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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:

International Union of Basic and Clinical Pharmacology. XC. Multisite Pharmacology: Recommendations for the Nomenclature of Receptor Allosterism and Allosteric Ligands
Arthur Christopoulos, Jean‐Pierre Changeux, William A. Catterall, et al.
Pharmacological Reviews (2014) Vol. 66, Iss. 4, pp. 918-947
Open Access | Times Cited: 223

Showing 1-25 of 223 citing articles:

Trends in GPCR drug discovery: new agents, targets and indications
Alexander S. Hauser, Misty M. Attwood, Mathias Rask‐Andersen, et al.
Nature Reviews Drug Discovery (2017) Vol. 16, Iss. 12, pp. 829-842
Open Access | Times Cited: 2266
Mechanisms of signalling and biased agonism in G protein-coupled receptors
Denise Wootten, Arthur Christopoulos, Maria Martí-Solano, et al.
Nature Reviews Molecular Cell Biology (2018) Vol. 19, Iss. 10, pp. 638-653
Open Access | Times Cited: 584
How Ligands Illuminate GPCR Molecular Pharmacology
Daniel Wacker, Raymond C. Stevens, Bryan L. Roth
Cell (2017) Vol. 170, Iss. 3, pp. 414-427
Open Access | Times Cited: 489
Ten things you should know about protein kinases: IUPHAR Review 14
Doriano Fabbro, Sandra W. Cowan‐Jacob, Henrik Moebitz
British Journal of Pharmacology (2015) Vol. 172, Iss. 11, pp. 2675-2700
Open Access | Times Cited: 308
Structural insights into G-protein-coupled receptor allostery
David M. Thal, Alisa Glukhova, Patrick M. Sexton, et al.
Nature (2018) Vol. 559, Iss. 7712, pp. 45-53
Closed Access | Times Cited: 303
GABAA receptor: Positive and negative allosteric modulators
Richard W. Olsen
Neuropharmacology (2018) Vol. 136, pp. 10-22
Open Access | Times Cited: 300
Allosteric Modulation as a Unifying Mechanism for Receptor Function and Regulation
Jean‐Pierre Changeux, Arthur Christopoulos
Cell (2016) Vol. 166, Iss. 5, pp. 1084-1102
Open Access | Times Cited: 285
LEAP2 Is an Endogenous Antagonist of the Ghrelin Receptor
Xuecai Ge, Hong Yang, Maria A. Bednarek, et al.
Cell Metabolism (2017) Vol. 27, Iss. 2, pp. 461-469.e6
Open Access | Times Cited: 282
Emerging Molecular Mechanisms of Signal Transduction in Pentameric Ligand-Gated Ion Channels
Ákos Nemecz, Marie S. Prevost, Anaïs Menny, et al.
Neuron (2016) Vol. 90, Iss. 3, pp. 452-470
Open Access | Times Cited: 226
Advances in G Protein-Coupled Receptor Allostery: From Function to Structure
Arthur Christopoulos
Molecular Pharmacology (2014) Vol. 86, Iss. 5, pp. 463-478
Open Access | Times Cited: 213
International Union of Basic and Clinical Pharmacology. CX. Classification of Receptors for 5-hydroxytryptamine; Pharmacology and Function
Nicholas M. Barnes, Gerard P. Ahern, Carine Bécamel, et al.
Pharmacological Reviews (2020) Vol. 73, Iss. 1, pp. 310-520
Open Access | Times Cited: 204
GPR40 (FFAR1) – Combined Gs and Gq signaling in vitro is associated with robust incretin secretagogue action ex vivo and in vivo
M. Hauge, M. A. Vestmar, Anna Sofie Husted, et al.
Molecular Metabolism (2014) Vol. 4, Iss. 1, pp. 3-14
Open Access | Times Cited: 200
Novel Allosteric Modulators of G Protein-coupled Receptors
Patrick R. Gentry, Patrick M. Sexton, Arthur Christopoulos
Journal of Biological Chemistry (2015) Vol. 290, Iss. 32, pp. 19478-19488
Open Access | Times Cited: 188
Biased Allosteric Modulators: New Frontiers in GPCR Drug Discovery
Lauren M. Slosky, Marc G. Caron, Lawrence S Barak
Trends in Pharmacological Sciences (2021) Vol. 42, Iss. 4, pp. 283-299
Open Access | Times Cited: 136
Structure-Based Virtual Screening for Ligands of G Protein–Coupled Receptors: What Can Molecular Docking Do for You?
Flavio Ballante, Albert J. Kooistra, Stefanie Kampen, et al.
Pharmacological Reviews (2021) Vol. 73, Iss. 4, pp. 1698-1736
Open Access | Times Cited: 104
Glycine: The Smallest Anti-Inflammatory Micronutrient
Karla Aidee Aguayo-Cerón, Fausto Sánchez‐Muñoz, Rocío Alejandra Gutiérrez-Rojas, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 14, pp. 11236-11236
Open Access | Times Cited: 47
Cardiotoxic effects of common and emerging drugs: role of cannabinoid receptors
Yi-Ming Bo, Xin Zhao, Liliang Li
Clinical Science (2024) Vol. 138, Iss. 6, pp. 413-434
Closed Access | Times Cited: 22
Functional dynamics of G protein-coupled receptors reveal new routes for drug discovery
Paolo Conflitti, Edward Lyman, Mark S.P. Sansom, et al.
Nature Reviews Drug Discovery (2025)
Closed Access | Times Cited: 2
Practical Strategies and Concepts in GPCR Allosteric Modulator Discovery: Recent Advances with Metabotropic Glutamate Receptors
Craig W. Lindsley, Kyle A. Emmitte, Corey R. Hopkins, et al.
Chemical Reviews (2016) Vol. 116, Iss. 11, pp. 6707-6741
Open Access | Times Cited: 166
A kinetic view of GPCR allostery and biased agonism
J. Robert Lane, Lauren T. May, Robert G. Parton, et al.
Nature Chemical Biology (2017) Vol. 13, Iss. 9, pp. 929-937
Open Access | Times Cited: 159
Allosteric “beta-blocker” isolated from a DNA-encoded small molecule library
Seungkirl Ahn, Alem W. Kahsai, Biswaranjan Pani, et al.
Proceedings of the National Academy of Sciences (2017) Vol. 114, Iss. 7, pp. 1708-1713
Open Access | Times Cited: 147
Endogenous Allosteric Modulators of G Protein–Coupled Receptors
Emma T. van der Westhuizen, Céline Valant, Patrick M. Sexton, et al.
Journal of Pharmacology and Experimental Therapeutics (2015) Vol. 353, Iss. 2, pp. 246-260
Open Access | Times Cited: 137
25 Years of Small Molecular Weight Kinase Inhibitors: Potentials and Limitations
Doriano Fabbro
Molecular Pharmacology (2014) Vol. 87, Iss. 5, pp. 766-775
Open Access | Times Cited: 129
International Union of Basic and Clinical Pharmacology. XCV. Recent Advances in the Understanding of the Pharmacology and Biological Roles of Relaxin Family Peptide Receptors 1–4, the Receptors for Relaxin Family Peptides
Michelle L. Halls, Ross A. D. Bathgate, Steve W. Sutton, et al.
Pharmacological Reviews (2015) Vol. 67, Iss. 2, pp. 389-440
Open Access | Times Cited: 128
What Can Crystal Structures of Aminergic Receptors Tell Us about Designing Subtype-Selective Ligands?
Mayako Michino, Thijs Beuming, Prashant Donthamsetti, et al.
Pharmacological Reviews (2014) Vol. 67, Iss. 1, pp. 198-213
Open Access | Times Cited: 118
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