Tetsuya Chujo

1.5k total citations
17 papers, 1.1k citations indexed

About

Tetsuya Chujo is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Tetsuya Chujo has authored 17 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Plant Science, 11 papers in Molecular Biology and 7 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Tetsuya Chujo's work include Plant Gene Expression Analysis (7 papers), Plant-Microbe Interactions and Immunity (6 papers) and Plant and fungal interactions (6 papers). Tetsuya Chujo is often cited by papers focused on Plant Gene Expression Analysis (7 papers), Plant-Microbe Interactions and Immunity (6 papers) and Plant and fungal interactions (6 papers). Tetsuya Chujo collaborates with scholars based in Japan, New Zealand and Iran. Tetsuya Chujo's co-authors include Barry Scott, Hisakazu Yamane, Kazunori Okada, Hideaki Nojiri, Eiichi Minami, Yoko Nishizawa, Takafumi Shimizu, Naoki Yokotani, Naoto Shibuya and Koji Miyamoto and has published in prestigious journals such as PLoS ONE, Journal of Experimental Botany and Molecular Microbiology.

In The Last Decade

Tetsuya Chujo

17 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tetsuya Chujo Japan 13 903 729 118 118 106 17 1.1k
Shiduku Taniguchi Japan 10 633 0.7× 293 0.4× 90 0.8× 40 0.3× 252 2.4× 11 786
Zejian Guo China 12 1.4k 1.5× 927 1.3× 28 0.2× 56 0.5× 108 1.0× 23 1.5k
Jiuhai Zhao China 13 813 0.9× 532 0.7× 92 0.8× 49 0.4× 233 2.2× 20 1.0k
Manzhu Bao China 17 595 0.7× 659 0.9× 110 0.9× 45 0.4× 23 0.2× 48 842
Martina Rickauer France 18 1.0k 1.1× 279 0.4× 41 0.3× 189 1.6× 96 0.9× 40 1.1k
Marina Varbanova United States 6 393 0.4× 386 0.5× 78 0.7× 51 0.4× 28 0.3× 6 609
L. Buchwaldt Canada 21 1.2k 1.3× 259 0.4× 185 1.6× 254 2.2× 46 0.4× 42 1.2k
Kevin D. Simcox United States 8 504 0.6× 308 0.4× 56 0.5× 26 0.2× 84 0.8× 11 701
Ziniu Deng China 6 582 0.6× 419 0.6× 67 0.6× 155 1.3× 52 0.5× 10 789
Dong Duan China 12 358 0.4× 396 0.5× 84 0.7× 93 0.8× 26 0.2× 21 587

Countries citing papers authored by Tetsuya Chujo

Since Specialization
Citations

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

Fields of papers citing papers by Tetsuya Chujo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tetsuya Chujo

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

All Works

17 of 17 papers shown
1.
Lee, Kate, Kimberly Green, David J. Winter, et al.. (2020). Regulation of host‐infection ability in the grass‐symbiotic fungus Epichloë festucae by histone H3K9 and H3K36 methyltransferases. Environmental Microbiology. 23(4). 2116–2131. 10 indexed citations
2.
Chujo, Tetsuya, Carla J. Eaton, Pierre‐Yves Dupont, et al.. (2019). Complex epigenetic regulation of alkaloid biosynthesis and host interaction by heterochromatin protein I in a fungal endophyte-plant symbiosis. Fungal Genetics and Biology. 125. 71–83. 20 indexed citations
3.
Chujo, Tetsuya, et al.. (2019). Regulation of subtelomeric fungal secondary metabolite genes by H3K4me3 regulators CclA and KdmB. Molecular Microbiology. 112(3). 837–853. 13 indexed citations
4.
Chujo, Tetsuya, et al.. (2015). Molecular and cellular analysis of the pH response transcription factor PacC in the fungal symbiont Epichloë festucae. Fungal Genetics and Biology. 85. 25–37. 12 indexed citations
5.
Miyamoto, Koji, Takashi Matsumoto, Atsushi Okada, et al.. (2014). Identification of Target Genes of the bZIP Transcription Factor OsTGAP1, Whose Overexpression Causes Elicitor-Induced Hyperaccumulation of Diterpenoid Phytoalexins in Rice Cells. PLoS ONE. 9(8). e105823–e105823. 36 indexed citations
6.
Chujo, Tetsuya, Koji Miyamoto, Satoshi Ogawa, et al.. (2014). Overexpression of Phosphomimic Mutated OsWRKY53 Leads to Enhanced Blast Resistance in Rice. PLoS ONE. 9(6). e98737–e98737. 114 indexed citations
7.
Chujo, Tetsuya & Barry Scott. (2014). Histone H3K9 and H3K27 methylation regulates fungal alkaloid biosynthesis in a fungal endophyte–plant symbiosis. Molecular Microbiology. 92(2). 413–434. 122 indexed citations
8.
Yokotani, Naoki, Yuko Sato, Shigeru Tanabe, et al.. (2013). WRKY76 is a rice transcriptional repressor playing opposite roles in blast disease resistance and cold stress tolerance. Journal of Experimental Botany. 64(16). 5085–5097. 261 indexed citations
9.
Chujo, Tetsuya, Koji Miyamoto, Takafumi Shimizu, et al.. (2013). OsWRKY28, a PAMP-responsive transrepressor, negatively regulates innate immune responses in rice against rice blast fungus. Plant Molecular Biology. 82(1-2). 23–37. 123 indexed citations
10.
Tanaka, Aiko, Daigo Takemoto, Tetsuya Chujo, & Barry Scott. (2012). Fungal endophytes of grasses. Current Opinion in Plant Biology. 15(4). 462–468. 62 indexed citations
11.
Chujo, Tetsuya, Naoto Shibuya, Tetsuo Takemura, et al.. (2009). Promoter Analysis of the Elicitor-Induced WRKY GeneOsWRKY53, Which Is Involved in Defense Responses in Rice. Bioscience Biotechnology and Biochemistry. 73(8). 1901–1904. 26 indexed citations
12.
Chujo, Tetsuya, Tomoaki Kato, Kazunari Yamada, et al.. (2008). Characterization of an Elicitor-Induced Rice WRKY Gene,OsWRKY71. Bioscience Biotechnology and Biochemistry. 72(1). 240–245. 41 indexed citations
13.
Chujo, Tetsuya, Kazunori Okada, Kazuya Suzuki, et al.. (2007). Identification of a Jasmonic Acid-Responsive Region in the Promoter of the Rice 12-Oxophytodienoic Acid Reductase 1 GeneOsOPR1. Bioscience Biotechnology and Biochemistry. 71(12). 3110–3115. 13 indexed citations
14.
Chujo, Tetsuya, Ryota Takai, Chiharu Akimoto‐Tomiyama, et al.. (2007). Involvement of the elicitor-induced gene OsWRKY53 in the expression of defense-related genes in rice. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1769(7-8). 497–505. 145 indexed citations
15.
Okada, Kazunori, Tetsuya Chujo, Shin‐ichi Arimura, et al.. (2007). Identification of the OsOPR7 gene encoding 12-oxophytodienoate reductase involved in the biosynthesis of jasmonic acid in rice. Planta. 227(3). 517–526. 130 indexed citations
16.
Yagi, Ken, Tetsuya Chujo, Hideaki Nojiri, et al.. (2001). Evidence for the Presence of DNA-Binding Proteins Involved in Regulation of the Gene Expression of Indole-3-Pyruvic Acid Decarboxylase, a Key Enzyme in Indole-3-Acetic Acid Biosynthesis in Azospirillum lipoferum FS. Bioscience Biotechnology and Biochemistry. 65(5). 1265–1269. 10 indexed citations
17.
Yagi, Ken, Tetsuya Chujo, Hideaki Nojiri, et al.. (2000). Isolation and Characterization of Low-indole-3-acetic Acid-producing Mutants fromBradyrhizobium elkanii. Bioscience Biotechnology and Biochemistry. 64(7). 1359–1364. 3 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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