A citation-based method for searching scientific literature

Elena M Stoffel, Pamela B Mangu, Stephen B Gruber, Stanley R Hamilton, Matthew F Kalady, Michelle Wan Yee Lau, Karen H Lu, Nancy Roach, Paul J Limburg. J Clin Oncol 2015
Times Cited: 175







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



Times Cited
  Times     Co-cited
Similarity


Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.
Isabel Spier, Stefanie Holzapfel, Janine Altmüller, Bixiao Zhao, Sukanya Horpaopan, Stefanie Vogt, Sophia Chen, Monika Morak, Susanne Raeder, Katrin Kayser,[...]. Int J Cancer 2015
89
4

Identification and characterization of the familial adenomatous polyposis coli gene.
J Groden, A Thliveris, W Samowitz, M Carlson, L Gelbert, H Albertsen, G Joslyn, J Stevens, L Spirio, M Robertson. Cell 1991
4

Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas.
Shilpa Grover, Fay Kastrinos, Ewout W Steyerberg, E Francis Cook, Akriti Dewanwala, Lynn Anne Burbidge, Richard J Wenstrup, Sapna Syngal. JAMA 2012
102
4

Expanded extracolonic tumor spectrum in MUTYH-associated polyposis.
Stefanie Vogt, Natalie Jones, Daria Christian, Christoph Engel, Maartje Nielsen, Astrid Kaufmann, Verena Steinke, Hans F Vasen, Peter Propping, Julian R Sampson,[...]. Gastroenterology 2009
167
4

Upper gastrointestinal cancer in patients with familial adenomatous polyposis.
A D Spigelman, C B Williams, I C Talbot, P Domizio, R K Phillips. Lancet 1989
490
4

Nonpolypoid colorectal neoplasms: a challenge in endoscopic surveillance of patients with Lynch syndrome.
E J A Rondagh, S Gulikers, E B Gómez-García, Y Vanlingen, Y Detisch, B Winkens, H F A Vasen, A A M Masclee, S Sanduleanu. Endoscopy 2013
38
10

Genetic alterations during colorectal-tumor development.
B Vogelstein, E R Fearon, S R Hamilton, S E Kern, A C Preisinger, M Leppert, Y Nakamura, R White, A M Smits, J L Bos. N Engl J Med 1988
4

A genetic model for colorectal tumorigenesis.
E R Fearon, B Vogelstein. Cell 1990
4



Multipopulation analysis of polymorphisms in five mononucleotide repeats used to determine the microsatellite instability status of human tumors.
Olivier Buhard, Francesca Cattaneo, Yick Fu Wong, So Fan Yim, Eitan Friedman, Jean-François Flejou, Alex Duval, Richard Hamelin. J Clin Oncol 2006
152
4

Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis.
Carlos J Gallego, Brian H Shirts, Caroline S Bennette, Greg Guzauskas, Laura M Amendola, Martha Horike-Pyne, Fuki M Hisama, Colin C Pritchard, William M Grady, Wylie Burke,[...]. J Clin Oncol 2015
88
4

Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors.
Arjen R Mensenkamp, Ingrid P Vogelaar, Wendy A G van Zelst-Stams, Monique Goossens, Hicham Ouchene, Sandra J B Hendriks-Cornelissen, Michael P Kwint, Nicoline Hoogerbrugge, Iris D Nagtegaal, Marjolijn J L Ligtenberg. Gastroenterology 2014
211
4

Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer.
Andrea E de Jong, Marjo van Puijenbroek, Yvonne Hendriks, Carli Tops, Juul Wijnen, Margreet G E M Ausems, Hanne Meijers-Heijboer, Anja Wagner, Theo A M van Os, Annette H J T Bröcker-Vriends,[...]. Clin Cancer Res 2004
178
4

Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts.
Daniel D Buchanan, Mark Clendenning, Christophe Rosty, Stine V Eriksen, Michael D Walsh, Rhiannon J Walters, Stephen N Thibodeau, Jenna Stewart, Susan Preston, Aung Ko Win,[...]. J Gastroenterol Hepatol 2017
25
16

Interpretation of immunohistochemistry for mismatch repair proteins is only reliable in a specialized setting.
Lucia I H Overbeek, Marjolijn J L Ligtenberg, Riki W Willems, Rosella P M G Hermens, Willeke A M Blokx, Stefan V Dubois, Hans van der Linden, Jos W R Meijer, Maria L Mlynek-Kersjes, Nicoline Hoogerbrugge,[...]. Am J Surg Pathol 2008
85
4

Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome).
Daniel D Buchanan, Christophe Rosty, Mark Clendenning, Amanda B Spurdle, Aung Ko Win. Appl Clin Genet 2014
59
6

Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results.
Laura C Beamer, Marcia L Grant, Carin R Espenschied, Kathleen R Blazer, Heather L Hampel, Jeffrey N Weitzel, Deborah J MacDonald. J Clin Oncol 2012
147
4



HSP110 T17 simplifies and improves the microsatellite instability testing in patients with colorectal cancer.
Olivier Buhard, Anaïs Lagrange, Agathe Guilloux, Chrystelle Colas, Mouna Chouchène, Kristell Wanherdrick, Florence Coulet, Erell Guillerm, Coralie Dorard, Laetitia Marisa,[...]. J Med Genet 2016
26
15

Comparison of the microsatellite instability analysis system and the Bethesda panel for the determination of microsatellite instability in colorectal cancers.
Kathleen M Murphy, Shengle Zhang, Tanya Geiger, Michael J Hafez, Jeff Bacher, Karin D Berg, James R Eshleman. J Mol Diagn 2006
161
4

A tailored approach to BRAF and MLH1 methylation testing in a universal screening program for Lynch syndrome.
Tomer Adar, Linda H Rodgers, Kristen M Shannon, Makoto Yoshida, Tianle Ma, Anthony Mattia, Gregory Y Lauwers, Anthony J Iafrate, Daniel C Chung. Mod Pathol 2017
29
13

MSIsensor: microsatellite instability detection using paired tumor-normal sequence data.
Beifang Niu, Kai Ye, Qunyuan Zhang, Charles Lu, Mingchao Xie, Michael D McLellan, Michael C Wendl, Li Ding. Bioinformatics 2014
272
4

Detection of Mismatch Repair Deficiency and Microsatellite Instability in Colorectal Adenocarcinoma by Targeted Next-Generation Sequencing.
Jonathan A Nowak, Matthew B Yurgelun, Jacqueline L Bruce, Vanesa Rojas-Rudilla, Dimity L Hall, Priyanka Shivdasani, Elizabeth P Garcia, Agoston T Agoston, Amitabh Srivastava, Shuji Ogino,[...]. J Mol Diagn 2017
82
4

CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome.
Aysel Ahadova, Magnus von Knebel Doeberitz, Hendrik Bläker, Matthias Kloor. Fam Cancer 2016
42
9



A Novel and Reliable Method to Detect Microsatellite Instability in Colorectal Cancer by Next-Generation Sequencing.
Lizhen Zhu, Yanqin Huang, Xuefeng Fang, Chenglin Liu, Wanglong Deng, Chenhan Zhong, Jinghong Xu, Dong Xu, Ying Yuan. J Mol Diagn 2018
37
10


Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database.
Pål Møller, Toni Seppälä, Inge Bernstein, Elke Holinski-Feder, Paola Sala, D Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf Sijmons,[...]. Gut 2017
69
5

Clues to the pathogenesis of familial colorectal cancer.
L A Aaltonen, P Peltomäki, F S Leach, P Sistonen, L Pylkkänen, J P Mecklin, H Järvinen, S M Powell, J Jen, S R Hamilton. Science 1993
4

Germline Genetic Features of Young Individuals With Colorectal Cancer.
Elena M Stoffel, Erika Koeppe, Jessica Everett, Peter Ulintz, Mark Kiel, Jenae Osborne, Linford Williams, Kristen Hanson, Stephen B Gruber, Laura S Rozek. Gastroenterology 2018
102
4

Cancer risk in Lynch Syndrome.
Emma Barrow, James Hill, D Gareth Evans. Fam Cancer 2013
105
4

Deleterious Germline Mutations in Patients With Apparently Sporadic Pancreatic Adenocarcinoma.
Koji Shindo, Jun Yu, Masaya Suenaga, Shahriar Fesharakizadeh, Christy Cho, Anne Macgregor-Das, Abdulrehman Siddiqui, P Dane Witmer, Koji Tamura, Tae Jun Song,[...]. J Clin Oncol 2017
170
4

Very high risk of cancer in familial Peutz-Jeghers syndrome.
F M Giardiello, J D Brensinger, A C Tersmette, S N Goodman, G M Petersen, S V Booker, M Cruz-Correa, J A Offerhaus. Gastroenterology 2000
791
4

Risk of pancreatic cancer in families with Lynch syndrome.
Fay Kastrinos, Bhramar Mukherjee, Nabihah Tayob, Fei Wang, Jennifer Sparr, Victoria M Raymond, Prathap Bandipalliam, Elena M Stoffel, Stephen B Gruber, Sapna Syngal. JAMA 2009
285
4

Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH.
Natalie Jones, Stefanie Vogt, Maartje Nielsen, Daria Christian, Petra A Wark, Diana Eccles, Emma Edwards, D Gareth Evans, Eamonn R Maher, Hans F Vasen,[...]. Gastroenterology 2009
74
5

Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors.
Nada Al-Tassan, Nikolas H Chmiel, Julie Maynard, Nick Fleming, Alison L Livingston, Geraint T Williams, Angela K Hodges, D Rhodri Davies, Sheila S David, Julian R Sampson,[...]. Nat Genet 2002
898
4

A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.
Robbert D A Weren, Marjolijn J L Ligtenberg, C Marleen Kets, Richarda M de Voer, Eugène T P Verwiel, Liesbeth Spruijt, Wendy A G van Zelst-Stams, Marjolijn C Jongmans, Christian Gilissen, Jayne Y Hehir-Kwa,[...]. Nat Genet 2015
193
4

Update on Lynch syndrome genomics.
Päivi Peltomäki. Fam Cancer 2016
82
4

A molecular portrait of microsatellite instability across multiple cancers.
Isidro Cortes-Ciriano, Sejoon Lee, Woong-Yang Park, Tae-Min Kim, Peter J Park. Nat Commun 2017
220
4

Two-stain immunohistochemical screening for Lynch syndrome in colorectal cancer may fail to detect mismatch repair deficiency.
Rachel Pearlman, Michael Markow, Deborah Knight, Wei Chen, Christina A Arnold, Colin C Pritchard, Heather Hampel, Wendy L Frankel. Mod Pathol 2018
26
15

A systematic review and economic evaluation of diagnostic strategies for Lynch syndrome.
Tristan Snowsill, Nicola Huxley, Martin Hoyle, Tracey Jones-Hughes, Helen Coelho, Chris Cooper, Ian Frayling, Chris Hyde. Health Technol Assess 2014
76
5

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
Leigha Senter, Mark Clendenning, Kaisa Sotamaa, Heather Hampel, Jane Green, John D Potter, Annika Lindblom, Kristina Lagerstedt, Stephen N Thibodeau, Noralane M Lindor,[...]. Gastroenterology 2008
343
4


Practical guidance for mismatch repair-deficiency testing in endometrial cancer.
E Stelloo, A M L Jansen, E M Osse, R A Nout, C L Creutzberg, D Ruano, D N Church, H Morreau, V T H B M Smit, T van Wezel,[...]. Ann Oncol 2017
86
4

Impact of chromoscopy on adenoma detection in patients with Lynch syndrome: a prospective, multicenter, blinded, tandem colonoscopy study.
Gabriel Rahmi, Thierry Lecomte, David Malka, Thibault Maniere, Marc Le Rhun, Rosine Guimbaud, Marie-Georges Lapalus, Anne Le Sidaner, Driffa Moussata, Olivier Caron,[...]. Am J Gastroenterol 2015
32
12


Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland.
P Lichtenstein, N V Holm, P K Verkasalo, A Iliadou, J Kaprio, M Koskenvuo, E Pukkala, A Skytthe, K Hemminki. N Engl J Med 2000
4


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.