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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:

Affinity selection mass spectrometry speeding drug discovery
Renaud Prudent, Hugues Lemoine, Jarrod Walsh, et al.
Drug Discovery Today (2023) Vol. 28, Iss. 11, pp. 103760-103760
Closed Access | Times Cited: 13

Showing 13 citing articles:

Emerging paradigms for target discovery of traditional medicines: A genome-wide pan-GPCR perspective
Zenghao Bi, Huan Li, Yuting Liang, et al.
The Innovation (2025), pp. 100774-100774
Open Access
Fragment-based drug discovery campaigns guided by native mass spectrometry
Louise M. Sternicki, Sally‐Ann Poulsen
RSC Medicinal Chemistry (2024) Vol. 15, Iss. 7, pp. 2270-2285
Closed Access | Times Cited: 3
How should we teach medicinal chemistry in higher education to prepare students for a future career as medicinal chemists and drug designers? - A teacher´s perspective.
Philipp Klahn
(2024)
Open Access | Times Cited: 1
Target-specific affinity separation of the bioactive compounds from herbal extract using the spin column packed with the immobilized protein microspheres prior to LC-MS analysis
Taotao Wang, Yunshan Wang, Shoucheng Zhao, et al.
Journal of Chromatography A (2024) Vol. 1734, pp. 465322-465322
Closed Access | Times Cited: 1
Ligand discovery by activity-based protein profiling
Micah J. Niphakis, Benjamin F. Cravatt
Cell chemical biology (2024) Vol. 31, Iss. 9, pp. 1636-1651
Closed Access | Times Cited: 1
Coupling of surface plasmon resonance and mass spectrometry for molecular interaction studies in drug discovery
Yuan-Di Zhao, Darya Hadavi, Ingrid Dijkgraaf, et al.
Drug Discovery Today (2024) Vol. 29, Iss. 7, pp. 104027-104027
Open Access
A review of biophysical strategies to investigate protein-ligand binding: What have we employed?
Zhen Zhao, Liang Zhao, C. Kong, et al.
International Journal of Biological Macromolecules (2024) Vol. 276, pp. 133973-133973
Closed Access
Optimizing the Affinity Selection Mass Spectrometry Workflow for Efficient Identification and Ranking of Potent USP1 Inhibitors
Yi Zhao, Meixian Liu, Tian Qin, et al.
SLAS TECHNOLOGY (2024) Vol. 29, Iss. 4, pp. 100174-100174
Open Access
Discovery of ICOS-targeted small molecules using affinity selection mass spectrometry screening
Longfei Zhang, Laura Calvo‐Barreiro, Victor S. Batista, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Discovery of ICOS‐targeted small molecules using affinity selection mass spectrometry screening
Longfei Zhang, Laura Calvo‐Barreiro, Victor S. Batista, et al.
ChemMedChem (2024) Vol. 19, Iss. 22
Open Access
Improved Rapid Equilibrium Dialysis-Mass Spectrometry (RED-MS) Method for Measuring Small Molecule–Protein Complex Binding Affinities in Solution
Bryan D. Choi, C.-C. Han, Jonathan R. LaRochelle, et al.
Journal of the American Society for Mass Spectrometry (2024)
Closed Access
How Should we Teach Medicinal Chemistry in Higher Education to Prepare Students for a Future Career as Medicinal Chemists and Drug Designers? – A Teacher's Perspective
Philipp Klahn
ChemMedChem (2024)
Open Access
Drug screening approaches for small-molecule compounds in cancer-targeted therapy
Yelin Zhao, Chengfu Yuan, Yuchen Shi, et al.
Journal of drug targeting (2024), pp. 1-16
Closed Access
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