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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:

ADAR1 RNA editing regulates endothelial cell functions via the MDA-5 RNA sensing signaling pathway
Xinfeng Guo, Silvia Liu, Rose Yan, et al.
Life Science Alliance (2021) Vol. 5, Iss. 3, pp. e202101191-e202101191
Open Access | Times Cited: 11

Showing 11 citing articles:

RNA modifications in cardiovascular health and disease
Aikaterini Gatsiou, Konstantinos Stellos
Nature Reviews Cardiology (2022) Vol. 20, Iss. 5, pp. 325-346
Closed Access | Times Cited: 34
ADAR1 Zα domain P195A mutation activates the MDA5-dependent RNA-sensing signaling pathway in brain without decreasing overall RNA editing
Xinfeng Guo, Silvia Liu, Sheng Yi, et al.
Cell Reports (2023) Vol. 42, Iss. 7, pp. 112733-112733
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: 20
The Ever‐Expanding Influence of the Endothelial Nitric Oxide Synthase
Riham Rafea, Mauro Siragusa, Ingrid Fleming
Basic & Clinical Pharmacology & Toxicology (2025) Vol. 136, Iss. 5
Open Access
Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification – Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous Mutations
Lingjuan Liu, Lu Zhang, Peng Huang, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 8
Role of ADAR1 on Proliferation and Differentiation in Porcine Preadipocytes
Menghuan Yang, Jun Jiang, Ruimin Ren, et al.
Animals (2024) Vol. 14, Iss. 8, pp. 1201-1201
Open Access | Times Cited: 1
Nuclear eNOS interacts with andS-nitrosates ADAR1 to modulate type I interferon signaling and endothelial function
Xiaozhu Zhou, Carsten Kuenne, Stefan Günther, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Functional roles of epitranscriptomic marks in the cardiovascular system and disease: a narrative review
Mirolyuba Ilieva, Shizuka Uchida
Annals of Translational Medicine (2022) Vol. 10, Iss. 13, pp. 753-753
Open Access | Times Cited: 4
ADAR1 suppression causes interferon signaling and transposable element transcript accumulation in human astrocytes
Cali M. McEntee, Alyssa N. Cavalier, Thomas J. LaRocca
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 2
Microbial RNA, the New PAMP of Many Faces
M. Ayelén Milillo, Lis N. Velásquez, Paula Barrionuevo
Frontiers in Tropical Diseases (2022) Vol. 3
Open Access | Times Cited: 2
An AGS-associated mutation in ADAR1 catalytic domain causes early-onset and MDA5- dependent encephalopathy with IFN pathway activation in the brain
Xinfeng Guo, Richard A. Steinman, Yi Sheng, et al.
Research Square (Research Square) (2022)
Open Access
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