Yasuhito Onodera

2.8k total citations
46 papers, 2.1k citations indexed

About

Yasuhito Onodera is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Yasuhito Onodera has authored 46 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 12 papers in Oncology and 9 papers in Cell Biology. Recurrent topics in Yasuhito Onodera's work include Cell Adhesion Molecules Research (8 papers), Cancer Cells and Metastasis (6 papers) and Ubiquitin and proteasome pathways (6 papers). Yasuhito Onodera is often cited by papers focused on Cell Adhesion Molecules Research (8 papers), Cancer Cells and Metastasis (6 papers) and Ubiquitin and proteasome pathways (6 papers). Yasuhito Onodera collaborates with scholars based in Japan, United States and United Kingdom. Yasuhito Onodera's co-authors include Jin‐Min Nam, Hisataka Sabe, Shigeru Hashimoto, Mina J. Bissell, Ari Hashimoto, Hiroki Shirato, Atsuko Yamada, Catherine C. Park, Yuichi Mazaki and Miwa Tanaka and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Yasuhito Onodera

46 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yasuhito Onodera Japan 25 1.3k 584 542 447 310 46 2.1k
Kamiar Moin United States 30 1.1k 0.8× 404 0.7× 743 1.4× 1.2k 2.6× 424 1.4× 50 2.4k
Vasilena Gocheva United States 21 1.3k 1.0× 289 0.5× 969 1.8× 1.2k 2.6× 289 0.9× 25 2.7k
Cosimo Commisso United States 16 1.9k 1.5× 680 1.2× 765 1.4× 1.1k 2.5× 66 0.2× 31 3.0k
Christopher S. Gondi United States 32 1.6k 1.2× 225 0.4× 772 1.4× 1.1k 2.5× 265 0.9× 70 2.8k
Jihe Zhao United States 27 2.1k 1.6× 635 1.1× 1.0k 1.8× 661 1.5× 763 2.5× 40 3.5k
Miguel Abal Spain 34 1.7k 1.3× 499 0.9× 1.1k 2.0× 882 2.0× 78 0.3× 83 3.1k
Jun Chung United States 24 1.6k 1.2× 305 0.5× 515 1.0× 546 1.2× 618 2.0× 39 2.3k
Marta Canel United Kingdom 20 1.0k 0.8× 480 0.8× 590 1.1× 320 0.7× 526 1.7× 27 1.9k
Mansoureh Sameni United States 36 1.7k 1.3× 745 1.3× 1.1k 2.1× 1.8k 4.1× 695 2.2× 58 3.7k
Ainhoa Mielgo United States 28 1.3k 1.0× 409 0.7× 1.2k 2.2× 473 1.1× 319 1.0× 38 2.7k

Countries citing papers authored by Yasuhito Onodera

Since Specialization
Citations

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

Fields of papers citing papers by Yasuhito Onodera

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yasuhito Onodera

This figure shows the co-authorship network connecting the top 25 collaborators of Yasuhito Onodera. A scholar is included among the top collaborators of Yasuhito Onodera 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 Yasuhito Onodera. Yasuhito Onodera 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.
Onozawa, Masahiro, Kohei Kasahara, Toshihiro Matsukawa, et al.. (2025). CML With Mutant ASXL1 Showed Decreased Sensitivity to TKI Treatment via Upregulation of the ALOX5‐BLTR Signaling Pathway. Cancer Science. 116(4). 1115–1125. 1 indexed citations
2.
Takada, Shingo, et al.. (2024). Development of a Myogenin minimal promoter-based system for visualizing the degree of myogenic differentiation. Biochemical and Biophysical Research Communications. 741. 151091–151091. 1 indexed citations
3.
Oikawa, Tsukasa, Junya Hasegawa, Haruka Handa, et al.. (2024). p53 ensures the normal behavior and modification of G1/S-specific histone H3.1 in the nucleus. Life Science Alliance. 7(9). e202402835–e202402835. 2 indexed citations
4.
Onodera, Yasuhito, et al.. (2024). In vivo CRISPR screening directly targeting testicular cells. Cell Genomics. 4(3). 100510–100510. 4 indexed citations
5.
Yu, Li, Nako Maishi, Akira Hasebe, et al.. (2022). The oral bacterium Streptococcus mutans promotes tumor metastasis by inducing vascular inflammation. Cancer Science. 113(11). 3980–3994. 32 indexed citations
6.
Koyasu, Sho, Keisuke Saito, Minoru Kobayashi, et al.. (2022). ZBTB2 links p53 deficiency to HIF ‐1‐mediated hypoxia signaling to promote cancer aggressiveness. EMBO Reports. 24(1). e54042–e54042. 9 indexed citations
7.
Kobayashi, Minoru, Sho Koyasu, Shusuke Akamatsu, et al.. (2021). Proteolysis of a histone acetyl reader, ATAD2, induces chemoresistance of cancer cells under severe hypoxia by inhibiting cell cycle progression in S phase. Cancer Letters. 528. 76–84. 11 indexed citations
8.
Onodera, Yasuhito, Amato J. Giaccia, Quynh‐Thu Le, et al.. (2020). Lysosomal trafficking mediated by Arl8b and BORC promotes invasion of cancer cells that survive radiation. Communications Biology. 3(1). 620–620. 31 indexed citations
9.
Hashimoto, Shigeru, Ari Hashimoto, Akira Fukao, et al.. (2019). ARF6 and AMAP1 are major targets of KRAS and TP53 mutations to promote invasion, PD-L1 dynamics, and immune evasion of pancreatic cancer. Proceedings of the National Academy of Sciences. 116(35). 17450–17459. 102 indexed citations
10.
Mazaki, Yuichi, Yasuhito Onodera, Tsunehito Higashi, et al.. (2017). ARF1 recruits RAC1 to leading edge in neutrophil chemotaxis. Cell Communication and Signaling. 15(1). 36–36. 10 indexed citations
11.
Onodera, Yasuhito, Erinn B. Rankin, Amato J. Giaccia, et al.. (2017). Targeting integrins with RGD-conjugated gold nanoparticles in radiotherapy decreases the invasive activity of breast cancer cells. International Journal of Nanomedicine. Volume 12. 5069–5085. 106 indexed citations
12.
Onodera, Yasuhito, Jin‐Min Nam, & Hisataka Sabe. (2013). Intracellular trafficking of integrins in cancer cells. Pharmacology & Therapeutics. 140(1). 1–9. 32 indexed citations
13.
Osawa, Takahiro, Noritaka Ohga, Kosuke Akiyama, et al.. (2013). Lysyl oxidase secreted by tumour endothelial cells promotes angiogenesis and metastasis. British Journal of Cancer. 109(8). 2237–2247. 67 indexed citations
14.
Nam, Jin‐Min, Kazi Mokim Ahmed, Sylvain V. Costes, et al.. (2013). β1-integrin via NF-κB signaling is essential for acquisition of invasiveness in a model of radiation treated in situ breast cancer. Breast Cancer Research. 15(4). R60–R60. 35 indexed citations
15.
Yamamoto, Kazuhiro, Noritaka Ohga, Yasuhiro Hida, et al.. (2012). Biglycan is a specific marker and an autocrine angiogenic factor of tumour endothelial cells. British Journal of Cancer. 106(6). 1214–1223. 84 indexed citations
16.
Nam, Jin‐Min, Yasuhito Onodera, Mina J. Bissell, & Catherine C. Park. (2010). Breast Cancer Cells in Three-dimensional Culture Display an Enhanced Radioresponse after Coordinate Targeting of Integrin α5β1 and Fibronectin. Cancer Research. 70(13). 5238–5248. 168 indexed citations
17.
Sabe, Hisataka, Shigeru Hashimoto, Masaki Morishige, et al.. (2009). The EGFR‐GEP100‐Arf6‐AMAP1 Signaling Pathway Specific to Breast Cancer Invasion and Metastasis†. Traffic. 10(8). 982–993. 89 indexed citations
18.
Onodera, Yasuhito, Shigeru Hashimoto, Ari Hashimoto, et al.. (2005). Expression of AMAP1, an ArfGAP, provides novel targets to inhibit breast cancer invasive activities. The EMBO Journal. 24(5). 963–973. 137 indexed citations
19.
Hashimoto, Shigeru, Yasuhito Onodera, Ari Hashimoto, et al.. (2004). Requirement for Arf6 in breast cancer invasive activities. Proceedings of the National Academy of Sciences. 101(17). 6647–6652. 222 indexed citations
20.
Koyama, Shin-ya, Shinichiro Sugiyama, Akiko Kondo, et al.. (2002). Interaction of POB1, a Downstream Molecule of Small G Protein Ral, with PAG2, a Paxillin-binding Protein, Is Involved in Cell Migration. Journal of Biological Chemistry. 277(41). 38618–38626. 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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