Ryosuke Sugiyama

1.3k total citations
29 papers, 989 citations indexed

About

Ryosuke Sugiyama is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Ryosuke Sugiyama has authored 29 papers receiving a total of 989 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Organic Chemistry and 10 papers in Pharmacology. Recurrent topics in Ryosuke Sugiyama's work include Microbial Natural Products and Biosynthesis (10 papers), Synthetic Organic Chemistry Methods (9 papers) and Metal-Catalyzed Oxygenation Mechanisms (6 papers). Ryosuke Sugiyama is often cited by papers focused on Microbial Natural Products and Biosynthesis (10 papers), Synthetic Organic Chemistry Methods (9 papers) and Metal-Catalyzed Oxygenation Mechanisms (6 papers). Ryosuke Sugiyama collaborates with scholars based in Japan, Singapore and France. Ryosuke Sugiyama's co-authors include Shinichi Nishimura, Hideaki Kakeya, Masami Yokota Hirai, Taro Ozaki, Hiroyasu Onaka, Shumpei Asamizu, Takeshi Sakurai, Kunishige Kataoka, Tetsuya Mori and Kazuki Saito and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Ryosuke Sugiyama

28 papers receiving 981 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ryosuke Sugiyama Japan 18 603 296 269 202 136 29 989
Juan He China 24 770 1.3× 673 2.3× 373 1.4× 375 1.9× 132 1.0× 101 1.7k
Hongwen Tao China 16 320 0.5× 332 1.1× 259 1.0× 141 0.7× 179 1.3× 32 937
F. Sima Sariaslani United States 22 981 1.6× 212 0.7× 192 0.7× 87 0.4× 244 1.8× 39 1.4k
Rui‐Yun Yang China 21 486 0.8× 561 1.9× 292 1.1× 160 0.8× 305 2.2× 80 1.3k
Marcel Frese Germany 21 602 1.0× 316 1.1× 154 0.6× 425 2.1× 164 1.2× 70 1.2k
Manuel González Sierra Argentina 18 437 0.7× 134 0.5× 217 0.8× 290 1.4× 94 0.7× 52 958
Nurettin Yaylı Türkiye 21 491 0.8× 150 0.5× 496 1.8× 379 1.9× 100 0.7× 126 1.4k
José F. Quı́lez del Moral Spain 21 429 0.7× 170 0.6× 170 0.6× 827 4.1× 133 1.0× 83 1.4k
Hansjörg Weber Austria 19 624 1.0× 92 0.3× 81 0.3× 248 1.2× 87 0.6× 55 940
Sumei Li China 24 696 1.2× 885 3.0× 171 0.6× 524 2.6× 496 3.6× 53 1.6k

Countries citing papers authored by Ryosuke Sugiyama

Since Specialization
Citations

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

Fields of papers citing papers by Ryosuke Sugiyama

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ryosuke Sugiyama

This figure shows the co-authorship network connecting the top 25 collaborators of Ryosuke Sugiyama. A scholar is included among the top collaborators of Ryosuke Sugiyama 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 Ryosuke Sugiyama. Ryosuke Sugiyama 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.
Yamaguchi, Masashi, Shuji Shigenobu, Katsushi Yamaguchi, et al.. (2025). LIPID RICH 1 modulates allocation of carbon between starch and triacylglycerol in Arabidopsis leaves. Journal of Experimental Botany. 76(8). 2144–2161. 1 indexed citations
2.
Nishimura, Hiroaki, et al.. (2024). Isolation of new indole alkaloid triglucoside from the aqueous extract of Uncaria rhynchophylla. Journal of Natural Medicines. 79(1). 28–35.
3.
Ma, Suze, E. De la Mora, He Li, et al.. (2024). Fused radical SAM and αKG-HExxH domain proteins contain a distinct structural fold and catalyse cyclophane formation and β-hydroxylation. Nature Chemistry. 16(11). 1882–1893. 9 indexed citations
4.
Sugiyama, Ryosuke, et al.. (2022). The Biosynthetic Landscape of Triceptides Reveals Radical SAM Enzymes That Catalyze Cyclophane Formation on Tyr- and His-Containing Motifs. Journal of the American Chemical Society. 144(26). 11580–11593. 44 indexed citations
5.
Yokoyama, Tadashi, Shinya Fushinobu, Akiko Maruyama, et al.. (2022). Glutathione degradation activity of γ‐glutamyl peptidase 1 manifests its dual roles in primary and secondary sulfur metabolism in Arabidopsis. The Plant Journal. 111(6). 1626–1642. 22 indexed citations
6.
Sugiyama, Ryosuke, Rui Li, Ayuko Kuwahara, et al.. (2021). Retrograde sulfur flow from glucosinolates to cysteine in Arabidopsis thaliana. Proceedings of the National Academy of Sciences. 118(22). 71 indexed citations
7.
Fujita, Kohei, et al.. (2021). Amphiol, an Antifungal Fungal Pigment from Pseudogymnoascus sp. PF1464. Journal of Natural Products. 84(4). 986–992. 11 indexed citations
8.
Nguyen, Thi Quynh Ngoc, Ryosuke Sugiyama, Fernaldo Richtia Winnerdy, et al.. (2020). Post-translational formation of strained cyclophanes in bacteria. Nature Chemistry. 12(11). 1042–1053. 84 indexed citations
9.
Tsugawa, Hiroshi, Ryo Nakabayashi, Tetsuya Mori, et al.. (2019). A cheminformatics approach to characterize metabolomes in stable-isotope-labeled organisms. Nature Methods. 16(4). 295–298. 208 indexed citations
10.
Sugiyama, Ryosuke, Shinichi Nishimura, Taro Ozaki, et al.. (2019). Chemical Interactions of Cryptic Actinomycete Metabolite 5‐Alkyl‐1,2,3,4‐tetrahydroquinolines through Aggregate Formation. Angewandte Chemie. 131(38). 13620–13625. 1 indexed citations
11.
Tsugawa, Hiroshi, Ryo Nakabayashi, Tetsuya Mori, et al.. (2019). Publisher Correction: A cheminformatics approach to characterize metabolomes in stable-isotope-labeled organisms. Nature Methods. 16(5). 446–446. 6 indexed citations
12.
Sugiyama, Ryosuke & Masami Yokota Hirai. (2019). Atypical Myrosinase as a Mediator of Glucosinolate Functions in Plants. Frontiers in Plant Science. 10. 1008–1008. 47 indexed citations
13.
Sugiyama, Ryosuke, Shinichi Nishimura, Taro Ozaki, et al.. (2019). Chemical Interactions of Cryptic Actinomycete Metabolite 5‐Alkyl‐1,2,3,4‐tetrahydroquinolines through Aggregate Formation. Angewandte Chemie International Edition. 58(38). 13486–13491. 12 indexed citations
14.
Yamada, Kenji, Tadashi Kunieda, Ryosuke Sugiyama, et al.. (2019). Leaf Endoplasmic Reticulum Bodies Identified in Arabidopsis Rosette Leaves Are Involved in Defense against Herbivory. PLANT PHYSIOLOGY. 179(4). 1515–1524. 52 indexed citations
15.
Sugiyama, Ryosuke, Shinichi Nishimura, Taro Ozaki, et al.. (2016). Discovery and Total Synthesis of Streptoaminals: Antimicrobial [5,5]‐Spirohemiaminals from the Combined‐Culture of Streptomyces nigrescens and Tsukamurella pulmonis. Angewandte Chemie International Edition. 55(35). 10278–10282. 43 indexed citations
16.
Sugiyama, Ryosuke, et al.. (2015). A novel resting form of the trinuclear copper center in the double mutant of a multicopper oxidase, CueO, Cys500Ser/Glu506Ala. Journal of Inorganic Biochemistry. 149. 88–90. 3 indexed citations
17.
Komori, Hirofumi, Ryosuke Sugiyama, Kunishige Kataoka, et al.. (2014). New insights into the catalytic active-site structure of multicopper oxidases. Acta Crystallographica Section D Biological Crystallography. 70(3). 772–779. 26 indexed citations
18.
Komori, Hirofumi, Ryosuke Sugiyama, Kunishige Kataoka, Yoshiki Higuchi, & Takeshi Sakurai. (2012). An O‐Centered Structure of the Trinuclear Copper Center in the Cys500Ser/Glu506Gln Mutant of CueO and Structural Changes in Low to High X‐Ray Dose Conditions. Angewandte Chemie International Edition. 51(8). 1861–1864. 26 indexed citations
19.
Iwaki, Masayo, et al.. (2010). ATR‐FTIR study of the protonation states of the Glu residue in the multicopper oxidases, CueO and bilirubin oxidase. FEBS Letters. 584(18). 4027–4031. 17 indexed citations
20.
Kataoka, Kunishige, Ryosuke Sugiyama, Shun Hirota, et al.. (2009). Four-electron Reduction of Dioxygen by a Multicopper Oxidase, CueO, and Roles of Asp112 and Glu506 Located Adjacent to the Trinuclear Copper Center. Journal of Biological Chemistry. 284(21). 14405–14413. 65 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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