Mitsuhiro Aida

10.3k total citations · 3 hit papers
52 papers, 8.0k citations indexed

About

Mitsuhiro Aida is a scholar working on Plant Science, Molecular Biology and Biochemistry. According to data from OpenAlex, Mitsuhiro Aida has authored 52 papers receiving a total of 8.0k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Plant Science, 48 papers in Molecular Biology and 2 papers in Biochemistry. Recurrent topics in Mitsuhiro Aida's work include Plant Molecular Biology Research (49 papers), Plant Reproductive Biology (43 papers) and Plant Gene Expression Analysis (12 papers). Mitsuhiro Aida is often cited by papers focused on Plant Molecular Biology Research (49 papers), Plant Reproductive Biology (43 papers) and Plant Gene Expression Analysis (12 papers). Mitsuhiro Aida collaborates with scholars based in Japan, United States and Germany. Mitsuhiro Aida's co-authors include Masao Tasaka, Tetsuya Ishida, Hidehiro Fukaki, Renze Heidstra, Ikram Blilou, Ben Scheres, Viola Willemsen, H. Fujisawa, Marjolein Wildwater and Jiřı́ Friml and has published in prestigious journals such as Nature, Cell and Nature Communications.

In The Last Decade

Mitsuhiro Aida

50 papers receiving 7.9k citations

Hit Papers

The PIN auxin efflux facilitator network controls growth ... 1997 2026 2006 2016 2005 1997 2004 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mitsuhiro Aida Japan 32 7.6k 6.5k 270 157 98 52 8.0k
Steven E. Clark United States 35 8.0k 1.1× 6.8k 1.1× 386 1.4× 213 1.4× 84 0.9× 58 8.5k
Naomi Ori Israel 41 5.6k 0.7× 4.3k 0.7× 297 1.1× 130 0.8× 92 0.9× 63 6.1k
Robert Sablowski United Kingdom 37 4.6k 0.6× 4.2k 0.6× 260 1.0× 148 0.9× 79 0.8× 55 5.1k
Thomas Berleth Canada 29 4.8k 0.6× 4.6k 0.7× 261 1.0× 164 1.0× 107 1.1× 54 5.4k
John Paul Alvarez Australia 29 7.8k 1.0× 6.7k 1.0× 643 2.4× 362 2.3× 93 0.9× 37 8.2k
Gwyneth Ingram France 32 3.6k 0.5× 2.8k 0.4× 210 0.8× 159 1.0× 113 1.2× 72 3.9k
Ari Pekka Mähönen Finland 30 5.3k 0.7× 4.0k 0.6× 139 0.5× 69 0.4× 93 0.9× 52 5.6k
Rebecca Schwab Germany 20 5.8k 0.8× 4.4k 0.7× 142 0.5× 165 1.1× 27 0.3× 31 6.5k
Michael Sauer Germany 35 8.2k 1.1× 6.8k 1.1× 244 0.9× 157 1.0× 94 1.0× 54 8.8k
Cristina Ferrándiz Spain 37 5.3k 0.7× 4.4k 0.7× 383 1.4× 229 1.5× 33 0.3× 73 5.7k

Countries citing papers authored by Mitsuhiro Aida

Since Specialization
Citations

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

Fields of papers citing papers by Mitsuhiro Aida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitsuhiro Aida

This figure shows the co-authorship network connecting the top 25 collaborators of Mitsuhiro Aida. A scholar is included among the top collaborators of Mitsuhiro Aida 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 Mitsuhiro Aida. Mitsuhiro Aida 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.
Tameshige, Toshiaki, Takashi Tsuchida, Mitsuhiro Aida, et al.. (2025). Mutual inhibition between EPFL2 and auxin extends the intervals of periodic leaf morphogenesis. Nature Communications. 16(1). 9753–9753.
2.
Yamada, Mizuki, Shigeru Tanaka, Tatsuya Miyazaki, & Mitsuhiro Aida. (2021). Expression of the auxin biosynthetic genes <i>YUCCA1</i> and <i>YUCCA4</i> is dependent on the boundary regulators <i>CUP-SHAPED COTYLEDON</i> genes in the <i>Arabidopsis thaliana</i> embryo. Plant Biotechnology. 39(1). 37–42. 4 indexed citations
3.
Ikeda, Yoshihisa, et al.. (2021). Interpreting Cytokinin Action as Anterograde Signaling and Beyond. Frontiers in Plant Science. 12. 641257–641257. 8 indexed citations
4.
Sugimoto, Kaoru, Paul T. Tarr, Yayoi Inui, et al.. (2019). Primed histone demethylation regulates shoot regenerative competency. Nature Communications. 10(1). 1786–1786. 60 indexed citations
5.
Scofield, Simon, Angharad Jones, John Fozard, et al.. (2018). Coordination of meristem and boundary functions by transcription factors in the SHOOT MERISTEMLESS regulatory network. Development. 145(9). 47 indexed citations
6.
Tameshige, Toshiaki, Satoshi Okamoto, Jin‐Suk Lee, et al.. (2016). A Secreted Peptide and Its Receptors Shape the Auxin Response Pattern and Leaf Margin Morphogenesis. Current Biology. 26(18). 2478–2485. 61 indexed citations
7.
Hasegawa, Junko, Yuki Sakamoto, Satoru Nakagami, et al.. (2016). Three-Dimensional Imaging of Plant Organs Using a Simple and Rapid Transparency Technique. Plant and Cell Physiology. 57(3). 462–472. 73 indexed citations
8.
Landrein, Benoît, Annamária Kiss, Massimiliano Sassi, et al.. (2015). Mechanical stress contributes to the expression of the STM homeobox gene in Arabidopsis shoot meristems. eLife. 4. e07811–e07811. 126 indexed citations
9.
Burian, Agata, et al.. (2015). The CUP-SHAPED COTYLEDON2 and 3 genes have a post-meristematic effect on Arabidopsis thaliana phyllotaxis. Annals of Botany. 115(5). 807–820. 16 indexed citations
10.
Ikawa, Yasuhiro, et al.. (2015). Phenotypic Variants of Differentiation-Inducible Friend Leukemia Lines: Isolation and Correlation between Inducibility and Virus Release. Proceedings of the International Symposium on Comparative Leukemia Research. 37–47.
11.
Takeda, Seiji, Satoko Shimizu, Li Zhao, et al.. (2011). CUP‐SHAPED COTYLEDON1 transcription factor activates the expression of LSH4 and LSH3 , two members of the ALOG gene family, in shoot organ boundary cells. The Plant Journal. 66(6). 1066–1077. 107 indexed citations
12.
Niihama, Mitsuru, et al.. (2010). gorgon, a Novel Missense Mutation in the SHOOT MERISTEMLESS Gene, Impairs Shoot Meristem Homeostasis in Arabidopsis. Plant and Cell Physiology. 51(4). 621–634. 21 indexed citations
13.
Karim, Md. Rezaul, et al.. (2009). A Role forArabidopsis PUCHIin Floral Meristem Identity and Bract Suppression    . The Plant Cell. 21(5). 1360–1372. 74 indexed citations
14.
Tabata, Ryo, Masaya Ikezaki, Takahiro Fujibe, et al.. (2009). Arabidopsis AUXIN RESPONSE FACTOR6 and 8 Regulate Jasmonic Acid Biosynthesis and Floral Organ Development via Repression of Class 1 KNOX Genes. Plant and Cell Physiology. 51(1). 164–175. 180 indexed citations
15.
Konishi, Mineko, et al.. (2008). Identification of novel meristem factors involved in shoot regeneration through the analysis of temperature‐sensitive mutants of Arabidopsis. The Plant Journal. 57(6). 1027–1039. 37 indexed citations
16.
Hibara, Ken‐ichiro, Md. Rezaul Karim, Shinobu Takada, et al.. (2006). Arabidopsis CUP-SHAPED COTYLEDON3 Regulates Postembryonic Shoot Meristem and Organ Boundary Formation. The Plant Cell. 18(11). 2946–2957. 292 indexed citations
17.
Nikovics, Krisztina, Thomas Blein, Alexis Peaucelle, et al.. (2006). The Balance between the MIR164A and CUC2 Genes Controls Leaf Margin Serration in Arabidopsis. The Plant Cell. 18(11). 2929–2945. 477 indexed citations
18.
Aida, Mitsuhiro, Dimitris Beis, Renze Heidstra, et al.. (2004). The PLETHORA Genes Mediate Patterning of the Arabidopsis Root Stem Cell Niche. Cell. 119(1). 109–120. 919 indexed citations breakdown →
19.
Taoka, Ken‐ichiro, et al.. (2004). The NAC domain mediates functional specificity of CUP‐SHAPED COTYLEDON proteins. The Plant Journal. 40(4). 462–473. 68 indexed citations
20.
Ishida, Tetsuya, Mitsuhiro Aida, Shinobu Takada, & Masao Tasaka. (2000). Involvement of CUP-SHAPED COTYLEDON Genes in Gynoecium and Ovule Development in Arabidopsis thaliana. Plant and Cell Physiology. 41(1). 60–67. 114 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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