Satoru Moritoh

909 total citations
17 papers, 669 citations indexed

About

Satoru Moritoh is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Plant Science. According to data from OpenAlex, Satoru Moritoh has authored 17 papers receiving a total of 669 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 4 papers in Plant Science. Recurrent topics in Satoru Moritoh's work include Retinal Development and Disorders (5 papers), Photoreceptor and optogenetics research (4 papers) and Neuroscience and Neuropharmacology Research (3 papers). Satoru Moritoh is often cited by papers focused on Retinal Development and Disorders (5 papers), Photoreceptor and optogenetics research (4 papers) and Neuroscience and Neuropharmacology Research (3 papers). Satoru Moritoh collaborates with scholars based in Japan, United States and Austria. Satoru Moritoh's co-authors include Amane Koizumi, Rie Terada, Kenji F. Tanaka, A. Ono, Ko Matsui, Katsushi Yamaguchi, Tetsuo Yamamori, Ko Shimamoto, Yusuke Komatsu and Chang‐Ho Eun and has published in prestigious journals such as Nature Communications, Nature Neuroscience and PLoS ONE.

In The Last Decade

Satoru Moritoh

17 papers receiving 660 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Satoru Moritoh Japan 14 327 223 207 101 69 17 669
Jong‐So Kim South Korea 13 396 1.2× 195 0.9× 181 0.9× 22 0.2× 15 0.2× 18 858
Monique Pena United States 6 583 1.8× 141 0.6× 180 0.9× 683 6.8× 17 0.2× 7 1.3k
Rui Gomes Portugal 13 610 1.9× 128 0.6× 116 0.6× 130 1.3× 4 0.1× 17 972
Deborah Duricka United States 9 139 0.4× 134 0.6× 54 0.3× 31 0.3× 9 0.1× 12 369
Zoya Katarova Hungary 15 323 1.0× 89 0.4× 353 1.7× 53 0.5× 4 0.1× 23 712
Catherine Choi United States 10 374 1.1× 51 0.2× 182 0.9× 119 1.2× 7 0.1× 21 702
Tanja Diemer United States 15 527 1.6× 25 0.1× 131 0.6× 28 0.3× 145 2.1× 20 826
Magali Hennion France 13 798 2.4× 80 0.4× 98 0.5× 47 0.5× 4 0.1× 16 973
Liana Artinian United States 12 273 0.8× 45 0.2× 195 0.9× 12 0.1× 22 0.3× 18 571

Countries citing papers authored by Satoru Moritoh

Since Specialization
Citations

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

Fields of papers citing papers by Satoru Moritoh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Satoru Moritoh

This figure shows the co-authorship network connecting the top 25 collaborators of Satoru Moritoh. A scholar is included among the top collaborators of Satoru Moritoh 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 Satoru Moritoh. Satoru Moritoh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Morizawa, Yosuke M., Mami Matsumoto, Tomomi Aida, et al.. (2022). Synaptic pruning through glial synapse engulfment upon motor learning. Nature Neuroscience. 25(11). 1458–1469. 35 indexed citations
2.
Shimoda, Yoshiteru, Kaoru Beppu, Yoko Ikoma, et al.. (2021). Optogenetic stimulus-triggered acquisition of seizure resistance. Neurobiology of Disease. 163. 105602–105602. 17 indexed citations
3.
Higo, Asuka, Fumihito Miura, Shojiro Tamaki, et al.. (2020). DNA methylation is reconfigured at the onset of reproduction in rice shoot apical meristem. Nature Communications. 11(1). 4079–4079. 45 indexed citations
4.
Kobayashi, Kensuke, Ryo Kitahara, Katsunori Kitano, et al.. (2019). Gene delivery to cone photoreceptors by subretinal injection of rAAV2/6 in the mouse retina. Biochemical and Biophysical Research Communications. 515(1). 222–227. 5 indexed citations
5.
Takeuchi, Haruki, Satoru Moritoh, Katsunori Kitano, et al.. (2018). Different Activity Patterns in Retinal Ganglion Cells of TRPM1 and mGluR6 Knockout Mice. BioMed Research International. 2018. 1–6. 12 indexed citations
6.
Nakamura, Orie, Satoru Moritoh, Kota Sato, et al.. (2017). Bilberry extract administration prevents retinal ganglion cell death in mice via the regulation of chaperone molecules under conditions of endoplasmic reticulum stress. Clinical ophthalmology. Volume 11. 1825–1834. 18 indexed citations
7.
Maekawa, Shigeto, Kota Sato, Kosuke Fujita, et al.. (2017). The neuroprotective effect of hesperidin in NMDA-induced retinal injury acts by suppressing oxidative stress and excessive calpain activation. Scientific Reports. 7(1). 6885–6885. 53 indexed citations
8.
Sato, Kota, Koji M. Nishiguchi, Kazuichi Maruyama, et al.. (2016). Topical ocular dexamethasone decreases intraocular pressure and body weight in rats. Journal of Negative Results in BioMedicine. 15(1). 5–5. 14 indexed citations
9.
Kanemaru, Kazunori, Hiroshi Sekiya, Ming Xu, et al.. (2014). In Vivo Visualization of Subtle, Transient, and Local Activity of Astrocytes Using an Ultrasensitive Ca2+ Indicator. Cell Reports. 8(1). 311–318. 142 indexed citations
10.
Maruyama, Yuko, Kazuichi Maruyama, Yukinari Kato, et al.. (2014). The Effect of Podoplanin Inhibition on Lymphangiogenesis Under Pathological Conditions. Investigative Ophthalmology & Visual Science. 55(8). 4813–4813. 27 indexed citations
11.
Moritoh, Satoru, Yusuke Komatsu, Tetsuo Yamamori, & Amane Koizumi. (2013). Diversity of Retinal Ganglion Cells Identified by Transient GFP Transfection in Organotypic Tissue Culture of Adult Marmoset Monkey Retina. PLoS ONE. 8(1). e54667–e54667. 42 indexed citations
12.
Moritoh, Satoru, Chang‐Ho Eun, A. Ono, et al.. (2012). Targeted disruption of an orthologue of DOMAINS REARRANGED METHYLASE 2, OsDRM2 , impairs the growth of rice plants by abnormal DNA methylation. The Plant Journal. 71(1). 85–98. 100 indexed citations
13.
Moritoh, Satoru, Kaori Sato, Yasunobu Okada, & Amane Koizumi. (2011). Endogenous arginine vasopressin-positive retinal cells in arginine vasopressin-eGFP transgenic rats identified by immunohistochemistry and reverse transcriptase-polymerase chain reaction.. PubMed. 17. 3254–61. 10 indexed citations
14.
Moritoh, Satoru, et al.. (2010). Organotypic Tissue Culture of Adult Rodent Retina Followed by Particle-Mediated Acute Gene Transfer In Vitro. PLoS ONE. 5(9). e12917–e12917. 27 indexed citations
15.
Yamauchi, Takaki, Satoru Moritoh, Yasuyo Johzuka‐Hisatomi, et al.. (2008). Alternative splicing of the rice OsMET1 genes encoding maintenance DNA methyltransferase. Journal of Plant Physiology. 165(17). 1774–1782. 32 indexed citations
16.
Sugiyama, Shin, Satoru Moritoh, Yoshimi Furukawa, et al.. (2007). Involvement of the Mitochondrial Protein Translocator Component Tim50 in Growth, Cell Proliferation and the Modulation of Respiration in Drosophila. Genetics. 176(2). 927–936. 30 indexed citations
17.
Moritoh, Satoru, Daisuke Miki, Masahiro Akiyama, et al.. (2005). RNAi-mediated Silencing of OsGEN-L (OsGEN-like), a New Member of the RAD2/XPG Nuclease Family, Causes Male Sterility by Defect of Microspore Development in Rice. Plant and Cell Physiology. 46(5). 699–715. 60 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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