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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:

Gasdermin D serves as a key executioner of pyroptosis in experimental cerebral ischemia and reperfusion model both in vivo and in vitro
Dongping Zhang, Jinhong Qian, Peng Zhang, et al.
Journal of Neuroscience Research (2019) Vol. 97, Iss. 6, pp. 645-660
Closed Access | Times Cited: 137

Showing 1-25 of 137 citing articles:

Channelling inflammation: gasdermins in physiology and disease
Xing Liu, Shiyu Xia, Zhibin Zhang, et al.
Nature Reviews Drug Discovery (2021) Vol. 20, Iss. 5, pp. 384-405
Open Access | Times Cited: 533
The IL-1 family of cytokines and receptors in rheumatic diseases
Charles A. Dinarello
Nature Reviews Rheumatology (2019) Vol. 15, Iss. 10, pp. 612-632
Closed Access | Times Cited: 310
Bone marrow mesenchymal stem cell-derived exosomes attenuate cerebral ischemia-reperfusion injury-induced neuroinflammation and pyroptosis by modulating microglia M1/M2 phenotypes
Xiaoli Liu, Meimei Zhang, Haining Liu, et al.
Experimental Neurology (2021) Vol. 341, pp. 113700-113700
Closed Access | Times Cited: 233
Activating cGAS–STING axis contributes to neuroinflammation in CVST mouse model and induces inflammasome activation and microglia pyroptosis
Rui Ding, Haiyan Li, Yaqi Liu, et al.
Journal of Neuroinflammation (2022) Vol. 19, Iss. 1
Open Access | Times Cited: 123
The Versatile Gasdermin Family: Their Function and Roles in Diseases
Ju Zou, Yixiang Zheng, Yan Huang, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 105
Pyroptosis-induced inflammation and tissue damage
Swathy O. Vasudevan, Bharat Behl, Vijay Rathinam
Seminars in Immunology (2023) Vol. 69, pp. 101781-101781
Open Access | Times Cited: 103
Mechanisms of immune response and cell death in ischemic stroke and their regulation by natural compounds
Zhaoyuan Gong, Jing Guo, Bin Liu, et al.
Frontiers in Immunology (2024) Vol. 14
Open Access | Times Cited: 27
Long-read sequencing of 945 Han individuals identifies structural variants associated with phenotypic diversity and disease susceptibility
Jiao Gong, Huiru Sun, Kaiyuan Wang, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 3
Low-density lipoprotein receptor (LDLR) regulates NLRP3-mediated neuronal pyroptosis following cerebral ischemia/reperfusion injury
Rui Sun, Mengna Peng, Pengfei Xu, et al.
Journal of Neuroinflammation (2020) Vol. 17, Iss. 1
Open Access | Times Cited: 128
Inhibition of PRMT5 Attenuates Oxidative Stress-Induced Pyroptosis via Activation of the Nrf2/HO-1 Signal Pathway in a Mouse Model of Renal Ischemia-Reperfusion Injury
Changhui Diao, Zhiyuan Chen, Tao Qiu, et al.
Oxidative Medicine and Cellular Longevity (2019) Vol. 2019, pp. 1-18
Open Access | Times Cited: 108
Do pyroptosis, apoptosis, and necroptosis (PANoptosis) exist in cerebral ischemia? Evidence from cell and rodent studies
Qí Zhāng, Kun Xiong, Weitao Yan, et al.
Neural Regeneration Research (2021) Vol. 17, Iss. 8, pp. 1761-1761
Open Access | Times Cited: 101
Inhibition of AIM2 inflammasome activation alleviates GSDMD-induced pyroptosis in early brain injury after subarachnoid haemorrhage
Bin Yuan, Xiaoming Zhou, Zong-qi You, et al.
Cell Death and Disease (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 99
Relevant mediators involved in and therapies targeting the inflammatory response induced by activation of the NLRP3 inflammasome in ischemic stroke
Qingxue Xu, Bo Zhao, Yingze Ye, et al.
Journal of Neuroinflammation (2021) Vol. 18, Iss. 1
Open Access | Times Cited: 92
Astragaloside IV Alleviates Cerebral Ischemia-Reperfusion Injury through NLRP3 Inflammasome-Mediated Pyroptosis Inhibition via Activating Nrf2
Lan Xiao, Ziwei Dai, Wenjing Tang, et al.
Oxidative Medicine and Cellular Longevity (2021) Vol. 2021, Iss. 1
Open Access | Times Cited: 89
Targeting the pathways of regulated necrosis: a potential strategy for alleviation of cardio-cerebrovascular injury
Liqun Lu, Jing Tian, Xiu‐Ju Luo, et al.
Cellular and Molecular Life Sciences (2020) Vol. 78, Iss. 1, pp. 63-78
Closed Access | Times Cited: 80
Melatonin Enhances the Therapeutic Effect of Plasma Exosomes Against Cerebral Ischemia-Induced Pyroptosis Through the TLR4/NF-κB Pathway
Kankai Wang, Junnan Ru, Hengli Zhang, et al.
Frontiers in Neuroscience (2020) Vol. 14
Open Access | Times Cited: 80
Oxidative Stress, Inflammation, and Autophagy: Potential Targets of Mesenchymal Stem Cells-Based Therapies in Ischemic Stroke
Jialin He, Jianyang Liu, Yan Huang, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 79
Amelioration of diabetes‐induced inflammation mediated pyroptosis, sarcopenia, and adverse muscle remodelling by bone morphogenetic protein‐7
Chandrakala Aluganti Narasimhulu, Dinender K. Singla
Journal of Cachexia Sarcopenia and Muscle (2021) Vol. 12, Iss. 2, pp. 403-420
Open Access | Times Cited: 76
Role of pyroptosis in liver diseases
Abdullah Al Mamun, Yanqing Wu, Chang Jia, et al.
International Immunopharmacology (2020) Vol. 84, pp. 106489-106489
Closed Access | Times Cited: 75
Medioresinol as a novel PGC-1α activator prevents pyroptosis of endothelial cells in ischemic stroke through PPARα-GOT1 axis
Yunjie Wang, Xin‐Yuan Guan, Chenglong Gao, et al.
Pharmacological Research (2021) Vol. 169, pp. 105640-105640
Closed Access | Times Cited: 72
Pyroptosis, and its Role in Central Nervous System Disease
Yingchao Hu, Bingwei Wang, Sheng Li, et al.
Journal of Molecular Biology (2021) Vol. 434, Iss. 4, pp. 167379-167379
Closed Access | Times Cited: 66
The Regulation and Modification of GSDMD Signaling in Diseases
Zihao Li, Senlin Ji, Meiling Jiang, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 62
NLRP3 Inflammasome Activation: A Therapeutic Target for Cerebral Ischemia–Reperfusion Injury
Lixia Wang, Wei Ren, Qing-Juan Wu, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 61
Salvianolic Acids for Injection alleviates cerebral ischemia/reperfusion injury by switching M1/M2 phenotypes and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia in vivo and in vitro
Dai-Chao Ma, Nannan Zhang, Yina Zhang, et al.
Journal of Ethnopharmacology (2021) Vol. 270, pp. 113776-113776
Closed Access | Times Cited: 60
Ginsenoside Rd attenuates cerebral ischemia/reperfusion injury by exerting an anti-pyroptotic effect via the miR-139-5p/FoxO1/Keap1/Nrf2 axis
Yiqin Yao, Sheng Hu, Chunxue Zhang, et al.
International Immunopharmacology (2022) Vol. 105, pp. 108582-108582
Open Access | Times Cited: 50
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