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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:

Assembly and regulation of ASC specks
Florian Hoß, Juan F. Rodríguez-Alcázar, Eicke Latz
Cellular and Molecular Life Sciences (2016) Vol. 74, Iss. 7, pp. 1211-1229
Open Access | Times Cited: 125

Showing 1-25 of 125 citing articles:

Targeting the NLRP3 inflammasome in inflammatory diseases
Matthew Mangan, Edward J. Olhava, William Roush, et al.
Nature Reviews Drug Discovery (2018) Vol. 17, Iss. 8, pp. 588-606
Closed Access | Times Cited: 1538
NLRP3 Inflammasome and the IL-1 Pathway in Atherosclerosis
Alena Grebe, Florian Hoß, Eicke Latz
Circulation Research (2018) Vol. 122, Iss. 12, pp. 1722-1740
Open Access | Times Cited: 726
A new research hot spot: The role of NLRP3 inflammasome activation, a key step in pyroptosis, in diabetes and diabetic complications
Zi-Wei Yu, Jing Zhang, Xin Li, et al.
Life Sciences (2019) Vol. 240, pp. 117138-117138
Closed Access | Times Cited: 149
The role of inflammasomes in vascular cognitive impairment
Luting Poh, Wei Liang Sim, Dong‐Gyu Jo, et al.
Molecular Neurodegeneration (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 91
The role of NLRP3 inflammasome activation in proinflammatory and cytotoxic effects of metal nanoparticles
Michael Aschner, Anatoly V. Skalny, Airton C. Martins, et al.
Archives of Toxicology (2025)
Closed Access | Times Cited: 2
β-Amyloid Clustering around ASC Fibrils Boosts Its Toxicity in Microglia
Lea L. Friker, Hannah Scheiblich, Inga V. Hochheiser, et al.
Cell Reports (2020) Vol. 30, Iss. 11, pp. 3743-3754.e6
Open Access | Times Cited: 138
Regulated Forms of Cell Death in Fungi
A. Pedro Gonçalves, Jens Heller, Asen Daskalov, et al.
Frontiers in Microbiology (2017) Vol. 8
Open Access | Times Cited: 118
Maf1 Ameliorates Sepsis-Associated Encephalopathy by Suppressing the NF-kB/NLRP3 Inflammasome Signaling Pathway
Shenglong Chen, Chaogang Tang, Hongguang Ding, et al.
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 96
Uncoupled pyroptosis and IL-1β secretion downstream of inflammasome signaling
Yang Li, Qianzhou Jiang
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 34
Quercetin, a natural flavonoid, protects against hepatic ischemia–reperfusion injury via inhibiting Caspase-8/ASC dependent macrophage pyroptosis
Jiacheng Lin, Fuyang Li, Junzhe Jiao, et al.
Journal of Advanced Research (2024)
Open Access | Times Cited: 12
Targeting inflammasomes and pyroptosis in retinal diseases—molecular mechanisms and future perspectives
Yimeng Sun, Fan Li, Yunfei Liu, et al.
Progress in Retinal and Eye Research (2024) Vol. 101, pp. 101263-101263
Open Access | Times Cited: 10
The dual role of PGAM5 in inflammation
Yuxin Qi, Bhavana Rajbanshi, Ruihan Hao, et al.
Experimental & Molecular Medicine (2025)
Open Access | Times Cited: 1
NLRP3 Inflammasome Targeting Offers a Novel Therapeutic Paradigm for Sepsis-Induced Myocardial Injury
Yuzi Jin, Joshua S. Fleishman, Yudong Ma, et al.
Drug Design Development and Therapy (2025) Vol. Volume 19, pp. 1025-1041
Open Access | Times Cited: 1
lncRNA NEAT1 ameliorates LPS‑induced inflammation in MG63 cells by activating autophagy and suppressing the NLRP3 inflammasome
Wenyu Dai, Manyi Wang, Peiqi Wang, et al.
International Journal of Molecular Medicine (2020) Vol. 47, Iss. 2, pp. 607-620
Open Access | Times Cited: 57
Alternative splicing regulates stochastic NLRP3 activity
Florian Hoß, James L. Mueller, Francisca Rojas, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 56
ASC deglutathionylation is a checkpoint for NLRP3 inflammasome activation
Shuhang Li, Linlin Wang, Zhihao Xu, et al.
The Journal of Experimental Medicine (2021) Vol. 218, Iss. 9
Open Access | Times Cited: 47
lncRNA PVT1 modulates NLRP3‑mediated pyroptosis in septic acute kidney injury by targeting miR‑20a‑5p
Long-Tian Deng, Qianlu Wang, Can Yu, et al.
Molecular Medicine Reports (2021) Vol. 23, Iss. 4
Open Access | Times Cited: 41
Contribution of adaptive immunity to human COPD and experimental models of emphysema
Farrah Kheradmand, Yun Zhang, David B. Corry
Physiological Reviews (2022) Vol. 103, Iss. 2, pp. 1059-1093
Closed Access | Times Cited: 33
L-plastin enhances NLRP3 inflammasome assembly and bleomycin-induced lung fibrosis
Hemant Joshi, Alison Almgren‐Bell, Edgar Anaya, et al.
Cell Reports (2022) Vol. 38, Iss. 11, pp. 110507-110507
Open Access | Times Cited: 31
ATP-binding and hydrolysis of human NLRP3
Rebecca Brinkschulte, David Fusshöller, Florian Hoß, et al.
Communications Biology (2022) Vol. 5, Iss. 1
Open Access | Times Cited: 29
MARCH5‐dependent NLRP3 ubiquitination is required for mitochondrial NLRP3‐NEK7 complex formation and NLRP3 inflammasome activation
Yeon‐Ji Park, Niranjan Dodantenna, Yonghyeon Kim, et al.
The EMBO Journal (2023) Vol. 42, Iss. 19
Open Access | Times Cited: 21
ASC specks exacerbate α‑synuclein pathology via amplifying NLRP3 inflammasome activities
Ran Zheng, Yiqun Yan, Shaobing Dai, et al.
Journal of Neuroinflammation (2023) Vol. 20, Iss. 1
Open Access | Times Cited: 20
Atranorin inhibits NLRP3 inflammasome activation by targeting ASC and protects NLRP3 inflammasome-driven diseases
Haoyu Wang, Xi Lin, Guan-gen Huang, et al.
Acta Pharmacologica Sinica (2023) Vol. 44, Iss. 8, pp. 1687-1700
Closed Access | Times Cited: 18
The Potential of NLRP3 Inflammasome as a Therapeutic Target in Neurological Diseases
Wenfang He, Zhiping Hu, Yanjun Zhong, et al.
Molecular Neurobiology (2023) Vol. 60, Iss. 5, pp. 2520-2538
Closed Access | Times Cited: 17
Inflammasome activation in patients with Kaposi sarcoma herpesvirus (KSHV)-associated disorders
Silvia Lucena Lage, Ramya Ramaswami, Joseph M. Rocco, et al.
Blood (2024) Vol. 144, Iss. 14, pp. 1496-1507
Closed Access | Times Cited: 8
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