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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:

DNA replication: the recombination connection
Esther A. Epum, James E. Haber
Trends in Cell Biology (2021) Vol. 32, Iss. 1, pp. 45-57
Open Access | Times Cited: 57

Showing 1-25 of 57 citing articles:

Causes and consequences of DNA single-strand breaks
Keith W. Caldecott
Trends in Biochemical Sciences (2023) Vol. 49, Iss. 1, pp. 68-78
Open Access | Times Cited: 43
Break-induced replication: unraveling each step
Liping Liu, Anna Malkova
Trends in Genetics (2022) Vol. 38, Iss. 7, pp. 752-765
Open Access | Times Cited: 43
Break-induced replication orchestrates resection-dependent template switching
Tianpeng Zhang, Yashpal Rawal, Haoyang Jiang, et al.
Nature (2023) Vol. 619, Iss. 7968, pp. 201-208
Closed Access | Times Cited: 24
Quantifying DNA replication speeds in single cells by scEdU-seq
Jeroen van den Berg, Vincent van Batenburg, Christoph Geisenberger, et al.
Nature Methods (2024) Vol. 21, Iss. 7, pp. 1175-1184
Open Access | Times Cited: 10
TERRA R-loops trigger a switch in telomere maintenance towards break-induced replication and PrimPol-dependent repair
Suna In, Patrícia Renck Nunes, Rita Valador Fernandes, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access | Times Cited: 1
Two-ended recombination at a Flp-nickase-broken replication fork
Rajula Elango, Namrata M. Nilavar, Andrew G. Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 7
Two-ended recombination at a Flp-nickase-broken replication fork
Rajula Elango, Namrata M. Nilavar, Andrew G. Li, et al.
Molecular Cell (2024)
Open Access | Times Cited: 6
TOP3A amplification and ATRX inactivation are mutually exclusive events in pediatric osteosarcomas using ALT
Alexandre de Nonneville, Sébastien Salas, François Bertucci, et al.
EMBO Molecular Medicine (2022) Vol. 14, Iss. 10
Open Access | Times Cited: 26
Stressed? Break-induced replication comes to the rescue!
Rosemary S. Lee, Jerzy Twarowski, Anna Malkova
DNA repair (2024) Vol. 142, pp. 103759-103759
Closed Access | Times Cited: 5
DNA nicks induce mutational signatures associated with BRCA1 deficiency
Yi-Li Feng, Qian Liu, Ruo-Dan Chen, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 21
Strategic targeting of Cas9 nickase expands tandem gene arrays
Hiroaki Takesue, Satoshi Okada, Goro Doi, et al.
Cell Genomics (2025), pp. 100811-100811
Open Access
A Rfa1-MN–based system reveals new factors involved in the rescue of broken replication forks
Ana Amiama-Roig, Marta Barrientos‐Moreno, Esther Cruz-Zambrano, et al.
PLoS Genetics (2025) Vol. 21, Iss. 4, pp. e1011405-e1011405
Open Access
The Safe Path at the Fork: Ensuring Replication-Associated DNA Double-Strand Breaks are Repaired by Homologous Recombination
Jac A. Nickoloff, Neelam Sharma, Lynn Taylor, et al.
Frontiers in Genetics (2021) Vol. 12
Open Access | Times Cited: 26
Telomere Length Regulation
Peter M. Lansdorp
Frontiers in Oncology (2022) Vol. 12
Open Access | Times Cited: 17
The Fission Yeast Mating-Type Switching Motto: “One-for-Two” and “Two-for-One”
Benoı̂t Arcangioli, Serge Gangloff
Microbiology and Molecular Biology Reviews (2023) Vol. 87, Iss. 1
Open Access | Times Cited: 10
Inducing multiple nicks promotes interhomolog homologous recombination to correct heterozygous mutations in somatic cells
Akiko Tomita, Hiroyuki Sasanuma, Tomoo Owa, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10
DNA Replication in Time and Space: The Archaeal Dimension
Anastasia Serdyuk, Thorsten Allers
DNA (2025) Vol. 5, Iss. 2, pp. 24-24
Open Access
GEN1 promotes common fragile site expression
Anaid Benitez, Marie Sebald, Radhakrishnan Kanagaraj, et al.
Cell Reports (2023) Vol. 42, Iss. 2, pp. 112062-112062
Open Access | Times Cited: 8
Potential Role of the Fragile Histidine Triad in Cancer Evo-Dev
Zheyun Niu, Dongming Jiang, Jiaying Shen, et al.
Cancers (2023) Vol. 15, Iss. 4, pp. 1144-1144
Open Access | Times Cited: 8
Regulator of telomere elongation helicase 1 gene and its association with malignancy
Mohammad Arian Hassani, Jamshid Murid, Jinsong Yan
Cancer Reports (2022) Vol. 6, Iss. 1
Open Access | Times Cited: 13
Interaction of human HelQ with DNA polymerase delta halts DNA synthesis and stimulates DNA single-strand annealing
He Liu, Rebecca Lever, Andrew Cubbon, et al.
Nucleic Acids Research (2023) Vol. 51, Iss. 4, pp. 1740-1749
Open Access | Times Cited: 7
Alternative Lengthening of Telomeres in Yeast: Old Questions and New Approaches
Kendra Musmaker, Jacob Wells, Meng-Chia Tsai, et al.
Biomolecules (2024) Vol. 14, Iss. 1, pp. 113-113
Open Access | Times Cited: 2
Cold Tumour Phenotype Explained Through Whole Genome Sequencing in Clinical Nasopharyngeal Cancer: A Preliminary Study
Handoko Handoko, Marlinda Adham, Lisnawati Rachmadi, et al.
ImmunoTargets and Therapy (2024) Vol. Volume 13, pp. 173-182
Open Access | Times Cited: 2
POLD3 as Controller of Replicative DNA Repair
Nezeka S. Alli, Anna Lou‐Hing, Edward L. Bolt, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 22, pp. 12417-12417
Open Access | Times Cited: 2
RAD51 paralogs: Expanding roles in replication stress responses and repair
Debanjali Bhattacharya, Satyaranjan Sahoo, Tarun Nagraj, et al.
Current Opinion in Pharmacology (2022) Vol. 67, pp. 102313-102313
Closed Access | Times Cited: 10
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