A citation-based method for searching scientific literature

José M Sogo, Massimo Lopes, Marco Foiani. Science 2002
Times Cited: 644







List of co-cited articles
1750 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Rad51-mediated replication fork reversal is a global response to genotoxic treatments in human cells.
Ralph Zellweger, Damian Dalcher, Karun Mutreja, Matteo Berti, Jonas A Schmid, Raquel Herrador, Alessandro Vindigni, Massimo Lopes. J Cell Biol 2015
370
36

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
754
32


Replication fork reversal in eukaryotes: from dead end to dynamic response.
Kai J Neelsen, Massimo Lopes. Nat Rev Mol Cell Biol 2015
278
27

The DNA replication checkpoint response stabilizes stalled replication forks.
M Lopes, C Cotta-Ramusino, A Pellicioli, G Liberi, P Plevani, M Muzi-Falconi, C S Newlon, M Foiani. Nature 2001
605
26

Causes and consequences of replication stress.
Michelle K Zeman, Karlene A Cimprich. Nat Cell Biol 2014
26

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
169
23

Replication Fork Slowing and Reversal upon DNA Damage Require PCNA Polyubiquitination and ZRANB3 DNA Translocase Activity.
Marko Vujanovic, Jana Krietsch, Maria Chiara Raso, Nastassja Terraneo, Ralph Zellweger, Jonas A Schmid, Angelo Taglialatela, Jen-Wei Huang, Cory L Holland, Katharina Zwicky,[...]. Mol Cell 2017
119
23

DNA2 drives processing and restart of reversed replication forks in human cells.
Saravanabhavan Thangavel, Matteo Berti, Maryna Levikova, Cosimo Pinto, Shivasankari Gomathinayagam, Marko Vujanovic, Ralph Zellweger, Hayley Moore, Eu Han Lee, Eric A Hendrickson,[...]. J Cell Biol 2015
205
21

Rad51 protects nascent DNA from Mre11-dependent degradation and promotes continuous DNA synthesis.
Yoshitami Hashimoto, Arnab Ray Chaudhuri, Massimo Lopes, Vincenzo Costanzo. Nat Struct Mol Biol 2010
338
21

Topoisomerase I poisoning results in PARP-mediated replication fork reversal.
Arnab Ray Chaudhuri, Yoshitami Hashimoto, Raquel Herrador, Kai J Neelsen, Daniele Fachinetti, Rodrigo Bermejo, Andrea Cocito, Vincenzo Costanzo, Massimo Lopes. Nat Struct Mol Biol 2012
309
21


ATR prohibits replication catastrophe by preventing global exhaustion of RPA.
Luis Ignacio Toledo, Matthias Altmeyer, Maj-Britt Rask, Claudia Lukas, Dorthe Helena Larsen, Lou Klitgaard Povlsen, Simon Bekker-Jensen, Niels Mailand, Jiri Bartek, Jiri Lukas. Cell 2013
490
21


Smarcal1-Mediated Fork Reversal Triggers Mre11-Dependent Degradation of Nascent DNA in the Absence of Brca2 and Stable Rad51 Nucleofilaments.
Arun Mouli Kolinjivadi, Vincenzo Sannino, Anna De Antoni, Karina Zadorozhny, Mairi Kilkenny, Hervé Técher, Giorgio Baldi, Rong Shen, Alberto Ciccia, Luca Pellegrini,[...]. Mol Cell 2017
172
20

Human RECQ1 promotes restart of replication forks reversed by DNA topoisomerase I inhibition.
Matteo Berti, Arnab Ray Chaudhuri, Saravanabhavan Thangavel, Shivasankari Gomathinayagam, Sasa Kenig, Marko Vujanovic, Federico Odreman, Timo Glatter, Simona Graziano, Ramiro Mendoza-Maldonado,[...]. Nat Struct Mol Biol 2013
261
19

ATR phosphorylates SMARCAL1 to prevent replication fork collapse.
Frank B Couch, Carol E Bansbach, Robert Driscoll, Jessica W Luzwick, Gloria G Glick, Rémy Bétous, Clinton M Carroll, Sung Yun Jung, Jun Qin, Karlene A Cimprich,[...]. Genes Dev 2013
246
19

MRE11 and EXO1 nucleases degrade reversed forks and elicit MUS81-dependent fork rescue in BRCA2-deficient cells.
Delphine Lemaçon, Jessica Jackson, Annabel Quinet, Joshua R Brickner, Shan Li, Stephanie Yazinski, Zhongsheng You, Grzegorz Ira, Lee Zou, Nima Mosammaparast,[...]. Nat Commun 2017
180
19

Functional uncoupling of MCM helicase and DNA polymerase activities activates the ATR-dependent checkpoint.
Tony S Byun, Marcin Pacek, Muh-ching Yee, Johannes C Walter, Karlene A Cimprich. Genes Dev 2005
543
19

Exo1 processes stalled replication forks and counteracts fork reversal in checkpoint-defective cells.
Cecilia Cotta-Ramusino, Daniele Fachinetti, Chiara Lucca, Ylli Doksani, Massimo Lopes, José Sogo, Marco Foiani. Mol Cell 2005
204
19

S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex.
Yuki Katou, Yutaka Kanoh, Masashige Bando, Hideki Noguchi, Hirokazu Tanaka, Toshihiko Ashikari, Katsunori Sugimoto, Katsuhiko Shirahige. Nature 2003
534
18

Replication fork stability confers chemoresistance in BRCA-deficient cells.
Arnab Ray Chaudhuri, Elsa Callen, Xia Ding, Ewa Gogola, Alexandra A Duarte, Ji-Eun Lee, Nancy Wong, Vanessa Lafarga, Jennifer A Calvo, Nicholas J Panzarino,[...]. Nature 2016
439
18

Signaling pathways of replication stress in yeast.
Benjamin Pardo, Laure Crabbé, Philippe Pasero. FEMS Yeast Res 2017
70
25

Polyubiquitinated PCNA recruits the ZRANB3 translocase to maintain genomic integrity after replication stress.
Alberto Ciccia, Amitabh V Nimonkar, Yiduo Hu, Ildiko Hajdu, Yathish Jagadheesh Achar, Lior Izhar, Sarah A Petit, Britt Adamson, John C Yoon, Stephen C Kowalczykowski,[...]. Mol Cell 2012
187
16

Restoration of Replication Fork Stability in BRCA1- and BRCA2-Deficient Cells by Inactivation of SNF2-Family Fork Remodelers.
Angelo Taglialatela, Silvia Alvarez, Giuseppe Leuzzi, Vincenzo Sannino, Lepakshi Ranjha, Jen-Wei Huang, Chioma Madubata, Roopesh Anand, Brynn Levy, Raul Rabadan,[...]. Mol Cell 2017
169
15


HLTF's Ancient HIRAN Domain Binds 3' DNA Ends to Drive Replication Fork Reversal.
Andrew C Kile, Diana A Chavez, Julien Bacal, Sherif Eldirany, Dmitry M Korzhnev, Irina Bezsonova, Brandt F Eichman, Karlene A Cimprich. Mol Cell 2015
117
15


RADX Promotes Genome Stability and Modulates Chemosensitivity by Regulating RAD51 at Replication Forks.
Huzefa Dungrawala, Kamakoti P Bhat, Rémy Le Meur, Walter J Chazin, Xia Ding, Shyam K Sharan, Sarah R Wessel, Aditya A Sathe, Runxiang Zhao, David Cortez. Mol Cell 2017
91
15

Error-free DNA damage tolerance and sister chromatid proximity during DNA replication rely on the Polα/Primase/Ctf4 Complex.
Marco Fumasoni, Katharina Zwicky, Fabio Vanoli, Massimo Lopes, Dana Branzei. Mol Cell 2015
94
14

Visualization of recombination-mediated damage bypass by template switching.
Michele Giannattasio, Katharina Zwicky, Cindy Follonier, Marco Foiani, Massimo Lopes, Dana Branzei. Nat Struct Mol Biol 2014
98
14

Hydroxyurea-stalled replication forks become progressively inactivated and require two different RAD51-mediated pathways for restart and repair.
Eva Petermann, Manuel Luís Orta, Natalia Issaeva, Niklas Schultz, Thomas Helleday. Mol Cell 2010
555
14

RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO.
Carsten Hoege, Boris Pfander, George-Lucian Moldovan, George Pyrowolakis, Stefan Jentsch. Nature 2002
13

Sae2, Exo1 and Sgs1 collaborate in DNA double-strand break processing.
Eleni P Mimitou, Lorraine S Symington. Nature 2008
732
13

Replication stress: getting back on track.
Matteo Berti, Alessandro Vindigni. Nat Struct Mol Biol 2016
154
13

The DNA damage response: making it safe to play with knives.
Alberto Ciccia, Stephen J Elledge. Mol Cell 2010
13

Maintaining genome stability at the replication fork.
Dana Branzei, Marco Foiani. Nat Rev Mol Cell Biol 2010
582
13


Replication Fork Reversal: Players and Guardians.
Annabel Quinet, Delphine Lemaçon, Alessandro Vindigni. Mol Cell 2017
127
13

RADX Modulates RAD51 Activity to Control Replication Fork Protection.
Kamakoti P Bhat, Archana Krishnamoorthy, Huzefa Dungrawala, Edwige B Garcin, Mauro Modesti, David Cortez. Cell Rep 2018
49
26

How the Eukaryotic Replisome Achieves Rapid and Efficient DNA Replication.
Joseph T P Yeeles, Agnieska Janska, Anne Early, John F X Diffley. Mol Cell 2017
182
12

Repriming of DNA synthesis at stalled replication forks by human PrimPol.
Silvana Mourón, Sara Rodriguez-Acebes, María I Martínez-Jiménez, Sara García-Gómez, Sandra Chocrón, Luis Blanco, Juan Méndez. Nat Struct Mol Biol 2013
174
12

PrimPol, an archaic primase/polymerase operating in human cells.
Sara García-Gómez, Aurelio Reyes, María I Martínez-Jiménez, E Sandra Chocrón, Silvana Mourón, Gloria Terrados, Christopher Powell, Eduardo Salido, Juan Méndez, Ian J Holt,[...]. Mol Cell 2013
233
12

Checkpoint Kinase Rad53 Couples Leading- and Lagging-Strand DNA Synthesis under Replication Stress.
Haiyun Gan, Chuanhe Yu, Sujan Devbhandari, Sushma Sharma, Junhong Han, Andrei Chabes, Dirk Remus, Zhiguo Zhang. Mol Cell 2017
33
36

dNTP pools determine fork progression and origin usage under replication stress.
Jérôme Poli, Olga Tsaponina, Laure Crabbé, Andrea Keszthelyi, Véronique Pantesco, Andrei Chabes, Armelle Lengronne, Philippe Pasero. EMBO J 2012
191
12

Mrc1 transduces signals of DNA replication stress to activate Rad53.
A A Alcasabas, A J Osborn, J Bachant, F Hu, P J Werler, K Bousset, K Furuya, J F Diffley, A M Carr, S J Elledge. Nat Cell Biol 2001
404
12

Replication fork stalling at natural impediments.
Ekaterina V Mirkin, Sergei M Mirkin. Microbiol Mol Biol Rev 2007
361
12

SMARCAL1 catalyzes fork regression and Holliday junction migration to maintain genome stability during DNA replication.
Rémy Bétous, Aaron C Mason, Robert P Rambo, Carol E Bansbach, Akosua Badu-Nkansah, Bianca M Sirbu, Brandt F Eichman, David Cortez. Genes Dev 2012
187
11

Substrate-selective repair and restart of replication forks by DNA translocases.
Rémy Bétous, Frank B Couch, Aaron C Mason, Brandt F Eichman, Maria Manosas, David Cortez. Cell Rep 2013
108
11

Independent and Stochastic Action of DNA Polymerases in the Replisome.
James E Graham, Kenneth J Marians, Stephen C Kowalczykowski. Cell 2017
83
13


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.