Ryota Kunita

759 total citations
14 papers, 612 citations indexed

About

Ryota Kunita is a scholar working on Cell Biology, Molecular Biology and Neurology. According to data from OpenAlex, Ryota Kunita has authored 14 papers receiving a total of 612 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cell Biology, 6 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in Ryota Kunita's work include Cellular transport and secretion (8 papers), Microtubule and mitosis dynamics (5 papers) and Amyotrophic Lateral Sclerosis Research (3 papers). Ryota Kunita is often cited by papers focused on Cellular transport and secretion (8 papers), Microtubule and mitosis dynamics (5 papers) and Amyotrophic Lateral Sclerosis Research (3 papers). Ryota Kunita collaborates with scholars based in Japan, Canada and United Kingdom. Ryota Kunita's co-authors include Asako Otomo, Shinji Hadano, Joh‐E Ikeda, Kyoko Suzuki-Utsunomiya, Hikaru Mizumura, Shigeki Mizuno, Yoshiko Yanagisawa, Junko Showguchi-Miyata, Shigeru Kakuta and Joh-E Ikeda and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Biochemical and Biophysical Research Communications.

In The Last Decade

Ryota Kunita

14 papers receiving 598 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ryota Kunita Japan 13 305 240 171 147 100 14 612
Junko Showguchi-Miyata Japan 5 430 1.4× 266 1.1× 108 0.6× 285 1.9× 130 1.3× 5 636
Minako Tateno Japan 9 303 1.0× 421 1.8× 81 0.5× 137 0.9× 106 1.1× 12 785
Matthew D. Figley United States 10 230 0.8× 429 1.8× 103 0.6× 90 0.6× 102 1.0× 12 680
Andrea Chai United Kingdom 7 205 0.7× 180 0.8× 112 0.7× 99 0.7× 67 0.7× 8 600
Jennifer Lévy United States 10 142 0.5× 415 1.7× 269 1.6× 89 0.6× 103 1.0× 11 619
Anna Birve Sweden 14 311 1.0× 411 1.7× 58 0.3× 186 1.3× 64 0.6× 20 729
Thomas A. Kwiatkowski United States 5 389 1.3× 235 1.0× 81 0.5× 258 1.8× 109 1.1× 6 606
Yasuhide Hayashi Japan 9 140 0.5× 374 1.6× 249 1.5× 68 0.5× 288 2.9× 9 741
Pippa A. Radcliffe United Kingdom 10 199 0.7× 761 3.2× 205 1.2× 168 1.1× 74 0.7× 12 955

Countries citing papers authored by Ryota Kunita

Since Specialization
Citations

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

Fields of papers citing papers by Ryota Kunita

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryota Kunita

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

All Works

14 of 14 papers shown
1.
Otomo, Asako, Ryota Kunita, Kyoko Suzuki-Utsunomiya, Joh‐E Ikeda, & Shinji Hadano. (2011). Defective relocalization of ALS2/alsin missense mutants to Rac1-induced macropinosomes accounts for loss of their cellular function and leads to disturbed amphisome formation. FEBS Letters. 585(5). 730–736. 36 indexed citations
2.
Hadano, Shinji, Asako Otomo, Ryota Kunita, et al.. (2010). Loss of ALS2/Alsin Exacerbates Motor Dysfunction in a SOD1H46R-Expressing Mouse ALS Model by Disturbing Endolysosomal Trafficking. PLoS ONE. 5(3). e9805–e9805. 88 indexed citations
3.
Hadano, Shinji, Yasuhiro Yoshii, Asako Otomo, et al.. (2010). Genetic background and gender effects on gross phenotypes in congenic lines of ALS2/alsin-deficient mice. Neuroscience Research. 68(2). 131–136. 12 indexed citations
4.
Otomo, Asako, Ryota Kunita, Kyoko Suzuki-Utsunomiya, et al.. (2008). ALS2/alsin deficiency in neurons leads to mild defects in macropinocytosis and axonal growth. Biochemical and Biophysical Research Communications. 370(1). 87–92. 34 indexed citations
5.
Suzuki-Utsunomiya, Kyoko, Shinji Hadano, Asako Otomo, et al.. (2007). ALS2CL, a novel ALS2-interactor, modulates ALS2-mediated endosome dynamics. Biochemical and Biophysical Research Communications. 354(2). 491–497. 22 indexed citations
6.
Kunita, Ryota, Asako Otomo, Hikaru Mizumura, et al.. (2007). The Rab5 Activator ALS2/alsin Acts as a Novel Rac1 Effector through Rac1-activated Endocytosis. Journal of Biological Chemistry. 282(22). 16599–16611. 65 indexed citations
7.
Hadano, Shinji, Ryota Kunita, Asako Otomo, Kyoko Suzuki-Utsunomiya, & Joh‐E Ikeda. (2007). Molecular and cellular function of ALS2/alsin: Implication of membrane dynamics in neuronal development and degeneration. Neurochemistry International. 51(2-4). 74–84. 68 indexed citations
8.
Hadano, Shinji, Susanna C. Benn, Shigeru Kakuta, et al.. (2005). Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking. Human Molecular Genetics. 15(2). 233–250. 109 indexed citations
9.
Kunita, Ryota, Asako Otomo, Hikaru Mizumura, et al.. (2004). Homo-oligomerization of ALS2 through Its Unique Carboxyl-terminal Regions Is Essential for the ALS2-associated Rab5 Guanine Nucleotide Exchange Activity and Its Regulatory Function on Endosome Trafficking. Journal of Biological Chemistry. 279(37). 38626–38635. 55 indexed citations
10.
Hadano, Shinji, Asako Otomo, Kyoko Suzuki-Utsunomiya, et al.. (2004). ALS2CL, the novel protein highly homologous to the carboxy‐terminal half of ALS2, binds to Rab5 and modulates endosome dynamics. FEBS Letters. 575(1-3). 64–70. 36 indexed citations
11.
Kunita, Ryota, Asako Otomo, & Joh‐E Ikeda. (2002). Identification and Characterization of Novel Members of the CREG Family, Putative Secreted Glycoproteins Expressed Specifically in Brain. Genomics. 80(5). 456–460. 16 indexed citations
12.
Kunita, Ryota, Osamu Nakabayashi, Shigeki Mizuno, & Tateki Kikuchi. (1997). Predominant expression of a Z-chromosome-linked immunoglobulin superfamily gene, ZOV3, in steroidogenic cells of ovarian follicles and in embryonic gonads of chickens. Differentiation. 62(2). 63–70. 16 indexed citations
13.
Kunita, Ryota, Osamu Nakabayashi, Jer‐Yuarn Wu, et al.. (1997). Molecular cloning of acid α-glucosidase cDNA of Japanese quail (Coturnix coturnix japonica) and the lack of its mRNA in acid maltase deficient quails. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1362(2-3). 269–278. 12 indexed citations
14.
Saitoh, Yasushi, Akira Ogawa, Tetsuya Hori, Ryota Kunita, & Shigeki Mizuno. (1993). Identification and localization of two genes on the chicken Z chromosome: implication of evolutionary conservation of the Z chromosome among avian species. Chromosome Research. 1(4). 239–251. 43 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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