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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:

Discovery of new GPCR ligands to illuminate new biology
Bryan L. Roth, John J. Irwin, Brian K. Shoichet
Nature Chemical Biology (2017) Vol. 13, Iss. 11, pp. 1143-1151
Open Access | Times Cited: 94

Showing 1-25 of 94 citing articles:

Common activation mechanism of class A GPCRs
Qingtong Zhou, Dehua Yang, Meng Wu, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 526
TRUPATH, an open-source biosensor platform for interrogating the GPCR transducerome
Reid H. J. Olsen, Jeffrey F. DiBerto, Justin G. English, et al.
Nature Chemical Biology (2020) Vol. 16, Iss. 8, pp. 841-849
Open Access | Times Cited: 428
Unexplored therapeutic opportunities in the human genome
Tudor I. Oprea, Cristian Bologa, Søren Brunak, et al.
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 5, pp. 317-332
Open Access | Times Cited: 339
Unexplored therapeutic opportunities in the human genome.
Tudor I. Oprea, Cristian Bologa, Søren Brunak, et al.
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 5, pp. 377-377
Open Access | Times Cited: 303
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
The Concise Guide to PHARMACOLOGY 2023/24: G protein-coupled receptors
S P H Alexander, Arthur Christopoulos, Anthony P. Davenport, et al.
British Journal of Pharmacology (2023) Vol. 180, Iss. S2
Open Access | Times Cited: 229
Discovery of Human Signaling Systems: Pairing Peptides to G Protein-Coupled Receptors
Simon R. Foster, Alexander S. Hauser, Line Vedel, et al.
Cell (2019) Vol. 179, Iss. 4, pp. 895-908.e21
Open Access | Times Cited: 220
New Insights into Modes of GPCR Activation
Wenjing Wang, Yuhui Qiao, Zijian Li
Trends in Pharmacological Sciences (2018) Vol. 39, Iss. 4, pp. 367-386
Closed Access | Times Cited: 202
The novel μ‐opioid receptor agonist PZM21 depresses respiration and induces tolerance to antinociception
R. W. Hill, Alex Disney, Alexandra E. Conibear, et al.
British Journal of Pharmacology (2018) Vol. 175, Iss. 13, pp. 2653-2661
Open Access | Times Cited: 165
Psychedelic-inspired drug discovery using an engineered biosensor
Chunyang Dong, Calvin Ly, Lee E. Dunlap, et al.
Cell (2021) Vol. 184, Iss. 10, pp. 2779-2792.e18
Open Access | Times Cited: 140
AlphaFold2 versus experimental structures: evaluation on G protein-coupled receptors
Xinheng He, Chongzhao You, Hualiang Jiang, et al.
Acta Pharmacologica Sinica (2022) Vol. 44, Iss. 1, pp. 1-7
Open Access | Times Cited: 88
Structure-based discovery of conformationally selective inhibitors of the serotonin transporter
Isha Singh, Anubha Seth, Christian B. Billesbølle, et al.
Cell (2023) Vol. 186, Iss. 10, pp. 2160-2175.e17
Open Access | Times Cited: 46
New Binding Sites, New Opportunities for GPCR Drug Discovery
H. C. Stephen Chan, Yi Li, Thamani Dahoun, et al.
Trends in Biochemical Sciences (2019) Vol. 44, Iss. 4, pp. 312-330
Open Access | Times Cited: 123
Nanobody-enabled monitoring of kappa opioid receptor states
Tao Che, Justin G. English, B. Krumm, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 117
Fungal G-protein-coupled receptors: mediators of pathogenesis and targets for disease control
Neil Brown, Sanne Schrevens, Patrick Van Dijck, et al.
Nature Microbiology (2018) Vol. 3, Iss. 4, pp. 402-414
Closed Access | Times Cited: 94
VEGAS as a Platform for Facile Directed Evolution in Mammalian Cells
Justin G. English, Reid H. J. Olsen, Katherine Lansu, et al.
Cell (2019) Vol. 178, Iss. 3, pp. 748-761.e17
Open Access | Times Cited: 91
The G protein-coupled receptors deorphanization landscape
Céline Laschet, Nadine Dupuis, Julien Hanson
Biochemical Pharmacology (2018) Vol. 153, pp. 62-74
Closed Access | Times Cited: 90
Allosteric drugs and mutations: chances, challenges, and necessity
Enrico Guarnera, Igor N. Berezovsky
Current Opinion in Structural Biology (2020) Vol. 62, pp. 149-157
Closed Access | Times Cited: 89
Structural insights into emergent signaling modes of G protein–coupled receptors
Ieva Sutkevičiu̅tė, Jean‐Pierre Vilardaga
Journal of Biological Chemistry (2020) Vol. 295, Iss. 33, pp. 11626-11642
Open Access | Times Cited: 73
Structural studies of phosphorylation-dependent interactions between the V2R receptor and arrestin-2
Qing‐tao He, Peng Xiao, Shen-Ming Huang, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 58
Chemogenetics defines receptor-mediated functions of short chain free fatty acids
Daniele Bolognini, Natasja Barki, Adrian J. Butcher, et al.
Nature Chemical Biology (2019) Vol. 15, Iss. 5, pp. 489-498
Open Access | Times Cited: 64
Structure of the dopamine D2 receptor in complex with the antipsychotic drug spiperone
Dohyun Im, Asuka Inoue, Takaaki Fujiwara, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 64
Molecular pharmacology of metabotropic receptors targeted by neuropsychiatric drugs
Bryan L. Roth
Nature Structural & Molecular Biology (2019) Vol. 26, Iss. 7, pp. 535-544
Open Access | Times Cited: 61
Rational design of agonists for bitter taste receptor TAS2R14: from modeling to bench and back
Antonella Di Pizio, Lukas Waterloo, Regine Brox, et al.
Cellular and Molecular Life Sciences (2019) Vol. 77, Iss. 3, pp. 531-542
Open Access | Times Cited: 58
Exploring the Allosteric Territory of Protein Function
Wei-Ven Tee, Zhen Wah Tan, Keene Lee, et al.
The Journal of Physical Chemistry B (2021) Vol. 125, Iss. 15, pp. 3763-3780
Closed Access | Times Cited: 41
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