Shogo Tanabe

616 total citations
21 papers, 444 citations indexed

About

Shogo Tanabe is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Shogo Tanabe has authored 21 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 8 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Shogo Tanabe's work include Neuroinflammation and Neurodegeneration Mechanisms (9 papers), Neurogenesis and neuroplasticity mechanisms (6 papers) and Multiple Sclerosis Research Studies (4 papers). Shogo Tanabe is often cited by papers focused on Neuroinflammation and Neurodegeneration Mechanisms (9 papers), Neurogenesis and neuroplasticity mechanisms (6 papers) and Multiple Sclerosis Research Studies (4 papers). Shogo Tanabe collaborates with scholars based in Japan and United States. Shogo Tanabe's co-authors include Toshihide Yamashita, Yuki Fujita, Takahide Itokazu, Rieko Muramatsu, M. Nııkura, Yasuhiro Moriwaki, Hidemi Misawa, Takashi Okuda, Sae Uchida and Koji Yamanaka and has published in prestigious journals such as Journal of Neuroscience, Nature Neuroscience and Scientific Reports.

In The Last Decade

Shogo Tanabe

21 papers receiving 443 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shogo Tanabe Japan 12 174 113 104 92 91 21 444
Karelle Bénardais Germany 11 167 1.0× 96 0.8× 122 1.2× 95 1.0× 128 1.4× 16 464
Jillian C. Nissen United States 12 277 1.6× 180 1.6× 139 1.3× 74 0.8× 52 0.6× 16 497
Nina Fainberg United States 7 153 0.9× 110 1.0× 124 1.2× 27 0.3× 52 0.6× 13 407
Siling Du United States 10 186 1.1× 107 0.9× 90 0.9× 27 0.3× 57 0.6× 16 420
Anne‐Laure Dubessy France 9 131 0.8× 65 0.6× 105 1.0× 99 1.1× 183 2.0× 17 419
Shalaka Wahane United States 10 211 1.2× 80 0.7× 208 2.0× 174 1.9× 129 1.4× 12 545
Teresa A. Evans United States 9 181 1.0× 81 0.7× 156 1.5× 150 1.6× 114 1.3× 13 584
Jose A. Mazzitelli United States 6 329 1.9× 113 1.0× 170 1.6× 26 0.3× 83 0.9× 7 646
Maria C. J. Vincenten Netherlands 9 189 1.1× 144 1.3× 114 1.1× 173 1.9× 89 1.0× 9 464

Countries citing papers authored by Shogo Tanabe

Since Specialization
Citations

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

Fields of papers citing papers by Shogo Tanabe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shogo Tanabe

This figure shows the co-authorship network connecting the top 25 collaborators of Shogo Tanabe. A scholar is included among the top collaborators of Shogo Tanabe 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 Shogo Tanabe. Shogo Tanabe 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.
Uyeda, Akiko, Lili Quan, Shogo Tanabe, et al.. (2024). Synaptotagmin 4 Supports Spontaneous Axon Sprouting after Spinal Cord Injury. Journal of Neuroscience. 44(43). e1593232024–e1593232024. 3 indexed citations
2.
Maruyama, Takashi, Shogo Tanabe, Akiko Uyeda, Tatsunori Suzuki, & Rieko Muramatsu. (2023). Free fatty acids support oligodendrocyte survival in a mouse model of amyotrophic lateral sclerosis. Frontiers in Cellular Neuroscience. 17. 1081190–1081190. 3 indexed citations
3.
Tanabe, Shogo, et al.. (2022). Lysophosphatidic acid stimulates pericyte migration via LPA receptor 1. Biochemical and Biophysical Research Communications. 618. 61–66. 2 indexed citations
4.
Tanabe, Shogo, et al.. (2022). Circulating factors that influence the central nervous system remyelination. Current Opinion in Pharmacology. 62. 130–136. 7 indexed citations
5.
Ito, Masumi, Rieko Muramatsu, Yuki Kato, et al.. (2021). Age-dependent decline in remyelination capacity is mediated by apelin–APJ signaling. Nature Aging. 1(3). 284–294. 23 indexed citations
6.
Tanabe, Shogo, et al.. (2021). Microglial ASD-related genes are involved in oligodendrocyte differentiation. Scientific Reports. 11(1). 17825–17825. 7 indexed citations
7.
Itokazu, Takahide, et al.. (2021). Interleukin-17A regulates ependymal cell proliferation and functional recovery after spinal cord injury in mice. Cell Death and Disease. 12(8). 766–766. 13 indexed citations
8.
Tanabe, Shogo, et al.. (2019). Microglia promote the proliferation of neural precursor cells by secreting osteopontin. Biochemical and Biophysical Research Communications. 513(4). 841–845. 14 indexed citations
9.
Tanabe, Shogo, et al.. (2019). Microglia suppress the secondary progression of autoimmune encephalomyelitis. Glia. 67(9). 1694–1704. 39 indexed citations
10.
Tanabe, Shogo & Toshihide Yamashita. (2019). Function of Lymphocytes in Oligodendrocyte Development. The Neuroscientist. 26(1). 74–86. 4 indexed citations
11.
Tanabe, Shogo & Toshihide Yamashita. (2018). B lymphocytes: Crucial contributors to brain development and neurological diseases. Neuroscience Research. 139. 37–41. 12 indexed citations
12.
Tanabe, Shogo & Toshihide Yamashita. (2018). B-1a lymphocytes promote oligodendrogenesis during brain development. Nature Neuroscience. 21(4). 506–516. 74 indexed citations
13.
Harada, Kana, Yuki Fujita, Tatsusada Okuno, et al.. (2018). Inhibition of RGMa alleviates symptoms in a rat model of neuromyelitis optica. Scientific Reports. 8(1). 34–34. 20 indexed citations
14.
Tanabe, Shogo, et al.. (2018). Inhibiting repulsive guidance molecule-a suppresses secondary progression in mouse models of multiple sclerosis. Cell Death and Disease. 9(11). 1061–1061. 40 indexed citations
15.
Tanabe, Shogo & Toshihide Yamashita. (2018). The role of immune cells in brain development and neurodevelopmental diseases. International Immunology. 30(10). 437–444. 44 indexed citations
16.
Tanabe, Shogo, et al.. (2016). QR-decomposed generalized belief propagation for MIMO detection. International Symposium on Information Theory and its Applications. 468–472. 3 indexed citations
17.
Nııkura, M., Shogo Tanabe, Yasuhiro Moriwaki, et al.. (2016). Selective Expression of Osteopontin in ALS-resistant Motor Neurons is a Critical Determinant of Late Phase Neurodegeneration Mediated by Matrix Metalloproteinase-9. Scientific Reports. 6(1). 27354–27354. 59 indexed citations
19.
Tanabe, Shogo & Toshihide Yamashita. (2014). Repulsive Guidance Molecule-a Is Involved in Th17-Cell-Induced Neurodegeneration in Autoimmune Encephalomyelitis. Cell Reports. 9(4). 1459–1470. 42 indexed citations
20.
Misawa, Hidemi, et al.. (2011). Osteopontin is an alpha motor neuron marker in the mouse spinal cord. Journal of Neuroscience Research. 90(4). 732–742. 30 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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