A citation-based method for searching scientific literature

Patrícia M Machado, Rita D Brandão, Branca M Cavaco, Joana Eugénio, Sandra Bento, Mónica Nave, Paula Rodrigues, Aires Fernandes, Fátima Vaz. J Clin Oncol 2007
Times Cited: 74







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



Times Cited
  Times     Co-cited
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The c.156_157insAlu BRCA2 rearrangement accounts for more than one-fourth of deleterious BRCA mutations in northern/central Portugal.
Ana Peixoto, Catarina Santos, Patrícia Rocha, Manuela Pinheiro, Sofia Príncipe, Deolinda Pereira, Helena Rodrigues, Fernando Castro, Joaquim Abreu, Leonor Gusmão,[...]. Breast Cancer Res Treat 2009
43
44

De novo Alu element insertions targeted to a sequence common to the BRCA1 and BRCA2 genes.
Erik Teugels, Sylvia De Brakeleer, Guido Goelen, Willy Lissens, Erica Sermijn, Jacques De Grève. Hum Mutat 2005
60
30

Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.
Tom Walsh, Silvia Casadei, Kathryn Hale Coats, Elizabeth Swisher, Sunday M Stray, Jake Higgins, Kevin C Roach, Jessica Mandell, Ming K Lee, Sona Ciernikova,[...]. JAMA 2006
435
20

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients.
A Petrij-Bosch, T Peelen, M van Vliet, R van Eijk, R Olmer, M Drüsedau, F B Hogervorst, S Hageman, P J Arts, M J Ligtenberg,[...]. Nat Genet 1997
348
14

Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method.
Frans B L Hogervorst, Petra M Nederlof, Johan J P Gille, Cathal J McElgunn, Maartje Grippeling, Roelof Pruntel, Rein Regnerus, Tibor van Welsem, Resie van Spaendonk, Fred H Menko,[...]. Cancer Res 2003
255
14

Founder mutations in BRCA1 and BRCA2 genes.
R Ferla, V Calò, S Cascio, G Rinaldi, G Badalamenti, I Carreca, E Surmacz, G Colucci, V Bazan, A Russo. Ann Oncol 2007
149
14


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
13

Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families.
Carolin Hartmann, Anika L John, Rüdiger Klaes, Wera Hofmann, Rainer Bielen, Rolf Koehler, Bart Janssen, Claus R Bartram, Norbert Arnold, Johannes Zschocke. Hum Mutat 2004
61
14

Low frequency of large genomic rearrangements of BRCA1 and BRCA2 in western Denmark.
Mads Thomassen, Anne-Marie Gerdes, Dorthe Cruger, Peter K A Jensen, Torben A Kruse. Cancer Genet Cytogenet 2006
40
22


A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family.
M Nordling, P Karlsson, J Wahlström, Y Engwall, A Wallgren, T Martinsson. Cancer Res 1998
69
13

High proportion of BRCA1/2 founder mutations in Hispanic breast/ovarian cancer families from Colombia.
Diana Torres, Muhammad Usman Rashid, Fabian Gil, Angela Umana, Giancarlo Ramelli, Jose Fernando Robledo, Mauricio Tawil, Lilian Torregrosa, Ignacio Briceno, Ute Hamann. Breast Cancer Res Treat 2007
67
13

Prevalence of BRCA1 and BRCA2 mutations in breast cancer patients from Brazil.
Magda C B Gomes, Mauricio M Costa, Radovan Borojevic, Alvaro N A Monteiro, Roberto Vieira, Sergio Koifman, Rosalina Jorge Koifman, Song Li, Robert Royer, Shiyu Zhang,[...]. Breast Cancer Res Treat 2007
55
16


Prevalence and type of BRCA mutations in Hispanics undergoing genetic cancer risk assessment in the southwestern United States: a report from the Clinical Cancer Genetics Community Research Network.
Jeffrey N Weitzel, Jessica Clague, Arelis Martir-Negron, Raquel Ogaz, Josef Herzog, Charité Ricker, Chelsy Jungbluth, Cheryl Cina, Paul Duncan, Gary Unzeitig,[...]. J Clin Oncol 2013
99
12

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.
D Ford, D F Easton, M Stratton, S Narod, D Goldgar, P Devilee, D T Bishop, B Weber, G Lenoir, J Chang-Claude,[...]. Am J Hum Genet 1998
10

Significant contribution of germline BRCA2 rearrangements in male breast cancer families.
Isabelle Tournier, Brigitte Bressac-de Paillerets, Hagay Sobol, Dominique Stoppa-Lyonnet, Rosette Lidereau, Michel Barrois, Sylvie Mazoyer, Florence Coulet, Agnès Hardouin, Agnès Chompret,[...]. Cancer Res 2004
80
10

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals.
Thomas S Frank, Amie M Deffenbaugh, Julia E Reid, Mark Hulick, Brian E Ward, Beth Lingenfelter, Kathi L Gumpper, Thomas Scholl, Sean V Tavtigian, Dmitry R Pruss,[...]. J Clin Oncol 2002
625
10

Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families.
Thomas v O Hansen, Lars Jønson, Anders Albrechtsen, Mette K Andersen, Bent Ejlertsen, Finn C Nielsen. Breast Cancer Res Treat 2009
49
16

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families.
Marco Montagna, Maurizia Dalla Palma, Chiara Menin, Simona Agata, Arcangela De Nicolo, Luigi Chieco-Bianchi, Emma D'Andrea. Hum Mol Genet 2003
150
10

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation.
Ana Peixoto, Catarina Santos, Manuela Pinheiro, Pedro Pinto, Maria José Soares, Patrícia Rocha, Leonor Gusmão, António Amorim, Annemarie van der Hout, Anne-Marie Gerdes,[...]. Breast Cancer Res Treat 2011
21
38

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.
Hanne Meijers-Heijboer, Ans van den Ouweland, Jan Klijn, Marijke Wasielewski, Anja de Snoo, Rogier Oldenburg, Antoinette Hollestelle, Mark Houben, Ellen Crepin, Monique van Veghel-Plandsoen,[...]. Nat Genet 2002
767
9

Prevalence of five previously reported and recurrent BRCA1 genetic rearrangement mutations in 20,000 patients from hereditary breast/ovarian cancer families.
Brant C Hendrickson, Thaddeus Judkins, Benjamin D Ward, Kristilyn Eliason, Amie E Deffenbaugh, Lynn Anne Burbidge, Kristin Pyne, Benoît Leclair, Brian E Ward, Thomas Scholl. Genes Chromosomes Cancer 2005
39
17

No Evidence of BRCA1/2 genomic rearrangements in high-risk French-Canadian breast/ovarian cancer families.
Anne-Marie Moisan, Jessyka Fortin, Martine Dumont, Carolle Samson, Paul Bessette, Jocelyne Chiquette, Rachel Laframboise, Jean Lépine, Bernard Lespérance, Roxane Pichette,[...]. Genet Test 2006
42
16


Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects.
Orland Díez, Ana Osorio, Mercedes Durán, José Ignacio Martinez-Ferrandis, Miguel de la Hoya, Raquel Salazar, Ana Vega, Berta Campos, Raquel Rodríguez-López, Eladio Velasco,[...]. Hum Mutat 2003
132
9

Caution should be used when interpreting alterations affecting the exon 3 of the BRCA2 gene in breast/ovarian cancer families.
Orland Díez, Sara Gutiérrez-Enríquez, Teresa Ramón y Cajal, Carmen Alonso, Judith Balmaña, Gemma Llort. J Clin Oncol 2007
10
70

Analysis of BRCA1 and BRCA2 mutations in Brazilian breast cancer patients with positive family history.
Rozany Mucha Dufloth, Sílvia Carvalho, Juliana Karina Heinrich, Júlia Yoriko Shinzato, César Cabello dos Santos, Luiz Carlos Zeferino, Fernando Schmitt. Sao Paulo Med J 2005
28
25

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
9

MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases.
Stefanie Engert, Barbara Wappenschmidt, Beate Betz, Karin Kast, Michael Kutsche, Heide Hellebrand, Timm O Goecke, Marion Kiechle, Dieter Niederacher, Rita K Schmutzler,[...]. Hum Mutat 2008
69
10

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification.
Jan P Schouten, Cathal J McElgunn, Raymond Waaijer, Danny Zwijnenburg, Filip Diepvens, Gerard Pals. Nucleic Acids Res 2002
9

Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1.
T M Smith, M K Lee, C I Szabo, N Jerome, M McEuen, M Taylor, L Hood, M C King. Genome Res 1996
222
9

Evidence for common ancestral origin of a recurring BRCA1 genomic rearrangement identified in high-risk Hispanic families.
Jeffrey N Weitzel, Veronica I Lagos, Josef S Herzog, Thaddeus Judkins, Brant Hendrickson, Jason S Ho, Charité N Ricker, Katrina J Lowstuter, Kathleen R Blazer, Gail Tomlinson,[...]. Cancer Epidemiol Biomarkers Prev 2007
74
9

Prevalence of BRCA1 and BRCA2 gene mutations in families with medium and high risk of breast and ovarian cancer in Brazil.
V F Esteves, L C S Thuler, L C Amêndola, R J Koifman, S Koifman, P P Frankel, R J S Vieira. Braz J Med Biol Res 2009
17
41

Prevalence of BRCA1 genomic rearrangements in a large cohort of Italian breast and breast/ovarian cancer families without detectable BRCA1 and BRCA2 point mutations.
Simona Agata, Alessandra Viel, Lara Della Puppa, Laura Cortesi, Giusi Fersini, Monia Callegaro, Maurizia Dalla Palma, Riccardo Dolcetti, Massimo Federico, Salvatore Venuta,[...]. Genes Chromosomes Cancer 2006
45
13

The contribution of germline rearrangements to the spectrum of BRCA2 mutations.
F Casilli, I Tournier, O M Sinilnikova, F Coulet, F Soubrier, C Houdayer, A Hardouin, P Berthet, H Sobol, V Bourdon,[...]. J Med Genet 2006
47
12

Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer.
Sara Gutiérrez-Enríquez, Miguel de la Hoya, Cristina Martínez-Bouzas, Ana Sanchez de Abajo, Teresa Ramón y Cajal, Gemma Llort, Ignacio Blanco, Elena Beristain, Eduardo Díaz-Rubio, Carmen Alonso,[...]. Breast Cancer Res Treat 2007
37
16


Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments.
Federica Casilli, Zorika Christiana Di Rocco, Sophie Gad, Isabelle Tournier, Dominique Stoppa-Lyonnet, Thierry Frebourg, Mario Tosi. Hum Mutat 2002
146
8

BRCA1 and BRCA2 mutations in a South American population.
Lilian Jara, Sandra Ampuero, Eudocia Santibáñez, Lorena Seccia, Juan Rodríguez, Mario Bustamante, Víctor Martínez, Alejandra Catenaccio, Guillermo Lay-Son, Rafael Blanco,[...]. Cancer Genet Cytogenet 2006
47
12

Screening BRCA1 and BRCA2 unclassified variants for splicing mutations using reverse transcription PCR on patient RNA and an ex vivo assay based on a splicing reporter minigene.
C Bonnet, S Krieger, M Vezain, A Rousselin, I Tournier, A Martins, P Berthet, A Chevrier, C Dugast, V Layet,[...]. J Med Genet 2008
91
8

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes.
S Thorlacius, G Olafsdottir, L Tryggvadottir, S Neuhausen, J G Jonasson, S V Tavtigian, H Tulinius, H M Ogmundsdottir, J E Eyfjörd. Nat Genet 1996
412
8

Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations.
James D Fackenthal, Olufunmilayo I Olopade. Nat Rev Cancer 2007
280
8

The R71G BRCA1 is a founder Spanish mutation and leads to aberrant splicing of the transcript.
A Vega, B Campos, B Bressac-De-Paillerets, P M Bond, N Janin, F S Douglas, M Domènech, M Baena, C Pericay, C Alonso,[...]. Hum Mutat 2001
69
8

Incidence of BRCA1 and BRCA2 mutations in 54 Chilean families with breast/ovarian cancer, genotype-phenotype correlations.
Marcela Gallardo, Antonia Silva, Lorena Rubio, Carolina Alvarez, Carolina Torrealba, Mauricio Salinas, Teresa Tapia, Paola Faundez, Lorena Palma, María Eugenia Riccio,[...]. Breast Cancer Res Treat 2006
50
12

Study of a single BRCA2 mutation with high carrier frequency in a small population.
S Thorlacius, S Sigurdsson, H Bjarnadottir, G Olafsdottir, J G Jonasson, L Tryggvadottir, H Tulinius, J E Eyfjörd. Am J Hum Genet 1997
203
8

BRCA1 and BRCA2 point mutations and large rearrangements in breast and ovarian cancer families in Northern Poland.
Magdalena Ratajska, Izabela Brozek, Elzbieta Senkus-Konefka, Jacek Jassem, Magdalena Stepnowska, Grazia Palomba, Marina Pisano, Milena Casula, Giuseppe Palmieri, Ake Borg,[...]. Oncol Rep 2008
50
12

The relative contribution of point mutations and genomic rearrangements in BRCA1 and BRCA2 in high-risk breast cancer families.
Maurizia Dalla Palma, Susan M Domchek, Jill Stopfer, Julie Erlichman, Jill D Siegfried, Jessica Tigges-Cardwell, Bernard A Mason, Timothy R Rebbeck, Katherine L Nathanson. Cancer Res 2008
76
8

Mutation analysis in the BRCA2 gene in primary breast cancers.
Y Miki, T Katagiri, F Kasumi, T Yoshimoto, Y Nakamura. Nat Genet 1996
239
8


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.