Noriko Saitoh

4.2k total citations
125 papers, 3.1k citations indexed

About

Noriko Saitoh is a scholar working on Molecular Biology, Statistical and Nonlinear Physics and Rheumatology. According to data from OpenAlex, Noriko Saitoh has authored 125 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 22 papers in Statistical and Nonlinear Physics and 14 papers in Rheumatology. Recurrent topics in Noriko Saitoh's work include Genomics and Chromatin Dynamics (29 papers), RNA Research and Splicing (22 papers) and Nonlinear Waves and Solitons (19 papers). Noriko Saitoh is often cited by papers focused on Genomics and Chromatin Dynamics (29 papers), RNA Research and Splicing (22 papers) and Nonlinear Waves and Solitons (19 papers). Noriko Saitoh collaborates with scholars based in Japan, United States and Egypt. Noriko Saitoh's co-authors include I. Goldberg, William C. Earnshaw, Mitsuyoshi Nakao, Kengo Gohchi, Edgar R. Wood, Moritaka Gotoh, Juzo Matsuda, Scott D. Patterson, Chris Spahr and David L. Spector and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Noriko Saitoh

121 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Noriko Saitoh Japan 29 2.1k 361 296 283 271 125 3.1k
Christopher M. Rose United States 36 2.3k 1.1× 364 1.0× 135 0.5× 69 0.2× 646 2.4× 117 4.4k
Alexandr P. Kornev United States 36 4.6k 2.2× 860 2.4× 196 0.7× 77 0.3× 161 0.6× 66 5.6k
E.J.J. van Zoelen Netherlands 32 2.9k 1.4× 303 0.8× 572 1.9× 174 0.6× 196 0.7× 125 3.9k
Martin Jakab Austria 23 3.2k 1.5× 572 1.6× 176 0.6× 43 0.2× 185 0.7× 66 4.5k
Danny M. Hatters Australia 35 2.6k 1.3× 524 1.5× 153 0.5× 56 0.2× 161 0.6× 79 4.0k
Jacob D. Jaffe United States 37 4.3k 2.1× 286 0.8× 370 1.3× 55 0.2× 419 1.5× 80 5.7k
Hauke Busch Germany 34 2.0k 1.0× 390 1.1× 288 1.0× 155 0.5× 731 2.7× 181 3.8k
Emidio Capriotti Italy 30 4.4k 2.1× 331 0.9× 1.6k 5.5× 110 0.4× 359 1.3× 74 5.7k
Natarajan Kannan United States 37 3.2k 1.6× 820 2.3× 289 1.0× 47 0.2× 258 1.0× 124 4.4k
K Murakami Japan 35 2.8k 1.3× 709 2.0× 507 1.7× 68 0.2× 173 0.6× 106 4.8k

Countries citing papers authored by Noriko Saitoh

Since Specialization
Citations

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

Fields of papers citing papers by Noriko Saitoh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Noriko Saitoh

This figure shows the co-authorship network connecting the top 25 collaborators of Noriko Saitoh. A scholar is included among the top collaborators of Noriko 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 Noriko Saitoh. Noriko 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.
Tanabe, Hideyuki, et al.. (2025). Condensin II collaborates with cohesin to establish and maintain interphase chromosome territories. The Journal of Cell Biology. 225(4).
2.
Watanabe, Kenji, Tatsuyoshi Yamamoto, Takeshi Fujita, et al.. (2024). Metabolically inducing defects in DNA repair sensitizes BRCA –wild-type cancer cells to replication stress. Science Signaling. 17(862). eadl6445–eadl6445. 2 indexed citations
3.
Saitoh, Noriko, et al.. (2023). Mathematical model of structural changes in nuclear speckle. Biophysics and Physicobiology. 20(2). n/a–n/a.
4.
Abe, Ryota, Miho Shimada, Tomonori Hirose, et al.. (2022). The 3′ Pol II pausing at replication-dependent histone genes is regulated by Mediator through Cajal bodies’ association with histone locus bodies. Nature Communications. 13(1). 18 indexed citations
5.
Matsumori, Haruka, Kenji Watanabe, Hiroaki Tachiwana, et al.. (2022). Ribosomal protein L5 facilitates rDNA-bundled condensate and nucleolar assembly. Life Science Alliance. 5(7). e202101045–e202101045. 10 indexed citations
6.
Maehara, Kazumitsu, Kosuke Tomimatsu, Akihito Harada, et al.. (2021). Modeling population size independent tissue epigenomes by ChIL‐seq with single thin sections. Molecular Systems Biology. 17(11). e10323–e10323. 3 indexed citations
7.
Tachiwana, Hiroaki, Kazumitsu Maehara, Akihito Harada, et al.. (2021). Chromatin structure-dependent histone incorporation revealed by a genome-wide deposition assay. eLife. 10. 5 indexed citations
8.
Kodama, Takashi, Atsushi Suenaga, Rashid Mehmood, et al.. (2021). Importin α2 association with chromatin: Direct DNA binding via a novel DNA‐binding domain. Genes to Cells. 26(12). 945–966. 7 indexed citations
9.
Ochiai, Hiroshi, Tetsutaro Hayashi, Mana Umeda, et al.. (2020). Genome-wide kinetic properties of transcriptional bursting in mouse embryonic stem cells. Science Advances. 6(25). eaaz6699–eaaz6699. 62 indexed citations
10.
Abdalla, Mohamed O., Tatsuro Yamamoto, Kazumitsu Maehara, et al.. (2019). The Eleanor ncRNAs activate the topological domain of the ESR1 locus to balance against apoptosis. Nature Communications. 10(1). 3778–3778. 29 indexed citations
11.
Ichikawa, Yuichi, Noriko Saitoh, & Paul D. Kaufman. (2018). An asymmetric centromeric nucleosome. eLife. 7. 4 indexed citations
12.
Tokunaga, Kazuaki, Noriko Saitoh, I. Goldberg, et al.. (2014). Computational image analysis of colony and nuclear morphology to evaluate human induced pluripotent stem cells. Scientific Reports. 4(1). 6996–6996. 52 indexed citations
13.
Liu, Lifeng, Ko Ishihara, Takaya Ichimura, et al.. (2008). MCAF1/AM Is Involved in Sp1-mediated Maintenance of Cancer-associated Telomerase Activity. Journal of Biological Chemistry. 284(8). 5165–5174. 45 indexed citations
14.
Kobayashi, Kayoko, et al.. (2003). General Anesthesia for a Patient with Brugada-pattern ECG : An Evaluation of Heart Rate Variability Using Power Spectrum. 31(1). 32–38. 2 indexed citations
15.
Matsuzaki, Kazuhito, Takeshi Minami, Masahide Tojo, et al.. (2003). PML‐nuclear bodies are involved in cellular serum response. Genes to Cells. 8(3). 275–286. 16 indexed citations
16.
Nagata, Koh-ichi, Aie Kawajiri, Takashi Shiromizu, et al.. (2003). Filament Formation of MSF-A, a Mammalian Septin, in Human Mammary Epithelial Cells Depends on Interactions with Microtubules. Journal of Biological Chemistry. 278(20). 18538–18543. 149 indexed citations
17.
18.
Togashi, Hideaki, et al.. (2000). Functions of a Rho-specific Guanine Nucleotide Exchange Factor in Neurite Retraction. Journal of Biological Chemistry. 275(38). 29570–29578. 42 indexed citations
19.
Matsuda, Juzo, et al.. (1993). β2-glycoprotein I -dependent and -independent anticardiolipin antibody in patients with end-stage renal disease. Thrombosis Research. 72(2). 109–117. 20 indexed citations
20.
Saitoh, Noriko & Satoru Saito. (1987). General Solutions to the Bäcklund Transformation of Hirota's Bilinear Difference Equation. Journal of the Physical Society of Japan. 56(5). 1664–1674. 13 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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