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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:

Identification and Characterization of the First Selective Y4 Receptor Positive Allosteric Modulator
Mario Schubert, Jan Stichel, Yu Du, et al.
Journal of Medicinal Chemistry (2017) Vol. 60, Iss. 17, pp. 7605-7612
Closed Access | Times Cited: 11

Showing 11 citing articles:

Allosteric Modulation of Class A GPCRs: Targets, Agents, and Emerging Concepts
Eric A. Wold, Jianping Chen, Kathryn A. Cunningham, et al.
Journal of Medicinal Chemistry (2018) Vol. 62, Iss. 1, pp. 88-127
Open Access | Times Cited: 132
Illuminating the neuropeptide Y4 receptor and its ligand pancreatic polypeptide from a structural, functional, and therapeutic perspective
Corinna Schüß, Victoria Behr, Annette G. Beck‐Sickinger
Neuropeptides (2024) Vol. 105, pp. 102416-102416
Open Access | Times Cited: 4
NPY1R-targeted peptide-mediated delivery of a dual PPARα/γ agonist to adipocytes enhances adipogenesis and prevents diabetes progression
Stefanie Wittrisch, Nora Klöting, Karin Mörl, et al.
Molecular Metabolism (2019) Vol. 31, pp. 163-180
Open Access | Times Cited: 29
Highly Selective Y4 Receptor Antagonist Binds in an Allosteric Binding Pocket
Corinna Schüß, Oanh Vu, Mario Schubert, et al.
Journal of Medicinal Chemistry (2021) Vol. 64, Iss. 5, pp. 2801-2814
Closed Access | Times Cited: 16
Cyclic Analogues of the Chemerin C-Terminus Mimic a Loop Conformation Essential for Activating the Chemokine-like Receptor 1
Tobias F. Fischer, Clara T. Schoeder, Tristan Zellmann, et al.
Journal of Medicinal Chemistry (2021) Vol. 64, Iss. 6, pp. 3048-3058
Closed Access | Times Cited: 15
Carbaboranylation of Truncated C‐Terminal Neuropeptide Y Analogue Leads to Full hY1 Receptor Agonism
Sven Hofmann, Josephin Lindner, Annette G. Beck‐Sickinger, et al.
ChemBioChem (2018) Vol. 19, Iss. 21, pp. 2300-2306
Closed Access | Times Cited: 13
Positive allosteric modulation of endogenous delta opioid receptor signaling in the enteric nervous system is a potential treatment for gastrointestinal motility disorders
Jesse J. DiCello, Simona Carbone, Ayame Saito, et al.
AJP Gastrointestinal and Liver Physiology (2021) Vol. 322, Iss. 1, pp. G66-G78
Open Access | Times Cited: 11
Biased agonists at the human Y1 receptor lead to prolonged membrane residency and extended receptor G protein interaction
Anette Kaiser, Lizzy Wanka, Isabelle Ziffert, et al.
Cellular and Molecular Life Sciences (2020) Vol. 77, Iss. 22, pp. 4675-4691
Open Access | Times Cited: 10
Structure–Activity Relationship Study of the High-Affinity Neuropeptide Y4 Receptor Positive Allosteric Modulator VU0506013
Corinna Schüß, Oanh Vu, Nigam M. Mishra, et al.
Journal of Medicinal Chemistry (2023) Vol. 66, Iss. 13, pp. 8745-8766
Closed Access | Times Cited: 3
Stereochemistry-Driven Interactions of α,γ-Peptide Ligands with the Neuropeptide Y Y4-Receptor
Eva Plut, Jacqueline C. Calderón, Vesna Stanojlović, et al.
Journal of Medicinal Chemistry (2023) Vol. 66, Iss. 14, pp. 9642-9657
Closed Access | Times Cited: 2
Heterodimeric Analogues of the Potent Y1R Antagonist 1229U91, Lacking One of the Pharmacophoric C-Terminal Structures, Retain Potent Y1R Affinity and Show Improved Selectivity over Y4R
Rachel Richardson, Marleen Groenen, Mengjie Liu, et al.
Journal of Medicinal Chemistry (2020) Vol. 63, Iss. 10, pp. 5274-5286
Open Access | Times Cited: 2
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