A citation-based method for searching scientific literature

Fiona Vaz, Helmut Hanenberg, Beatrice Schuster, Karen Barker, Constanze Wiek, Verena Erven, Kornelia Neveling, Daniela Endt, Ian Kesterton, Flavia Autore, Franca Fraternali, Marcel Freund, Linda Hartmann, David Grimwade, Roland G Roberts, Heiner Schaal, Shehla Mohammed, Nazneen Rahman, Detlev Schindler, Christopher G Mathew. Nat Genet 2010
Times Cited: 294







List of co-cited articles
1140 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
Alfons Meindl, Heide Hellebrand, Constanze Wiek, Verena Erven, Barbara Wappenschmidt, Dieter Niederacher, Marcel Freund, Peter Lichtner, Linda Hartmann, Heiner Schaal,[...]. Nat Genet 2010
481
38

Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.
Agata Smogorzewska, Shuhei Matsuoka, Patrizia Vinciguerra, E Robert McDonald, Kristen E Hurov, Ji Luo, Bryan A Ballif, Steven P Gygi, Kay Hofmann, Alan D D'Andrea,[...]. Cell 2007
533
26

Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype.
Sarah L Sawyer, Lei Tian, Marketta Kähkönen, Jeremy Schwartzentruber, Martin Kircher, Jacek Majewski, David A Dyment, A Micheil Innes, Kym M Boycott, Lisa A Moreau,[...]. Cancer Discov 2015
206
26

Mutations in ERCC4, encoding the DNA-repair endonuclease XPF, cause Fanconi anemia.
Massimo Bogliolo, Beatrice Schuster, Chantal Stoepker, Burak Derkunt, Yan Su, Anja Raams, Juan P Trujillo, Jordi Minguillón, María J Ramírez, Roser Pujol,[...]. Am J Hum Genet 2013
226
24

Mutations of the SLX4 gene in Fanconi anemia.
Yonghwan Kim, Francis P Lach, Rohini Desetty, Helmut Hanenberg, Arleen D Auerbach, Agata Smogorzewska. Nat Genet 2011
253
22

Biallelic inactivation of BRCA2 in Fanconi anemia.
Niall G Howlett, Toshiyasu Taniguchi, Susan Olson, Barbara Cox, Quinten Waisfisz, Christine De Die-Smulders, Nicole Persky, Markus Grompe, Hans Joenje, Gerard Pals,[...]. Science 2002
871
22

A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination.
Anderson T Wang, Taeho Kim, John E Wagner, Brooke A Conti, Francis P Lach, Athena L Huang, Henrik Molina, Erica M Sanborn, Heather Zierhut, Belinda K Cornes,[...]. Mol Cell 2015
168
22

Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway.
I Garcia-Higuera, T Taniguchi, S Ganesan, M S Meyn, C Timmers, J Hejna, M Grompe, A D D'Andrea. Mol Cell 2001
966
21

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype.
Chantal Stoepker, Karolina Hain, Beatrice Schuster, Yvonne Hilhorst-Hofstee, Martin A Rooimans, Jurgen Steltenpool, Anneke B Oostra, Katharina Eirich, Elisabeth T Korthof, Aggie W M Nieuwint,[...]. Nat Genet 2011
225
20

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
Bing Xia, Josephine C Dorsman, Najim Ameziane, Yne de Vries, Martin A Rooimans, Qing Sheng, Gerard Pals, Abdellatif Errami, Eliane Gluckman, Julian Llera,[...]. Nat Genet 2007
344
19


Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia.
Asuka Hira, Kenichi Yoshida, Koichi Sato, Yusuke Okuno, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Akira Shimamoto, Hidetoshi Tahara,[...]. Am J Hum Genet 2015
79
22

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
Sarah Reid, Detlev Schindler, Helmut Hanenberg, Karen Barker, Sandra Hanks, Reinhard Kalb, Kornelia Neveling, Patrick Kelly, Sheila Seal, Marcel Freund,[...]. Nat Genet 2007
445
18

Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia.
Kimberly A Rickman, Francis P Lach, Avinash Abhyankar, Frank X Donovan, Erica M Sanborn, Jennifer A Kennedy, Carrie Sougnez, Stacey B Gabriel, Olivier Elemento, Settara C Chandrasekharappa,[...]. Cell Rep 2015
91
18

A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51.
Najim Ameziane, Patrick May, Anneke Haitjema, Henri J van de Vrugt, Sari E van Rossum-Fikkert, Dejan Ristic, Gareth J Williams, Jesper Balk, Davy Rockx, Hong Li,[...]. Nat Commun 2015
91
18

Identification and purification of two distinct complexes containing the five RAD51 paralogs.
J Y Masson, M C Tarsounas, A Z Stasiak, A Stasiak, R Shah, M J McIlwraith, F E Benson, S C West. Genes Dev 2001
282
16

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.
Elizabeth L Virts, Anna Jankowska, Craig Mackay, Marcel F Glaas, Constanze Wiek, Stephanie L Kelich, Nadine Lottmann, Felicia M Kennedy, Christophe Marchal, Erik Lehnert,[...]. Hum Mol Genet 2015
52
30

Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs.
M Takata, M S Sasaki, S Tachiiri, T Fukushima, E Sonoda, D Schild, L H Thompson, S Takeda. Mol Cell Biol 2001
438
16

Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families.
Ana Osorio, Daniela Endt, Fernando Fernández, Katharina Eirich, Miguel de la Hoya, Rita Schmutzler, Trinidad Caldés, Alfons Meindl, Detlev Schindler, Javier Benitez. Hum Mol Genet 2012
60
25


Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2.
Bing Xia, Qing Sheng, Koji Nakanishi, Akihiro Ohashi, Jianmin Wu, Nicole Christ, Xinggang Liu, Maria Jasin, Fergus J Couch, David M Livingston. Mol Cell 2006
573
15

Germline mutations in RAD51D confer susceptibility to ovarian cancer.
Chey Loveday, Clare Turnbull, Emma Ramsay, Deborah Hughes, Elise Ruark, Jessica R Frankum, Georgina Bowden, Bolot Kalmyrzaev, Margaret Warren-Perry, Katie Snape,[...]. Nat Genet 2011
343
15

Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation.
Hanan E Shamseldin, Mohamed Elfaki, Fowzan S Alkuraya. J Med Genet 2012
61
24

RAD51 paralogs: roles in DNA damage signalling, recombinational repair and tumorigenesis.
Natsuko Suwaki, Kerstin Klare, Madalena Tarsounas. Semin Cell Dev Biol 2011
189
14

Germline RAD51C mutations confer susceptibility to ovarian cancer.
Chey Loveday, Clare Turnbull, Elise Ruark, Rosa Maria Munoz Xicola, Emma Ramsay, Deborah Hughes, Margaret Warren-Perry, Katie Snape, Diana Eccles, D Gareth Evans,[...]. Nat Genet 2012
173
14

A novel ubiquitin ligase is deficient in Fanconi anemia.
Amom Ruhikanta Meetei, Johan P de Winter, Annette L Medhurst, Michael Wallisch, Quinten Waisfisz, Henri J van de Vrugt, Anneke B Oostra, Zhijiang Yan, Chen Ling, Colin E Bishop,[...]. Nat Genet 2003
450
14

Fanconi anemia and its diagnosis.
Arleen D Auerbach. Mutat Res 2009
356
14

Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene.
Jung-Young Park, Elizabeth L Virts, Anna Jankowska, Constanze Wiek, Mohamed Othman, Sujata C Chakraborty, Gail H Vance, Fowzan S Alkuraya, Helmut Hanenberg, Paul R Andreassen. J Med Genet 2016
58
24

The Fanconi anaemia pathway: new players and new functions.
Raphael Ceccaldi, Prabha Sarangi, Alan D D'Andrea. Nat Rev Mol Cell Biol 2016
383
14


Mammalian RAD51 paralogs protect nascent DNA at stalled forks and mediate replication restart.
Kumar Somyajit, Sneha Saxena, Sharath Babu, Anup Mishra, Ganesh Nagaraju. Nucleic Acids Res 2015
77
16

Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase.
Helen E Bryant, Niklas Schultz, Huw D Thomas, Kayan M Parker, Dan Flower, Elena Lopez, Suzanne Kyle, Mark Meuth, Nicola J Curtin, Thomas Helleday. Nature 2005
13

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
782
13

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Marieke Levitus, Quinten Waisfisz, Barbara C Godthelp, Yne de Vries, Shobbir Hussain, Wouter W Wiegant, Elhaam Elghalbzouri-Maghrani, Jûrgen Steltenpool, Martin A Rooimans, Gerard Pals,[...]. Nat Genet 2005
333
13

How the fanconi anemia pathway guards the genome.
George-Lucian Moldovan, Alan D D'Andrea. Annu Rev Genet 2009
418
12

DNA interstrand crosslink repair and cancer.
Andrew J Deans, Stephen C West. Nat Rev Cancer 2011
648
12

RAD51C is a susceptibility gene for ovarian cancer.
Liisa M Pelttari, Tuomas Heikkinen, Deborah Thompson, Anne Kallioniemi, Johanna Schleutker, Kaija Holli, Carl Blomqvist, Kristiina Aittomäki, Ralf Bützow, Heli Nevanlinna. Hum Mol Genet 2011
96
12

A 20-year perspective on the International Fanconi Anemia Registry (IFAR).
David I Kutler, Bhuvanesh Singh, Jaya Satagopan, Sat Dev Batish, Marianne Berwick, Philip F Giampietro, Helmut Hanenberg, Arleen D Auerbach. Blood 2003
498
12

FANCI is a second monoubiquitinated member of the Fanconi anemia pathway.
Ashley E Sims, Elizabeth Spiteri, Robert J Sims, Adriana G Arita, Francis P Lach, Thomas Landers, Melanie Wurm, Marcel Freund, Kornelia Neveling, Helmut Hanenberg,[...]. Nat Struct Mol Biol 2007
211
12

Positional cloning of a novel Fanconi anemia gene, FANCD2.
C Timmers, T Taniguchi, J Hejna, C Reifsteck, L Lucas, D Bruun, M Thayer, B Cox, S Olson, A D D'Andrea,[...]. Mol Cell 2001
313
12

Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population.
Honglin Song, Ed Dicks, Susan J Ramus, Jonathan P Tyrer, Maria P Intermaggio, Jane Hayward, Christopher K Edlund, David Conti, Patricia Harrington, Lindsay Fraser,[...]. J Clin Oncol 2015
183
12

Biallelic inactivation of REV7 is associated with Fanconi anemia.
Dominique Bluteau, Julien Masliah-Planchon, Connor Clairmont, Alix Rousseau, Raphael Ceccaldi, Catherine Dubois d'Enghien, Olivier Bluteau, Wendy Cuccuini, Stéphanie Gachet, Régis Peffault de Latour,[...]. J Clin Invest 2016
86
13

Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia.
Kerstin Knies, Shojiro Inano, María J Ramírez, Masamichi Ishiai, Jordi Surrallés, Minoru Takata, Detlev Schindler. J Clin Invest 2017
121
12

Mechanism of RAD51-dependent DNA interstrand cross-link repair.
David T Long, Markus Räschle, Vladimir Joukov, Johannes C Walter. Science 2011
164
11


Loss of Rad51c leads to embryonic lethality and modulation of Trp53-dependent tumorigenesis in mice.
Sergey G Kuznetsov, Diana C Haines, Betty K Martin, Shyam K Sharan. Cancer Res 2009
62
17

UBE2T is the E2 in the Fanconi anemia pathway and undergoes negative autoregulation.
Yuichi J Machida, Yuka Machida, Yuefeng Chen, Allan M Gurtan, Gary M Kupfer, Alan D D'Andrea, Anindya Dutta. Mol Cell 2006
201
11

Fanconi anaemia and the repair of Watson and Crick DNA crosslinks.
Molly C Kottemann, Agata Smogorzewska. Nature 2013
405
11

Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.
Alberto Ciccia, Chen Ling, Rachel Coulthard, Zhijiang Yan, Yutong Xue, Amom Ruhikanta Meetei, El Houari Laghmani, Hans Joenje, Neil McDonald, Johan P de Winter,[...]. Mol Cell 2007
225
11

Fancd2 counteracts the toxic effects of naturally produced aldehydes in mice.
Frédéric Langevin, Gerry P Crossan, Ivan V Rosado, Mark J Arends, Ketan J Patel. Nature 2011
349
11


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.