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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:

NLRP3 Inflammasome Assembly in Neutrophils Is Supported by PAD4 and Promotes NETosis Under Sterile Conditions
Patrick Münzer, Roberto Negro, Shoichi Fukui, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 118

Showing 1-25 of 118 citing articles:

Neutrophil phenotypes and functions in cancer: A consensus statement
Daniela F. Quail, Borko Amulic, Monowar Aziz, et al.
The Journal of Experimental Medicine (2022) Vol. 219, Iss. 6
Open Access | Times Cited: 207
Neutrophil extracellular traps: from physiology to pathology
Andrés Hidalgo, Peter Libby, Oliver Soehnlein, et al.
Cardiovascular Research (2021) Vol. 118, Iss. 13, pp. 2737-2753
Open Access | Times Cited: 195
Receptor-Mediated NETosis on Neutrophils
Tao Chen, Yanhong Li, Rui Sun, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 106
Molecular mechanisms and therapeutic target of NETosis in diseases
Jiayu Huang, Weiqi Hong, Meihua Wan, et al.
MedComm (2022) Vol. 3, Iss. 3
Open Access | Times Cited: 95
Neutrophil intrinsic and extrinsic regulation of NETosis in health and disease
Valentina Poli, Ivan Zanoni
Trends in Microbiology (2022) Vol. 31, Iss. 3, pp. 280-293
Open Access | Times Cited: 89
Interleukin-1 and the NLRP3 inflammasome in COVID-19: Pathogenetic and therapeutic implications
Nicola Potere, Marco Giuseppe Del Buono, Roberto Caricchio, et al.
EBioMedicine (2022) Vol. 85, pp. 104299-104299
Open Access | Times Cited: 80
Inflammasome activation in neutrophils of patients with severe COVID-19
Karen Aymonnier, Julie Ng, Laura E. Fredenburgh, et al.
Blood Advances (2022) Vol. 6, Iss. 7, pp. 2001-2013
Open Access | Times Cited: 75
Thromboinflammation: From Atherosclerosis to COVID-19
Denisa D. Wagner, Lukas Andreas Heger
Arteriosclerosis Thrombosis and Vascular Biology (2022) Vol. 42, Iss. 9, pp. 1103-1112
Open Access | Times Cited: 53
Identification of renal ischemia reperfusion injury subtypes and predictive strategies for delayed graft function and graft survival based on neutrophil extracellular trap-related genes
Jiyue Wu, Feilong Zhang, Zheng Xiang, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 52
Cholesterol accumulation in macrophages drives NETosis in atherosclerotic plaques via IL-1β secretion
Mustafa Yalcınkaya, Panagiotis Fotakis, Wenli Liu, et al.
Cardiovascular Research (2022) Vol. 119, Iss. 4, pp. 969-981
Open Access | Times Cited: 40
Inflammasomes and Atherosclerosis: a Mixed Picture
Alan R. Tall, Karin Bornfeldt
Circulation Research (2023) Vol. 132, Iss. 11, pp. 1505-1520
Open Access | Times Cited: 40
Post-COVID Syndrome in Adults—An Overview
Rüdiger E. Scharf, Juan‐Manuel Anaya
Viruses (2023) Vol. 15, Iss. 3, pp. 675-675
Open Access | Times Cited: 34
Inflammasome Signaling, Thromboinflammation, and Venous Thromboembolism
Nicola Potere, Antonio Abbate, Yogendra Kanthi, et al.
JACC Basic to Translational Science (2023) Vol. 8, Iss. 9, pp. 1245-1261
Open Access | Times Cited: 31
Alleviation of arthritis through prevention of neutrophil extracellular traps by an orally available inhibitor of protein arginine deiminase 4
Chandru Gajendran, Shoichi Fukui, Naveen M. Sadhu, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 30
NLRP3 inflammasome and interleukin-1 contributions to COVID-19-associated coagulopathy and immunothrombosis
Nicola Potere, Evan C. Garrad, Yogendra Kanthi, et al.
Cardiovascular Research (2023) Vol. 119, Iss. 11, pp. 2046-2060
Open Access | Times Cited: 30
Pyroptosis in neutrophils: Multimodal integration of inflammasome and regulated cell death signaling pathways
George Dubyak, Brandon A. Miller, Eric Pearlman
Immunological Reviews (2023) Vol. 314, Iss. 1, pp. 229-249
Open Access | Times Cited: 28
Neutrophil extracellular traps mediate deep vein thrombosis: from mechanism to therapy
Mengting Yao, Jiacheng Ma, Dongwen Wu, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 26
Role and Therapeutic Targeting Strategies of Neutrophil Extracellular Traps in Inflammation
Xiang Li, Shanghua Xiao, Nina Filipczak, et al.
International Journal of Nanomedicine (2023) Vol. Volume 18, pp. 5265-5287
Open Access | Times Cited: 24
Understanding thrombosis: the critical role of oxidative stress
Peiming Li, Xueru Ma, Guofei Huang
Hematology (2024) Vol. 29, Iss. 1
Open Access | Times Cited: 10
Toll-like receptor 4 in pancreatic damage and immune infiltration in acute pancreatitis
Jordan Mattke, Carly M. Darden, Michael C. Lawrence, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 10
How Do ROS Induce NETosis? Oxidative DNA Damage, DNA Repair, and Chromatin Decondensation
Dhia Azzouz, Nades Palaniyar
Biomolecules (2024) Vol. 14, Iss. 10, pp. 1307-1307
Open Access | Times Cited: 10
Neutrophil extracellular traps in cancer
Yuxi Ma, Jielin Wei, Wenshan He, et al.
MedComm (2024) Vol. 5, Iss. 8
Open Access | Times Cited: 9
Neutrophil peptidylarginine deiminase 4 plays a systemic role in obesity-induced chronic inflammation in mice
Stijn Van Bruggen, Casey E. Sheehy, Sirima Kraisin, et al.
Journal of Thrombosis and Haemostasis (2024) Vol. 22, Iss. 5, pp. 1496-1509
Closed Access | Times Cited: 8
Litomosoides sigmodontis microfilariae-induced eosinophil ETosis is dependent on the canonical inflammasome pathway
Alexandra Ehrens, Benjamin Lenz, Celia Nieto-Pérez, et al.
Cell Reports (2025) Vol. 44, Iss. 1, pp. 115164-115164
Closed Access | Times Cited: 1
Caspase-1-driven neutrophil pyroptosis and its role in host susceptibility to Pseudomonas aeruginosa
Karin Santoni, David Péricat, Léana Gorse, et al.
PLoS Pathogens (2022) Vol. 18, Iss. 7, pp. e1010305-e1010305
Open Access | Times Cited: 37
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