Maho Tanaka

6.2k total citations · 1 hit paper
76 papers, 4.2k citations indexed

About

Maho Tanaka is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Maho Tanaka has authored 76 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Plant Science, 46 papers in Molecular Biology and 8 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Maho Tanaka's work include Plant Molecular Biology Research (43 papers), Plant Stress Responses and Tolerance (27 papers) and Photosynthetic Processes and Mechanisms (13 papers). Maho Tanaka is often cited by papers focused on Plant Molecular Biology Research (43 papers), Plant Stress Responses and Tolerance (27 papers) and Photosynthetic Processes and Mechanisms (13 papers). Maho Tanaka collaborates with scholars based in Japan, United States and Vietnam. Maho Tanaka's co-authors include Motoaki Seki, Kazuo Shinozaki, Akihiro Matsui, Lam‐Son Phan Tran, Yasuko Watanabe, Rie Nishiyama, Chien Van Ha, Kazuko Yamaguchi‐Shinozaki, Luís Herrera‐Estrella and Marco Antonio Leyva‐González and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and PLoS ONE.

In The Last Decade

Maho Tanaka

76 papers receiving 4.2k citations

Hit Papers

Positive regulatory role ... 2013 2026 2017 2021 2013 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maho Tanaka Japan 36 3.6k 2.0k 534 93 87 76 4.2k
Yuri Kanno Japan 33 2.9k 0.8× 1.6k 0.8× 261 0.5× 148 1.6× 74 0.9× 53 3.5k
Ming‐Tsair Chan Taiwan 37 3.1k 0.9× 2.7k 1.3× 498 0.9× 64 0.7× 127 1.5× 73 4.1k
Hye Ryun Woo South Korea 27 4.1k 1.1× 3.2k 1.6× 212 0.4× 97 1.0× 133 1.5× 45 4.5k
Stefan de Folter Mexico 39 5.6k 1.5× 4.5k 2.2× 341 0.6× 73 0.8× 197 2.3× 129 6.2k
Richard G. H. Immink Netherlands 44 6.0k 1.7× 5.2k 2.5× 428 0.8× 154 1.7× 230 2.6× 87 6.8k
Punita Nagpal United States 20 4.8k 1.3× 3.7k 1.8× 230 0.4× 119 1.3× 142 1.6× 29 5.2k
Rie Nishiyama Japan 22 2.4k 0.7× 1.3k 0.6× 433 0.8× 32 0.3× 150 1.7× 26 2.8k
Hong‐Quan Yang China 40 5.5k 1.5× 3.9k 1.9× 265 0.5× 74 0.8× 105 1.2× 70 6.0k
Xingliang Hou China 28 3.3k 0.9× 2.1k 1.0× 161 0.3× 279 3.0× 86 1.0× 51 3.9k
Guiling Sun China 27 1.5k 0.4× 1.2k 0.6× 287 0.5× 175 1.9× 121 1.4× 55 2.3k

Countries citing papers authored by Maho Tanaka

Since Specialization
Citations

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

Fields of papers citing papers by Maho Tanaka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maho Tanaka

This figure shows the co-authorship network connecting the top 25 collaborators of Maho Tanaka. A scholar is included among the top collaborators of Maho Tanaka 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 Maho Tanaka. Maho Tanaka 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.
Sulieman, Saad, Chien Van Ha, Dung Tien Le, et al.. (2024). Comparative transcriptome analysis of respiration-related genes in nodules of phosphate-deficient soybean (Glycine max cv. Williams 82). Plant Stress. 11. 100368–100368. 1 indexed citations
2.
Ha, Chien Van, Mohammad Golam Mostofa, Kien Huu Nguyen, et al.. (2022). The histidine phosphotransfer AHP4 plays a negative role in Arabidopsis plant response to drought. The Plant Journal. 111(6). 1732–1752. 14 indexed citations
3.
Kim, Jong-Myong, Imma Pérez‐Salamó, Taiko Kim To, et al.. (2022). Jasmonates and Histone deacetylase 6 activate Arabidopsis genome-wide histone acetylation and methylation during the early acute stress response. BMC Biology. 20(1). 83–83. 14 indexed citations
4.
Watanabe, Yasuko, Kien Huu Nguyen, Cuong Duy Tran, et al.. (2022). SUPPRESSOR of MAX2 1 (SMAX1) and SMAX1-LIKE2 (SMXL2) Negatively Regulate Drought Resistance in Arabidopsis thaliana. Plant and Cell Physiology. 63(12). 1900–1913. 21 indexed citations
5.
Sakamoto, Takuya, Yuki Sakamoto, Stefan Grob, et al.. (2022). Two-step regulation of centromere distribution by condensin II and the nuclear envelope proteins. Nature Plants. 8(8). 940–953. 18 indexed citations
6.
Utsumi, Yoshinori, Chikako Utsumi, Maho Tanaka, et al.. (2022). Ethanol treatment enhances drought stress avoidance in cassava (Manihot esculenta Crantz). Plant Molecular Biology. 110(3). 269–285. 8 indexed citations
7.
Bashir, Khurram, Akihiro Matsui, Maho Tanaka, et al.. (2021). Overexpression of nicotinamidase 3 (NIC3) gene and the exogenous application of nicotinic acid (NA) enhance drought tolerance and increase biomass in Arabidopsis. Plant Molecular Biology. 107(1-2). 63–84. 22 indexed citations
8.
Utsumi, Yoshinori, Chikako Utsumi, Maho Tanaka, et al.. (2021). Agrobacterium-mediated cassava transformation for the Asian elite variety KU50. Plant Molecular Biology. 109(3). 271–282. 4 indexed citations
9.
Sako, Kaori, Yushi Futamura, Takeshi Shimizu, et al.. (2020). Inhibition of mitochondrial complex I by the novel compound FSL0260 enhances high salinity-stress tolerance in Arabidopsis thaliana. Scientific Reports. 10(1). 8691–8691. 14 indexed citations
10.
Sakamoto, Kazunori, Mitsuru Ueno, Masatoshi Sonoda, et al.. (2019). Transcriptome analysis of soybean (Glycine max) root genes differentially expressed in rhizobial, arbuscular mycorrhizal, and dual symbiosis. Journal of Plant Research. 132(4). 541–568. 25 indexed citations
11.
Takahashi, Naoki, Nobuo Ogita, Shoji Taniguchi, et al.. (2019). A regulatory module controlling stress-induced cell cycle arrest in Arabidopsis. eLife. 8. 91 indexed citations
12.
Watanabe, Shunsuke, Muneo Sato, Yuji Sawada, et al.. (2018). Arabidopsis molybdenum cofactor sulfurase ABA3 contributes to anthocyanin accumulation and oxidative stress tolerance in ABA-dependent and independent ways. Scientific Reports. 8(1). 16592–16592. 44 indexed citations
13.
Matsuda, Fumio, Ryo Nakabayashi, Masanori Okamoto, et al.. (2017). A Highly Specific Genome-Wide Association Study Integrated with Transcriptome Data Reveals the Contribution of Copy Number Variations to Specialized Metabolites in Arabidopsis thaliana Accessions. Molecular Biology and Evolution. 34(12). 3111–3122. 9 indexed citations
14.
Matsui, Akihiro, Kei Iida, Maho Tanaka, et al.. (2017). Novel Stress-Inducible Antisense RNAs of Protein-Coding Loci Are Synthesized by RNA-Dependent RNA Polymerase. PLANT PHYSIOLOGY. 175(1). 457–472. 11 indexed citations
15.
Rasheed, Sultana, Khurram Bashir, Akihiro Matsui, Maho Tanaka, & Motoaki Seki. (2016). Transcriptomic Analysis of Soil-Grown Arabidopsis thaliana Roots and Shoots in Response to a Drought Stress. Frontiers in Plant Science. 7. 180–180. 92 indexed citations
16.
Sako, Kaori, Jong-Myong Kim, Akihiro Matsui, et al.. (2015). Ky-2, a Histone Deacetylase Inhibitor, Enhances High-Salinity Stress Tolerance inArabidopsis thaliana. Plant and Cell Physiology. 57(4). 776–783. 52 indexed citations
17.
Nakaminami, Kentaro, Akihiro Matsui, Hirofumi Nakagami, et al.. (2014). Analysis of Differential Expression Patterns of mRNA and Protein During Cold-acclimation and De-acclimation in Arabidopsis. Molecular & Cellular Proteomics. 13(12). 3602–3611. 66 indexed citations
18.
Nishiyama, Rie, Yasuko Watanabe, Marco Antonio Leyva‐González, et al.. (2013). Arabidopsis AHP2, AHP3, and AHP5 histidine phosphotransfer proteins function as redundant negative regulators of drought stress response. Proceedings of the National Academy of Sciences. 110(12). 4840–4845. 161 indexed citations
19.
Okamoto, Masanori, Kiyoshi Tatematsu, Akihiro Matsui, et al.. (2010). Genome-wide analysis of endogenous abscisic acid-mediated transcription in dry and imbibed seeds of Arabidopsis using tiling arrays. The Plant Journal. 62(1). 39–51. 105 indexed citations
20.
Kurihara, Yukio, Akihiro Matsui, Kousuke Hanada, et al.. (2009). Genome-wide suppression of aberrant mRNA-like noncoding RNAs by NMD in Arabidopsis. Proceedings of the National Academy of Sciences. 106(7). 2453–2458. 154 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026