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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:

Binding kinetics of ligands acting at GPCRs
David A. Sykes, Leigh A. Stoddart, Laura E. Kilpatrick, et al.
Molecular and Cellular Endocrinology (2019) Vol. 485, pp. 9-19
Open Access | Times Cited: 101

Showing 1-25 of 101 citing articles:

Molecular Dynamics Simulations in Drug Discovery and Pharmaceutical Development
Outi M. H. Salo‐Ahen, Ida Alanko, Rajendra Bhadane, et al.
Processes (2020) Vol. 9, Iss. 1, pp. 71-71
Open Access | Times Cited: 373
New Advances in Targeting the Resolution of Inflammation: Implications for Specialized Pro-Resolving Mediator GPCR Drug Discovery
Julia Park, Christopher J. Langmead, Darren Riddy
ACS Pharmacology & Translational Science (2020) Vol. 3, Iss. 1, pp. 88-106
Open Access | Times Cited: 97
Intrinsically disordered proteins and proteins with intrinsically disordered regions in neurodegenerative diseases
Orkid Coskuner‐Weber, Ozan Mirzanli, Vladimir N. Uversky
Biophysical Reviews (2022) Vol. 14, Iss. 3, pp. 679-707
Open Access | Times Cited: 45
Quantifying Target Occupancy of Small Molecules Within Living Cells
Matthew B. Robers, Rachel Friedman‐Ohana, K. Huber, et al.
Annual Review of Biochemistry (2020) Vol. 89, Iss. 1, pp. 557-581
Open Access | Times Cited: 61
Does the Lipid Bilayer Orchestrate Access and Binding of Ligands to Transmembrane Orthosteric/Allosteric Sites of G Protein-Coupled Receptors?
Christopher T. Szlenk, B. Jeevan, Senthil Natesan
Molecular Pharmacology (2019) Vol. 96, Iss. 5, pp. 527-541
Open Access | Times Cited: 59
The luminescent HiBiT peptide enables selective quantitation of G protein–coupled receptor ligand engagement and internalization in living cells
Michelle E. Boursier, Sergiy Levin, Kris Zimmerman, et al.
Journal of Biological Chemistry (2020) Vol. 295, Iss. 15, pp. 5124-5135
Open Access | Times Cited: 49
100 years of modelling ligand–receptor binding and response: A focus on GPCRs
David B. Finlay, Stephen B. Duffull, Michelle Glass
British Journal of Pharmacology (2020) Vol. 177, Iss. 7, pp. 1472-1484
Open Access | Times Cited: 47
Perspective: Implications of Ligand–Receptor Binding Kinetics for Therapeutic Targeting of G Protein-Coupled Receptors
Wijnand J. C. van der Velden, Laura H. Heitman, Mette M. Rosenkilde
ACS Pharmacology & Translational Science (2020) Vol. 3, Iss. 2, pp. 179-189
Open Access | Times Cited: 46
A combination of machine learning and infrequent metadynamics to efficiently predict kinetic rates, transition states, and molecular determinants of drug dissociation from G protein-coupled receptors
João Marcelo Lamim Ribeiro, Davide Provasi, Marta Filizola
The Journal of Chemical Physics (2020) Vol. 153, Iss. 12
Open Access | Times Cited: 42
Perspectives on High-Throughput Ligand/Protein Docking With Martini MD Simulations
Paulo C. T. Souza, Vittorio Limongelli, Sangwook Wu, et al.
Frontiers in Molecular Biosciences (2021) Vol. 8
Open Access | Times Cited: 38
Computational Workflow for Refining AlphaFold Models in Drug Design Using Kinetic and Thermodynamic Binding Calculations: A Case Study for the Unresolved Inactive Human Adenosine A3 Receptor
Margarita Stampelou, Graham Ladds, Antonios Kolocouris
The Journal of Physical Chemistry B (2024) Vol. 128, Iss. 4, pp. 914-936
Closed Access | Times Cited: 5
Signaling by neutrophil G protein-coupled receptors that regulate the release of superoxide anions
Cláes Dahlgren, Huamei Forsman, Martina Sundqvist, et al.
Journal of Leukocyte Biology (2024)
Open Access | Times Cited: 5
G Protein-Coupled Receptor–Ligand Dissociation Rates and Mechanisms from τRAMD Simulations
Daria B. Kokh, Rebecca C. Wade
Journal of Chemical Theory and Computation (2021) Vol. 17, Iss. 10, pp. 6610-6623
Open Access | Times Cited: 29
The Impact of the Secondary Binding Pocket on the Pharmacology of Class A GPCRs
Attila Egyed, Dóra Kiss, György M. Keserü
Frontiers in Pharmacology (2022) Vol. 13
Open Access | Times Cited: 21
Membrane Lipids Are an Integral Part of Transmembrane Allosteric Sites in GPCRs: A Case Study of Cannabinoid CB1 Receptor Bound to a Negative Allosteric Modulator, ORG27569, and Analogs
Peter Obi, Senthil Natesan
Journal of Medicinal Chemistry (2022) Vol. 65, Iss. 18, pp. 12240-12255
Open Access | Times Cited: 21
Ligand selectivity hotspots in serotonin GPCRs
Ícaro A. Simon, Walden E. Bjørn‐Yoshimoto, Kasper Harpsøe, et al.
Trends in Pharmacological Sciences (2023) Vol. 44, Iss. 12, pp. 978-990
Open Access | Times Cited: 12
Highly Selective Drug-Derived Fluorescent Probes for the Cannabinoid Receptor Type 1 (CB1R)
Leonard Mach, Anahid Omran, Jara Bouma, et al.
Journal of Medicinal Chemistry (2024)
Open Access | Times Cited: 4
Application of FRET- and BRET-based live-cell biosensors in deorphanization and ligand discovery studies on orphan G protein-coupled receptors
Joanna J. Sajkowska, C. Tsang, Paweł Kozielewicz
SLAS DISCOVERY (2024) Vol. 29, Iss. 6, pp. 100174-100174
Open Access | Times Cited: 4
Redefining Roles: A Paradigm Shift in Tryptophan–Kynurenine Metabolism for Innovative Clinical Applications
Masaru Tanaka, Ágnes Szabó, László Vécsei
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 23, pp. 12767-12767
Open Access | Times Cited: 4
A universal cannabinoid CB1 and CB2 receptor TR-FRET kinetic ligand-binding assay
Leire Borrega‐Román, Bradley L. Hoare, Miroslav Kosar, et al.
Frontiers in Pharmacology (2025) Vol. 16
Open Access
Subtype-Selective Fluorescent Ligands as Pharmacological Research Tools for the Human Adenosine A2A Receptor
Eleonora Comeo, Nicholas D. Kindon, Mark Soave, et al.
Journal of Medicinal Chemistry (2019) Vol. 63, Iss. 5, pp. 2656-2672
Open Access | Times Cited: 33
Pharmacological characterisation of novel adenosine A3 receptor antagonists
Kerry Barkan, Panagiotis Lagarias, Margarita Stampelou, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 28
Highly Selective Drug-Derived Fluorescent Probes for the Cannabinoid Receptor Type 1 (CB1R)
Leonard Mach, Anahid Omran, Jara Bouma, et al.
(2024)
Open Access | Times Cited: 3
Synergistic, multi-level understanding of psychedelics: three systematic reviews and meta-analyses of their pharmacology, neuroimaging and phenomenology
Kenneth Shinozuka, Katarina Jerotic, Pedro A. M. Mediano, et al.
Translational Psychiatry (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 3
The importance of target binding kinetics for measuring target binding affinity in drug discovery: a case study from a CRF1 receptor antagonist program
Sam R.J. Hoare, Beth A. Fleck, John P. Williams, et al.
Drug Discovery Today (2019) Vol. 25, Iss. 1, pp. 7-14
Closed Access | Times Cited: 29
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