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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:

A structural atlas of druggable sites on Na v channels
Zhangqiang Li, Qiurong Wu, Nieng Yan
Channels (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 16

Showing 16 citing articles:

Structural biology and molecular pharmacology of voltage-gated ion channels
Jian Huang, Xiaojing Pan, Nieng Yan
Nature Reviews Molecular Cell Biology (2024) Vol. 25, Iss. 11, pp. 904-925
Closed Access | Times Cited: 23
Drugs exhibit diverse binding modes and access routes in the Nav1.5 cardiac sodium channel pore
Elaine Tao, Ben Corry
The Journal of General Physiology (2025) Vol. 157, Iss. 2
Closed Access | Times Cited: 2
Structural basis for human Cav3.2 inhibition by selective antagonists
Jian Huang, Xiao Fan, Xueqin Jin, et al.
Cell Research (2024) Vol. 34, Iss. 6, pp. 440-450
Open Access | Times Cited: 11
Peptide toxins as tools in ion channel biology
S. Bandyopadhyay, Satyajit Mishra, Jeet Kalia
Current Opinion in Chemical Biology (2025) Vol. 84, pp. 102568-102568
Closed Access | Times Cited: 1
Dissection of the structure–function relationship of Na v channels
Zhangqiang Li, Qiurong Wu, Gaoxingyu Huang, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 9
Open Access | Times Cited: 4
Differential Inhibition by Cenobamate of Canonical Human Nav1.5 Ion Channels and Several Point Mutants
Teodor Asvadur Şulea, Sorin Draga, Maria Mernea, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 1, pp. 358-358
Open Access
Inhibition of NMDA receptors and other ion channel types by membrane-associated drugs
Elizabeth G. Neureiter, M. Quincy Erickson-Oberg, Aparna Nigam, et al.
Frontiers in Pharmacology (2025) Vol. 16
Open Access
A versatile residue numbering scheme for Nav and Cav channels
Xueqin Jin, Jian Huang, Huan Wang, et al.
Cell chemical biology (2024) Vol. 31, Iss. 8, pp. 1394-1404
Closed Access | Times Cited: 2
Multiple hERG channel blocking pathways: implications for macromolecules
Bernd J. Zünkler
Trends in Pharmacological Sciences (2024) Vol. 45, Iss. 8, pp. 671-677
Open Access | Times Cited: 1
ω-Grammotoxin-SIA inhibits voltage-gated Na+ channel currents
Rita de Cássia Collaço, Filip Van Petegem, Frank Bosmans
The Journal of General Physiology (2024) Vol. 156, Iss. 10
Closed Access | Times Cited: 1
Inhibitory Effects of Cenobamate on Multiple Human Cardiac Ion Channels and Possible Arrhythmogenic Consequences
Andreea Larisa Mateias, Florian Armasescu, Bogdan Amuzescu, et al.
Biomolecules (2024) Vol. 14, Iss. 12, pp. 1582-1582
Open Access | Times Cited: 1
Scorpion α-toxin LqhαIT specifically interacts with a glycan at the pore domain of voltage-gated sodium channels
Swastik Phulera, Callum J. Dickson, Christopher J. Schwalen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
20S-Ginsenoside Rh2, the major bioactive saponin in Panax notoginseng flowers, ameliorates cough by inhibition of NaV1.7 and TRPV1 channel currents and downregulation of TRPV1 expression
Xiao Liu, Jie Xiang, Shuyuan Fan, et al.
Journal of Ethnopharmacology (2024) Vol. 336, pp. 118716-118716
Closed Access
Scorpion α-toxin LqhαIT specifically interacts with a glycan at the pore domain of voltage-gated sodium channels
Swastik Phulera, Callum J. Dickson, Christopher J. Schwalen, et al.
Structure (2024) Vol. 32, Iss. 10, pp. 1611-1620.e4
Open Access
Harnessing Deep Learning Methods for Voltage-Gated Ion Channel Drug Discovery
Diego López Mateos, B. Harris, Adriana Hernández González, et al.
Physiology (2024) Vol. 40, Iss. 1, pp. 67-87
Closed Access
Drug discovery targeting Nav1.8: Structural insights and therapeutic potential
Huan Wang, Jian Huang, Jie Zang, et al.
Current Opinion in Chemical Biology (2024) Vol. 83, pp. 102538-102538
Closed Access
Discovery of E0199: A novel compound targeting both peripheral NaV and KV7 channels to alleviate neuropathic pain
Boxuan Zhang, Xiaoxing Shi, Xingang Liu, et al.
Journal of Pharmaceutical Analysis (2024) Vol. 15, Iss. 1, pp. 101132-101132
Open Access
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