Hisato Saitoh

6.2k total citations · 1 hit paper
92 papers, 5.3k citations indexed

About

Hisato Saitoh is a scholar working on Molecular Biology, Oncology and Immunology. According to data from OpenAlex, Hisato Saitoh has authored 92 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 22 papers in Oncology and 13 papers in Immunology. Recurrent topics in Hisato Saitoh's work include Ubiquitin and proteasome pathways (54 papers), Peptidase Inhibition and Analysis (13 papers) and DNA Repair Mechanisms (10 papers). Hisato Saitoh is often cited by papers focused on Ubiquitin and proteasome pathways (54 papers), Peptidase Inhibition and Analysis (13 papers) and DNA Repair Mechanisms (10 papers). Hisato Saitoh collaborates with scholars based in Japan, United States and Switzerland. Hisato Saitoh's co-authors include Joseph Hinchey, Mary Dasso, Yasuhiro Uchimura, William C. Earnshaw, Robert T. Pu, John E. Tomkiel, Mitsuyoshi Nakao, Carol Cooke, Hong Zhang and Michael J. Matunis and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Hisato Saitoh

92 papers receiving 5.2k citations

Hit Papers

Functional Heterogeneity ... 2000 2026 2008 2017 2000 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hisato Saitoh Japan 38 4.6k 1.3k 772 726 621 92 5.3k
Erica S. Johnson United States 26 5.6k 1.2× 1.7k 1.3× 625 0.8× 1.1k 1.4× 712 1.1× 33 5.9k
Michael J. Matunis United States 46 10.3k 2.2× 1.7k 1.3× 910 1.2× 997 1.4× 697 1.1× 94 11.2k
Olivier Coux France 25 4.9k 1.1× 1.5k 1.2× 671 0.9× 1.5k 2.0× 1.1k 1.7× 65 5.6k
Andreas Bachmair Austria 33 5.1k 1.1× 1.3k 1.0× 495 0.6× 955 1.3× 631 1.0× 72 6.5k
Alfred C.O. Vertegaal Netherlands 44 5.5k 1.2× 1.9k 1.5× 527 0.7× 637 0.9× 459 0.7× 98 6.1k
Michael H. Tatham United Kingdom 31 4.5k 1.0× 1.6k 1.3× 490 0.6× 526 0.7× 602 1.0× 53 4.9k
Alexei F. Kisselev United States 35 5.7k 1.2× 2.2k 1.8× 489 0.6× 1.1k 1.5× 871 1.4× 57 6.4k
Ellis Jaffray United Kingdom 39 4.6k 1.0× 1.6k 1.2× 576 0.7× 502 0.7× 492 0.8× 57 5.3k
Peter Zwickl Germany 25 4.3k 0.9× 1.5k 1.1× 441 0.6× 1.3k 1.8× 722 1.2× 38 4.8k
Deanna M. Koepp United States 18 4.2k 0.9× 1.2k 1.0× 437 0.6× 893 1.2× 469 0.8× 33 4.8k

Countries citing papers authored by Hisato Saitoh

Since Specialization
Citations

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

Fields of papers citing papers by Hisato Saitoh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hisato Saitoh

This figure shows the co-authorship network connecting the top 25 collaborators of Hisato Saitoh. A scholar is included among the top collaborators of Hisato Saitoh 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 Hisato Saitoh. Hisato Saitoh 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.
Morotomi‐Yano, Keiko, et al.. (2019). Nanosecond pulsed electric fields induce extracellular release of chromosomal DNA and histone citrullination in neutrophil-differentiated HL-60 cells. Scientific Reports. 9(1). 8451–8451. 16 indexed citations
2.
Fukuda, Isao, Mikako Hirohama, Akihiro Ito, et al.. (2016). Inhibition of protein SUMOylation by natural quinones. The Journal of Antibiotics. 69(10). 776–779. 3 indexed citations
3.
Shimura, Tsutomu, S. Matsumoto, Yuichiro Shimizu, et al.. (2015). SUMOylation of xeroderma pigmentosum group C protein regulates DNA damage recognition during nucleotide excision repair. Scientific Reports. 5(1). 10984–10984. 31 indexed citations
4.
Mihara, Keiko, et al.. (2015). A Convenient Technique to Fix Suspension Cells on a Coverslip for Microscopy. Current Protocols in Cell Biology. 68(1). 4.30.1–4.30.10. 7 indexed citations
5.
Saito, Masayuki, et al.. (2014). Construction of a mouse Aos1-Uba2 chimeric SUMO-E1 enzyme, mAU, and its expression in baculovirus-insect cells. Bioengineered. 5(2). 133–137. 1 indexed citations
6.
Mihara, Keiko, et al.. (2014). Adhesion of suspension cells on a coverslip in serum-free conditions. Analytical Biochemistry. 466. 1–3. 10 indexed citations
7.
Shimizu, Yuichiro, Yasuhiro Uchimura, Naoshi Dohmae, et al.. (2010). Stimulation of DNA Glycosylase Activities by XPC Protein Complex: Roles of Protein‐Protein Interactions. Journal of Nucleic Acids. 2010(1). 26 indexed citations
8.
Uwada, Junsuke, et al.. (2010). A Simplein SituCell-Based SUMOylation Assay with Potential Application to Drug Screening. Bioscience Biotechnology and Biochemistry. 74(7). 1473–1475. 8 indexed citations
9.
Saitoh, Hisato, et al.. (2010). A Real-Time SUMO-Binding Assay for the Analysis of the SUMO-SIM Protein Interaction Network. Bioscience Biotechnology and Biochemistry. 74(6). 1302–1305. 6 indexed citations
10.
Fukuda, Isao, Akihiro Ito, Go Hirai, et al.. (2009). Ginkgolic Acid Inhibits Protein SUMOylation by Blocking Formation of the E1-SUMO Intermediate. Chemistry & Biology. 16(2). 133–140. 277 indexed citations
11.
Motohashi, Hozumi, Fumiki Katsuoka, Chika Miyoshi, et al.. (2006). MafG Sumoylation Is Required for Active Transcriptional Repression. Molecular and Cellular Biology. 26(12). 4652–4663. 45 indexed citations
12.
Uchimura, Yasuhiro, Makoto Nakamura, Kaoru Sugasawa, Mitsuyoshi Nakao, & Hisato Saitoh. (2004). Overproduction of eukaryotic SUMO-1- and SUMO-2-conjugated proteins in Escherichia coli. Analytical Biochemistry. 331(1). 204–206. 99 indexed citations
13.
Uchimura, Yasuhiro, Mitsuyoshi Nakao, & Hisato Saitoh. (2004). Generation of SUMO‐1 modified proteins in E. coli: towards understanding the biochemistry/structural biology of the SUMO‐1 pathway. FEBS Letters. 564(1-2). 85–90. 53 indexed citations
14.
Işık, Sevim, Kuniaki Sano, Kimiko Tsutsui, et al.. (2003). The SUMO pathway is required for selective degradation of DNA topoisomerase IIβ induced by a catalytic inhibitor ICRF‐1931. FEBS Letters. 546(2-3). 374–378. 42 indexed citations
15.
Matsuzaki, Kazuhito, Takeshi Minami, Masahide Tojo, et al.. (2003). Serum response factor is modulated by the SUMO-1 conjugation system. Biochemical and Biophysical Research Communications. 306(1). 32–38. 48 indexed citations
16.
Kim, Keun Il, Sung Hee Baek, Young Joo Jeon, et al.. (2000). A New SUMO-1-specific Protease, SUSP1, That Is Highly Expressed in Reproductive Organs. Journal of Biological Chemistry. 275(19). 14102–14106. 124 indexed citations
17.
Saitoh, Hisato & Mary Dasso. (1995). The RCC1 Protein Interacts with Ran, RanBP1, hsc70, and a 340-kDa Protein in Xenopus Extracts. Journal of Biological Chemistry. 270(18). 10658–10663. 32 indexed citations
18.
Uryu, Noboru, et al.. (1989). Research Note: Determination of the Sex of Chickens by a Biotin-Labeled Deoxyribonucleic Acid Probe. Poultry Science. 68(6). 850–853. 18 indexed citations
19.
Esashi, Y., et al.. (1985). CO2Enhancement of Aerobic and Hypoxic C2H4 Production in the Tissues of Cocklebur Seeds at Different Dormant States. Australian Journal of Plant Physiology. 12(1). 59–68. 8 indexed citations
20.

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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