A citation-based method for searching scientific literature


List of co-cited articles
60 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Replication stress activates DNA repair synthesis in mitosis.
Sheroy Minocherhomji, Songmin Ying, Victoria A Bjerregaard, Sara Bursomanno, Aiste Aleliunaite, Wei Wu, Hocine W Mankouri, Huahao Shen, Ying Liu, Ian D Hickson. Nature 2015
293
83

Mammalian RAD52 Functions in Break-Induced Replication Repair of Collapsed DNA Replication Forks.
Sotirios K Sotiriou, Irene Kamileri, Natalia Lugli, Konstantinos Evangelou, Caterina Da-Ré, Florian Huber, Laura Padayachy, Sebastien Tardy, Noemie L Nicati, Samia Barriot,[...]. Mol Cell 2016
159
83

RAD52 Facilitates Mitotic DNA Synthesis Following Replication Stress.
Rahul Bhowmick, Sheroy Minocherhomji, Ian D Hickson. Mol Cell 2016
184
83

RAD52 and SLX4 act nonepistatically to ensure telomere stability during alternative telomere lengthening.
Priyanka Verma, Robert L Dilley, Tianpeng Zhang, Melina T Gyparaki, Yiwen Li, Roger A Greenberg. Genes Dev 2019
43
66

Small-molecule inhibitors identify the RAD52-ssDNA interaction as critical for recovery from replication stress and for survival of BRCA2 deficient cells.
Sarah R Hengel, Eva Malacaria, Laura Folly da Silva Constantino, Fletcher E Bain, Andrea Diaz, Brandon G Koch, Liping Yu, Meng Wu, Pietro Pichierri, M Ashley Spies,[...]. Elife 2016
43
66

The DNA damage response: making it safe to play with knives.
Alberto Ciccia, Stephen J Elledge. Mol Cell 2010
66

Alternative Lengthening of Telomeres through Two Distinct Break-Induced Replication Pathways.
Jia-Min Zhang, Tribhuwan Yadav, Jian Ouyang, Li Lan, Lee Zou. Cell Rep 2019
91
66

Causes and consequences of replication stress.
Michelle K Zeman, Karlene A Cimprich. Nat Cell Biol 2014
967
66

DNA synthesis by Pol η promotes fragile site stability by preventing under-replicated DNA in mitosis.
Valérie Bergoglio, Anne-Sophie Boyer, Erin Walsh, Valeria Naim, Gaëlle Legube, Marietta Y W T Lee, Laurie Rey, Filippo Rosselli, Christophe Cazaux, Kristin A Eckert,[...]. J Cell Biol 2013
125
66


Rad52 inactivation is synthetically lethal with BRCA2 deficiency.
Zhihui Feng, Shaun P Scott, Wendy Bussen, Girdhar G Sharma, Gongshe Guo, Tej K Pandita, Simon N Powell. Proc Natl Acad Sci U S A 2011
206
50

Replication fork reversal triggers fork degradation in BRCA2-defective cells.
Sofija Mijic, Ralph Zellweger, Nagaraja Chappidi, Matteo Berti, Kurt Jacobs, Karun Mutreja, Sebastian Ursich, Arnab Ray Chaudhuri, Andre Nussenzweig, Pavel Janscak,[...]. Nat Commun 2017
159
50

When RAD52 Allows Mitosis to Accept Unscheduled DNA Synthesis.
Camille Franchet, Jean-Sébastien Hoffmann. Cancers (Basel) 2019
10
50

Break-induced replication repair of damaged forks induces genomic duplications in human cells.
Lorenzo Costantino, Sotirios K Sotiriou, Juha K Rantala, Simon Magin, Emil Mladenov, Thomas Helleday, James E Haber, George Iliakis, Olli P Kallioniemi, Thanos D Halazonetis. Science 2014
277
50


Replication Fork Reversal: Players and Guardians.
Annabel Quinet, Delphine Lemaçon, Alessandro Vindigni. Mol Cell 2017
116
33


The essential kinase ATR: ensuring faithful duplication of a challenging genome.
Joshua C Saldivar, David Cortez, Karlene A Cimprich. Nat Rev Mol Cell Biol 2017
302
33

Double-strand break repair-independent role for BRCA2 in blocking stalled replication fork degradation by MRE11.
Katharina Schlacher, Nicole Christ, Nicolas Siaud, Akinori Egashira, Hong Wu, Maria Jasin. Cell 2011
719
33

Rad52 SUMOylation affects the efficiency of the DNA repair.
Veronika Altmannova, Nadine Eckert-Boulet, Milica Arneric, Peter Kolesar, Radka Chaloupkova, Jiri Damborsky, Patrick Sung, Xiaolan Zhao, Michael Lisby, Lumir Krejci. Nucleic Acids Res 2010
71
33

Cell-type-specific replication initiation programs set fragility of the FRA3B fragile site.
Anne Letessier, Gaël A Millot, Stéphane Koundrioukoff, Anne-Marie Lachagès, Nicolas Vogt, R Scott Hansen, Bernard Malfoy, Olivier Brison, Michelle Debatisse. Nature 2011
290
33

Distinct RAD51 associations with RAD52 and BCCIP in response to DNA damage and replication stress.
Justin Wray, Jingmei Liu, Jac A Nickoloff, Zhiyuan Shen. Cancer Res 2008
44
33


Targeted inactivation of mouse RAD52 reduces homologous recombination but not resistance to ionizing radiation.
T Rijkers, J Van Den Ouweland, B Morolli, A G Rolink, W M Baarends, P P Van Sloun, P H Lohman, A Pastink. Mol Cell Biol 1998
250
33


Rad52 prevents excessive replication fork reversal and protects from nascent strand degradation.
Eva Malacaria, Giusj Monia Pugliese, Masayoshi Honda, Veronica Marabitti, Francesca Antonella Aiello, Maria Spies, Annapaola Franchitto, Pietro Pichierri. Nat Commun 2019
39
33

Identification of a second DNA binding site in the human Rad52 protein.
Wataru Kagawa, Ako Kagawa, Kengo Saito, Shukuko Ikawa, Takehiko Shibata, Hitoshi Kurumizaka, Shigeyuki Yokoyama. J Biol Chem 2008
49
33

Repair Pathway Choices and Consequences at the Double-Strand Break.
Raphael Ceccaldi, Beatrice Rondinelli, Alan D D'Andrea. Trends Cell Biol 2016
666
33


Distinct roles of RAD52 and POLQ in chromosomal break repair and replication stress response.
Andrew A Kelso, Felicia Wednesday Lopezcolorado, Ragini Bhargava, Jeremy M Stark. PLoS Genet 2019
26
33

Small-Molecule Disruption of RAD52 Rings as a Mechanism for Precision Medicine in BRCA-Deficient Cancers.
Gurushankar Chandramouly, Shane McDevitt, Katherine Sullivan, Tatiana Kent, Antonio Luz, J Fraser Glickman, Mark Andrake, Tomasz Skorski, Richard T Pomerantz. Chem Biol 2015
56
33

RAD52 as a Potential Target for Synthetic Lethality-Based Anticancer Therapies.
Monika Toma, Katherine Sullivan-Reed, Tomasz Śliwiński, Tomasz Skorski. Cancers (Basel) 2019
20
33

Emerging Roles of RAD52 in Genome Maintenance.
Manisha Jalan, Kyrie S Olsen, Simon N Powell. Cancers (Basel) 2019
24
33

DNA replication stress as a hallmark of cancer.
Morgane Macheret, Thanos D Halazonetis. Annu Rev Pathol 2015
337
33

DNA repair by a Rad22-Mus81-dependent pathway that is independent of Rhp51.
Claudette L Doe, Fekret Osman, Julie Dixon, Matthew C Whitby. Nucleic Acids Res 2004
73
33

DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells.
Andreas Sturzenegger, Kamila Burdova, Radhakrishnan Kanagaraj, Maryna Levikova, Cosimo Pinto, Petr Cejka, Pavel Janscak. J Biol Chem 2014
118
33

Survival of the replication checkpoint deficient cells requires MUS81-RAD52 function.
Ivana Murfuni, Giorgia Basile, Shyamal Subramanyam, Eva Malacaria, Margherita Bignami, Maria Spies, Annapaola Franchitto, Pietro Pichierri. PLoS Genet 2013
48
33


Targeting BRCA1- and BRCA2-deficient cells with RAD52 small molecule inhibitors.
Fei Huang, Nadish Goyal, Katherine Sullivan, Kritika Hanamshet, Mikir Patel, Olga M Mazina, Charles X Wang, W Frank An, James Spoonamore, Shailesh Metkar,[...]. Nucleic Acids Res 2016
51
33


Physiological and Pathological Roles of RAD52 at DNA Replication Forks.
Eva Malacaria, Masayoshi Honda, Annapaola Franchitto, Maria Spies, Pietro Pichierri. Cancers (Basel) 2020
9
33

The concerted roles of FANCM and Rad52 in the protection of common fragile sites.
Hailong Wang, Shibo Li, Joshua Oaks, Jianping Ren, Lei Li, Xiaohua Wu. Nat Commun 2018
31
33


TRAIP drives replisome disassembly and mitotic DNA repair synthesis at sites of incomplete DNA replication.
Remi Sonneville, Rahul Bhowmick, Saskia Hoffmann, Niels Mailand, Ian D Hickson, Karim Labib. Elife 2019
28
33

RTEL1 suppresses G-quadruplex-associated R-loops at difficult-to-replicate loci in the human genome.
Wei Wu, Rahul Bhowmick, Ivan Vogel, Özgün Özer, Fiorella Ghisays, Roshan S Thakur, Esther Sanchez de Leon, Philipp H Richter, Liqun Ren, John H Petrini,[...]. Nat Struct Mol Biol 2020
29
33

Nuclear body phase separation drives telomere clustering in ALT cancer cells.
Huaiying Zhang, Rongwei Zhao, Jason Tones, Michel Liu, Robert L Dilley, David M Chenoweth, Roger A Greenberg, Michael A Lampson. Mol Biol Cell 2020
30
33


Alternative lengthening of human telomeres is a conservative DNA replication process with features of break-induced replication.
Fani-Marlen Roumelioti, Sotirios K Sotiriou, Vasiliki Katsini, Maria Chiourea, Thanos D Halazonetis, Sarantis Gagos. EMBO Rep 2016
84
33

Genome-wide high-resolution mapping of mitotic DNA synthesis sites and common fragile sites by direct sequencing.
Fang Ji, Hongwei Liao, Sheng Pan, Liujian Ouyang, Fang Jia, Zaiyang Fu, Fengjiao Zhang, Xinwei Geng, Xinming Wang, Tingting Li,[...]. Cell Res 2020
14
33

Break-induced telomere synthesis underlies alternative telomere maintenance.
Robert L Dilley, Priyanka Verma, Nam Woo Cho, Harrison D Winters, Anne R Wondisford, Roger A Greenberg. Nature 2016
209
33


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.