A citation-based method for searching scientific literature

Yoko Katsuki, Minoru Takata. Endocr Relat Cancer 2016
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity


Hereditary breast and ovarian cancer: new genes in confined pathways.
Finn Cilius Nielsen, Thomas van Overeem Hansen, Claus Storgaard Sørensen. Nat Rev Cancer 2016
211
25

BRCA1 and BRCA2: different roles in a common pathway of genome protection.
Rohini Roy, Jarin Chun, Simon N Powell. Nat Rev Cancer 2011
836
25

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
873
20

Mechanism of Ubiquitination and Deubiquitination in the Fanconi Anemia Pathway.
Sylvie van Twest, Vincent J Murphy, Charlotte Hodson, Winnie Tan, Paolo Swuec, Julienne J O'Rourke, Jörg Heierhorst, Wayne Crismani, Andrew J Deans. Mol Cell 2017
84
20

The Fanconi anaemia pathway: new players and new functions.
Raphael Ceccaldi, Prabha Sarangi, Alan D D'Andrea. Nat Rev Mol Cell Biol 2016
396
20

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
211
20

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
20

Identification of the breast cancer susceptibility gene BRCA2.
R Wooster, G Bignell, J Lancaster, S Swift, S Seal, J Mangion, N Collins, S Gregory, C Gumbs, G Micklem. Nature 1995
15

Breast-cancer risk in families with mutations in PALB2.
Antonis C Antoniou, Silvia Casadei, Tuomas Heikkinen, Daniel Barrowdale, Katri Pylkäs, Jonathan Roberts, Andrew Lee, Deepak Subramanian, Kim De Leeneer, Florentia Fostira,[...]. N Engl J Med 2014
522
15


Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers.
Peter C Fong, David S Boss, Timothy A Yap, Andrew Tutt, Peijun Wu, Marja Mergui-Roelvink, Peter Mortimer, Helen Swaisland, Alan Lau, Mark J O'Connor,[...]. N Engl J Med 2009
15

BRCA2 functions: from DNA repair to replication fork stabilization.
Amélie Fradet-Turcotte, Justine Sitz, Damien Grapton, Alexandre Orthwein. Endocr Relat Cancer 2016
42
15

Homologous recombination and human health: the roles of BRCA1, BRCA2, and associated proteins.
Rohit Prakash, Yu Zhang, Weiran Feng, Maria Jasin. Cold Spring Harb Perspect Biol 2015
458
15

Fanconi anaemia and the repair of Watson and Crick DNA crosslinks.
Molly C Kottemann, Agata Smogorzewska. Nature 2013
409
15

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
536
15


FANCI phosphorylation functions as a molecular switch to turn on the Fanconi anemia pathway.
Masamichi Ishiai, Hiroyuki Kitao, Agata Smogorzewska, Junya Tomida, Aiko Kinomura, Emi Uchida, Alihossein Saberi, Eiji Kinoshita, Emiko Kinoshita-Kikuta, Tohru Koike,[...]. Nat Struct Mol Biol 2008
178
15

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
448
15

Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer.
Guido Neidhardt, Jan Hauke, Juliane Ramser, Eva Groß, Andrea Gehrig, Clemens R Müller, Anne-Karin Kahlert, Karl Hackmann, Ellen Honisch, Dieter Niederacher,[...]. JAMA Oncol 2017
58
15

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
15

Germline RECQL mutations are associated with breast cancer susceptibility.
Cezary Cybulski, Jian Carrot-Zhang, Wojciech Kluźniak, Barbara Rivera, Aniruddh Kashyap, Dominika Wokołorczyk, Sylvie Giroux, Javad Nadaf, Nancy Hamel, Shiyu Zhang,[...]. Nat Genet 2015
131
15

Secondary mutations as a mechanism of cisplatin resistance in BRCA2-mutated cancers.
Wataru Sakai, Elizabeth M Swisher, Beth Y Karlan, Mukesh K Agarwal, Jake Higgins, Cynthia Friedman, Emily Villegas, Céline Jacquemont, Daniel J Farrugia, Fergus J Couch,[...]. Nature 2008
732
15

Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer.
Johanna I Kiiski, Liisa M Pelttari, Sofia Khan, Edda S Freysteinsdottir, Inga Reynisdottir, Steven N Hart, Hermela Shimelis, Sara Vilske, Anne Kallioniemi, Johanna Schleutker,[...]. Proc Natl Acad Sci U S A 2014
125
15


Repair Pathway Choices and Consequences at the Double-Strand Break.
Raphael Ceccaldi, Beatrice Rondinelli, Alan D D'Andrea. Trends Cell Biol 2016
800
15

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.
R Wooster, S L Neuhausen, J Mangion, Y Quirk, D Ford, N Collins, K Nguyen, S Seal, T Tran, D Averill. Science 1994
15

Modifiers of breast and ovarian cancer risks for BRCA1 and BRCA2 mutation carriers.
Roger L Milne, Antonis C Antoniou. Endocr Relat Cancer 2016
44
10

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
80
10

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
806
10

FANCD2 binds CtIP and regulates DNA-end resection during DNA interstrand crosslink repair.
Junya Unno, Akiko Itaya, Masato Taoka, Koichi Sato, Junya Tomida, Wataru Sakai, Kaoru Sugasawa, Masamichi Ishiai, Tsuyoshi Ikura, Toshiaki Isobe,[...]. Cell Rep 2014
64
10


What is the DNA repair defect underlying Fanconi anemia?
Julien P Duxin, Johannes C Walter. Curr Opin Cell Biol 2015
104
10

The FA Core Complex Contains a Homo-dimeric Catalytic Module for the Symmetric Mono-ubiquitination of FANCI-FANCD2.
Paolo Swuec, Ludovic Renault, Aaron Borg, Fenil Shah, Vincent J Murphy, Sylvie van Twest, Ambrosius P Snijders, Andrew J Deans, Alessandro Costa. Cell Rep 2017
39
10

Regulation of FANCD2 and FANCI monoubiquitination by their interaction and by DNA.
Simonne Longerich, Youngho Kwon, Miaw-Sheue Tsai, Aye Su Hlaing, Gary M Kupfer, Patrick Sung. Nucleic Acids Res 2014
60
10

Involvement of SLX4 in interstrand cross-link repair is regulated by the Fanconi anemia pathway.
Kimiyo N Yamamoto, Shunsuke Kobayashi, Masataka Tsuda, Hitoshi Kurumizaka, Minoru Takata, Koichi Kono, Josef Jiricny, Shunichi Takeda, Kouji Hirota. Proc Natl Acad Sci U S A 2011
148
10

FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2.
Maria Castella, Celine Jacquemont, Elizabeth L Thompson, Jung Eun Yeo, Ronald S Cheung, Jen-Wei Huang, Alexandra Sobeck, Eric A Hendrickson, Toshiyasu Taniguchi. PLoS Genet 2015
51
10

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
92
10

Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations.
Maria Castella, Roser Pujol, Elsa Callén, Juan P Trujillo, José A Casado, Hans Gille, Francis P Lach, Arleen D Auerbach, Detlev Schindler, Javier Benítez,[...]. Blood 2011
91
10

The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription.
Rebekka A Schwab, Jadwiga Nieminuszczy, Fenil Shah, Jamie Langton, David Lopez Martinez, Chih-Chao Liang, Martin A Cohn, Richard J Gibbons, Andrew J Deans, Wojciech Niedzwiedz. Mol Cell 2015
216
10

Fanconi anemia FANCG protein in mitigating radiation- and enzyme-induced DNA double-strand breaks by homologous recombination in vertebrate cells.
Kazuhiko Yamamoto, Masamichi Ishiai, Nobuko Matsushita, Hiroshi Arakawa, Jane E Lamerdin, Jean-Marie Buerstedde, Mitsune Tanimoto, Mine Harada, Larry H Thompson, Minoru Takata. Mol Cell Biol 2003
117
10

DNA robustly stimulates FANCD2 monoubiquitylation in the complex with FANCI.
Koichi Sato, Kazue Toda, Masamichi Ishiai, Minoru Takata, Hitoshi Kurumizaka. Nucleic Acids Res 2012
66
10

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
172
10

Structure of the FANCI-FANCD2 complex: insights into the Fanconi anemia DNA repair pathway.
Woo Joo, Guozhou Xu, Nicole S Persky, Agata Smogorzewska, Derek G Rudge, Olga Buzovetsky, Stephen J Elledge, Nikola P Pavletich. Science 2011
115
10

Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice.
Scott Houghtaling, Cynthia Timmers, Meenakshi Noll, Milton J Finegold, Stephen N Jones, M Stephen Meyn, Markus Grompe. Genes Dev 2003
210
10

Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4.
Yonghwan Kim, Gabriella S Spitz, Uma Veturi, Francis P Lach, Arleen D Auerbach, Agata Smogorzewska. Blood 2013
124
10

Repair of strand breaks by homologous recombination.
Maria Jasin, Rodney Rothstein. Cold Spring Harb Perspect Biol 2013
518
10

Update of the human and mouse Fanconi anemia genes.
Hongbin Dong, Daniel W Nebert, Elspeth A Bruford, David C Thompson, Hans Joenje, Vasilis Vasiliou. Hum Genomics 2015
99
10

RING finger and WD repeat domain 3 (RFWD3) associates with replication protein A (RPA) and facilitates RPA-mediated DNA damage response.
Shangfeng Liu, Jessica Chu, Nur Yucer, Mei Leng, Shih-Ya Wang, Benjamin P C Chen, Walter N Hittelman, Yi Wang. J Biol Chem 2011
48
10

SnapShot: Fanconi anemia and associated proteins.
Anderson T Wang, Agata Smogorzewska. Cell 2015
112
10

Hereditary breast and ovarian cancer due to mutations in BRCA1 and BRCA2.
Nancie Petrucelli, Mary B Daly, Gerald L Feldman. Genet Med 2010
200
10


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.