A citation-based method for searching scientific literature

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
Times Cited: 76







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



Times Cited
  Times     Co-cited
Similarity


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
38

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
27

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
19

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
19

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
32

Meta-analysis of BRCA1 and BRCA2 penetrance.
Sining Chen, Giovanni Parmigiani. J Clin Oncol 2007
18

Clinical significance of large rearrangements in BRCA1 and BRCA2.
Thaddeus Judkins, Eric Rosenthal, Christopher Arnell, Lynn Anne Burbidge, Wade Geary, Toby Barrus, Jeremy Schoenberger, Jeffrey Trost, Richard J Wenstrup, Benjamin B Roa. Cancer 2012
79
18

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
17

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


Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2.
Mary-Claire King, Joan H Marks, Jessica B Mandell. Science 2003
15

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
15

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
15


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
14

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

Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations.
Timothy R Rebbeck, Henry T Lynch, Susan L Neuhausen, Steven A Narod, Laura Van't Veer, Judy E Garber, Gareth Evans, Claudine Isaacs, Mary B Daly, Ellen Matloff,[...]. N Engl J Med 2002
994
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
74
13


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
22

Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada.
Harvey A Risch, John R McLaughlin, David E C Cole, Barry Rosen, Linda Bradley, Isabel Fan, James Tang, Song Li, Shiyu Zhang, Patricia A Shaw,[...]. J Natl Cancer Inst 2006
438
13

Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.
Susan M Domchek, Tara M Friebel, Christian F Singer, D Gareth Evans, Henry T Lynch, Claudine Isaacs, Judy E Garber, Susan L Neuhausen, Ellen Matloff, Rosalind Eeles,[...]. JAMA 2010
824
13

Large BRCA1 and BRCA2 genomic rearrangements in Malaysian high risk breast-ovarian cancer families.
Peter Kang, Shivaani Mariapun, Sze Yee Phuah, Linda Shushan Lim, Jianjun Liu, Sook-Yee Yoon, Meow Keong Thong, Nur Aishah Mohd Taib, Cheng Har Yip, Soo-Hwang Teo. Breast Cancer Res Treat 2010
32
31

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
13


American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
Mark E Robson, Courtney D Storm, Jeffrey Weitzel, Dana S Wollins, Kenneth Offit. J Clin Oncol 2010
295
11

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
11

Genomic rearrangements in BRCA1 and BRCA2: A literature review.
Ingrid Petroni Ewald, Patricia Lisboa Izetti Ribeiro, Edenir Inêz Palmero, Silvia Liliana Cossio, Roberto Giugliani, Patricia Ashton-Prolla. Genet Mol Biol 2009
61
14


Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years.
Kathleen E Malone, Janet R Daling, David R Doody, Li Hsu, Leslie Bernstein, Ralph J Coates, Polly A Marchbanks, Michael S Simon, Jill A McDonald, Sandra A Norman,[...]. Cancer Res 2006
204
10

Frequency of BRCA1/BRCA2 mutations in a population-based sample of young breast carcinoma cases.
K E Malone, J R Daling, C Neal, N M Suter, C O'Brien, K Cushing-Haugen, T J Jonasdottir, J D Thompson, E A Ostrander. Cancer 2000
170
10

BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer.
Michael J Hall, Julia E Reid, Lynn A Burbidge, Dmitry Pruss, Amie M Deffenbaugh, Cynthia Frye, Richard J Wenstrup, Brian E Ward, Thomas A Scholl, Walter W Noll. Cancer 2009
223
10

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
14

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
11

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
19

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

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
147
10

Limited family structure and BRCA gene mutation status in single cases of breast cancer.
Jeffrey N Weitzel, Veronica I Lagos, Carey A Cullinane, Patricia J Gambol, Julie O Culver, Kathleen R Blazer, Melanie R Palomares, Katrina J Lowstuter, Deborah J MacDonald. JAMA 2007
130
10

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
25

Prevalence of BRCA mutations and founder effect in high-risk Hispanic families.
Jeffrey N Weitzel, Veronica Lagos, Kathleen R Blazer, Rebecca Nelson, Charité Ricker, Josef Herzog, Colleen McGuire, Susan Neuhausen. Cancer Epidemiol Biomarkers Prev 2005
121
9

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
14

Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups.
Esther M John, Alexander Miron, Gail Gong, Amanda I Phipps, Anna Felberg, Frederick P Li, Dee W West, Alice S Whittemore. JAMA 2007
219
9


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
17

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
11

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
9

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
14

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
13

Identification and comprehensive characterization of large genomic rearrangements in the BRCA1 and BRCA2 genes.
Jesús del Valle, Lídia Feliubadaló, Marga Nadal, Alex Teulé, Rosa Miró, Raquel Cuesta, Eva Tornero, Mireia Menéndez, Esther Darder, Joan Brunet,[...]. Breast Cancer Res Treat 2010
28
25

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
16


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.