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 of the adenosine A2A receptor bound to an engineered G protein
Byron Carpenter, Rony Nehmé, Tony Warne, et al.
Nature (2016) Vol. 536, Iss. 7614, pp. 104-107
Open Access | Times Cited: 426

Showing 1-25 of 426 citing articles:

The Molecular Basis of G Protein–Coupled Receptor Activation
William I. Weis, Brian K. Kobilka
Annual Review of Biochemistry (2018) Vol. 87, Iss. 1, pp. 897-919
Open Access | Times Cited: 983

Structure and dynamics of GPCR signaling complexes
Daniel Hilger, Matthieu Masureel, Brian K. Kobilka
Nature Structural & Molecular Biology (2017) Vol. 25, Iss. 1, pp. 4-12
Open Access | Times Cited: 796

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: 643

Pharmacology of Adenosine Receptors: The State of the Art
Pier Andrea Borea, Stefania Gessi, Stefania Merighi, et al.
Physiological Reviews (2018) Vol. 98, Iss. 3, pp. 1591-1625
Open Access | Times Cited: 620

Illuminating G-Protein-Coupling Selectivity of GPCRs
Asuka Inoue, Francesco Raimondi, Francois Marie Ngako Kadji, et al.
Cell (2019) Vol. 177, Iss. 7, pp. 1933-1947.e25
Open Access | Times Cited: 533

Common activation mechanism of class A GPCRs
Qingtong Zhou, Dehua Yang, Meng Wu, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 522

GPCR Signaling Regulation: The Role of GRKs and Arrestins
Vsevolod V. Gurevich, Eugenia V. Gurevich
Frontiers in Pharmacology (2019) Vol. 10
Open Access | Times Cited: 461

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

Cryo-EM in drug discovery: achievements, limitations and prospects
Jean‐Paul Renaud, Ashwin Chari, Claudio Ciferri, et al.
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 7, pp. 471-492
Closed Access | Times Cited: 386

Selectivity determinants of GPCR–G-protein binding
Tilman Flock, Alexander S. Hauser, Nadia Lund, et al.
Nature (2017) Vol. 545, Iss. 7654, pp. 317-322
Open Access | Times Cited: 356

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

Structure of the adenosine-bound human adenosine A1 receptor–Gi complex
Christopher J. Draper-Joyce, Maryam Khoshouei, David M. Thal, et al.
Nature (2018) Vol. 558, Iss. 7711, pp. 559-563
Closed Access | Times Cited: 321

Single-molecule analysis of ligand efficacy in β2AR–G-protein activation
G. Glenn Gregorio, Matthieu Masureel, Daniel Hilger, et al.
Nature (2017) Vol. 547, Iss. 7661, pp. 68-73
Open Access | Times Cited: 312

Structures of the M1 and M2 muscarinic acetylcholine receptor/G-protein complexes
Shoji Maeda, Qianhui Qu, Michael J. Robertson, et al.
Science (2019) Vol. 364, Iss. 6440, pp. 552-557
Open Access | Times Cited: 302

Impact of GPCR Structures on Drug Discovery
Miles Congreve, Chris de Graaf, Nigel A. Swain, et al.
Cell (2020) Vol. 181, Iss. 1, pp. 81-91
Open Access | Times Cited: 299

PtdIns(4,5)P2 stabilizes active states of GPCRs and enhances selectivity of G-protein coupling
Hsin‐Yung Yen, Kin Kuan Hoi, Idlir Liko, et al.
Nature (2018) Vol. 559, Iss. 7714, pp. 423-427
Open Access | Times Cited: 282

Structure of the Adenosine A1 Receptor Reveals the Basis for Subtype Selectivity
Alisa Glukhova, David M. Thal, Thi Nguyen, et al.
Cell (2017) Vol. 168, Iss. 5, pp. 867-877.e13
Open Access | Times Cited: 270

Mini-G proteins: Novel tools for studying GPCRs in their active conformation
Rony Nehmé, Byron Carpenter, Ankita Singhal, et al.
PLoS ONE (2017) Vol. 12, Iss. 4, pp. e0175642-e0175642
Open Access | Times Cited: 262

Cryo-EM structure of the adenosine A2A receptor coupled to an engineered heterotrimeric G protein
Javier García‐Nafría, Yang Lee, Xiao‐chen Bai, et al.
eLife (2018) Vol. 7
Open Access | Times Cited: 257

Human GLP-1 receptor transmembrane domain structure in complex with allosteric modulators
Gaojie Song, Dehua Yang, Yuxia Wang, et al.
Nature (2017) Vol. 546, Iss. 7657, pp. 312-315
Closed Access | Times Cited: 222

GPCR drug discovery: integrating solution NMR data with crystal and cryo-EM structures
Ichio Shimada, Takumi Ueda, Yutaka Kofuku, et al.
Nature Reviews Drug Discovery (2018) Vol. 18, Iss. 1, pp. 59-82
Open Access | Times Cited: 217

Molecular mechanism of biased signaling in a prototypical G protein–coupled receptor
Carl‐Mikael Suomivuori, Naomi R. Latorraca, Laura M. Wingler, et al.
Science (2020) Vol. 367, Iss. 6480, pp. 881-887
Open Access | Times Cited: 211

Cryo-EM structure of the serotonin 5-HT1B receptor coupled to heterotrimeric Go
Javier García‐Nafría, Rony Nehmé, Patricia C. Edwards, et al.
Nature (2018) Vol. 558, Iss. 7711, pp. 620-623
Open Access | Times Cited: 208

Assembly of a GPCR-G Protein Complex
Yang Du, Nguyen Minh Duc, Søren G. F. Rasmussen, et al.
Cell (2019) Vol. 177, Iss. 5, pp. 1232-1242.e11
Open Access | Times Cited: 206

Structures of Human A 1 and A 2A Adenosine Receptors with Xanthines Reveal Determinants of Selectivity
R.K. Cheng, Elena Segala, N.J. Robertson, et al.
Structure (2017) Vol. 25, Iss. 8, pp. 1275-1285.e4
Open Access | Times Cited: 201

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