A citation-based method for searching scientific literature

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, H Meijers-Heijboer, J G Klijn, H F Vasen, C J Cornelisse, L J van 't Veer, E Bakker, G J van Ommen, P Devilee. Nat Genet 1997
Times Cited: 348







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



Times Cited
  Times     Co-cited
Similarity


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
31

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
440
29

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
26

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
256
26

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
25


A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17.
N Puget, D Torchard, O M Serova-Sinilnikova, H T Lynch, J Feunteun, G M Lenoir, S Mazoyer. Cancer Res 1997
148
21

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
32

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.
A Antoniou, P D P Pharoah, S Narod, H A Risch, J E Eyfjord, J L Hopper, N Loman, H Olsson, O Johannsson, A Borg,[...]. Am J Hum Genet 2003
19

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
47

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
17

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
17

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
227
17

Gross rearrangements in BRCA1 but not BRCA2 play a notable role in predisposition to breast and ovarian cancer in high-risk families of German origin.
Sabine Preisler-Adams, Ines Schönbuchner, Britta Fiebig, Brigitte Welling, Bernd Dworniczak, Bernhard H F Weber. Cancer Genet Cytogenet 2006
43
39


Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2.
Mary-Claire King, Joan H Marks, Jessica B Mandell. Science 2003
17

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
24

Novel genomic rearrangements in the BRCA1 gene detected in Greek breast/ovarian cancer patients.
Sophia Armaou, Irene Konstantopoulou, Theodore Anagnostopoulos, Evangelia Razis, Ioannis Boukovinas, Nikolaos Xenidis, George Fountzilas, Drakoulis Yannoukakos. Eur J Cancer 2007
42
38

Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spot.
Nadine Puget, Sophie Gad, Laure Perrin-Vidoz, Olga M Sinilnikova, Dominique Stoppa-Lyonnet, Gilbert M Lenoir, Sylvie Mazoyer. Am J Hum Genet 2002
77
20

High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic.
Petra Vasickova, Eva Machackova, Miroslava Lukesova, Jiri Damborsky, Ondrej Horky, Hana Pavlu, Jitka Kuklova, Veronika Kosinova, Marie Navratilova, Lenka Foretova. BMC Med Genet 2007
42
38

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
35

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
50
32


Identification of novel BRCA large genomic rearrangements in Singapore Asian breast and ovarian patients with cancer.
Y K Lim, P T C Lau, A B Ali, S C Lee, J E-L Wong, T C Putti, J-H Sng. Clin Genet 2007
43
34

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
17

Genomic rearrangements at the BRCA1 locus in Spanish families with breast/ovarian cancer.
Miguel de la Hoya, Sara Gutiérrez-Enríquez, Eladio Velasco, Ana Osorio, Ana Sanchez de Abajo, Ana Vega, Raquel Salazar, Eva Esteban, Gemma Llort, Rogelio Gonzalez-Sarmiento,[...]. Clin Chem 2006
55
25

An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?
N Puget, O M Sinilnikova, D Stoppa-Lyonnet, C Audoynaud, S Pagès, H T Lynch, D Goldgar, G M Lenoir, S Mazoyer. Am J Hum Genet 1999
114
14

Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families.
Sophie Gad, Virginie Caux-Moncoutier, Sabine Pagès-Berhouet, Marion Gauthier-Villars, Isabelle Coupier, Pascal Pujol, Marc Frénay, Brigitte Gilbert, Christine Maugard, Yves-Jean Bignon,[...]. Oncogene 2002
76
18

Large genomic deletions inactivate the BRCA2 gene in breast cancer families.
S Agata, M Dalla Palma, M Callegaro, M C Scaini, C Menin, C Ghiotto, O Nicoletto, G Zavagno, L Chieco-Bianchi, E D'Andrea,[...]. J Med Genet 2005
52
26

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
29

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
28

Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family.
J Swensen, M Hoffman, M H Skolnick, S L Neuhausen. Hum Mol Genet 1997
109
13

Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions.
N Puget, D Stoppa-Lyonnet, O M Sinilnikova, S Pagès, H T Lynch, G M Lenoir, S Mazoyer. Cancer Res 1999
151
13

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
630
13

Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families.
J Lahti-Domenici, K Rapakko, K Pääkkönen, M Allinen, H Nevanlinna, M Kujala, P Huusko, R Winqvist. Cancer Genet Cytogenet 2001
39
30


Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing.
M A Unger, K L Nathanson, K Calzone, D Antin-Ozerkis, H A Shih, A M Martin, G M Lenoir, S Mazoyer, B L Weber. Am J Hum Genet 2000
118
11

Screening for a BRCA2 rearrangement in high-risk breast/ovarian cancer families: evidence for a founder effect and analysis of the associated phenotypes.
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
75
14

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
75
14

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
26

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
77
14

Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene.
Ivana Ticha, Zdenek Kleibl, Jana Stribrna, Jaroslav Kotlas, Martina Zimovjanova, Martin Mateju, Michal Zikan, Petr Pohlreich. Breast Cancer Res Treat 2010
32
34


Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families.
P N Tonin, A M Mes-Masson, P A Futreal, K Morgan, M Mahon, W D Foulkes, D E Cole, D Provencher, P Ghadirian, S A Narod. Am J Hum Genet 1998
128
10

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
10


Contribution of BRCA1 and BRCA2 mutations to inherited ovarian cancer.
Susan J Ramus, Patricia A Harrington, Carole Pye, Richard A DiCioccio, Mark J Cox, Kim Garlinghouse-Jones, Ingrid Oakley-Girvan, Ian J Jacobs, Richard M Hardy, Alice S Whittemore,[...]. Hum Mutat 2007
57
17

Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification.
D J Bunyan, D M Eccles, J Sillibourne, E Wilkins, N Simon Thomas, J Shea-Simonds, P J Duncan, C E Curtis, D O Robinson, J F Harvey,[...]. Br J Cancer 2004
148
10

Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.
J Peto, N Collins, R Barfoot, S Seal, W Warren, N Rahman, D F Easton, C Evans, J Deacon, M R Stratton. J Natl Cancer Inst 1999
636
9

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
414
9


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.