Ritsuko Katoh‐Semba

4.0k total citations
87 papers, 3.4k citations indexed

About

Ritsuko Katoh‐Semba is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Developmental Neuroscience. According to data from OpenAlex, Ritsuko Katoh‐Semba has authored 87 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Cellular and Molecular Neuroscience, 39 papers in Molecular Biology and 31 papers in Developmental Neuroscience. Recurrent topics in Ritsuko Katoh‐Semba's work include Nerve injury and regeneration (37 papers), Neurogenesis and neuroplasticity mechanisms (31 papers) and Glycosylation and Glycoproteins Research (16 papers). Ritsuko Katoh‐Semba is often cited by papers focused on Nerve injury and regeneration (37 papers), Neurogenesis and neuroplasticity mechanisms (31 papers) and Glycosylation and Glycoproteins Research (16 papers). Ritsuko Katoh‐Semba collaborates with scholars based in Japan, United States and Poland. Ritsuko Katoh‐Semba's co-authors include Reiji Semba, Ikuo Takeuchi, Kanefusa Kato, Akihiko Oohira, F. Matsui, Stephen D. Skaper, Silvio Varon, Shigeo Kashiwamata, Teiichi Furuichi and Tetsushi Sadakata and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Ritsuko Katoh‐Semba

86 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ritsuko Katoh‐Semba Japan	29	1.9k	1.4k	959	771	366	87	3.4k
Jessica A. Gorski United States	19	2.0k 1.1×	2.0k 1.4×	1.1k 1.1×	541 0.7×	390 1.1×	23	4.1k
Albert Martı́nez Spain	31	2.0k 1.0×	1.3k 0.9×	1.3k 1.3×	308 0.4×	403 1.1×	50	3.2k
Pradeep G. Bhide United States	39	2.2k 1.1×	2.3k 1.6×	1.1k 1.1×	446 0.6×	469 1.3×	112	4.8k
Sophia A. Colamarino United States	8	2.3k 1.2×	2.0k 1.4×	1.9k 2.0×	567 0.7×	377 1.0×	8	4.0k
Gustavo Paratcha Argentina	30	2.0k 1.1×	1.3k 0.9×	982 1.0×	273 0.4×	470 1.3×	55	3.2k
Deanna L. Benson United States	40	3.5k 1.9×	2.7k 1.9×	788 0.8×	1.1k 1.4×	683 1.9×	96	5.3k
Riccardo Brambilla Italy	37	2.5k 1.3×	2.8k 2.0×	628 0.7×	649 0.8×	534 1.5×	75	5.0k
Kurt Gottmann Germany	30	3.1k 1.6×	2.0k 1.4×	922 1.0×	569 0.7×	807 2.2×	70	4.5k
Serge Marty France	25	1.9k 1.0×	983 0.7×	834 0.9×	447 0.6×	348 1.0×	38	2.7k
Virginia M. Tennyson United States	29	2.3k 1.2×	1.7k 1.2×	651 0.7×	635 0.8×	411 1.1×	48	4.6k

Countries citing papers authored by Ritsuko Katoh‐Semba

Since Specialization

Citations

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

Fields of papers citing papers by Ritsuko Katoh‐Semba

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ritsuko Katoh‐Semba. 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 Ritsuko Katoh‐Semba. The network helps show where Ritsuko Katoh‐Semba may publish in the future.

Co-authorship network of co-authors of Ritsuko Katoh‐Semba

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

All Works

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20 of 20 papers shown

Shinoda, Yo, Tetsushi Sadakata, Emi Kinameri, et al.. (2018). Aspects of excitatory/inhibitory synapses in multiple brain regions are correlated with levels of brain-derived neurotrophic factor/neurotrophin-3. Biochemical and Biophysical Research Communications. 509(2). 429–434. 5 indexed citations

Mizuno, Shota, Ritsuko Katoh‐Semba, Tetsushi Sadakata, et al.. (2017). CAPS2 deficiency affects environmental enrichment-induced adult neurogenesis and differentiation/survival of newborn neurons in the hippocampal dentate gyrus. Neuroscience Letters. 661. 121–125. 7 indexed citations

Adachi, Naoki, Tadahiro Numakawa, Emi Kumamaru, et al.. (2012). Phencyclidine-Induced Decrease of Synaptic Connectivity via Inhibition of BDNF Secretion in Cultured Cortical Neurons. Cerebral Cortex. 23(4). 847–858. 31 indexed citations

Miyazaki, Noriko, Kaori Sudo, Motoko Matsuda, et al.. (2011). Phase Advance of the Light-Dark Cycle Perturbs Diurnal Rhythms of Brain-derived Neurotrophic Factor and Neurotrophin-3 Protein Levels, Which Reduces Synaptophysin-positive Presynaptic Terminals in the Cortex of Juvenile Rats. Journal of Biological Chemistry. 286(24). 21478–21487. 14 indexed citations

Katoh‐Semba, Ritsuko, Satoko Kitajima, Masako Tsuzuki, et al.. (2009). Activation of p38 mitogen-activated protein kinase is required for in vivo brain-derived neurotrophic factor production in the rat hippocampus. Neuroscience. 163(1). 352–361. 25 indexed citations

Ito, Hidenori, Kimie Atsuzawa, Rika Morishita, et al.. (2008). Sept8 controls the binding of vesicle‐associated membrane protein 2 to synaptophysin. Journal of Neurochemistry. 108(4). 867–880. 48 indexed citations

Katoh‐Semba, Ritsuko, Masako Tsuzuki, Noriko Miyazaki, et al.. (2007). Distribution and immunohistochemical localization of GDNF protein in selected neural and non-neural tissues of rats during development and changes in unilateral 6-hydroxydopamine lesions. Neuroscience Research. 59(3). 277–287. 22 indexed citations

Sadakata, Tetsushi, Miwa Washida, Yoshimi Iwayama, et al.. (2007). Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients. Journal of Clinical Investigation. 117(4). 931–943. 146 indexed citations

Ito, Hidenori, Nobuteru Usuda, Kimie Atsuzawa, et al.. (2006). Phosphorylation by extracellular signal‐regulated kinase of a multidomain adaptor protein, vinexin, at synapses. Journal of Neurochemistry. 100(2). 545–554. 19 indexed citations

10.

Katoh‐Semba, Ritsuko, Satoshi Ichisaka, Yoshio Hata, et al.. (2003). NT‐4 protein is localized in neuronal cells in the brain stem as well as the dorsal root ganglion of embryonic and adult rats. Journal of Neurochemistry. 86(3). 660–668. 9 indexed citations

11.

Asano, Tomiko, Haruo Shinohara, Rika Morishita, et al.. (2001). Selective localization of G protein γ₅ subunit in the subventricular zone of the lateral ventricle and rostral migratory stream of the adult rat brain. Journal of Neurochemistry. 79(6). 1129–1135. 12 indexed citations

12.

Katoh‐Semba, Ritsuko, Ikuo Takeuchi, Yutaka Inaguma, Hidenori Ito, & Kanefusa Kato. (1999). Brain-derived neurotrophic factor, nerve growth factor and neurotrophin-3 in selected regions of the rat brain following kainic acid-induced seizure activity. Neuroscience Research. 35(1). 19–29. 54 indexed citations

13.

Katoh‐Semba, Ritsuko, Reiji Semba, Ikuo Takeuchi, & Kanefusa Kato. (1998). Age-related changes in levels of brain-derived neurotrophic factor in selected brain regions of rats, normal mice and senescence-accelerated mice: a comparison to those of nerve growth factor and neurotrophin-3. Neuroscience Research. 31(3). 227–234. 142 indexed citations

14.

Matsuda, Motoko, Ritsuko Katoh‐Semba, Hiroshi Kitani, & Yasuhiro Tomooka. (1996). A possible role of the nestin protein in the developing central nervous system in rat embryos. Brain Research. 723(1-2). 177–189. 25 indexed citations

15.

Katoh‐Semba, Ritsuko, Reiji Semba, Hiroyuki Kato, et al.. (1994). Regulation by Androgen of Levels of the β Subunit of Nerve Growth Factor and Its mRNA in Selected Regions of the Mouse Brain. Journal of Neurochemistry. 62(6). 2141–2147. 30 indexed citations

16.

Katoh‐Semba, Ritsuko & Atsuhiko Oohira. (1993). Core proteins of soluble chondroitin sulfate proteoglycans purified from the rat brain block the cell cycle of PC12D cells. Journal of Cellular Physiology. 156(1). 17–23. 20 indexed citations

17.

Yoshino, Hiide, et al.. (1993). Activation of UDP-galactose:globotriaosylceramide .alpha.1-3-galactosyltransferase during PC12D cell differentiation induced by galactosyl ceramides. Biochemistry. 32(31). 7904–7908. 5 indexed citations

18.

Katoh‐Semba, Ritsuko, Reiji Semba, Shigeo Kashiwamata, & Kanefusa Kato. (1993). An acceleration of age-related increases in levels of the β-subunit of nerve growth factor in selected tissues from senescence-accelerated mice (SAM-P/8). Journal of Molecular Neuroscience. 4(2). 107–115. 4 indexed citations

19.

Watanabe, Kimi, Atsuhiko Oohira, Ritsuko Katoh‐Semba, Tsuyoshi Totsuka, & Keiichi Yoshida. (1989). Sulfated proteoglycans synthesized by Neuro 2a neuroblastoma cells: Comparison between cells with and without ganglioside-induced neurites. Neurochemical Research. 14(8). 707–716. 8 indexed citations

20.

Sano, Mamoru, Kanefusa Kato, Tsuyoshi Totsuka, & Ritsuko Katoh‐Semba. (1988). A convenient bioassay for NGF using a new subline of PC12 pheochromocytoma cells (PC12D). Brain Research. 459(2). 404–406. 21 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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