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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Roles of leader and follower cells in collective cell migration
Lei Qin, Dazhi Yang, Weihong Yi, et al.
Molecular Biology of the Cell (2021) Vol. 32, Iss. 14, pp. 1267-1272
Open Access | Times Cited: 65

Showing 1-25 of 65 citing articles:

Cancer metabolism and carcinogenesis
Jianqiang Yang, Chloe Shay, Nabil F. Saba, et al.
Experimental Hematology and Oncology (2024) Vol. 13, Iss. 1
Open Access | Times Cited: 35
Modeling the extracellular matrix in cell migration and morphogenesis: a guide for the curious biologist
Rebecca M. Crossley, Samuel Johnson, Erika Tsingos, et al.
Frontiers in Cell and Developmental Biology (2024) Vol. 12
Open Access | Times Cited: 25
Microfluidics meets 3D cancer cell migration
Pranav Mehta, Zaid Rahman, Peter ten Dijke, et al.
Trends in cancer (2022) Vol. 8, Iss. 8, pp. 683-697
Open Access | Times Cited: 48
Deposited footprints let cells switch between confined, oscillatory, and exploratory migration
Emiliano Pérez Ipiña, D. D. Joseph, Benoît Ladoux, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 22
Open Access | Times Cited: 9
Cytokinesis machinery promotes cell dissociation from collectively migrating strands in confinement
Robert A. Law, Alexander Kiepas, Habben E. Desta, et al.
Science Advances (2023) Vol. 9, Iss. 2
Open Access | Times Cited: 19
Who's really in charge: Diverse follower cell behaviors in collective cell migration
Joseph P. Campanale, Denise J. Montell
Current Opinion in Cell Biology (2023) Vol. 81, pp. 102160-102160
Open Access | Times Cited: 15
The Rac pathway prevents cell fragmentation in a nonprotrusively migrating leader cell during C. elegans gonad organogenesis
Noor Singh, Pu Zhang, Karen Jian Li, et al.
Current Biology (2024) Vol. 34, Iss. 11, pp. 2387-2402.e5
Closed Access | Times Cited: 5
An evolutionary and physiological perspective on cell-substrate adhesion machinery for cell migration
Julio C. Fierro Morales, Qian Xue, Minna Roh‐Johnson
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 19
The Migration and the Fate of Dental Pulp Stem Cells
Nadia Lampiasi
Biology (2023) Vol. 12, Iss. 5, pp. 742-742
Open Access | Times Cited: 12
The Drosophila hematopoietic niche assembles through collective cell migration controlled by neighbor tissues and Slit-Robo signaling
Kara A Nelson, Kari F. Lenhart, Lauren Anllo, et al.
eLife (2025) Vol. 13
Open Access
Internal cohesion gradient as a novel mechanism of collective cell migration
Larissa M. Oprysk, Maribel Vázquez, Troy Shinbrot
PLoS Computational Biology (2025) Vol. 21, Iss. 3, pp. e1012769-e1012769
Open Access
The Impact of Different Degrees of Leadership on Collective Navigation in Follower-Leader Systems
Sara Bernardi, Kevin J. Painter
Bulletin of Mathematical Biology (2025) Vol. 87, Iss. 5
Open Access
The cellular slime mold Fonticula alba forms a dynamic, multicellular collective while feeding on bacteria
Christopher P. Toret, Andrea Picco, Micaela Boiero Sanders, et al.
Current Biology (2022) Vol. 32, Iss. 9, pp. 1961-1973.e4
Open Access | Times Cited: 17
A Scribble/Cdep/Rac pathway controls follower-cell crawling and cluster cohesion during collective border-cell migration
Joseph P. Campanale, James A. Mondo, Denise J. Montell
Developmental Cell (2022) Vol. 57, Iss. 21, pp. 2483-2496.e4
Open Access | Times Cited: 16
Collective rotational motion of freely expanding T84 epithelial cell colonies
Flora Ascione, Sergio Caserta, Speranza Esposito, et al.
Journal of The Royal Society Interface (2023) Vol. 20, Iss. 199
Open Access | Times Cited: 9
Leader Cells: Invade and Evade—The Frontline of Cancer Progression
Brittany R. Doran, Laura R. Moffitt, Amy L. Wilson, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 19, pp. 10554-10554
Open Access | Times Cited: 3
Scale-free correlations and potential criticality in weakly ordered populations of brain cancer cells
Kevin B. Wood, Andrea Comba, Sébastien Motsch, et al.
Science Advances (2023) Vol. 9, Iss. 26
Open Access | Times Cited: 7
Meningeal origins and dynamics of perivascular fibroblast development on the mouse cerebral vasculature
Hannah E. Jones, Vanessa Coelho‐Santos, Stephanie Bonney, et al.
Development (2023) Vol. 150, Iss. 19
Open Access | Times Cited: 7
Engineering anisotropic tissue analogues: harnessing synergistic potential of extrusion-based bioprinting and extracellular matrix-based bioink
Ashis Kumar Bera, Mohd Suhail Rizvi, Vijayasankar Kn, et al.
Biofabrication (2024) Vol. 17, Iss. 1, pp. 015003-015003
Closed Access | Times Cited: 2
Epithelial–Mesenchymal Transition by Synergy between Transforming Growth Factor-β and Growth Factors in Cancer Progression
Masao Saitoh
Diagnostics (2022) Vol. 12, Iss. 9, pp. 2127-2127
Open Access | Times Cited: 10
Disentangling cadherin-mediated cell-cell interactions in collective cancer cell migration
Themistoklis Zisis, David B. Brückner, Tom Brandstätter, et al.
Biophysical Journal (2021) Vol. 121, Iss. 1, pp. 44-60
Open Access | Times Cited: 14
Optical Cellular Micromotion: A New Paradigm to Measure Tumor Cells Invasion within Gels Mimicking the 3D Tumor Environments
Zhaobin Guo, Chih‐Tsung Yang, Chia‐Chi Chien, et al.
Small Methods (2022) Vol. 6, Iss. 8
Open Access | Times Cited: 9
Interplay between Partial EMT and Cisplatin Resistance as the Drivers for Recurrence in HNSCC
Julia Ingruber, József Dudás, Susanne Sprung, et al.
Biomedicines (2022) Vol. 10, Iss. 10, pp. 2482-2482
Open Access | Times Cited: 9
Meningeal origins and dynamics of perivascular fibroblast development on the mouse cerebral vasculature
Hannah E. Jones, Vanessa Coelho‐Santos, Stephanie Bonney, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 5
CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells
Xiaoqiang Liu, Jinrui Yang, Meng Kong, et al.
Burns & Trauma (2023) Vol. 11
Open Access | Times Cited: 5
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