Satoru Ito

427 total citations
11 papers, 312 citations indexed

About

Satoru Ito is a scholar working on Molecular Biology, Plant Science and Surgery. According to data from OpenAlex, Satoru Ito has authored 11 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Plant Science and 3 papers in Surgery. Recurrent topics in Satoru Ito's work include Phytochemistry and Biological Activities (4 papers), Natural product bioactivities and synthesis (4 papers) and Phytochemistry and Bioactive Compounds (2 papers). Satoru Ito is often cited by papers focused on Phytochemistry and Biological Activities (4 papers), Natural product bioactivities and synthesis (4 papers) and Phytochemistry and Bioactive Compounds (2 papers). Satoru Ito collaborates with scholars based in Japan and United States. Satoru Ito's co-authors include Yonathan Asikin, Naoto Hirose, Kōji Wada, Hirosuke Oku, Hajime Tamaki, Hirokazu Ohsawa, Kaoru Funabashi, Takeshi Sagara, Kenjiro Ito and Sachie Otsuki and has published in prestigious journals such as Cancer Research, Phytochemistry and Molecular Cancer Therapeutics.

In The Last Decade

Satoru Ito

11 papers receiving 307 citations

Peers

Satoru Ito

MB

SURGE

PS

ONCOL

FS

Motohiro Kanazawa Japan

Ken Tsuboi Japan

Wenquan Lu China

Naftali Presser United States

Prasan Bhandari India

Desen Liang China

Maria Vittoria Sepporta Italy

Marwa G. A. Hegazy Egypt

Nur Dina Amalina Indonesia

Phung Thanh Huong Vietnam

Motohiro Kanazawa Japan

Satoru Ito

234 ×1.5

MB

49 ×0.4

SURGE

58 ×0.8

PS

41 ×0.7

ONCOL

19 ×0.4

FS

Citations per year, relative to Satoru Ito Satoru Ito (= 1×) peers Motohiro Kanazawa

Countries citing papers authored by Satoru Ito

Since Specialization

Citations

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

Fields of papers citing papers by Satoru Ito

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Satoru Ito

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

All Works

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11 of 11 papers shown

1.

Ito, Satoru, Sachie Otsuki, Hirokazu Ohsawa, et al.. (2023). Discovery of Futibatinib: The First Covalent FGFR Kinase Inhibitor in Clinical Use. ACS Medicinal Chemistry Letters. 14(4). 396–404. 16 indexed citations

2.

Tang, Wentao, Keigo Hanada, Yoshiharu Motoo, et al.. (2023). Budget impact analysis of comprehensive genomic profiling for untreated advanced or recurrent solid cancers in Japan. Journal of Medical Economics. 26(1). 614–626. 1 indexed citations

3.

Sootome, Hiroshi, Hidenori Fujita, Kenjiro Ito, et al.. (2020). Futibatinib Is a Novel Irreversible FGFR 1–4 Inhibitor That Shows Selective Antitumor Activity against FGFR-Deregulated Tumors. Cancer Research. 80(22). 4986–4997. 137 indexed citations

4.

Ito, Kimihiro, Makoto Nishio, Masanori Kato, et al.. (2019). TAS-121, A Selective Mutant EGFR Inhibitor, Shows Activity Against Tumors Expressing Various EGFR Mutations Including T790M and Uncommon Mutations G719X. Molecular Cancer Therapeutics. 18(5). 920–928. 10 indexed citations

5.

Asikin, Yonathan, et al.. (2016). Compositional and Electronic Discrimination Analyses of Taste and Aroma Profiles of Non-Centrifugal Cane Brown Sugars. Food Analytical Methods. 10(6). 1844–1856. 29 indexed citations

6.

Asikin, Yonathan, Naoto Hirose, Hajime Tamaki, et al.. (2015). Effects of different drying–solidification processes on physical properties, volatile fraction, and antioxidant activity of non-centrifugal cane brown sugar. LWT. 66. 340–347. 69 indexed citations

7.

Baba, Masaki, et al.. (2012). New triterpenoid saponins from cacti and anti-type I allergy activity of saponins from cactus. Bioorganic & Medicinal Chemistry Letters. 22(14). 4793–4800. 14 indexed citations

8.

Takahashi, Kunio, et al.. (2012). New Triterpenoid Saponins from Stenocereus eruca. Heterocycles. 85(6). 1377–1377. 4 indexed citations

9.

Koike, Takeshi, et al.. (2012). ChemInform Abstract: New Triterpenoid Saponins from Stenocereus eruca.. ChemInform. 43(41). 1 indexed citations

10.

Kinoshita, Kaoru, et al.. (2010). Triterpenoid saponins from Echinopsis macrogona (Cactaceae). Phytochemistry. 72(1). 136–146. 15 indexed citations

11.

Hamada, Hiroki, et al.. (1988). Enantioselectivity in the reduction of α-dicarvelone by cell suspension cultures of Nicotiana tabacum. Phytochemistry. 27(12). 3807–3808. 16 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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