Natsuko Kumamoto

1.2k total citations
28 papers, 935 citations indexed

About

Natsuko Kumamoto is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Natsuko Kumamoto has authored 28 papers receiving a total of 935 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 7 papers in Genetics. Recurrent topics in Natsuko Kumamoto's work include Receptor Mechanisms and Signaling (7 papers), Phosphodiesterase function and regulation (7 papers) and Neuropeptides and Animal Physiology (6 papers). Natsuko Kumamoto is often cited by papers focused on Receptor Mechanisms and Signaling (7 papers), Phosphodiesterase function and regulation (7 papers) and Neuropeptides and Animal Physiology (6 papers). Natsuko Kumamoto collaborates with scholars based in Japan, United States and Vietnam. Natsuko Kumamoto's co-authors include Shinsuke Matsuzaki, Taiichi Katayama, Tsuyoshi Hattori, Masaya Tohyama, Yan Gu, Joel M. Levine, Ken‐Ichi Takemaru, Shaoyu Ge, Shoko Shimizu and Ryota Hashimoto and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and Nature Neuroscience.

In The Last Decade

Natsuko Kumamoto

27 papers receiving 925 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Natsuko Kumamoto Japan 17 487 387 271 135 124 28 935
Elaine C. Budreck United States 10 376 0.8× 475 1.2× 154 0.6× 106 0.8× 156 1.3× 10 835
Parizad M. Bilimoria United States 12 554 1.1× 299 0.8× 142 0.5× 130 1.0× 69 0.6× 13 1.0k
James Gilbert United States 15 559 1.1× 343 0.9× 305 1.1× 107 0.8× 249 2.0× 18 1.1k
Martijn P. J. Dekkers Switzerland 11 426 0.9× 362 0.9× 207 0.8× 212 1.6× 116 0.9× 18 943
Eleonora Calcagno Italy 21 649 1.3× 702 1.8× 446 1.6× 87 0.6× 270 2.2× 25 1.4k
Toshihiro Nomura United States 17 440 0.9× 457 1.2× 206 0.8× 84 0.6× 221 1.8× 28 859
Mamoru Fukuchi Japan 19 518 1.1× 482 1.2× 153 0.6× 157 1.2× 122 1.0× 56 1.0k
Sophie Reibel France 18 377 0.8× 677 1.7× 116 0.4× 266 2.0× 108 0.9× 25 1.1k
Hideo Hagihara Japan 19 530 1.1× 437 1.1× 153 0.6× 263 1.9× 155 1.3× 43 1.2k

Countries citing papers authored by Natsuko Kumamoto

Since Specialization
Citations

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

Fields of papers citing papers by Natsuko Kumamoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natsuko Kumamoto

This figure shows the co-authorship network connecting the top 25 collaborators of Natsuko Kumamoto. A scholar is included among the top collaborators of Natsuko Kumamoto 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 Natsuko Kumamoto. Natsuko Kumamoto 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.
Kanemitsu, Yoshihiro, Takashi Ueda, Takeshi Kamiya, et al.. (2024). Comorbid functional dyspepsia reflects IL-33–mediated airway neuronal dysfunction in asthma. Journal of Allergy and Clinical Immunology. 154(6). 1422–1433. 4 indexed citations
2.
Yamamoto, Takashi, et al.. (2024). GPRC6A as a novel kokumi receptor responsible for enhanced taste preferences by ornithine. eLife. 13. 2 indexed citations
3.
Kumamoto, Natsuko, et al.. (2021). Additive Effects of L-Ornithine on Preferences to Basic Taste Solutions in Mice. Nutrients. 13(11). 3749–3749. 12 indexed citations
4.
Ieda, Daisuke, Yutaka Negishi, Tomomi Miyamoto, et al.. (2020). Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes. PLoS ONE. 15(8). e0237814–e0237814. 7 indexed citations
5.
Sawada, Masato, Mami Matsumoto, Keishi Narita, et al.. (2020). In vitro Time-lapse Imaging of Primary Cilium in Migrating Neuroblasts. BIO-PROTOCOL. 10(22). e3823–e3823. 3 indexed citations
6.
Matsumoto, Mami, Masato Sawada, Diego García‐González, et al.. (2019). Dynamic Changes in Ultrastructure of the Primary Cilium in Migrating Neuroblasts in the Postnatal Brain. Journal of Neuroscience. 39(50). 9967–9988. 37 indexed citations
7.
Kato, Atsuko, Hironori Hojo, Yasuyuki Shibata, et al.. (2017). Distribution of ASIC4 transcripts in the adult wild-type mouse brain. Neuroscience Letters. 651. 57–64. 12 indexed citations
8.
Watanabe, Masaya, Takashi Ueda, Yasuhiro Shibata, Natsuko Kumamoto, & Shinya Ugawa. (2015). The role of TRPV1 channels in carrageenan-induced mechanical hyperalgesia in mice. Neuroreport. 26(3). 173–178. 28 indexed citations
9.
Ueda, Takashi, et al.. (2015). Basal cells express functional TRPV4 channels in the mouse nasal epithelium. Biochemistry and Biophysics Reports. 4. 169–174. 4 indexed citations
10.
Miyoshi, Ko, Shinki Murakami, Mika Takeshima, et al.. (2014). Lack of Dopaminergic Inputs Elongates the Primary Cilia of Striatal Neurons. PLoS ONE. 9(5). e97918–e97918. 39 indexed citations
11.
Koyama, Yoshihisa, Tsuyoshi Hattori, Shoko Shimizu, et al.. (2013). DBZ (DISC1-binding zinc finger protein)-deficient mice display abnormalities in basket cells in the somatosensory cortices. Journal of Chemical Neuroanatomy. 53. 1–10. 19 indexed citations
12.
Ishikawa, Toru, Shingo Miyata, Yoshihisa Koyama, et al.. (2012). Transient expression of Xpn, an XLMR protein related to neurite extension, during brain development and participation in neurite outgrowth. Neuroscience. 214. 181–191. 25 indexed citations
13.
Kumamoto, Natsuko, et al.. (2012). A role for primary cilia in glutamatergic synaptic integration of adult-born neurons. SHILAP Revista de lepidopterología. 1(S1). 60 indexed citations
14.
Hattori, Tsuyoshi, Shoko Shimizu, Yoshihisa Koyama, et al.. (2010). DISC1 regulates cell–cell adhesion, cell–matrix adhesion and neurite outgrowth. Molecular Psychiatry. 15(8). 798–809. 44 indexed citations
15.
Yamada, Kohei, Shinsuke Matsuzaki, Tsuyoshi Hattori, et al.. (2010). Increased Stathmin1 Expression in the Dentate Gyrus of Mice Causes Abnormal Axonal Arborizations. PLoS ONE. 5(1). e8596–e8596. 50 indexed citations
16.
Hattori, Tsuyoshi, Yoshihisa Koyama, Kenneth M. Yamada, et al.. (2010). DISC1 regulates N-cadherin and β1-integrin expression in neurons. Molecular Psychiatry. 15(8). 778–778. 10 indexed citations
17.
Kubota, Kyoko, Kiyoshi Inoue, Ryota Hashimoto, et al.. (2009). Tumor necrosis factor receptor‐associated protein 1 regulates cell adhesion and synaptic morphology via modulation of N‐cadherin expression. Journal of Neurochemistry. 110(2). 496–508. 43 indexed citations
18.
Shimizu, Shoko, Shinsuke Matsuzaki, Tsuyoshi Hattori, et al.. (2008). DISC1–kendrin interaction is involved in centrosomal microtubule network formation. Biochemical and Biophysical Research Communications. 377(4). 1051–1056. 28 indexed citations
19.
Kubota, Kyoko, Natsuko Kumamoto, Shinsuke Matsuzaki, et al.. (2008). Dysbindin engages in c-Jun N-terminal kinase activity and cytoskeletal organization. Biochemical and Biophysical Research Communications. 379(2). 191–195. 36 indexed citations
20.
Hattori, Satoko, Tomotaka Murotani, Shinsuke Matsuzaki, et al.. (2008). Behavioral abnormalities and dopamine reductions in sdy mutant mice with a deletion in Dtnbp1, a susceptibility gene for schizophrenia. Biochemical and Biophysical Research Communications. 373(2). 298–302. 77 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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