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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:

Interferon-independent STING signaling promotes resistance to HSV-1 in vivo
Lívia H. Yamashiro, Stephen C. Wilson, Huntly M. Morrison, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 147

Showing 1-25 of 147 citing articles:

The cGAS–STING pathway as a therapeutic target in inflammatory diseases
Alexiane Decout, Jason D. Katz, Shankar Venkatraman, et al.
Nature reviews. Immunology (2021) Vol. 21, Iss. 9, pp. 548-569
Open Access | Times Cited: 1369
Autophagy in inflammation, infection, and immunometabolism
Vojo Deretić
Immunity (2021) Vol. 54, Iss. 3, pp. 437-453
Open Access | Times Cited: 576
TBK1 recruitment to STING activates both IRF3 and NF-κB that mediate immune defense against tumors and viral infections
Seoyun Yum, Minghao Li, Yan Fang, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 14
Open Access | Times Cited: 369
The type I interferonopathies: 10 years on
Yanick J. Crow, Daniel B. Stetson
Nature reviews. Immunology (2021) Vol. 22, Iss. 8, pp. 471-483
Open Access | Times Cited: 309
Cellular functions of cGAS-STING signaling
Chen Chen, Pinglong Xu
Trends in Cell Biology (2022) Vol. 33, Iss. 8, pp. 630-648
Closed Access | Times Cited: 204
The STING1 network regulates autophagy and cell death
Ruoxi Zhang, Rui Kang, Daolin Tang
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 171
Role of the cGAS–STING pathway in systemic and organ-specific diseases
Sladjana Skopelja‐Gardner, Jie An, Keith B. Elkon
Nature Reviews Nephrology (2022) Vol. 18, Iss. 9, pp. 558-572
Open Access | Times Cited: 170
STING induces LC3B lipidation onto single-membrane vesicles via the V-ATPase and ATG16L1-WD40 domain
Tara D. Fischer, Chunxin Wang, Benjamin Scott Padman, et al.
The Journal of Cell Biology (2020) Vol. 219, Iss. 12
Open Access | Times Cited: 149
A diamidobenzimidazole STING agonist protects against SARS-CoV-2 infection
Fiachra Humphries, Liraz Shmuel-Galia, Zhaozhao Jiang, et al.
Science Immunology (2021) Vol. 6, Iss. 59
Open Access | Times Cited: 135
Organellar homeostasis and innate immune sensing
Cassandra R. Harapas, Elina Idiiatullina, Mahmoud Al‐Azab, et al.
Nature reviews. Immunology (2022) Vol. 22, Iss. 9, pp. 535-549
Closed Access | Times Cited: 96
Multifaceted functions of STING in human health and disease: from molecular mechanism to targeted strategy
Zili Zhang, Haifeng Zhou, Xiaohu Ouyang, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 93
Biochemistry, Cell Biology, and Pathophysiology of the Innate Immune cGAS–cGAMP–STING Pathway
Christopher Ritchie, Jacqueline A. Carozza, Lingyin Li
Annual Review of Biochemistry (2022) Vol. 91, Iss. 1, pp. 599-628
Open Access | Times Cited: 82
Early cellular mechanisms of type I interferon-driven susceptibility to tuberculosis
Dmitri I. Kotov, Ophelia V. Lee, Stefan A. Fattinger, et al.
Cell (2023) Vol. 186, Iss. 25, pp. 5536-5553.e22
Open Access | Times Cited: 53
STING trafficking as a new dimension of immune signaling
Devon Jeltema, Kennady Abbott, Nan Yan
The Journal of Experimental Medicine (2023) Vol. 220, Iss. 3
Open Access | Times Cited: 52
Current understanding of the cGAS-STING signaling pathway: Structure, regulatory mechanisms, and related diseases
Jing Pan, Chen-Jie Fei, Yang Hu, et al.
动物学研究 (2023) Vol. 44, Iss. 1, pp. 183-218
Open Access | Times Cited: 51
The balance of STING signaling orchestrates immunity in cancer
Klara Rasmussen Bollerup Lanng, Emil Leth Lauridsen, Martin R. Jakobsen
Nature Immunology (2024) Vol. 25, Iss. 7, pp. 1144-1157
Closed Access | Times Cited: 42
Human life within a narrow range: The lethal ups and downs of type I interferons
Yanick J. Crow, Jean‐Laurent Casanova
Science Immunology (2024) Vol. 9, Iss. 97
Closed Access | Times Cited: 19
STING, the Endoplasmic Reticulum, and Mitochondria: Is Three a Crowd or a Conversation?
Judith A. Smith
Frontiers in Immunology (2021) Vol. 11
Open Access | Times Cited: 79
Herpes Simplex Virus 1 Infection of Neuronal and Non-Neuronal Cells Elicits Specific Innate Immune Responses and Immune Evasion Mechanisms
Amanda L. Verzosa, Lea A. McGeever, Shun‐Je Bhark, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 70
STING-Mediated Lung Inflammation and Beyond
Marie‐Louise Frémond, Yanick J. Crow
Journal of Clinical Immunology (2021) Vol. 41, Iss. 3, pp. 501-514
Open Access | Times Cited: 69
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy
Elise M. N. Ferré, Monica M. Schmitt, Michail S. Lionakis
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 58
A guide to membrane atg8ylation and autophagy with reflections on immunity
Vojo Deretić, Michael Lazarou
The Journal of Cell Biology (2022) Vol. 221, Iss. 7
Open Access | Times Cited: 57
SGLT2 inhibitor activates the STING/IRF3/IFN-β pathway and induces immune infiltration in osteosarcoma
Wei Wu, Zhenghao Zhang, Doudou Jing, et al.
Cell Death and Disease (2022) Vol. 13, Iss. 6
Open Access | Times Cited: 42
Termination of STING responses is mediated via ESCRT‐dependent degradation
Katherine R. Balka, Rajan Venkatraman, Tahnee L. Saunders, et al.
The EMBO Journal (2023) Vol. 42, Iss. 12
Open Access | Times Cited: 41
The ubiquitin E3 ligase TRIM10 promotes STING aggregation and activation in the Golgi apparatus
Lingli Kong, Chao Sui, Tian Chen, et al.
Cell Reports (2023) Vol. 42, Iss. 4, pp. 112306-112306
Open Access | Times Cited: 40
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