Dennis W. Zhou

1.1k total citations
16 papers, 816 citations indexed

About

Dennis W. Zhou is a scholar working on Cell Biology, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Dennis W. Zhou has authored 16 papers receiving a total of 816 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cell Biology, 6 papers in Molecular Biology and 5 papers in Immunology and Allergy. Recurrent topics in Dennis W. Zhou's work include Cellular Mechanics and Interactions (8 papers), Cell Adhesion Molecules Research (5 papers) and Force Microscopy Techniques and Applications (3 papers). Dennis W. Zhou is often cited by papers focused on Cellular Mechanics and Interactions (8 papers), Cell Adhesion Molecules Research (5 papers) and Force Microscopy Techniques and Applications (3 papers). Dennis W. Zhou collaborates with scholars based in United States, Germany and United Kingdom. Dennis W. Zhou's co-authors include Andrés J. Garcı́a, Jianping Fu, Amy Y. Clark, Jeffrey J. Werner, Christopher Johnson, Rob Knight, Karen E. Martin, Woojin M. Han, Edward A. Botchwey and José R. García and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Biomaterials.

In The Last Decade

Dennis W. Zhou

16 papers receiving 809 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dennis W. Zhou United States 14 278 272 219 118 100 16 816
Elly M. M. Versteeg Netherlands 19 467 1.7× 459 1.7× 104 0.5× 126 1.1× 93 0.9× 45 1.0k
Kari Törrönen Finland 14 444 1.6× 417 1.5× 111 0.5× 120 1.0× 79 0.8× 16 926
Stéphane Galiacy France 20 144 0.5× 271 1.0× 84 0.4× 70 0.6× 65 0.7× 31 1.1k
Г. П. Пинаев Russia 15 135 0.5× 300 1.1× 108 0.5× 82 0.7× 55 0.6× 75 653
Katsumi Mochitate Japan 16 170 0.6× 271 1.0× 125 0.6× 193 1.6× 90 0.9× 32 773
Leigh West United States 20 344 1.2× 353 1.3× 122 0.6× 65 0.6× 66 0.7× 30 1.0k
Yong Woo Ji South Korea 21 78 0.3× 294 1.1× 199 0.9× 136 1.2× 93 0.9× 74 1.4k
Jiansong Xie United States 15 129 0.5× 299 1.1× 135 0.6× 86 0.7× 34 0.3× 32 789
Giancarlo Nastasi Italy 17 474 1.7× 303 1.1× 56 0.3× 103 0.9× 66 0.7× 23 1.0k

Countries citing papers authored by Dennis W. Zhou

Since Specialization
Citations

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

Fields of papers citing papers by Dennis W. Zhou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dennis W. Zhou. 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 Dennis W. Zhou. The network helps show where Dennis W. Zhou may publish in the future.

Co-authorship network of co-authors of Dennis W. Zhou

This figure shows the co-authorship network connecting the top 25 collaborators of Dennis W. Zhou. A scholar is included among the top collaborators of Dennis W. Zhou 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 Dennis W. Zhou. Dennis W. Zhou is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Fernández, Marc, Dennis W. Zhou, Eric B. O’Neill, et al.. (2024). FAK, vinculin, and talin control mechanosensitive YAP nuclear localization. Biomaterials. 308. 122542–122542. 15 indexed citations
2.
Goodman, Max, et al.. (2023). A National Medical Student Diagnostic Radiology Competition Initiative: Survey and Outcomes of the RadiOlympics. Academic Radiology. 30(11). 2741–2748. 2 indexed citations
3.
Zheng, Yijun, Mitchell K. L. Han, Renping Zhao, et al.. (2021). Optoregulated force application to cellular receptors using molecular motors. Nature Communications. 12(1). 3580–3580. 27 indexed citations
4.
Zhou, Dennis W., Marc Fernández, Eric B. O’Neill, et al.. (2021). Force-FAK signaling coupling at individual focal adhesions coordinates mechanosensing and microtissue repair. Nature Communications. 12(1). 2359–2359. 59 indexed citations
5.
Clark, Amy Y., Karen E. Martin, José R. García, et al.. (2020). Integrin-specific hydrogels modulate transplanted human bone marrow-derived mesenchymal stem cell survival, engraftment, and reparative activities. Nature Communications. 11(1). 114–114. 164 indexed citations
6.
Flemming, Sven, Anny‐Claude Luissint, Dennis H. M. Kusters, et al.. (2020). Desmocollin-2 promotes intestinal mucosal repair by controlling integrin-dependent cell adhesion and migration. Molecular Biology of the Cell. 31(6). 407–418. 34 indexed citations
7.
Cantini, Marco, Yuan Yan Sin, Dennis W. Zhou, et al.. (2020). Material-driven fibronectin assembly rescues matrix defects due to mutations in collagen IV in fibroblasts. Biomaterials. 252. 120090–120090. 8 indexed citations
8.
Quirós, Miguel, Rachit Agarwal, Dennis W. Zhou, et al.. (2020). Resolvin E1 is a pro-repair molecule that promotes intestinal epithelial wound healing. Proceedings of the National Academy of Sciences. 117(17). 9477–9482. 70 indexed citations
9.
Quirós, Miguel, Vicky García‐Hernández, Dennis W. Zhou, et al.. (2019). TNFα promotes mucosal wound repair through enhanced platelet activating factor receptor signaling in the epithelium. Mucosal Immunology. 12(4). 909–918. 37 indexed citations
10.
Zhou, Dennis W., Ted T. Lee, Shinuo Weng, Jianping Fu, & Andrés J. Garcı́a. (2017). Effects of substrate stiffness and actomyosin contractility on coupling between force transmission and vinculin–paxillin recruitment at single focal adhesions. Molecular Biology of the Cell. 28(14). 1901–1911. 83 indexed citations
11.
Weaver, Jessica D., Amy Y. Clark, Soledad Pérez‐Amodio, et al.. (2017). PEG hydrogel containing calcium-releasing particles and mesenchymal stromal cells promote vessel maturation. Acta Biomaterialia. 67. 53–65. 19 indexed citations
12.
Kohn, Julie C., Dennis W. Zhou, François Bordeleau, et al.. (2015). Cooperative Effects of Matrix Stiffness and Fluid Shear Stress on Endothelial Cell Behavior. Biophysical Journal. 108(3). 471–478. 131 indexed citations
13.
Fernández, Isabel Cuesta, Abel Martín-Garrido, Dennis W. Zhou, et al.. (2015). Hic-5 Mediates TGFβ–Induced Adhesion in Vascular Smooth Muscle Cells by a Nox4-Dependent Mechanism. Arteriosclerosis Thrombosis and Vascular Biology. 35(5). 1198–1206. 17 indexed citations
14.
Zhou, Dennis W. & Andrés J. Garcı́a. (2014). Measurement Systems for Cell Adhesive Forces. Journal of Biomechanical Engineering. 137(2). 20908–20908. 23 indexed citations
15.
Ellerbroek, Shawn M., et al.. (2014). Vinculin-dependent actin bundling regulates cell migration and traction forces. Biochemical Journal. 465(3). 383–393. 37 indexed citations
16.
Werner, Jeffrey J., Dennis W. Zhou, J. Gregory Caporaso, Rob Knight, & Largus T. Angenent. (2011). Comparison of Illumina paired-end and single-direction sequencing for microbial 16S rRNA gene amplicon surveys. The ISME Journal. 6(7). 1273–1276. 90 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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