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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:

Poly(ADP-ribosyl)ation of acetyltransferase NAT10 by PARP1 is required for its nucleoplasmic translocation and function in response to DNA damage
Hongyi Liu, Yingying Liu, Yinling Zhang, et al.
Cell Communication and Signaling (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 25

Showing 25 citing articles:

Emerging role of RNA acetylation modification ac4C in diseases: Current advances and future challenges
Jie Luo, Jingsong Cao, Cong Chen, et al.
Biochemical Pharmacology (2023) Vol. 213, pp. 115628-115628
Closed Access | Times Cited: 34
Human PARP1 substrates and regulators of its catalytic activity: An updated overview
Tao Zhu, Juyan Zheng, Lingling Huang, et al.
Frontiers in Pharmacology (2023) Vol. 14
Open Access | Times Cited: 22
NAT10-mediated RNA acetylation enhances HNRNPUL1 mRNA stability to contribute cervical cancer progression
Yingfei Long, Yifei Ren, Qinglv Wei, et al.
International Journal of Medical Sciences (2023) Vol. 20, Iss. 8, pp. 1079-1090
Open Access | Times Cited: 22
Emerging roles of RNA ac4C modification and NAT10 in mammalian development and human diseases
Yigan Zhang, Yumei Lei, Yanbin Dong, et al.
Pharmacology & Therapeutics (2023) Vol. 253, pp. 108576-108576
Closed Access | Times Cited: 22
PARP1 at the crossroad of cellular senescence and nucleolar processes
Kinga Kołacz, Agnieszka Robaszkiewicz
Ageing Research Reviews (2024) Vol. 94, pp. 102206-102206
Closed Access | Times Cited: 8
NAT10, an RNA Cytidine Acetyltransferase, Regulates Ferroptosis in Cancer Cells
Mahmood Hassan Dalhat, Hani Choudhry, Mohammad Imran Khan
Antioxidants (2023) Vol. 12, Iss. 5, pp. 1116-1116
Open Access | Times Cited: 14
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
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
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
Short-chain fatty acids in breast milk and their relationship with the infant gut microbiota
Menglu Xi, Yalu Yan, Sufang Duan, et al.
Frontiers in Microbiology (2024) Vol. 15
Open Access | Times Cited: 3
NAT10 inhibition promotes ac4C‐dependent ferroptosis to counteract sorafenib resistance in nasopharyngeal carcinoma
Ziyi Xue, Haijing Xie, Ying Shan, et al.
Cancer Science (2024) Vol. 115, Iss. 10, pp. 3256-3272
Open Access | Times Cited: 3
N4-acetylcytidine and other RNA modifications in epitranscriptome: insight into DNA repair and cancer development
Eva Bártová, Lenka Stixová, Alena Svobodová Kovaříková
Epigenomics (2025), pp. 1-12
Open Access
Targeting NAT10 attenuates homologous recombination via destabilizing DNA:RNA hybrids and overcomes PARP inhibitor resistance in cancers
Zhu Xu, Mingming Zhu, Longpo Geng, et al.
Drug Resistance Updates (2025), pp. 101241-101241
Closed Access
MORC2 and MAX contributes to the expression of glycolytic enzymes, breast cancer cell proliferation and migration
Rohith Kumar Guddeti, Himavani Pacharla, Nanda Kumar Yellapu, et al.
Medical Oncology (2023) Vol. 40, Iss. 3
Open Access | Times Cited: 8
Monitoring nucleolar-nucleoplasmic protein shuttling in living cells by high-content microscopy and automated image analysis
Marina Engbrecht, David Grundei, Asisa M Dilger, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. 15, pp. e72-e72
Open Access | Times Cited: 2
Destabilization of microrchidia family CW‐type zinc finger 2 via the cyclin‐dependent kinase 1‐chaperone‐mediated autophagy pathway promotes mitotic arrest and enhances cancer cellular sensitivity to microtubule‐targeting agents
Shu‐Yuan Hu, Jin‐Xian Qian, Shao‐Ying Yang, et al.
Clinical and Translational Medicine (2023) Vol. 13, Iss. 3
Open Access | Times Cited: 6
The Complex Network of ADP-Ribosylation and DNA Repair: Emerging Insights and Implications for Cancer Therapy
Ziyuan Li, Aiqin Luo, Bingteng Xie
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 19, pp. 15028-15028
Open Access | Times Cited: 4
Modulatory Potential of Poly (ADP‐Ribose) Polymerase 1 (PARP1) in BRCA‐Mutated Tumors
Valens Munyembaraga, Delphine Cyuzuzo, Tran Nhat Phong Dao, et al.
European Journal of Cancer Care (2024) Vol. 2024, Iss. 1
Open Access | Times Cited: 1
Novel Insights into the Role of Chromatin Remodeler MORC2 in Cancer
Namita Chutani, Sandhya Ragula, Khajamohiddin Syed, et al.
Biomolecules (2023) Vol. 13, Iss. 10, pp. 1527-1527
Open Access | Times Cited: 2
Emerging roles of the chromatin remodeler MORC2 in cancer metabolism
Bibhukalyan Mohapatra, Suresh B. Pakala
Medical Oncology (2024) Vol. 41, Iss. 9
Closed Access
Biological Functions and Molecular Mechanisms of MORC2 in Human Diseases
Xin Zhao, Jinfeng Miao
Molecules and Cells (2024), pp. 100166-100166
Open Access
The role and mechanism of NAT10‐mediated ac4C modification in tumor development and progression
Zhuoran Gu, Libin Zou, Xinjian Pan, et al.
MedComm (2024) Vol. 5, Iss. 12
Closed Access
­­­MORC2 interaction with MAX contributes to the expression of Glycolytic enzymes, Breast Cancer Cell Proliferation and Migration
Rohith Kumar Guddeti, Himavani Pacharla, Nanda Kumar Yellapu, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
NAT10, an RNA acetyl cytidine transferase restrains ferroptosis in cancer cells by maintaining SLC7A11 RNA stability
Mahmood Hassan Dalhat, Hani Choudhry, Mohammad Imran Khan
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 1
PARP1 inhibition protects mice against Japanese encephalitis virus infection
Perumal Arumugam Desingu, Sneha Mishra, Lavanya Dindi, et al.
Cell Reports (2023) Vol. 42, Iss. 9, pp. 113103-113103
Open Access
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