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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:

Structure-based discovery of opioid analgesics with reduced side effects
Aashish Manglik, Henry J. Lin, Dipendra K. Aryal, et al.
Nature (2016) Vol. 537, Iss. 7619, pp. 185-190
Open Access | Times Cited: 866

Showing 1-25 of 866 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: 2253
Molecular Dynamics Simulation for All
Scott A. Hollingsworth, Ron O. Dror
Neuron (2018) Vol. 99, Iss. 6, pp. 1129-1143
Open Access | Times Cited: 1911
Poorly controlled postoperative pain: prevalence, consequences, and prevention
Tong J. Gan
Journal of Pain Research (2017) Vol. Volume 10, pp. 2287-2298
Open Access | Times Cited: 1093
Ultra-large library docking for discovering new chemotypes
Jiankun Lyu, Sheng Wang, Trent E. Balius, et al.
Nature (2019) Vol. 566, Iss. 7743, pp. 224-229
Open Access | Times Cited: 770
GPCR Dynamics: Structures in Motion
Naomi R. Latorraca, AJ Venkatakrishnan, Ron O. Dror
Chemical Reviews (2016) Vol. 117, Iss. 1, pp. 139-155
Open Access | Times Cited: 672
Biased signalling: from simple switches to allosteric microprocessors
Jeffrey S. Smith, Robert J. Lefkowitz, Sudarshan Rajagopal
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 4, pp. 243-260
Open Access | Times Cited: 642
Structure of the µ-opioid receptor–Gi protein complex
Antoine Koehl, Hongli Hu, Shoji Maeda, et al.
Nature (2018) Vol. 558, Iss. 7711, pp. 547-552
Open Access | Times Cited: 608
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: 580
Computational approaches streamlining drug discovery
Anastasiia Sadybekov, Vsevolod Katritch
Nature (2023) Vol. 616, Iss. 7958, pp. 673-685
Open Access | Times Cited: 533
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: 488
Bias Factor and Therapeutic Window Correlate to Predict Safer Opioid Analgesics
Cullen L. Schmid, Nicole Kennedy, Nicolette C. Ross, et al.
Cell (2017) Vol. 171, Iss. 5, pp. 1165-1175.e13
Open Access | Times Cited: 471
Perioperative opioid analgesia—when is enough too much? A review of opioid-induced tolerance and hyperalgesia
Lesley Colvin, Fiona A. Bull, Tim G. Hales
The Lancet (2019) Vol. 393, Iss. 10180, pp. 1558-1568
Open Access | Times Cited: 429
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: 423
G protein-coupled receptors: structure- and function-based drug discovery
Dehua Yang, Qingtong Zhou, Viktorija Labroska, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 415
Crystal Structure of an LSD-Bound Human Serotonin Receptor
Daniel Wacker, Sheng Wang, John D. McCorvy, et al.
Cell (2017) Vol. 168, Iss. 3, pp. 377-389.e12
Open Access | Times Cited: 405
Structure of the D2 dopamine receptor bound to the atypical antipsychotic drug risperidone
Sheng Wang, Tao Che, Anat Levit, et al.
Nature (2018) Vol. 555, Iss. 7695, pp. 269-273
Open Access | Times Cited: 390
A practical guide to large-scale docking
Brian J. Bender, Stefan Gahbauer, Andreas Luttens, et al.
Nature Protocols (2021) Vol. 16, Iss. 10, pp. 4799-4832
Open Access | Times Cited: 370
Endogenous and Exogenous Opioids in Pain
Gregory Corder, Daniel C. Castro, Michael R. Bruchas, et al.
Annual Review of Neuroscience (2018) Vol. 41, Iss. 1, pp. 453-473
Open Access | Times Cited: 366
Structure of the Nanobody-Stabilized Active State of the Kappa Opioid Receptor
Tao Che, Susruta Majumdar, Saheem A. Zaidi, et al.
Cell (2018) Vol. 172, Iss. 1-2, pp. 55-67.e15
Open Access | Times Cited: 338
An amygdalar neural ensemble that encodes the unpleasantness of pain
Gregory Corder, Biafra Ahanonu, Benjamin F. Grewe, et al.
Science (2019) Vol. 363, Iss. 6424, pp. 276-281
Open Access | Times Cited: 324
Breaking barriers to novel analgesic drug development
Ajay Yekkirala, David P. Roberson, Bruce P. Bean, et al.
Nature Reviews Drug Discovery (2017) Vol. 16, Iss. 8, pp. 545-564
Open Access | Times Cited: 313
The changing opioid crisis: development, challenges and opportunities
Nora D. Volkow, Carlos Blanco
Molecular Psychiatry (2020) Vol. 26, Iss. 1, pp. 218-233
Open Access | Times Cited: 313
Low intrinsic efficacy for G protein activation can explain the improved side effect profiles of new opioid agonists
Alexander Gillis, Arisbel B. Gondin, Andrea Kliewer, et al.
Science Signaling (2020) Vol. 13, Iss. 625
Open Access | Times Cited: 310
Tailored Approaches in Drug Development and Diagnostics: From Molecular Design to Biological Model Systems
Cecilia Sahlgren, Annika Meinander, Hongbo Zhang, et al.
Advanced Healthcare Materials (2017) Vol. 6, Iss. 21
Open Access | Times Cited: 307
Loss of μ opioid receptor signaling in nociceptors, but not microglia, abrogates morphine tolerance without disrupting analgesia
Gregory Corder, Vivianne L. Tawfik, Dong Wang, et al.
Nature Medicine (2017) Vol. 23, Iss. 2, pp. 164-173
Open Access | Times Cited: 306
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