the subparafascicular thalamic nucleus in the rat. Experimental Brain Research. 90(1). 175–9. 14 indexed citations
13.
14.
Moriizumi, T. & T. Hattori. (1992). Choline acetyltransferase-immunoreactive neurons in the rat entopeduncular nucleus. Neuroscience. 46(3). 721–728. 18 indexed citations
15.
Moriizumi, T. & T. Hattori. (1991). Pallidotectal projection to the inferior colliculus of the rat. Experimental Brain Research. 87(1). 223–6. 22 indexed citations
16.
Moriizumi, T., Masahiko Takada, & T. Hattori. (1991). Morphological changes of striatal dopaminergic presynaptic boutons following intrastriatal kainate injection. Neuropharmacology. 30(7). 813–817. 4 indexed citations
17.
Moriizumi, T. & T. Hattori. (1991). Non-dopaminergic projection from the subparafascicular area to the temporal cortex in the rat. Neuroscience Letters. 129(1). 127–130. 8 indexed citations
18.
Hattori, T., Masahiko Takada, T. Moriizumi, & Derek van der Kooy. (1991). Single dopaminergic nigrostriatal neurons form two chemically distinct synaptic types: Possible transmitter segregation within neurons. The Journal of Comparative Neurology. 309(3). 391–401. 76 indexed citations
19.
Takada, Masahiko, et al.. (1990). On the origin of the dopaminergic innervation of the paraventricular thalamic nucleus. Neuroscience Letters. 115(1). 33–36. 42 indexed citations
20.

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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