A citation-based method for searching scientific literature

Lucia Perez-Cabornero, Eladio Velasco, Mar Infante, David Sanz, Enrique Lastra, Lara Hernández, Cristina Miner, Mercedes Duran. Eur J Cancer 2009
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer.
H J Järvinen, M Aarnio, H Mustonen, K Aktan-Collan, L A Aaltonen, P Peltomäki, A De La Chapelle, J P Mecklin. Gastroenterology 2000
942
33


Rapid mutation detection in complex genes by heteroduplex analysis with capillary array electrophoresis.
Eladio Velasco, Mar Infante, Mercedes Durán, Eva Esteban-Cardeñosa, Enrique Lastra, Carlos García-Girón, Cristina Miner. Electrophoresis 2005
18
25

High proportion of large genomic rearrangements in hMSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families of the Basque Country.
Cristina Martínez-Bouzas, Enrique Ojembarrena, Elena Beristain, Javier Errasti, Noelia Viguera, Maria-Isabel Tejada Minguéz. Cancer Lett 2007
14
25

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines.
M A Rodriguez-Bigas, C R Boland, S R Hamilton, D E Henson, J R Jass, P M Khan, H Lynch, M Perucho, T Smyrk, L Sobin,[...]. J Natl Cancer Inst 1997
798
25

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
25

MSH2 genomic deletions are a frequent cause of HNPCC.
J Wijnen, H van der Klift, H Vasen, P M Khan, F Menko, C Tops, H Meijers Heijboer, D Lindhout, P Møller, R Fodde. Nat Genet 1998
182
25


Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications.
H T Lynch, P M Lynch, S J Lanspa, C L Snyder, J F Lynch, C R Boland. Clin Genet 2009
512
25

Low prevalence of germline hMSH6 mutations in colorectal cancer families from Spain.
Ana Sánchez de Abajo, Miguel de la Hoya, Alicia Tosar, Javier Godino, Juan-Manuel Fernández, Jose-Lopez Asenjo, Beatriz-Perez Villamil, Pedro-Perez Segura, Eduardo Diaz-Rubio, Trinidad Caldes. World J Gastroenterol 2005
16
25

Tumor characteristics as an analytic tool for classifying genetic variants of uncertain clinical significance.
Robert M W Hofstra, Amanda B Spurdle, Diana Eccles, William D Foulkes, Niels de Wind, Nicoline Hoogerbrugge, Frans B L Hogervorst. Hum Mutat 2008
40
16



Characterization of hMLH1 and hMSH2 gene dosage alterations in Lynch syndrome patients.
Linnea M Baudhuin, Matthew J Ferber, Jennifer L Winters, Kelle J Steenblock, Russell L Swanson, Amy J French, Malinda L Butz, Stephen N Thibodeau. Gastroenterology 2005
36
16

Heteroduplex analysis by capillary array electrophoresis for rapid mutation detection in large multiexon genes.
Eladio Velasco, Mar Infante, Mercedes Durán, Lucía Pérez-Cabornero, David J Sanz, Eva Esteban-Cardeñosa, Cristina Miner. Nat Protoc 2007
33
16

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer.
C R Boland, S N Thibodeau, S R Hamilton, D Sidransky, J R Eshleman, R W Burt, S J Meltzer, M A Rodriguez-Bigas, R Fodde, G N Ranzani,[...]. Cancer Res 1998
16

Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review.
H T Lynch, T C Smyrk, P Watson, S J Lanspa, J F Lynch, P M Lynch, R J Cavalieri, C R Boland. Gastroenterology 1993
914
16

Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC).
Johanne Geary, Peter Sasieni, Richard Houlston, Louise Izatt, Ros Eeles, Stewart J Payne, Samantha Fisher, Shirley V Hodgson. Fam Cancer 2008
101
16

MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families.
Ester Borràs, Marta Pineda, Ignacio Blanco, Ethan M Jewett, Fei Wang, Alex Teulé, Trinidad Caldés, Miguel Urioste, Cristina Martínez-Bouzas, Joan Brunet,[...]. Cancer Res 2010
26
16

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC).
H F Vasen, J P Mecklin, P M Khan, H T Lynch. Dis Colon Rectum 1991
16

Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).
Heleen van der Klift, Juul Wijnen, Anja Wagner, Paul Verkuilen, Carli Tops, Robyn Otway, Maija Kohonen-Corish, Hans Vasen, Cristina Oliani, Daniela Barana,[...]. Genes Chromosomes Cancer 2005
98
16

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.
C E Bronner, S M Baker, P T Morrison, G Warren, L G Smith, M K Lescoe, M Kane, C Earabino, J Lipford, A Lindblom. Nature 1994
16

Mechanisms of change in gene copy number.
P J Hastings, James R Lupski, Susan M Rosenberg, Grzegorz Ira. Nat Rev Genet 2009
760
16

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
N C Nicolaides, N Papadopoulos, B Liu, Y F Wei, K C Carter, S M Ruben, C A Rosen, W A Haseltine, R D Fleischmann, C M Fraser. Nature 1994
16

A large fraction of unclassified variants of the mismatch repair genes MLH1 and MSH2 is associated with splicing defects.
Isabelle Tournier, Myriam Vezain, Alexandra Martins, Françoise Charbonnier, Stéphanie Baert-Desurmont, Sylviane Olschwang, Qing Wang, Marie Pierre Buisine, Johann Soret, Jamal Tazi,[...]. Hum Mutat 2008
125
16

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).
H F A Vasen, G Möslein, A Alonso, I Bernstein, L Bertario, I Blanco, J Burn, G Capella, C Engel, I Frayling,[...]. J Med Genet 2007
364
16


Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Hidewaki Nakagawa, Kaisa Sotamaa, Thomas W Prior, Judith Westman,[...]. N Engl J Med 2005
958
16

Microsatellite instability in colorectal cancer.
C Richard Boland, Ajay Goel. Gastroenterology 2010
16

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
Asad Umar, C Richard Boland, Jonathan P Terdiman, Sapna Syngal, Albert de la Chapelle, Josef Rüschoff, Richard Fishel, Noralane M Lindor, Lawrence J Burgart, Richard Hamelin,[...]. J Natl Cancer Inst 2004
16

BRAF V600E mutation analysis simplifies the testing algorithm for Lynch syndrome.
Ming Jin, Heather Hampel, Xiaoping Zhou, Lisa Schunemann, Martha Yearsley, Wendy L Frankel. Am J Clin Pathol 2013
29
16

Constant denaturant capillary electrophoresis (CDCE): a high resolution approach to mutational analysis.
K Khrapko, J S Hanekamp, W G Thilly, A Belenkii, F Foret, B L Karger. Nucleic Acids Res 1994
131
8

Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve analysis.
Tú Nguyen-Dumont, Florence Le Calvez-Kelm, Nathalie Forey, Sandrine McKay-Chopin, Sonia Garritano, Lydie Gioia-Patricola, Deepika De Silva, Ron Weigel, Suleeporn Sangrajrang, Fabienne Lesueur,[...]. Hum Mutat 2009
35
8


Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations.
T Wagner, D Stoppa-Lyonnet, E Fleischmann, D Muhr, S Pagès, T Sandberg, V Caux, R Moeslinger, G Langbauer, A Borg,[...]. Genomics 1999
172
8

Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: a proof-of-concept trial.
M William Audeh, James Carmichael, Richard T Penson, Michael Friedlander, Bethan Powell, Katherine M Bell-McGuinn, Clare Scott, Jeffrey N Weitzel, Ana Oaknin, Niklas Loman,[...]. Lancet 2010
991
8

Multiplex single-nucleotide primer extension analysis to simultaneously detect eleven BRCA1 mutations in breast cancer families.
Françoise Révillion, Alain Verdière, Joëlle Fournier, Louis Hornez, Jean-Philippe Peyrat. Clin Chem 2004
7
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
71
8

Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study.
Virginie Caux-Moncoutier, Sabine Pagès-Berhouet, Dorothée Michaux, Bernard Asselain, Laurent Castéra, Antoine De Pauw, Bruno Buecher, Marion Gauthier-Villars, Dominique Stoppa-Lyonnet, Claude Houdayer. Eur J Hum Genet 2009
29
8

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
8

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
8

High-accuracy DNA sequence variation screening by DHPLC.
J I Spiegelman, M N Mindrinos, P J Oefner. Biotechniques 2000
51
8

Evaluation of in silico splice tools for decision-making in molecular diagnosis.
Claude Houdayer, Catherine Dehainault, Christophe Mattler, Dorothée Michaux, Virginie Caux-Moncoutier, Sabine Pagès-Berhouet, Catherine Dubois d'Enghien, Anthony Laugé, Laurent Castera, Marion Gauthier-Villars,[...]. Hum Mutat 2008
130
8

Analysis of genomic CFTR DNA.
Claude Férec, Cédric Le Maréchal, Marie-Pierre Audrézet, Carlos M Farinha, Margarida D Amaral, Sabina Gallati, Javier Sanz, Bernhard Steiner, Nathalie Mouchel, Ann Harris,[...]. J Cyst Fibros 2004
6
16


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
48
8


Interlaboratory diagnostic validation of conformation-sensitive capillary electrophoresis for mutation scanning.
Christopher J Mattocks, Gemma Watkins, Daniel Ward, Tom Janssens, Ermanno A J Bosgoed, Kim van der Donk, Marjolijn J Ligtenberg, Bruno Pot, Joop Theelen, Nicholas C P Cross,[...]. Clin Chem 2010
11
9

Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF.
C Houdayer, M Gauthier-Villars, A Laugé, S Pagès-Berhouet, C Dehainault, V Caux-Moncoutier, P Karczynski, M Tosi, F Doz, L Desjardins,[...]. Hum Mutat 2004
101
8

Improving sensitivity of electrophoretic heteroduplex analysis using nucleosides as additives: Application to the breast cancer predisposition gene BRCA2.
Jérémie Weber, Rachelle Looten, Claude Houdayer, Dominique Stoppa-Lyonnet, Jean-Louis Viovy. Electrophoresis 2006
7
14


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.