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:

Probing small ribosomal subunit RNA helix 45 acetylation across eukaryotic evolution
Marie‐Line Bortolin‐Cavaillé, Aurélie Quillien, Supuni Thalalla Gamage, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 11, pp. 6284-6299
Open Access | Times Cited: 44

Showing 1-25 of 44 citing articles:

RNA modifications: importance in immune cell biology and related diseases
Lian Cui, Rui Ma, Jiangluyi Cai, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 200

Epigenetic regulation in the tumor microenvironment: molecular mechanisms and therapeutic targets
Jing Yang, Jin Xu, Wei Wang, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 152

Direct epitranscriptomic regulation of mammalian translation initiation through N4-acetylcytidine
Daniel Arango, David Sturgill, Renbin Yang, et al.
Molecular Cell (2022) Vol. 82, Iss. 15, pp. 2797-2814.e11
Open Access | Times Cited: 101

Lysine 2-hydroxyisobutyrylation of NAT10 promotes cancer metastasis in an ac4C-dependent manner
Long Liao, Yan He, Shujun Li, et al.
Cell Research (2023) Vol. 33, Iss. 5, pp. 355-371
Open Access | Times Cited: 79

RNA modifications in cellular metabolism: implications for metabolism-targeted therapy and immunotherapy
Weiwei Liu, Si-Qing Zheng, Li Tian, et al.
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 33

NAT10-mediated N4-acetylcytidine mRNA modification regulates self-renewal in human embryonic stem cells
Rucong Liu, Zibaguli Wubulikasimu, Runze Cai, et al.
Nucleic Acids Research (2023) Vol. 51, Iss. 16, pp. 8514-8531
Open Access | Times Cited: 33

RNA modification in cardiovascular disease: implications for therapeutic interventions
Cong Wang, Xuyang Hou, Qing Guan, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 31

Detection of ac4C in human mRNA is preserved upon data reassessment
Hamid Beiki, David Sturgill, Daniel Arango, et al.
Molecular Cell (2024) Vol. 84, Iss. 8, pp. 1611-1625.e3
Closed Access | Times Cited: 12

Activity reconstitution of Kre33 and Tan1 reveals a molecular ruler mechanism in eukaryotic tRNA acetylation
Chun-Rui Ma, Na Liu, Hong Li, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 9, pp. 5226-5240
Open Access | Times Cited: 10

Cytidine Acetylation Across the Tree of Life
Supuni Thalalla Gamage, Shereen A. Howpay Manage, Chu T. Thu, et al.
Accounts of Chemical Research (2024) Vol. 57, Iss. 3, pp. 338-348
Closed Access | Times Cited: 9

Recent advances in the potential role of RNA N4-acetylcytidine in cancer progression
Shujun Zhang, Yafeng Liu, Xiao Ma, et al.
Cell Communication and Signaling (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 8

N4-acetylcytidine (ac4C) promotes mRNA localization to stress granules
Pavel Kudrin, Ankita Singh, David Meierhofer, et al.
EMBO Reports (2024) Vol. 25, Iss. 4, pp. 1814-1834
Open Access | Times Cited: 8

ac4C: a fragile modification with stabilizing functions in RNA metabolism
Sarah Schiffers, Shalini Oberdoerffer
RNA (2024) Vol. 30, Iss. 5, pp. 583-594
Open Access | Times Cited: 8

Decoding the ribosome's hidden language: rRNA modifications as key players in cancer dynamics and targeted therapies
Li Cui, Jiarong Zheng, Yunfan Lin, et al.
Clinical and Translational Medicine (2024) Vol. 14, Iss. 5
Open Access | Times Cited: 8

Targeting N4‐acetylcytidine suppresses hepatocellular carcinoma progression by repressing eEF2‐mediated HMGB2 mRNA translation
Hailing Liu, Lei Xu, Shiwei Yue, et al.
Cancer Communications (2024) Vol. 44, Iss. 9, pp. 1018-1041
Open Access | Times Cited: 8

Advances in the mechanism of small nucleolar RNA and its role in DNA damage response
Liping Shen, Wencheng Zhang, Jia-Rong Deng, et al.
Military Medical Research (2024) Vol. 11, Iss. 1
Open Access | Times Cited: 7

Dissecting the oncogenic properties of essential RNA-modifying enzymes: a focus on NAT10
Mahmood Hassan Dalhat, Sharath Narayan, Hannah Serio, et al.
Oncogene (2024) Vol. 43, Iss. 15, pp. 1077-1086
Closed Access | Times Cited: 5

Molecular Basis for RNA Cytidine Acetylation by NAT10
Mingyang Zhou, Supuni Thalalla Gamage, Khoa Tran, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

NAT10 and cytidine acetylation in mRNA: intersecting paths in development and disease
Cyrinne Achour, Shalini Oberdoerffer
Current Opinion in Genetics & Development (2024) Vol. 87, pp. 102207-102207
Closed Access | Times Cited: 5

Antisense pairing and SNORD13 structure guide RNA cytidine acetylation
Supuni Thalalla Gamage, Marie‐Line Bortolin‐Cavaillé, Courtney N. Link, et al.
RNA (2022), pp. rna.079254.122-rna.079254.122
Open Access | Times Cited: 19

Biological function and mechanism of NAT10 in cancer
Yufeng Han, Xinxin Zhang, Lei Miao, et al.
Cancer Innovation (2025) Vol. 4, Iss. 1
Open Access

NAT10 primes a post-transcriptional repertoire essential for the maintenance of spermatogonial homeostasis
Xiaoli Zhu, Caoling Xu, Xue Jiang, et al.
Science Bulletin (2025)
Closed Access

From Function to Mechanism: Unveiling the Role of Small Nucleolar Ribonucleic Acids in Digestive Tumours
D. M. Xi, Guli Shayila Dui Sanbai, Min Jiang, et al.
Clinical Genetics (2025)
Closed Access

Transfer RNA acetylation regulates in vivo mammalian stress signaling
Supuni Thalalla Gamage, Roxane Khoogar, Shereen Howpay Manage, et al.
Science Advances (2025) Vol. 11, Iss. 12
Open Access

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