Takao Koeduka

2.5k total citations
62 papers, 1.9k citations indexed

About

Takao Koeduka is a scholar working on Molecular Biology, Plant Science and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Takao Koeduka has authored 62 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 19 papers in Plant Science and 12 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Takao Koeduka's work include Plant biochemistry and biosynthesis (34 papers), Plant Gene Expression Analysis (21 papers) and Biochemical and biochemical processes (12 papers). Takao Koeduka is often cited by papers focused on Plant biochemistry and biosynthesis (34 papers), Plant Gene Expression Analysis (21 papers) and Biochemical and biochemical processes (12 papers). Takao Koeduka collaborates with scholars based in Japan, United States and France. Takao Koeduka's co-authors include Kenji Matsui, Eran Pichersky, T.J. Baiga, Joseph P. Noel, Natalia Dudareva, Christine M. Kish, Tadahiko Kajiwara, Irina Orlova, Daniel G. Vassão and Norman Lewis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Takao Koeduka

62 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Takao Koeduka Japan 25 1.2k 781 300 293 247 62 1.9k
Joshua R. Widhalm United States 22 1.4k 1.2× 945 1.2× 218 0.7× 288 1.0× 164 0.7× 36 2.2k
Heiko Rischer Finland 29 1.5k 1.2× 1.0k 1.3× 302 1.0× 187 0.6× 204 0.8× 93 2.7k
Pascaline Ullmann France 20 1.6k 1.4× 1.0k 1.3× 262 0.9× 160 0.5× 128 0.5× 26 2.2k
John C. D’Auria Germany 23 2.4k 2.0× 1.6k 2.0× 303 1.0× 379 1.3× 232 0.9× 51 3.3k
Rachel Davidovich‐Rikanati Israel 18 1.2k 1.1× 864 1.1× 244 0.8× 157 0.5× 596 2.4× 37 2.1k
Mwafaq Ibdah Israel 24 943 0.8× 681 0.9× 131 0.4× 191 0.7× 361 1.5× 44 1.7k
Christine M. Kish United States 16 2.2k 1.9× 1.1k 1.4× 512 1.7× 682 2.3× 385 1.6× 18 2.9k
Christoph Crocoll Denmark 26 1.0k 0.9× 1.1k 1.4× 109 0.4× 165 0.6× 269 1.1× 61 1.8k
Romain Larbat France 26 825 0.7× 1.1k 1.3× 97 0.3× 153 0.5× 397 1.6× 44 1.9k
Nanna Bjarnholt Denmark 21 1.1k 1.0× 1.1k 1.5× 118 0.4× 108 0.4× 164 0.7× 40 2.1k

Countries citing papers authored by Takao Koeduka

Since Specialization
Citations

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

Fields of papers citing papers by Takao Koeduka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takao Koeduka

This figure shows the co-authorship network connecting the top 25 collaborators of Takao Koeduka. A scholar is included among the top collaborators of Takao Koeduka 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 Takao Koeduka. Takao Koeduka 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.
Koeduka, Takao. (2024). Research advances in regulation and genetic engineering of floral scents. Plant Biotechnology. 41(2). 103–110. 1 indexed citations
3.
Shitan, Nobukazu, et al.. (2022). Gene expression analysis of the ATP-binding cassette transporter ABCD1 in petunia (Petunia hybrida) and tobacco (Nicotiana spp.). Plant Gene. 33. 100391–100391. 1 indexed citations
4.
Ohnishi, Toshiyuki, et al.. (2021). 1-Octen-3-ol is formed from its primeveroside after mechanical wounding of soybean leaves. Plant Molecular Biology. 109(4-5). 551–561. 12 indexed citations
5.
Yamashita, Yüko, Katsuyuki T. Yamato, Ryuichi Nishihama, et al.. (2020). Fungal-Type Terpene Synthases in Marchantia polymorpha Are Involved in Sesquiterpene Biosynthesis in Oil Body Cells. Plant and Cell Physiology. 62(3). 528–537. 10 indexed citations
6.
Koeduka, Takao, Hideyuki Suzuki, Goro Taguchi, & Kenji Matsui. (2020). Biochemical characterization of the jasmonic acid methyltransferase gene from wasabi (<i>Eutrema japonicum</i>). Plant Biotechnology. 37(3). 389–392. 7 indexed citations
7.
Yamada, Naohiro, Takashi Sayama, Kenji Inagaki, et al.. (2020). Suppressed Methionine γ-Lyase Expression Causes Hyperaccumulation of S-Methylmethionine in Soybean Seeds. PLANT PHYSIOLOGY. 183(3). 943–956. 6 indexed citations
8.
Takai, Hiroki, Rika Ozawa, Junji Takabayashi, et al.. (2018). Silkworms suppress the release of green leaf volatiles by mulberry leaves with an enzyme from their spinnerets. Scientific Reports. 8(1). 11942–11942. 29 indexed citations
9.
Tanaka, Toshiyuki, Kaori Shiojiri, Rika Ozawa, et al.. (2018). Identification of a Hexenal Reductase That Modulates the Composition of Green Leaf Volatiles. PLANT PHYSIOLOGY. 178(2). 552–564. 48 indexed citations
11.
Mano, Jun’ichi, Chihiro Morita, Hiroki Sakai, et al.. (2016). Acrolein-detoxifying isozymes of glutathione transferase in plants. Planta. 245(2). 255–264. 15 indexed citations
12.
Ono, Eiichiro, Takao Koeduka, Hiromi Toyonaga, et al.. (2015). CYP74B24 is the 13-hydroperoxide lyase involved in biosynthesis of green leaf volatiles in tea (Camellia sinensis). Plant Physiology and Biochemistry. 98. 112–118. 13 indexed citations
13.
Matsuki, Atsushi, et al.. (2015). Spatial expression of the Arabidopsishydroperoxide lyasegene is controlled differently from that of theallene oxide synthasegene. Journal of Plant Interactions. 10(1). 1–10. 12 indexed citations
14.
Koeduka, Takao, et al.. (2015). Glutathionylation and reduction of methacrolein in tomato plants account for its absorption from the vapor phase. PLANT PHYSIOLOGY. 169(3). pp.01045.2015–pp.01045.2015. 16 indexed citations
15.
Kawasaki, Takashi, Takao Koeduka, Akifumi Sugiyama, et al.. (2014). Metabolic engineering of flavonoids with prenyltransferase and chalcone isomerase genes in tomato fruits. Plant Biotechnology. 31(5). 567–571. 4 indexed citations
16.
Koeduka, Takao, Bunta Watanabe, Shiro Suzuki, et al.. (2011). Characterization of raspberry ketone/zingerone synthase, catalyzing the alpha, beta-hydrogenation of phenylbutenones in raspberry fruits. Biochemical and Biophysical Research Communications. 412(1). 104–108. 42 indexed citations
17.
Koeduka, Takao. (2010). Molecular mechanism underlying how plants produce aromatic constituents of spices - evolution of phenylpropene synthases.. 11(2). 132–137. 1 indexed citations
18.
Koeduka, Takao, Nobukazu Shitan, Takuto Kumano, et al.. (2010). Production of prenylated flavonoids in tomato fruits expressing a prenyltransferase gene from Streptomyces coelicolor A3(2). Plant Biology. 13(2). 411–415. 15 indexed citations
19.
Koeduka, Takao, Kenji Matsui, Morifumi Hasegawa, Yoshihiko Akakabe, & Tadahiko Kajiwara. (2005). Rice fatty acid α-dioxygenase is induced by pathogen attack and heavy metal stress: activation through jasmonate signaling. Journal of Plant Physiology. 162(8). 912–920. 46 indexed citations
20.
Koeduka, Takao, Michael Stumpe, Tadahiko Kajiwara, & Ivo Feußner. (2003). Kinetics of barley FA hydroperoxide lyase are modulated by salts and detergents. Lipids. 38(11). 1167–1172. 22 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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