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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:

Biophysical Fragment Screening of the β1-Adrenergic Receptor: Identification of High Affinity Arylpiperazine Leads Using Structure-Based Drug Design
J.A. Christopher, Jason Brown, A.S. Dore, et al.
Journal of Medicinal Chemistry (2013) Vol. 56, Iss. 9, pp. 3446-3455
Open Access | Times Cited: 155

Showing 1-25 of 155 citing articles:

Twenty years on: the impact of fragments on drug discovery
Daniel A. Erlanson, Stephen W. Fesik, Roderick E. Hubbard, et al.
Nature Reviews Drug Discovery (2016) Vol. 15, Iss. 9, pp. 605-619
Closed Access | Times Cited: 871
Allosteric sodium in class A GPCR signaling
Vsevolod Katritch, Gustavo Fenalti, Enrique E. Abola, et al.
Trends in Biochemical Sciences (2014) Vol. 39, Iss. 5, pp. 233-244
Open Access | Times Cited: 467
Surface plasmon resonance spectroscopy for characterisation of membrane protein–ligand interactions and its potential for drug discovery
Simon G. Patching
Biochimica et Biophysica Acta (BBA) - Biomembranes (2013) Vol. 1838, Iss. 1, pp. 43-55
Open Access | Times Cited: 413
Biophysics in drug discovery: impact, challenges and opportunities
Jean‐Paul Renaud, Chun‐wa Chung, U. Helena Danielson, et al.
Nature Reviews Drug Discovery (2016) Vol. 15, Iss. 10, pp. 679-698
Open Access | Times Cited: 336
Surface Plasmon Resonance (SPR) Biosensors in Pharmaceutical Analysis
Andreea Olaru, Camelia Bala, Nicole Jaffrézic‐Renault, et al.
Critical Reviews in Analytical Chemistry (2014) Vol. 45, Iss. 2, pp. 97-105
Closed Access | Times Cited: 333
Kinetics for Drug Discovery: an industry-driven effort to target drug residence time
Doris A. Schuetz, Wilhelmus E. A. de Witte, Yin Cheong Wong, et al.
Drug Discovery Today (2017) Vol. 22, Iss. 6, pp. 896-911
Open Access | Times Cited: 208
Accurate determination of protein:ligand standard binding free energies from molecular dynamics simulations
Haohao Fu, Haochuan Chen, Marharyta Blazhynska, et al.
Nature Protocols (2022) Vol. 17, Iss. 4, pp. 1114-1141
Open Access | Times Cited: 106
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
Cholesterol, sphingolipids, and glycolipids: What do we know about their role in raft-like membranes?
Tomasz Róg, Ilpo Vattulainen
Chemistry and Physics of Lipids (2014) Vol. 184, pp. 82-104
Closed Access | Times Cited: 171
New paradigms in GPCR drug discovery
Kenneth A. Jacobson
Biochemical Pharmacology (2015) Vol. 98, Iss. 4, pp. 541-555
Open Access | Times Cited: 163
Structure-inspired design of β-arrestin-biased ligands for aminergic GPCRs
John D. McCorvy, Kyle V. Butler, Brendan Kelly, et al.
Nature Chemical Biology (2017) Vol. 14, Iss. 2, pp. 126-134
Open Access | Times Cited: 154
Fragment and Structure-Based Drug Discovery for a Class C GPCR: Discovery of the mGlu5 Negative Allosteric Modulator HTL14242 (3-Chloro-5-[6-(5-fluoropyridin-2-yl)pyrimidin-4-yl]benzonitrile)
J.A. Christopher, Sarah J. Aves, K.A. Bennett, et al.
Journal of Medicinal Chemistry (2015) Vol. 58, Iss. 16, pp. 6653-6664
Closed Access | Times Cited: 150
Predicting Binding Affinities for GPCR Ligands Using Free-Energy Perturbation
Eelke B. Lenselink, Julien Louvel, Anna F. Forti, et al.
ACS Omega (2016) Vol. 1, Iss. 2, pp. 293-304
Open Access | Times Cited: 138
The Role of a Sodium Ion Binding Site in the Allosteric Modulation of the A2A Adenosine G Protein-Coupled Receptor
Hugo Gutiérrez‐de‐Terán, Arnault Massink, David Rodríguez, et al.
Structure (2013) Vol. 21, Iss. 12, pp. 2175-2185
Open Access | Times Cited: 133
Exploring G Protein-Coupled Receptors (GPCRs) Ligand Space via Cheminformatics Approaches: Impact on Rational Drug Design
Shaherin Basith, Minghua Cui, Stephani Joy Y. Macalino, et al.
Frontiers in Pharmacology (2018) Vol. 9
Open Access | Times Cited: 126
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: 119
Structural features of the G-protein/GPCR interactions
Irina S. Moreira
Biochimica et Biophysica Acta (BBA) - General Subjects (2013) Vol. 1840, Iss. 1, pp. 16-33
Closed Access | Times Cited: 110
GPCR crystal structures: Medicinal chemistry in the pocket
Jeremy Shonberg, Ralf C. Kling, Peter Gmeiner, et al.
Bioorganic & Medicinal Chemistry (2014) Vol. 23, Iss. 14, pp. 3880-3906
Closed Access | Times Cited: 104
Recent Advances in Structure-Based Drug Design Targeting Class A G Protein-Coupled Receptors Utilizing Crystal Structures and Computational Simulations
Yoonji Lee, Shaherin Basith, Sun Choi
Journal of Medicinal Chemistry (2017) Vol. 61, Iss. 1, pp. 1-46
Open Access | Times Cited: 101
A mutagenesis and screening strategy to generate optimally thermostabilized membrane proteins for structural studies
Francesca Magnani, María J. Serrano‐Vega, Yoko Shibata, et al.
Nature Protocols (2016) Vol. 11, Iss. 8, pp. 1554-1571
Open Access | Times Cited: 95
Towards high throughput GPCR crystallography: In Meso soaking of Adenosine A2A Receptor crystals
Prakash Rucktooa, R.K. Cheng, Elena Segala, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 90
Intracellular Transfer of Na+ in an Active-State G-Protein-Coupled Receptor
Owen N. Vickery, Catarina A. Carvalheda, Saheem A. Zaidi, et al.
Structure (2017) Vol. 26, Iss. 1, pp. 171-180.e2
Open Access | Times Cited: 89
Function-specific virtual screening for GPCR ligands using a combined scoring method
Albert J. Kooistra, Henry F. Vischer, Daniel A. McNaught-Flores, et al.
Scientific Reports (2016) Vol. 6, Iss. 1
Open Access | Times Cited: 88
Ligands of Adrenergic Receptors: A Structural Point of View
Yiran Wu, Liting Zeng, Suwen Zhao
Biomolecules (2021) Vol. 11, Iss. 7, pp. 936-936
Open Access | Times Cited: 69
Nonantimicrobial Actions of Macrolides: Overview and Perspectives for Future Development
Jennifer Kricker, Clive P. Page, Fridrik Runar Gardarsson, et al.
Pharmacological Reviews (2021) Vol. 73, Iss. 4, pp. 1404-1433
Open Access | Times Cited: 59
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