Toshimitsu Fuse

982 total citations
9 papers, 689 citations indexed

About

Toshimitsu Fuse is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Toshimitsu Fuse has authored 9 papers receiving a total of 689 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Toshimitsu Fuse's work include Stress Responses and Cortisol (2 papers), Neuroendocrine regulation and behavior (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Toshimitsu Fuse is often cited by papers focused on Stress Responses and Cortisol (2 papers), Neuroendocrine regulation and behavior (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Toshimitsu Fuse collaborates with scholars based in Japan and United States. Toshimitsu Fuse's co-authors include Haruhiko Bito, Mikio Hoshino, Masahiko Watanabe, Yo-ichi Nabeshima, Yoshiya Kawaguchi, Christopher V.E. Wright, Toshio Terashima, Shoko Nakamura, Mami Terao and Akihisa Fukuda and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Journal of Neuroscience.

In The Last Decade

Toshimitsu Fuse

9 papers receiving 681 citations

Peers

Toshimitsu Fuse

CMN

GENET

Theo Schouten Netherlands

Lisa A. Ehrman United States

José Luis Nieto-González Spain

Alfredo Cabrera‐Socorro Belgium

Hans Lipp Switzerland

DM Chikaraishi United States

Margarethe Bittins Norway

Lawrence T. O’Connor United States

Susanne C. Bleckmann Germany

Tanya Nekrasova United States

Theo Schouten Netherlands

Toshimitsu Fuse

375 ×0.9

174 ×0.7

CMN

188 ×1.1

97 ×1.1

120 ×1.4

GENET

Citations per year, relative to Toshimitsu Fuse Toshimitsu Fuse (= 1×) peers Theo Schouten

Countries citing papers authored by Toshimitsu Fuse

Since Specialization

Citations

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

Fields of papers citing papers by Toshimitsu Fuse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toshimitsu Fuse

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

All Works

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9 of 9 papers shown

Uchida, Katsuya, et al.. (2021). Thyroid hormone insufficiency alters the expression of psychiatric disorder-related molecules in the hypothyroid mouse brain during the early postnatal period. Scientific Reports. 11(1). 6723–6723. 13 indexed citations

Konno, Kohtarou, Toshimitsu Fuse, Manabu Abe, et al.. (2016). Distribution of corticotropin-releasing factor neurons in the mouse brain: a study using corticotropin-releasing factor-modified yellow fluorescent protein knock-in mouse. Brain Structure and Function. 222(4). 1705–1732. 46 indexed citations

Itoi, Keiichi, Toshimitsu Fuse, Ryo Ozawa, et al.. (2014). Visualization of Corticotropin-Releasing Factor Neurons by Fluorescent Proteins in the Mouse Brain and Characterization of Labeled Neurons in the Paraventricular Nucleus of the Hypothalamus. Endocrinology. 155(10). 4054–4060. 32 indexed citations

Itoi, Keiichi, Naoya Sugimoto, Keisuke Sawada, et al.. (2011). Targeting of Locus Ceruleus Noradrenergic Neurons Expressing Human Interleukin-2 Receptor α-Subunit in Transgenic Mice by a Recombinant Immunotoxin anti-Tac(Fv)-PE38: A Study for Exploring Noradrenergic Influence upon Anxiety-Like and Depression-Like Behaviors. Journal of Neuroscience. 31(16). 6132–6139. 18 indexed citations

Takemoto‐Kimura, Sayaka, Natsumi Ageta‐Ishihara, Mio Nonaka, et al.. (2007). Regulation of Dendritogenesis via a Lipid-Raft-Associated Ca2+/Calmodulin-Dependent Protein Kinase CLICK-III/CaMKIγ. Neuron. 54(5). 755–770. 104 indexed citations

Ohmae, Shogo, Sayaka Takemoto‐Kimura, Michiko Okamura, et al.. (2006). Molecular Identification and Characterization of a Family of Kinases with Homology to Ca2+/Calmodulin-dependent Protein Kinases I/IV. Journal of Biological Chemistry. 281(29). 20427–20439. 29 indexed citations

Hoshino, Mikio, Shoko Nakamura, Kiyoshi Mori, et al.. (2005). Ptf1a, a bHLH Transcriptional Gene, Defines GABAergic Neuronal Fates in Cerebellum. Neuron. 47(2). 201–213. 364 indexed citations

Fuse, Toshimitsu, Yoshiakira Kanai, Masami Kanai‐Azuma, et al.. (2004). Conditional activation of RhoA suppresses the epithelial to mesenchymal transition at the primitive streak during mouse gastrulation. Biochemical and Biophysical Research Communications. 318(3). 665–672. 28 indexed citations

Takeuchi, Tomonori, Mika Tsujita, Misao Suzuki, et al.. (2002). Flp recombinase transgenic mice of C57BL/6 strain for conditional gene targeting. Biochemical and Biophysical Research Communications. 293(3). 953–957. 55 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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