Iori Sakakibara

2.0k total citations
33 papers, 1.3k citations indexed

About

Iori Sakakibara is a scholar working on Molecular Biology, Physiology and Rehabilitation. According to data from OpenAlex, Iori Sakakibara has authored 33 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 6 papers in Physiology and 4 papers in Rehabilitation. Recurrent topics in Iori Sakakibara's work include Muscle Physiology and Disorders (16 papers), Ubiquitin and proteasome pathways (7 papers) and Exercise and Physiological Responses (4 papers). Iori Sakakibara is often cited by papers focused on Muscle Physiology and Disorders (16 papers), Ubiquitin and proteasome pathways (7 papers) and Exercise and Physiological Responses (4 papers). Iori Sakakibara collaborates with scholars based in Japan, France and United States. Iori Sakakibara's co-authors include Pascal Maire, Takeshi Nikawa, Anayt Ulla, Juro Sakai, Takao Hamakubo, Tatsuhiko Kodama, Toshiya Tanaka, Masashi Okamura, Hiroyuki Aburatani and Ken‐ichi Wakabayashi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Iori Sakakibara

30 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Iori Sakakibara Japan 20 842 364 126 121 115 33 1.3k
George A. Kyriazis United States 17 533 0.6× 267 0.7× 150 1.2× 91 0.8× 117 1.0× 38 1.4k
Sigalit Boura‐Halfon Israel 20 799 0.9× 421 1.2× 121 1.0× 139 1.1× 106 0.9× 32 1.9k
Kechun Tang United States 20 707 0.8× 342 0.9× 123 1.0× 187 1.5× 106 0.9× 36 1.4k
Serge Summermatter Switzerland 21 709 0.8× 848 2.3× 183 1.5× 77 0.6× 67 0.6× 25 1.3k
Juan C. Bournat United States 11 441 0.5× 478 1.3× 64 0.5× 161 1.3× 85 0.7× 19 1.1k
Abolfazl Asadi Sweden 13 586 0.7× 603 1.7× 146 1.2× 62 0.5× 44 0.4× 18 1.4k
Antonello Lorenzini Italy 22 667 0.8× 670 1.8× 131 1.0× 72 0.6× 40 0.3× 57 1.6k
Zhenheng Guo United States 22 624 0.7× 486 1.3× 297 2.4× 77 0.6× 83 0.7× 35 1.4k
Val A. Fajardo Canada 22 765 0.9× 628 1.7× 199 1.6× 58 0.5× 117 1.0× 95 1.3k
Jessica Segalés Spain 15 1.4k 1.6× 582 1.6× 259 2.1× 75 0.6× 95 0.8× 16 1.7k

Countries citing papers authored by Iori Sakakibara

Since Specialization
Citations

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

Fields of papers citing papers by Iori Sakakibara

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iori Sakakibara

This figure shows the co-authorship network connecting the top 25 collaborators of Iori Sakakibara. A scholar is included among the top collaborators of Iori Sakakibara 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 Iori Sakakibara. Iori Sakakibara 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.
Watanabe, Masato, Ekaterina A. Semenova, Rinat Sultanov, et al.. (2025). Large MAF transcription factors reawaken evolutionarily dormant fast-glycolytic type IIb myofibers in human skeletal muscle. Skeletal Muscle. 15(1). 19–19. 1 indexed citations
2.
Fukawa, Tomoya, Kosuke Sugiura, Hirohisa Tsuda, et al.. (2025). Critical role of mitochondrial aconitase in skeletal muscle maturation. Scientific Reports. 15(1). 42957–42957.
3.
Sakai, Hiroshi, Iori Sakakibara, Akiyoshi Uezumi, et al.. (2024). Epidermal growth factor receptor contributes to indirect regulation of skeletal muscle mass by androgen. Endocrine Journal. 72(3). 259–272.
4.
Hasegawa, Yuka, et al.. (2024). PHF2 regulates sarcomeric gene transcription in myogenesis. PLoS ONE. 19(5). e0301690–e0301690. 1 indexed citations
5.
Masuda, Masashi, Iori Sakakibara, Takayuki Uchida, et al.. (2022). All-trans retinoic acid changes muscle fiber type via increasing GADD34 dependent on MAPK signal. Life Science Alliance. 5(7). e202101345–e202101345. 2 indexed citations
6.
Sakai, Hiroshi, Naohito Tokunaga, Kaori Tanaka, et al.. (2022). Uhrf1 governs the proliferation and differentiation of muscle satellite cells. iScience. 25(3). 103928–103928. 9 indexed citations
7.
Sakakibara, Iori, Takashi Yamada, Hiroshi Sakai, et al.. (2021). Myofiber androgen receptor increases muscle strength mediated by a skeletal muscle splicing variant of Mylk4. iScience. 24(4). 102303–102303. 37 indexed citations
8.
Ulla, Anayt, Takayuki Uchida, Yukari Miki, et al.. (2021). Morin attenuates dexamethasone-mediated oxidative stress and atrophy in mouse C2C12 skeletal myotubes. Archives of Biochemistry and Biophysics. 704. 108873–108873. 34 indexed citations
9.
10.
Maire, Pascal, et al.. (2020). Myogenesis control by SIX transcriptional complexes. Seminars in Cell and Developmental Biology. 104. 51–64. 23 indexed citations
11.
Inoue, Kazuki, Iori Sakakibara, Ji‐Won Lee, et al.. (2017). Uhrf1 is indispensable for normal limb growth by regulating chondrocyte differentiation through specific gene expression. Development. 145(1). 23 indexed citations
12.
Sakaue, Tomohisa, Iori Sakakibara, Koh‐ichi Nakashiro, et al.. (2017). The CUL3-SPOP-DAXX axis is a novel regulator of VEGFR2 expression in vascular endothelial cells. Scientific Reports. 7(1). 42845–42845. 25 indexed citations
13.
Yamasaki, Miwako, Keizo Takao, Shingo Soya, et al.. (2016). QRFP-Deficient Mice Are Hypophagic, Lean, Hypoactive and Exhibit Increased Anxiety-Like Behavior. PLoS ONE. 11(11). e0164716–e0164716. 25 indexed citations
14.
Sakakibara, Iori, Maud Wurmser, Matthieu Dos Santos, et al.. (2016). Six1 homeoprotein drives myofiber type IIA specialization in soleus muscle. Skeletal Muscle. 6(1). 30–30. 24 indexed citations
15.
Sakakibara, Iori, Marc Santolini, Arnaud Ferry, Vincent Hakim, & Pascal Maire. (2014). Six Homeoproteins and a linc-RNA at the Fast MYH Locus Lock Fast Myofiber Terminal Phenotype. PLoS Genetics. 10(5). e1004386–e1004386. 50 indexed citations
16.
Silvestre, Marta P., Benoı̂t Viollet, Paul Caton, et al.. (2014). The AMPK-SIRT signaling network regulates glucose tolerance under calorie restriction conditions. Life Sciences. 100(1). 55–60. 38 indexed citations
17.
Horikawa, Daiki D., John Cumbers, Iori Sakakibara, et al.. (2013). Analysis of DNA Repair and Protection in the Tardigrade Ramazzottius varieornatus and Hypsibius dujardini after Exposure to UVC Radiation. PLoS ONE. 8(6). e64793–e64793. 60 indexed citations
18.
Demignon, Josiane, Iori Sakakibara, Maryline Favier, et al.. (2011). Genesis of muscle fiber-type diversity during mouse embryogenesis relies on Six1 and Six4 gene expression. Developmental Biology. 359(2). 303–320. 59 indexed citations
19.
Okamura, Masashi, Hiromi Kudo, Ken‐ichi Wakabayashi, et al.. (2009). COUP-TFII acts downstream of Wnt/β-catenin signal to silence PPARγ gene expression and repress adipogenesis. Proceedings of the National Academy of Sciences. 106(14). 5819–5824. 150 indexed citations
20.
Ohguchi, Hiroto, Toshiya Tanaka, Aoi Uchida, et al.. (2008). Hepatocyte Nuclear Factor 4α Contributes to Thyroid Hormone Homeostasis by Cooperatively Regulating the Type 1 Iodothyronine Deiodinase Gene with GATA4 and Krüppel-Like Transcription Factor 9. Molecular and Cellular Biology. 28(12). 3917–3931. 36 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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