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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:

Regulation of endogenous transmembrane receptors through optogenetic Cry2 clustering
Lukasz J. Bugaj, Dawn P. Spelke, Colin K Mesuda, et al.
Nature Communications (2015) Vol. 6, Iss. 1
Open Access | Times Cited: 98

Showing 1-25 of 98 citing articles:

Optogenetic Tools for Subcellular Applications in Neuroscience
Benjamin R. Rost, Franziska Schneider‐Warme, Dietmar Schmitz, et al.
Neuron (2017) Vol. 96, Iss. 3, pp. 572-603
Open Access | Times Cited: 304
Blue-Light Receptors for Optogenetics
Aba Losi, Kevin H. Gardner, Andreas Möglich
Chemical Reviews (2018) Vol. 118, Iss. 21, pp. 10659-10709
Open Access | Times Cited: 224
New developments in the biology of fibroblast growth factors
David M. Ornitz, Nobuyuki Itoh
WIREs Mechanisms of Disease (2022) Vol. 14, Iss. 4
Open Access | Times Cited: 98
At Light Speed: Advances in Optogenetic Systems for Regulating Cell Signaling and Behavior
Nicole Repina, Alyssa B. Rosenbloom, Abhirup Mukherjee, et al.
Annual Review of Chemical and Biomolecular Engineering (2017) Vol. 8, Iss. 1, pp. 13-39
Open Access | Times Cited: 149
An open-hardware platform for optogenetics and photobiology
Karl P. Gerhardt, Evan J. Olson, Sebastian M. Castillo-Hair, et al.
Scientific Reports (2016) Vol. 6, Iss. 1
Open Access | Times Cited: 134
Extracellular matrix protein 1 promotes cell metastasis and glucose metabolism by inducing integrin β4/FAK/SOX2/HIF-1α signaling pathway in gastric cancer
Lu Gan, Jun Meng, Midie Xu, et al.
Oncogene (2017) Vol. 37, Iss. 6, pp. 744-755
Closed Access | Times Cited: 131
Membrane-associated periodic skeleton is a signaling platform for RTK transactivation in neurons
Ruobo Zhou, Boran Han, Chenglong Xia, et al.
Science (2019) Vol. 365, Iss. 6456, pp. 929-934
Open Access | Times Cited: 120
Near-Infrared Light-Activated DNA-Agonist Nanodevice for Nongenetically and Remotely Controlled Cellular Signaling and Behaviors in Live Animals
Miao Wang, Fang He, Hao Li, et al.
Nano Letters (2019) Vol. 19, Iss. 4, pp. 2603-2613
Open Access | Times Cited: 89
Light‐Controlled Mammalian Cells and Their Therapeutic Applications in Synthetic Biology
Maysam Mansouri, Tobias Strittmatter, Martin Fussenegger
Advanced Science (2018) Vol. 6, Iss. 1
Open Access | Times Cited: 86
Rapid Optogenetic Clustering in the Cytoplasm with BcLOVclust
Zikang Huang, William Benman, Liang Dong, et al.
Journal of Molecular Biology (2024) Vol. 436, Iss. 3, pp. 168452-168452
Closed Access | Times Cited: 9
Protein Design Accelerates the Development and Application of Optogenetic Tools
Lingyun Zhu, Yuxuan Wang, Xiaomin Wu, et al.
Computational and Structural Biotechnology Journal (2025) Vol. 27, pp. 717-732
Open Access | Times Cited: 1
Modular engineering of cellular signaling proteins and networks
Russell M. Gordley, Lukasz J. Bugaj, Wendell A. Lim
Current Opinion in Structural Biology (2016) Vol. 39, pp. 106-114
Open Access | Times Cited: 77
Single-Molecule Analysis and Engineering of DNA Motors
Sonisilpa Mohapatra, Chang-Ting Lin, Xinyu A. Feng, et al.
Chemical Reviews (2019) Vol. 120, Iss. 1, pp. 36-78
Closed Access | Times Cited: 76
Optogenetically controlled protein kinases for regulation of cellular signaling
Anna V. Leopold, Konstantin G. Chernov, Vladislav V. Verkhusha
Chemical Society Reviews (2018) Vol. 47, Iss. 7, pp. 2454-2484
Open Access | Times Cited: 66
Cell-matrix adhesion and cell-cell adhesion differentially control basal myosin oscillation and Drosophila egg chamber elongation
Xiang Qin, Byung Ouk Park, Jiaying Liu, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 65
Engineered Illumination Devices for Optogenetic Control of Cellular Signaling Dynamics
Nicole Repina, Thomas McClave, Hunter J. Johnson, et al.
Cell Reports (2020) Vol. 31, Iss. 10, pp. 107737-107737
Open Access | Times Cited: 61
Structural insights into BIC-mediated inactivation of Arabidopsis cryptochrome 2
Ling Ma, Xiang Wang, Zeyuan Guan, et al.
Nature Structural & Molecular Biology (2020) Vol. 27, Iss. 5, pp. 472-479
Closed Access | Times Cited: 54
Layilin augments integrin activation to promote antitumor immunity
Kelly M. Mahuron, J. Moreau, Jeff E. Glasgow, et al.
The Journal of Experimental Medicine (2020) Vol. 217, Iss. 9
Open Access | Times Cited: 52
Simple visualization of submicroscopic protein clusters with a phase-separation-based fluorescent reporter
Thomas R. Mumford, Diarmid Rae, Emily Brackhahn, et al.
Cell Systems (2024) Vol. 15, Iss. 2, pp. 166-179.e7
Open Access | Times Cited: 8
Optogenetic toolkit for precise control of calcium signaling
Guolin Ma, Shufan Wen, Lian He, et al.
Cell Calcium (2017) Vol. 64, pp. 36-46
Open Access | Times Cited: 61
Engineering genetically-encoded tools for optogenetic control of protein activity
Qi Liu, Chandra L. Tucker
Current Opinion in Chemical Biology (2017) Vol. 40, pp. 17-23
Open Access | Times Cited: 54
Synthetic biological approaches to optogenetically control cell signaling
Katja Kolar, Wilfried Weber
Current Opinion in Biotechnology (2017) Vol. 47, pp. 112-119
Closed Access | Times Cited: 54
Optogenetics in plants
John M. Christie, Matías D. Zurbriggen
New Phytologist (2020) Vol. 229, Iss. 6, pp. 3108-3115
Open Access | Times Cited: 41
Intracellular microbial rhodopsin-based optogenetics to control metabolism and cell signaling
Anastasiia D. Vlasova, Siarhei Bukhalovich, Diana F. Bagaeva, et al.
Chemical Society Reviews (2024) Vol. 53, Iss. 7, pp. 3327-3349
Closed Access | Times Cited: 5
Application of optogenetic Amyloid-β distinguishes between metabolic and physical damages in neurodegeneration
Chu Hsien Lim, Prameet Kaur, Emelyne Teo, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 38
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