Nae Saito

640 total citations
10 papers, 476 citations indexed

About

Nae Saito is a scholar working on Molecular Biology, Organic Chemistry and Oncology. According to data from OpenAlex, Nae Saito has authored 10 papers receiving a total of 476 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Organic Chemistry and 3 papers in Oncology. Recurrent topics in Nae Saito's work include Cancer Mechanisms and Therapy (2 papers), Peptidase Inhibition and Analysis (2 papers) and Molecular Junctions and Nanostructures (2 papers). Nae Saito is often cited by papers focused on Cancer Mechanisms and Therapy (2 papers), Peptidase Inhibition and Analysis (2 papers) and Molecular Junctions and Nanostructures (2 papers). Nae Saito collaborates with scholars based in Japan, France and United States. Nae Saito's co-authors include Takayoshi Okabe, Tetsuo Nagano, Takuya Terai, Kenjiro Hanaoka, Yasuteru Urano, Wen Piao, Moriaki Kusakabe, Yuichiro Koide, Hirotatsu Kojima and Hirofumi Nakano and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Medicinal Chemistry and Bioorganic & Medicinal Chemistry.

In The Last Decade

Nae Saito

10 papers receiving 472 citations

Peers

Nae Saito
Shane M. Hickey Australia
Shaojuan Zhang Netherlands
Bumhee Lim South Korea
Md. Imam Uddin United States
Lynette A. Smyth United Kingdom
Shane M. Hickey Australia
Nae Saito
Citations per year, relative to Nae Saito Nae Saito (= 1×) peers Shane M. Hickey

Countries citing papers authored by Nae Saito

Since Specialization
Citations

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

Fields of papers citing papers by Nae Saito

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nae Saito

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

All Works

10 of 10 papers shown
1.
Tachibana, Ryo, Takuya Terai, Gaëlle Boncompain, et al.. (2016). Improving the Solubility of Artificial Ligands of Streptavidin to Enable More Practical Reversible Switching of Protein Localization in Cells. ChemBioChem. 18(4). 358–362. 1 indexed citations
2.
Nakano, Hirofumi, Tsukasa Hasegawa, Riyo Imamura, et al.. (2016). Development of a potent and selective FLT3 kinase inhibitor by systematic expansion of a non-selective fragment-screening hit. Bioorganic & Medicinal Chemistry Letters. 26(9). 2370–2374. 8 indexed citations
3.
Nakano, Hirofumi, Tsukasa Hasegawa, Nae Saito, et al.. (2015). Design and synthesis of an in vivo-efficacious PIM3 kinase inhibitor as a candidate anti-pancreatic cancer agent. Bioorganic & Medicinal Chemistry Letters. 25(24). 5687–5693. 7 indexed citations
4.
Terai, Takuya, Gaëlle Boncompain, Shigeru Sugiyama, et al.. (2015). Artificial Ligands of Streptavidin (ALiS): Discovery, Characterization, and Application for Reversible Control of Intracellular Protein Transport. Journal of the American Chemical Society. 137(33). 10464–10467. 21 indexed citations
5.
Kimura, Yasuaki, Nae Saito, Jiaan Liu, et al.. (2015). Supramolecular Ligands for Histone Tails by Employing a Multivalent Display of Trisulfonated Calix[4]arenes. ChemBioChem. 16(18). 2599–2604. 13 indexed citations
6.
Sakamoto, Hiroki, Shinichiro Egashira, Nae Saito, et al.. (2014). Gliotoxin Suppresses NF-κB Activation by Selectively Inhibiting Linear Ubiquitin Chain Assembly Complex (LUBAC). ACS Chemical Biology. 10(3). 675–681. 71 indexed citations
7.
Nakano, Hirofumi, Nae Saito, L.J. Parker, et al.. (2012). Rational Evolution of a Novel Type of Potent and Selective Proviral Integration Site in Moloney Murine Leukemia Virus Kinase 1 (PIM1) Inhibitor from a Screening-Hit Compound. Journal of Medicinal Chemistry. 55(11). 5151–5164. 64 indexed citations
8.
Koide, Yuichiro, Yasuteru Urano, Kenjiro Hanaoka, et al.. (2012). Development of NIR Fluorescent Dyes Based on Si–rhodamine for in Vivo Imaging. Journal of the American Chemical Society. 134(11). 5029–5031. 258 indexed citations
9.
Okamoto, Masako, Hirotatsu Kojima, Nae Saito, et al.. (2011). Virtual screening and further development of novel ALK inhibitors. Bioorganic & Medicinal Chemistry. 19(10). 3086–3095. 12 indexed citations
10.
Okamoto, Masako, Nae Saito, Hirotatsu Kojima, et al.. (2010). Identification of novel ASK1 inhibitors using virtual screening. Bioorganic & Medicinal Chemistry. 19(1). 486–489. 21 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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