A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first 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
230
50

Familial colorectal cancer type X: genetic profiles and phenotypic features.
Mev Dominguez-Valentin, Christina Therkildsen, Sabrina Da Silva, Mef Nilbert. Mod Pathol 2015
23
50

Hereditary breast and ovarian cancer susceptibility genes (review).
Hiroshi Kobayashi, Sumire Ohno, Yoshikazu Sasaki, Miyuki Matsuura. Oncol Rep 2013
81
50

Differential features of colorectal cancers fulfilling Amsterdam criteria without involvement of the mutator pathway.
Xavier Llor, Elisenda Pons, Rosa M Xicola, Antoni Castells, Cristina Alenda, Virgínia Piñol, Montserrat Andreu, Sergi Castellví-Bel, Artemio Payá, Rodrigo Jover,[...]. Clin Cancer Res 2005
93
50

Risk of cancer in cases of suspected lynch syndrome without germline mutation.
María Rodríguez-Soler, Lucía Pérez-Carbonell, Carla Guarinos, Pedro Zapater, Adela Castillejo, Victor M Barberá, Miriam Juárez, Xavier Bessa, Rosa M Xicola, Juan Clofent,[...]. Gastroenterology 2013
134
50


American Gastroenterological Association Institute Guideline on the Diagnosis and Management of Lynch Syndrome.
Joel H Rubenstein, Robert Enns, Joel Heidelbaugh, Alan Barkun. Gastroenterology 2015
92
50

Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing.
Daniel D Buchanan, Yen Y Tan, Michael D Walsh, Mark Clendenning, Alexander M Metcalf, Kaltin Ferguson, Sven T Arnold, Bryony A Thompson, Felicity A Lose, Michael T Parsons,[...]. J Clin Oncol 2014
127
50

Familial colorectal cancer risk: ESMO Clinical Practice Guidelines.
J Balmaña, A Castells, A Cervantes. Ann Oncol 2010
25
50

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
783
50

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Matthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, Brian A Allen, Hajime Uno, Jason L Hornick, Chinedu I Ukaegbu, Lauren K Brais, Philip G McNamara, Robert J Mayer,[...]. J Clin Oncol 2017
165
50

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
Rachel Pearlman, Wendy L Frankel, Benjamin Swanson, Weiqiang Zhao, Ahmet Yilmaz, Kristin Miller, Jason Bacher, Christopher Bigley, Lori Nelsen, Paul J Goodfellow,[...]. JAMA Oncol 2017
247
50

Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
Lisa R Susswein, Megan L Marshall, Rachel Nusbaum, Kristen J Vogel Postula, Scott M Weissman, Lauren Yackowski, Erica M Vaccari, Jeffrey Bissonnette, Jessica K Booker, M Laura Cremona,[...]. Genet Med 2016
152
50

The promise of biomarkers in colorectal cancer detection.
Asad Umar, Sudhir Srivastava. Dis Markers 2004
10
25

Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.
Sigurdis Haraldsdottir, Heather Hampel, Jerneja Tomsic, Wendy L Frankel, Rachel Pearlman, Albert de la Chapelle, Colin C Pritchard. Gastroenterology 2014
226
25

Lynch syndrome in the 21st century: clinical perspectives.
A K Tiwari, H K Roy, H T Lynch. QJM 2016
59
25

Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
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
171
25

Worldwide variations in colorectal cancer.
Melissa M Center, Ahmedin Jemal, Robert A Smith, Elizabeth Ward. CA Cancer J Clin 2009
768
25


Gain of chromosomal region 20q and loss of 18 discriminates between Lynch syndrome and familial colorectal cancer.
Christina Therkildsen, Göran Jönsson, Mev Dominguez-Valentin, Anja Nissen, Eva Rambech, Britta Halvarsson, Inge Bernstein, Ke Borg, Mef Nilbert. Eur J Cancer 2013
19
25

Effect of daily aspirin on long-term risk of death due to cancer: analysis of individual patient data from randomised trials.
Peter M Rothwell, F Gerald R Fowkes, Jill F F Belch, Hisao Ogawa, Charles P Warlow, Tom W Meade. Lancet 2011
965
25


Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X.
Noralane M Lindor, Kari Rabe, Gloria M Petersen, Robert Haile, Graham Casey, John Baron, Steve Gallinger, Bharati Bapat, Melyssa Aronson, John Hopper,[...]. JAMA 2005
383
25


Clinicopathologic and pedigree differences in amsterdam I-positive hereditary nonpolyposis colorectal cancer families according to tumor microsatellite instability status.
Laura Valle, Jose Perea, Pablo Carbonell, Victoria Fernandez, Ana M Dotor, Javier Benitez, Miguel Urioste. J Clin Oncol 2007
53
25


Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
Heather Hampel, Wendy Frankel, Jenny Panescu, Janet Lockman, Kaisa Sotamaa, Daniel Fix, Ilene Comeras, Jennifer La Jeunesse, Hidewaki Nakagawa, Judith A Westman,[...]. Cancer Res 2006
379
25

Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers.
Wenche Sjursen, Bjørn Ivar Haukanes, Eli Marie Grindedal, Harald Aarset, Astrid Stormorken, Lars F Engebretsen, Christoffer Jonsrud, Inga Bjørnevoll, Per Arne Andresen, Sarah Ariansen,[...]. J Med Genet 2010
56
25

Epigenetic signatures of familial cancer are characteristic of tumor type and family category.
Emmi I Joensuu, Wael M Abdel-Rahman, Miina Ollikainen, Salla Ruosaari, Sakari Knuutila, Päivi Peltomäki. Cancer Res 2008
68
25

Concepts in familial colorectal cancer: where do we stand and what is the future?
Antoni Castells, Sergi Castellví-Bel, Francesc Balaguer. Gastroenterology 2009
50
25

Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.
Renée C Niessen, Robert M W Hofstra, Helga Westers, Marjolijn J L Ligtenberg, Krista Kooi, Paul O J Jager, Marloes L de Groote, Trijnie Dijkhuizen, Maran J W Olderode-Berends, Harry Hollema,[...]. Genes Chromosomes Cancer 2009
122
25

Comparison of clinical features between suspected familial colorectal cancer type X and Lynch syndrome in Japanese patients with colorectal cancer: a cross-sectional study conducted by the Japanese Society for Cancer of the Colon and Rectum.
Tatsuro Yamaguchi, Yoichi Furukawa, Yusuke Nakamura, Nagahide Matsubara, Hideki Ishikawa, Masami Arai, Naohiro Tomita, Kazuo Tamura, Kokichi Sugano, Chikashi Ishioka,[...]. Jpn J Clin Oncol 2015
24
25

Molecular information defines a new entity of hereditary colorectal cancer.
Rodrigo Jover, Antoni Castells. Gastroenterology 2008
4
25

A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.
Qing Liu, Luke B Hesson, Andrea C Nunez, Deborah Packham, Rachel Williams, Robyn L Ward, Mathew A Sloane. Carcinogenesis 2016
20
25

Identification of a Japanese Lynch syndrome patient with large deletion in the 3' region of the EPCAM gene.
Hidetaka Eguchi, Kensuke Kumamoto, Okihide Suzuki, Masakazu Kohda, Yuhki Tada, Yasushi Okazaki, Hideyuki Ishida. Jpn J Clin Oncol 2016
7
25

Genome-wide linkage analysis and tumoral characterization reveal heterogeneity in familial colorectal cancer type X.
E Sánchez-Tomé, B Rivera, J Perea, G Pita, D Rueda, F Mercadillo, A Canal, A Gonzalez-Neira, J Benitez, M Urioste. J Gastroenterol 2015
11
25

Familial colonic cancer without antecedent polyposis.
C R Boland, F J Troncale. Ann Intern Med 1984
101
25

Familial risk-colorectal cancer: ESMO Clinical Practice Guidelines.
J Balmaña, F Balaguer, A Cervantes, D Arnold. Ann Oncol 2013
87
25

EPCAM germ line deletions as causes of Lynch syndrome in Spanish patients.
Carla Guarinos, Adela Castillejo, Víctor-Manuel Barberá, Lucía Pérez-Carbonell, Ana-Beatriz Sánchez-Heras, Angel Segura, Carmen Guillén-Ponce, Ana Martínez-Cantó, María-Isabel Castillejo, Cecilia-Magdalena Egoavil,[...]. J Mol Diagn 2010
22
25

Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancer.
Y Mueller-Koch, H Vogelsang, R Kopp, P Lohse, G Keller, D Aust, M Muders, M Gross, J Daum, U Schiemann,[...]. Gut 2005
72
25

Familial colorectal cancer type X syndrome: two distinct molecular entities?
Inês Francisco, Cristina Albuquerque, Pedro Lage, Hélio Belo, Inês Vitoriano, Bruno Filipe, Isabel Claro, Sara Ferreira, Paula Rodrigues, Paula Chaves,[...]. Fam Cancer 2011
22
25

Clinical relevance of microsatellite instability in colorectal cancer.
Albert de la Chapelle, Heather Hampel. J Clin Oncol 2010
182
25

Screening adherence and cancer risk perceptions in colorectal cancer survivors with Lynch-like syndrome.
L H Katz, A M Burton-Chase, S Advani, B Fellman, K M Polivka, Y Yuan, P M Lynch, S K Peterson. Clin Genet 2016
9
25

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.
Marjolijn J L Ligtenberg, Roland P Kuiper, Tsun Leung Chan, Monique Goossens, Konnie M Hebeda, Marsha Voorendt, Tracy Y H Lee, Danielle Bodmer, Eveline Hoenselaar, Sandra J B Hendriks-Cornelissen,[...]. Nat Genet 2009
468
25

Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations.
Wael M Abdel-Rahman, Miina Ollikainen, Reetta Kariola, Heikki J Järvinen, Jukka-Pekka Mecklin, Minna Nyström-Lahti, Sakari Knuutila, Päivi Peltomäki. Oncogene 2005
71
25


Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.
Marietta E Kovacs, Janos Papp, Zoltan Szentirmay, Szabolcs Otto, Edith Olah. Hum Mutat 2009
114
25

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
208
25


Clinicopathological comparison of colorectal and endometrial carcinomas in patients with Lynch-like syndrome versus patients with Lynch syndrome.
Jenny Mas-Moya, Beth Dudley, Randall E Brand, Darcy Thull, Nathan Bahary, Marina N Nikiforova, Reetesh K Pai. Hum Pathol 2015
44
25


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.