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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:

Treatments in Aicardi–Goutières syndrome
Yanick J. Crow, Jay Shetty, John H. Livingston
Developmental Medicine & Child Neurology (2019) Vol. 62, Iss. 1, pp. 42-47
Open Access | Times Cited: 93

Showing 1-25 of 93 citing articles:

The role of RNA editing enzyme ADAR1 in human disease
Brian Song, Yusuke Shiromoto, Moeko Minakuchi, et al.
Wiley Interdisciplinary Reviews - RNA (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 107
Nucleic Acid Sensors as Therapeutic Targets for Human Disease
Sarah M. McWhirter, Caroline A. Jefferies
Immunity (2020) Vol. 53, Iss. 1, pp. 78-97
Open Access | Times Cited: 76
Cellular and molecular mechanisms breaking immune tolerance in inborn errors of immunity
Georgios Sogkas, Faranaz Atschekzei, Ignatius Ryan Adriawan, et al.
Cellular and Molecular Immunology (2021) Vol. 18, Iss. 5, pp. 1122-1140
Open Access | Times Cited: 62
The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology points to consider for diagnosis and management of autoinflammatory type I interferonopathies: CANDLE/PRAAS, SAVI and AGS
Kader Cetin Gedik, Lovro Lamot, Micol Romano, et al.
Annals of the Rheumatic Diseases (2022) Vol. 81, Iss. 5, pp. 601-613
Open Access | Times Cited: 59
RNA sensing via the RIG‐I‐like receptor LGP2 is essential for the induction of a type I IFN response in ADAR1 deficiency
Jorn E. Stok, Timo Oosenbrug, Laurens R. ter Haar, et al.
The EMBO Journal (2022) Vol. 41, Iss. 6
Open Access | Times Cited: 43
The cytokines interleukin-6 and interferon-α induce distinct microglia phenotypes
Phillip K. West, Andrew N. McCorkindale, Boris Guennewig, et al.
Journal of Neuroinflammation (2022) Vol. 19, Iss. 1
Open Access | Times Cited: 43
Significance of the cGAS-STING Pathway in Health and Disease
Jinglin Zhou, Zhan Zhuang, Jiamian Li, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 17, pp. 13316-13316
Open Access | Times Cited: 40
Breaking down the cellular responses to type I interferon neurotoxicity in the brain
Barney Viengkhou, Markus J. Hofer
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 25
Interferon-α receptor antisense oligonucleotides reduce neuroinflammation and neuropathology in a mouse model of cerebral interferonopathy
Barney Viengkhou, Christine Hong, Curt Mazur, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 4
Open Access | Times Cited: 10
The brain microvasculature is a primary mediator of interferon-α neurotoxicity in human cerebral interferonopathies
Barney Viengkhou, Emina Hayashida, Sarah McGlasson, et al.
Immunity (2024) Vol. 57, Iss. 7, pp. 1696-1709.e10
Open Access | Times Cited: 10
Regulation and inhibition of the DNA sensor cGAS
Jonny Hertzog, Jan Rehwinkel
EMBO Reports (2020) Vol. 21, Iss. 12
Open Access | Times Cited: 50
Aicardi-Goutières syndrome-associated mutation at ADAR1 gene locus activates innate immune response in mouse brain
Xinfeng Guo, Clayton A. Wiley, Richard A. Steinman, et al.
Journal of Neuroinflammation (2021) Vol. 18, Iss. 1
Open Access | Times Cited: 41
Gain-of-function mutations inALPK1cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome
Christina Torres Kozycki, Shilpa Kodati, Laryssa A. Huryn, et al.
Annals of the Rheumatic Diseases (2022) Vol. 81, Iss. 10, pp. 1453-1464
Open Access | Times Cited: 38
Aicardi–Goutières syndrome: A monogenic type I interferonopathy
Anran Liu, Songcheng Ying
Scandinavian Journal of Immunology (2023) Vol. 98, Iss. 4
Open Access | Times Cited: 22
The Role of cGAS-STING in Age-Related Diseases from Mechanisms to Therapies
Weitao Zheng, Dechao Feng, Xingyu Xiong, et al.
Aging and Disease (2023)
Open Access | Times Cited: 19
Brain organoid: a 3D technology for investigating cellular composition and interactions in human neurological development and disease models in vitro
Oluwafemi Solomon Agboola, Xinglin Hu, Zhiyan Shan, et al.
Stem Cell Research & Therapy (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 39
The Role of Nucleases and Nucleic Acid Editing Enzymes in the Regulation of Self-Nucleic Acid Sensing
Pauline Santa, Anne Garreau, Lee Serpas, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 34
The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE/PRAAS, SAVI, and AGS
Kader Cetin Gedik, Lovro Lamot, Micol Romano, et al.
Arthritis & Rheumatology (2022) Vol. 74, Iss. 5, pp. 735-751
Closed Access | Times Cited: 28
Dysregulation of the cGAS-STING Pathway in Monogenic Autoinflammation and Lupus
Holly Wobma, Daniel S. Shin, Janet Chou, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 24
Clinical spectrum and currently available treatment of type I interferonopathy Aicardi–Goutières syndrome
Giovanni Battista Dell’Isola, Gianluca Dini, Kaleb Logan Culpepper, et al.
World Journal of Pediatrics (2023) Vol. 19, Iss. 7, pp. 635-643
Open Access | Times Cited: 13
MEF2A suppresses stress responses that trigger DDX41-dependent IFN production
Julian R. Smith, Jack W. Dowling, Matthew I. McFadden, et al.
Cell Reports (2023) Vol. 42, Iss. 8, pp. 112805-112805
Open Access | Times Cited: 13
Crucial Roles of RSAD2/viperin in Immunomodulation, Mitochondrial Metabolism and Autoimmune Diseases
Siyan Chen, Jiani Ye, Yinfang Lin, et al.
Inflammation (2024)
Open Access | Times Cited: 5
Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
Mathieu Barbier, Melanie Bahlo, Alessandra Pennisi, et al.
Annals of Neurology (2022) Vol. 92, Iss. 1, pp. 122-137
Open Access | Times Cited: 19
An AGS-associated mutation in ADAR1 catalytic domain results in early-onset and MDA5-dependent encephalopathy with IFN pathway activation in the brain
Xinfeng Guo, Richard A. Steinman, Sheng Yi, et al.
Journal of Neuroinflammation (2022) Vol. 19, Iss. 1
Open Access | Times Cited: 19
Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus (jSLE)
Valentina Natoli, Amandine Charras, Gabriele Hahn, et al.
Molecular and Cellular Pediatrics (2023) Vol. 10, Iss. 1
Open Access | Times Cited: 12
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