Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Moonlighting at replication forks – a new life for homologous recombination proteins BRCA1, BRCA2 and RAD51
Arun Mouli Kolinjivadi, Vincenzo Sannino, Anna De Antoni, et al.
FEBS Letters (2017) Vol. 591, Iss. 8, pp. 1083-1100
Open Access | Times Cited: 149

Showing 1-25 of 149 citing articles:

The essential kinase ATR: ensuring faithful duplication of a challenging genome
Joshua C. Saldivar, David Cortez, Karlene A. Cimprich
Nature Reviews Molecular Cell Biology (2017) Vol. 18, Iss. 10, pp. 622-636
Open Access | Times Cited: 717
Homology-Directed Repair and the Role of BRCA1, BRCA2, and Related Proteins in Genome Integrity and Cancer
Chun-Chin Chen, Weiran Feng, Pei Xin Lim, et al.
Annual Review of Cancer Biology (2017) Vol. 2, Iss. 1, pp. 313-336
Open Access | Times Cited: 285
Replication gaps are a key determinant of PARP inhibitor synthetic lethality with BRCA deficiency
Ke Cong, Min Peng, Arne Nedergaard Kousholt, et al.
Molecular Cell (2021) Vol. 81, Iss. 15, pp. 3128-3144.e7
Open Access | Times Cited: 241
The impact of replication stress on replication dynamics and DNA damage in vertebrate cells
Hervé Técher, Stéphane Koundrioukoff, Alain Nicolas, et al.
Nature Reviews Genetics (2017) Vol. 18, Iss. 9, pp. 535-550
Closed Access | Times Cited: 233
BRCA1 and BRCA2 mutations and treatment strategies for breast cancer
Inês Godet, Daniele M. Gilkes
Integrative Cancer Science and Therapeutics (2017) Vol. 4, Iss. 1
Open Access | Times Cited: 223
Replication Catastrophe: When a Checkpoint Fails because of Exhaustion
Luis Toledo, Kai J. Neelsen, Jiří Lukáš
Molecular Cell (2017) Vol. 66, Iss. 6, pp. 735-749
Open Access | Times Cited: 193
RADX Promotes Genome Stability and Modulates Chemosensitivity by Regulating RAD51 at Replication Forks
Huzefa Dungrawala, Kamakoti P. Bhat, Rémy Le Meur, et al.
Molecular Cell (2017) Vol. 67, Iss. 3, pp. 374-386.e5
Open Access | Times Cited: 187
Replication Gaps Underlie BRCA Deficiency and Therapy Response
Nicholas J. Panzarino, John J. Krais, Ke Cong, et al.
Cancer Research (2020) Vol. 81, Iss. 5, pp. 1388-1397
Open Access | Times Cited: 156
Lesion Bypass and the Reactivation of Stalled Replication Forks
Kenneth J. Marians
Annual Review of Biochemistry (2018) Vol. 87, Iss. 1, pp. 217-238
Open Access | Times Cited: 158
Exploring the links between cancer and placenta development
Vincenzo Costanzo, Alberto Bardelli, Salvatore Siena, et al.
Open Biology (2018) Vol. 8, Iss. 6
Open Access | Times Cited: 145
Small-Molecule Inhibitors Targeting DNA Repair and DNA Repair Deficiency in Research and Cancer Therapy
Sarah R Hengel, Maria Spies, Maria Spies
Cell chemical biology (2017) Vol. 24, Iss. 9, pp. 1101-1119
Open Access | Times Cited: 128
The BRCA Tumor Suppressor Network in Chromosome Damage Repair by Homologous Recombination
Weixing Zhao, Claudia Wiese, Youngho Kwon, et al.
Annual Review of Biochemistry (2019) Vol. 88, Iss. 1, pp. 221-245
Open Access | Times Cited: 128
Non-enzymatic roles of human RAD51 at stalled replication forks
Jennifer M. Mason, Yuen‐Ling Chan, Ralph Weichselbaum, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 113
Replication Fork Breakage and Restart in Escherichia coli
Bénédicte Michel, Anurag Kumar Sinha, David R. F. Leach
Microbiology and Molecular Biology Reviews (2018) Vol. 82, Iss. 3
Open Access | Times Cited: 89
Rad52 prevents excessive replication fork reversal and protects from nascent strand degradation
Eva Malacaria, Giusj Monia Pugliese, Masayoshi Honda, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 77
POLθ prevents MRE11-NBS1-CtIP-dependent fork breakage in the absence of BRCA2/RAD51 by filling lagging-strand gaps
Anjali Mann, Miguel Angel Ramírez-Otero, Anna De Antoni, et al.
Molecular Cell (2022) Vol. 82, Iss. 22, pp. 4218-4231.e8
Open Access | Times Cited: 57
Building up and breaking down: mechanisms controlling recombination during replication
Dana Branzei, Barnabás Szakál
Critical Reviews in Biochemistry and Molecular Biology (2017) Vol. 52, Iss. 4, pp. 381-394
Open Access | Times Cited: 82
The BRCT Domains of the BRCA1 and BARD1 Tumor Suppressors Differentially Regulate Homology-Directed Repair and Stalled Fork Protection
David Billing, Michiko Horiguchi, Foon Wu-Baer, et al.
Molecular Cell (2018) Vol. 72, Iss. 1, pp. 127-139.e8
Open Access | Times Cited: 74
Emerging roles of CST in maintaining genome stability and human disease
Jason A. Stewart
Frontiers in bioscience (2018) Vol. 23, Iss. 8, pp. 1564-1586
Open Access | Times Cited: 60
PDS5 proteins are required for proper cohesin dynamics and participate in replication fork protection
Carmen del Rocío Monedero Morales, Miguel Ruiz‐Torres, Sara Rodríguez‐Acebes, et al.
Journal of Biological Chemistry (2019) Vol. 295, Iss. 1, pp. 146-157
Open Access | Times Cited: 55
Shaping the BRCAness mutational landscape by alternative double-strand break repair, replication stress and mitotic aberrancies
Colin Stok, Yannick P. Kok, Nathalie van den Tempel, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 8, pp. 4239-4257
Open Access | Times Cited: 52
The Brilliance of Borrelia: Mechanisms of Host Immune Evasion by Lyme Disease-Causing Spirochetes
Cassidy Anderson, Catherine A. Brissette
Pathogens (2021) Vol. 10, Iss. 3, pp. 281-281
Open Access | Times Cited: 48
Revisiting the BRCA-pathway through the lens of replication gap suppression
Sharon B. Cantor
DNA repair (2021) Vol. 107, pp. 103209-103209
Open Access | Times Cited: 46
BRCA1 deficiency specific base substitution mutagenesis is dependent on translesion synthesis and regulated by 53BP1
Dan Chen, Judit Z. Gervai, Ádám Póti, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 31
FIRRM/C1orf112 is synthetic lethal with PICH and mediates RAD51 dynamics
Colin Stok, Stavroula Tsaridou, Nathalie van den Tempel, et al.
Cell Reports (2023) Vol. 42, Iss. 7, pp. 112668-112668
Open Access | Times Cited: 22
Page 1 - Next Page

Scroll to top