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:

MRP1-Dependent Extracellular Release of Glutathione Induces Cardiomyocyte Ferroptosis After Ischemia-Reperfusion
Genki Ichihara, Yoshinori Katsumata, Yuki Sugiura, et al.
Circulation Research (2023) Vol. 133, Iss. 10, pp. 861-876
Closed Access | Times Cited: 21

Showing 21 citing articles:

Iron homeostasis and ferroptosis in human diseases: mechanisms and therapeutic prospects
Qin Ru, Yusheng Li, Lin Chen, et al.
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 50

Isoliquiritigenin alleviates myocardial ischemia-reperfusion injury by regulating the Nrf2/HO-1/SLC7a11/GPX4 axis in mice
Deshan Yao, Liuxiang Bao, Sichuan Wang, et al.
Free Radical Biology and Medicine (2024) Vol. 221, pp. 1-12
Closed Access | Times Cited: 21

Serpina3k lactylation protects from cardiac ischemia reperfusion injury
Le Wang, Dandan Li, Fang Yao, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2

Mitochondrial calcium in cardiac ischemia/reperfusion injury and cardioprotection
Edoardo Bertero, Tudor-Alexandru Popoiu, Christoph Maack
Basic Research in Cardiology (2024) Vol. 119, Iss. 4, pp. 569-585
Open Access | Times Cited: 13

Management of ROS and Regulatory Cell Death in Myocardial Ischemia–Reperfusion Injury
Ge Gong, Wenhui Wan, Xinghu Zhang, et al.
Molecular Biotechnology (2024)
Closed Access | Times Cited: 10

Pyroptosis in myocardial ischemia/reperfusion and its therapeutic implications
Yin Liu, Xi Li, Tingting Sun, et al.
European Journal of Pharmacology (2024) Vol. 971, pp. 176464-176464
Closed Access | Times Cited: 9

GSH and Ferroptosis: Side-by-Side Partners in the Fight against Tumors
Yulang Jiang, Christian Glandorff, Mingyu Sun
Antioxidants (2024) Vol. 13, Iss. 6, pp. 697-697
Open Access | Times Cited: 9

Deciphering the link: ferroptosis and its role in glioma
He Wang, Yingfeng Liu, Shusheng Che, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 4

TNFSF9 Silence Impedes Cerebral Ischemia–Reperfusion Injury via Modulating SLC3A2 Expression in Brain Microvascular Endothelial Cells
Shunli Liang, You Wu, Rongbo Zhang, et al.
Journal of Molecular Neuroscience (2025) Vol. 75, Iss. 1
Closed Access

HnRNPA2B1 promotes cardiac ferroptosis via m6A-dependent stabilization of PFN2 mRNA in myocardial ischemia-reperfusion injury
Shuotao Shi, Quan Chen, Ying Yang, et al.
Free Radical Biology and Medicine (2025)
Closed Access

Advances in Mechanisms of Ferroptosis in Cardiovascular Disease
婷 李
Advances in Clinical Medicine (2025) Vol. 15, Iss. 04, pp. 1433-1440
Closed Access

Natural products and ferroptosis: A novel approach for heart failure management
Zeyu Zhang, Zhihua Yang, Shuai Wang, et al.
Phytomedicine (2025), pp. 156783-156783
Closed Access

Ferroptosis in diabetic cardiomyopathy: Advances in cardiac fibroblast-cardiomyocyte interactions
Mengmeng Wang, De-Gang Mo, Ning Zhang, et al.
Heliyon (2024) Vol. 10, Iss. 15, pp. e35219-e35219
Open Access | Times Cited: 3

Salvianolic acid B alleviated myocardial ischemia-reperfusion injury via modulating SIRT3-mediated crosstalk between mitochondrial ROS and NLRP3
Xiao-Hong Wei, Jie Chen, Xue-Fen Wu, et al.
Phytomedicine (2024) Vol. 136, pp. 156260-156260
Closed Access | Times Cited: 3

Ins and Outs of Glutathione in Cardiac Ischemia/Reperfusion Injury
Edoardo Bertero, Christoph Maack
Circulation Research (2023) Vol. 133, Iss. 10, pp. 877-879
Closed Access | Times Cited: 6

Immunometabolic checkpoint-mediated macrophage metabolic reprogramming accelerates infected wound healing
Mingzhang Li, Zhengjiang Feng, Boyong Wang, et al.
Nano Today (2024) Vol. 57, pp. 102324-102324
Closed Access | Times Cited: 1

Aryl Hydrocarbon Receptor Alleviates Hepatic Fibrosis by Inducing Hepatic Stellate Cell Ferroptosis
Shenghui Liu
Journal of Cellular and Molecular Medicine (2024) Vol. 28, Iss. 23
Open Access | Times Cited: 1

Lipid-derived electrophiles inhibit the function of membrane channels during ferroptosis
Antonius Van Kessel, Gonzalo Cosa
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 21
Open Access

Role of gasotransmitters in necroptosis
Lei Cao, Xueli Wang, Ti Chu, et al.
Experimental Cell Research (2024) Vol. 442, Iss. 2, pp. 114233-114233
Closed Access

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