Yoshiaki Iwadate

1.0k total citations
52 papers, 718 citations indexed

About

Yoshiaki Iwadate is a scholar working on Cell Biology, Biomedical Engineering and Molecular Biology. According to data from OpenAlex, Yoshiaki Iwadate has authored 52 papers receiving a total of 718 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Cell Biology, 12 papers in Biomedical Engineering and 11 papers in Molecular Biology. Recurrent topics in Yoshiaki Iwadate's work include Cellular Mechanics and Interactions (20 papers), 3D Printing in Biomedical Research (8 papers) and Protist diversity and phylogeny (7 papers). Yoshiaki Iwadate is often cited by papers focused on Cellular Mechanics and Interactions (20 papers), 3D Printing in Biomedical Research (8 papers) and Protist diversity and phylogeny (7 papers). Yoshiaki Iwadate collaborates with scholars based in Japan, United States and South Korea. Yoshiaki Iwadate's co-authors include Shigehiko Yumura, Akira Nagasaki, Taro Q.P. Uyeda, Nobuhisa Umeki, Md. Kamruzzaman Pramanik, Miho Iijima, Hiroshi Asai, Thomas Egelhoff, Lucila S. Licate and Woontack Woo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Scientific Reports.

In The Last Decade

Yoshiaki Iwadate

46 papers receiving 705 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoshiaki Iwadate Japan 14 449 190 189 95 70 52 718
Matthew B. Smith United Kingdom 10 490 1.1× 236 1.2× 152 0.8× 88 0.9× 41 0.6× 18 727
Michael G. Vicker Germany 16 388 0.9× 243 1.3× 185 1.0× 31 0.3× 50 0.7× 23 688
Andrea Dimitracopoulos United Kingdom 9 478 1.1× 247 1.3× 158 0.8× 55 0.6× 45 0.6× 11 668
Jim H. Veldhuis Canada 15 746 1.7× 238 1.3× 435 2.3× 67 0.7× 38 0.5× 25 968
Krithika Mohan United States 9 338 0.8× 140 0.7× 107 0.6× 89 0.9× 56 0.8× 22 475
David Richmond United States 11 251 0.6× 659 3.5× 340 1.8× 78 0.8× 32 0.5× 19 1.0k
Loïc LeGoff France 12 490 1.1× 291 1.5× 204 1.1× 110 1.2× 39 0.6× 22 866
Daisuke Inoue Japan 21 515 1.1× 433 2.3× 280 1.5× 46 0.5× 23 0.3× 56 1.3k
Stéphane Rigaud France 5 329 0.7× 341 1.8× 157 0.8× 23 0.2× 37 0.5× 11 782
William A. Marganski United States 11 750 1.7× 329 1.7× 430 2.3× 110 1.2× 82 1.2× 15 1.1k

Countries citing papers authored by Yoshiaki Iwadate

Since Specialization
Citations

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

Fields of papers citing papers by Yoshiaki Iwadate

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshiaki Iwadate

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshiaki Iwadate. A scholar is included among the top collaborators of Yoshiaki Iwadate 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 Yoshiaki Iwadate. Yoshiaki Iwadate 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.
Sakurai, Tatsunari, et al.. (2025). Linear contraction of stress fibers generates cell body rotation. Cell Reports Physical Science. 6(2). 102429–102429. 1 indexed citations
2.
Kozawa, Satoshi, et al.. (2023). Bayesian traction force estimation using cell boundary-dependent force priors. Biophysical Journal. 122(23). 4542–4554. 1 indexed citations
3.
Sakurai, Tatsunari, et al.. (2022). Leading-edge elongation by follower cell interruption in advancing epithelial cell sheets. Proceedings of the National Academy of Sciences. 119(18). e2119903119–e2119903119. 9 indexed citations
4.
Saito, Nen, Akihiko Nakajima, Sayaka Ishihara, et al.. (2021). Comparative mapping of crawling-cell morphodynamics in deep learning-based feature space. PLoS Computational Biology. 17(8). e1009237–e1009237. 16 indexed citations
5.
Ueno, Tasuku, Daisuke Asanuma, Yusuke Nomura, et al.. (2021). Discovery of an F-actin–binding small molecule serving as a fluorescent probe and a scaffold for functional probes. Science Advances. 7(47). eabg8585–eabg8585. 15 indexed citations
6.
Tsujioka, Masatsune, Taro Q.P. Uyeda, Yoshiaki Iwadate, et al.. (2019). Actin-binding domains mediate the distinct distribution of two Dictyostelium Talins through different affinities to specific subsets of actin filaments during directed cell migration. PLoS ONE. 14(4). e0214736–e0214736. 4 indexed citations
7.
Sakumura, Yuichi, et al.. (2018). Sensing of substratum rigidity and directional migration by fast-crawling cells. Physical review. E. 97(5). 52401–52401. 7 indexed citations
8.
Iwadate, Yoshiaki, et al.. (2016). Hybrid mechanosensing system to generate the polarity needed for migration in fish keratocytes. Cell Adhesion & Migration. 10(4). 1–13. 11 indexed citations
9.
Mizuno, Takafumi, et al.. (2016). The Role of Stress Fibers in the Shape Determination Mechanism of Fish Keratocytes. Biophysical Journal. 110(2). 481–492. 11 indexed citations
10.
Adachi, Kenta, et al.. (2016). Kinetics of Coloration in Photochromic Tungsten(VI) Oxide/Silicon Oxycarbide/Silica Hybrid Xerogel: Insight into Cation Self-diffusion Mechanisms. ACS Applied Materials & Interfaces. 8(22). 14019–14028. 27 indexed citations
11.
Iwadate, Yoshiaki, et al.. (2013). Myosin-II-Mediated Directional Migration of Dictyostelium Cells in Response to Cyclic Stretching of Substratum. Biophysical Journal. 104(4). 748–758. 16 indexed citations
12.
Uyeda, Taro Q.P., Yoshiaki Iwadate, Nobuhisa Umeki, Akira Nagasaki, & Shigehiko Yumura. (2011). Stretching Actin Filaments within Cells Enhances their Affinity for the Myosin II Motor Domain. PLoS ONE. 6(10). e26200–e26200. 123 indexed citations
13.
Iwadate, Yoshiaki & Shigehiko Yumura. (2009). Cyclic stretch of the substratum using a shape-memory alloy induces directional migration in Dictyostelium cells. BioTechniques. 47(3). 757–767. 31 indexed citations
14.
Iwadate, Yoshiaki & Yasuo Nakaoka. (2008). Calcium regulates independently ciliary beat and cell contraction in Paramecium cells. Cell Calcium. 44(2). 169–179. 13 indexed citations
15.
Yumura, Shigehiko, Masashi Yoshida, Venkaiah Betapudi, et al.. (2005). Multiple Myosin II Heavy Chain Kinases: Roles in Filament Assembly Control and Proper Cytokinesis in Dictyostelium. Molecular Biology of the Cell. 16(9). 4256–4266. 73 indexed citations
16.
Iwadate, Yoshiaki & Toshinobu Suzaki. (2004). Ciliary reorientation is evoked by a rise in calcium level over the entire cilium. Cell Motility and the Cytoskeleton. 57(4). 197–206. 8 indexed citations
17.
Iwadate, Yoshiaki, et al.. (2003). VRML animation from multi-view images. 881–884. 5 indexed citations
18.
Inoue, Tomoyoshi, et al.. (2002). Transmitting visual information: icons become words. 244–249. 1 indexed citations
19.
Iwadate, Yoshiaki, Kaoru Katoh, M. Kikuyama, & Hiroshi Asai. (1999). Ca2+ triggers toxicyst discharge inDidinium nasutum. PROTOPLASMA. 206(1-3). 20–26. 8 indexed citations
20.
Iwadate, Yoshiaki & Hiroshi Asai. (1996). Improved preparation and swimming behavior of Triton-extracted models ofDidinium nasutum. Cell Motility and the Cytoskeleton. 33(3). 175–182. 3 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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