Masayuki Satake

10.6k total citations
172 papers, 8.5k citations indexed

About

Masayuki Satake is a scholar working on Environmental Chemistry, Molecular Biology and Biotechnology. According to data from OpenAlex, Masayuki Satake has authored 172 papers receiving a total of 8.5k indexed citations (citations by other indexed papers that have themselves been cited), including 125 papers in Environmental Chemistry, 75 papers in Molecular Biology and 37 papers in Biotechnology. Recurrent topics in Masayuki Satake's work include Marine Toxins and Detection Methods (123 papers), Marine Sponges and Natural Products (36 papers) and Protist diversity and phylogeny (33 papers). Masayuki Satake is often cited by papers focused on Marine Toxins and Detection Methods (123 papers), Marine Sponges and Natural Products (36 papers) and Protist diversity and phylogeny (33 papers). Masayuki Satake collaborates with scholars based in Japan, United States and Ireland. Masayuki Satake's co-authors include Takeshi Yasumoto, Michio Murata, Hideo Naoki, Yasukatsu Oshima, Kevin J. James, Terry McMahon, Katsuya Ofuji, Lincoln MacKenzie, Ambrose Furey and Hiroshi Nagai and has published in prestigious journals such as Science, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Masayuki Satake

167 papers receiving 8.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masayuki Satake Japan 55 6.8k 3.4k 2.2k 1.9k 1.5k 172 8.5k
Yasukatsu Oshima Japan 41 5.7k 0.8× 2.4k 0.7× 787 0.4× 2.3k 1.2× 625 0.4× 135 6.8k
Daniel G. Baden United States 44 4.2k 0.6× 2.6k 0.8× 744 0.3× 1.4k 0.7× 401 0.3× 141 6.1k
Jeffrey L. C. Wright Canada 40 3.5k 0.5× 2.2k 0.7× 1.0k 0.5× 1.6k 0.8× 932 0.6× 150 5.7k
Michael A. Quilliam Canada 59 7.4k 1.1× 3.9k 1.2× 810 0.4× 3.1k 1.6× 364 0.2× 216 10.1k
Patrizia Ciminiello Italy 43 3.3k 0.5× 1.8k 0.5× 768 0.3× 1.7k 0.9× 936 0.6× 125 4.8k
Christopher O. Miles Norway 44 3.8k 0.6× 2.1k 0.6× 588 0.3× 1.7k 0.9× 372 0.3× 181 6.0k
Ernesto Fattorusso Italy 59 3.1k 0.5× 4.3k 1.3× 4.1k 1.8× 1.7k 0.9× 4.5k 3.0× 385 12.5k
Takeshi Yasumoto Japan 81 17.0k 2.5× 8.3k 2.5× 3.8k 1.7× 4.4k 2.3× 2.5k 1.7× 365 20.8k
John A. Walter Canada 36 2.5k 0.4× 2.1k 0.6× 640 0.3× 1.1k 0.6× 551 0.4× 105 4.7k
Mari Yotsu‐Yamashita Japan 41 2.9k 0.4× 1.9k 0.6× 988 0.4× 302 0.2× 591 0.4× 162 4.4k

Countries citing papers authored by Masayuki Satake

Since Specialization
Citations

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

Fields of papers citing papers by Masayuki Satake

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masayuki Satake

This figure shows the co-authorship network connecting the top 25 collaborators of Masayuki Satake. A scholar is included among the top collaborators of Masayuki Satake 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 Masayuki Satake. Masayuki Satake 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.
Murata, Michio, Masayuki Satake, & Nobuaki Matsumori. (2025). Conformational dynamics and molecular interactions of natural products: unveiling functional structures in biological membranes. Proceedings of the Japan Academy Series B. 101(5). 249–273.
2.
Zhang, Botao, Michiya Kamio, Hajime Uchida, et al.. (2024). Okeaniazole A: Thiazole-containing cyclopeptide from the marine cyanobacterium Okeania hirsuta with antileishmanial activity. Tetrahedron Letters. 150. 155284–155284. 5 indexed citations
3.
Zhang, Botao, et al.. (2024). (10E,15Z)-12-(Dimethylsulfonio)-9,13-dihydroxyoctadeca-10,15-dienoate. SHILAP Revista de lepidopterología. 2024(1). M1784–M1784.
4.
Kamio, Michiya, et al.. (2024). N-Desmethylmajusculamide B, a lipopeptide isolated from the Okinawan cyanobacterium Okeania hirsuta. Bioscience Biotechnology and Biochemistry. 88(5). 517–521. 1 indexed citations
5.
Hamada, Keisuke, Dinh Thanh Nguyen, Masayuki Satake, et al.. (2022). LimF is a versatile prenyltransferase for histidine-C-geranylation on diverse non-natural substrates. Nature Catalysis. 5(8). 682–693. 31 indexed citations
6.
Twiner, Michael J., James C. Ryan, Jeanine S. Morey, et al.. (2008). Transcriptional profiling and inhibition of cholesterol biosynthesis in human T lymphocyte cells by the marine toxin azaspiracid. Genomics. 91(3). 289–300. 30 indexed citations
7.
Kotaki, Yuichi, Masayuki Satake, Nina Lundholm, et al.. (2006). New stage of the study on domoic acid-producing diatoms : A finding of Nitzschia navis-varingica that produces domoic acid derivatives as major toxin components. 30(1). 116–120. 8 indexed citations
8.
Alfonso, Amparo, Mercedes R. Vieytes, Katsuya Ofuji, et al.. (2006). Azaspiracids modulate intracellular pH levels in human lymphocytes. Biochemical and Biophysical Research Communications. 346(3). 1091–1099. 22 indexed citations
9.
Kulagina, Nadezhda V., Michael J. Twiner, Philipp Heß, et al.. (2006). Azaspiracid-1 inhibits bioelectrical activity of spinal cord neuronal networks. Toxicon. 47(7). 766–773. 37 indexed citations
10.
Aune, Tore, Stig Larsen, John Aasen, et al.. (2006). Relative toxicity of dinophysistoxin-2 (DTX-2) compared with okadaic acid, based on acute intraperitoneal toxicity in mice. Toxicon. 49(1). 1–7. 82 indexed citations
11.
Obara, Shigeru, et al.. (2005). The First Heart Sound Amplitude Has a Breaking Point and Positive Relationships With Blood Lactate Concentration and Double Product in Graded Exercise. 11(1). 33–39. 1 indexed citations
12.
Kotaki, Yuichi, Masayuki Satake, Nina Lundholm, et al.. (2005). Production of isodomoic acids A and B as major toxin components of a pennate diatom Nitzschia navis-varingica. Toxicon. 46(8). 946–953. 32 indexed citations
13.
Twiner, Michael J., Philipp Heß, Marie‐Yasmine Dechraoui Bottein, et al.. (2005). Cytotoxic and cytoskeletal effects of azaspiracid-1 on mammalian cell lines. Toxicon. 45(7). 891–900. 83 indexed citations
14.
Li, Yushan, et al.. (2004). Flavonoid Glycosides from Cecropia adenopus. 58(1). 46. 2 indexed citations
15.
Nicolaou, K. C., Štěpán Vyskočil, Theocharis V. Koftis, et al.. (2004). Structural Revision and Total Synthesis of Azaspiracid‐1, Part 1: Intelligence Gathering and Tentative Proposal. Angewandte Chemie International Edition. 43(33). 4312–4318. 84 indexed citations
16.
Fuwa, Haruhiko, et al.. (2003). Synthesis and biological evaluation of gambierol analogues. Bioorganic & Medicinal Chemistry Letters. 13(15). 2519–2522. 27 indexed citations
17.
Draisci, R., Luca Palleschi, Emanuele Ferretti, et al.. (2000). Development of a method for the identification of azaspiracid in shellfish by liquid chromatography–tandem mass spectrometry. Journal of Chromatography A. 871(1-2). 13–21. 45 indexed citations
18.
Morohashi, Akio, Masayuki Satake, Hideo Naoki, et al.. (1999). Brevetoxin B4 isolated from greenshell musselsPerna canaliculus, the major toxin involved in neurotoxic shellfish poisoning in New Zealand. Natural Toxins. 7(2). 45–48. 60 indexed citations
19.
Satake, Masayuki, Aurelia Tubaro, Jongsoo Lee, & Takeshi Yasumoto. (1998). Two new analogs of yessotoxin, homoyessotoxin and 45-hydroxyhomoyessotoxin, isolated from mussels of the Adriatic sea. Natural Toxins. 5(3). 107–110. 71 indexed citations
20.
Tsuchida, Takaaki, Takehito Yamamoto, Kōji Yamamoto, et al.. (1995). Analysis of the chemical constituents of 'Kijitsu (Zhishi)' and 'Kikoku (Zhiqiao)'. 49(3). 249–254. 1 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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