A citation-based method for searching scientific literature

Lyn Schofield, Fabienne Grieu, Benhur Amanuel, Amerigo Carrello, Dominic Spagnolo, Cathy Kiraly, Nicholas Pachter, Jack Goldblatt, Cameron Platell, Michael Levitt, Colin Stewart, Paul Salama, Hooi Ee, Spiro Raftopoulous, Paul Katris, Tim Threlfall, Edward Edkins, Marina Wallace, Barry Iacopetta. Int J Cancer 2014
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


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
80


Hereditary colorectal cancer.
Henry T Lynch, Albert de la Chapelle. N Engl J Med 2003
40

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
Valérie Bonadona, Bernard Bonaïti, Sylviane Olschwang, Sophie Grandjouan, Laetitia Huiart, Michel Longy, Rosine Guimbaud, Bruno Buecher, Yves-Jean Bignon, Olivier Caron,[...]. JAMA 2011
593
40


Population-based detection of Lynch syndrome in young colorectal cancer patients using microsatellite instability as the initial test.
Lyn Schofield, Natasha Watson, Fabienne Grieu, Wei Qi Li, Nik Zeps, Jennet Harvey, Colin Stewart, Michael Abdo, Jack Goldblatt, Barry Iacopetta. Int J Cancer 2009
56
40

Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis.
Uri Ladabaum, Grace Wang, Jonathan Terdiman, Amie Blanco, Miriam Kuppermann, C Richard Boland, James Ford, Elena Elkin, Kathryn A Phillips. Ann Intern Med 2011
239
33

A model-based assessment of the cost-utility of strategies to identify Lynch syndrome in early-onset colorectal cancer patients.
Tristan Snowsill, Nicola Huxley, Martin Hoyle, Tracey Jones-Hughes, Helen Coelho, Chris Cooper, Ian Frayling, Chris Hyde. BMC Cancer 2015
23
33

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
928
33

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
481
26

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
Bryony A Thompson, Amanda B Spurdle, John-Paul Plazzer, Marc S Greenblatt, Kiwamu Akagi, Fahd Al-Mulla, Bharati Bapat, Inge Bernstein, Gabriel Capellá, Johan T den Dunnen,[...]. Nat Genet 2014
304
26

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
79
26


Milestones of Lynch syndrome: 1895-2015.
Henry T Lynch, Carrie L Snyder, Trudy G Shaw, Christopher D Heinen, Megan P Hitchins. Nat Rev Cancer 2015
345
26

Risks of Lynch syndrome cancers for MSH6 mutation carriers.
Laura Baglietto, Noralane M Lindor, James G Dowty, Darren M White, Anja Wagner, Encarna B Gomez Garcia, Annette H J T Vriends, Nicola R Cartwright, Rebecca A Barnetson, Susan M Farrington,[...]. J Natl Cancer Inst 2010
232
26

The InSiGHT database: utilizing 100 years of insights into Lynch syndrome.
J P Plazzer, R H Sijmons, M O Woods, P Peltomäki, B Thompson, J T Den Dunnen, F Macrae. Fam Cancer 2013
70
20

Dominantly inherited constitutional epigenetic silencing of MLH1 in a cancer-affected family is linked to a single nucleotide variant within the 5'UTR.
Megan P Hitchins, Robert W Rapkins, Chau-To Kwok, Sameer Srivastava, Justin J L Wong, Levon M Khachigian, Patsie Polly, Jack Goldblatt, Robyn L Ward. Cancer Cell 2011
109
20

Inheritance of a cancer-associated MLH1 germ-line epimutation.
Megan P Hitchins, Justin J L Wong, Graeme Suthers, Catherine M Suter, David I K Martin, Nicholas J Hawkins, Robyn L Ward. N Engl J Med 2007
281
20

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
20

Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting.
Cecelia A Bellcross, Sara R Bedrosian, Elvan Daniels, Debra Duquette, Heather Hampel, Kory Jasperson, Djenaba A Joseph, Celia Kaye, Ira Lubin, Laurence J Meyer,[...]. Genet Med 2012
68
20

Impact of age cutoffs on a lynch syndrome screening program.
James M Gudgeon, Thomas W Belnap, Janet L Williams, Marc S Williams. J Oncol Pract 2013
14
21

Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
Francis M Giardiello, John I Allen, Jennifer E Axilbund, C Richard Boland, Carol A Burke, Randall W Burt, James M Church, Jason A Dominitz, David A Johnson, Tonya Kaltenbach,[...]. Am J Gastroenterol 2014
269
20

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.
Hans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, Jessica P Gopie, Angel Alonso, Stefan Aretz, Inge Bernstein, Lucio Bertario, John Burn, Gabriel Capella,[...]. Gut 2013
427
20

Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk.
Sanne W ten Broeke, Richard M Brohet, Carli M Tops, Heleen M van der Klift, Mary E Velthuizen, Inge Bernstein, Gabriel Capellá Munar, Encarna Gomez Garcia, Nicoline Hoogerbrugge, Tom G W Letteboer,[...]. J Clin Oncol 2015
122
20

The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer.
W S Samowitz, K Curtin, H H Lin, M A Robertson, D Schaffer, M Nichols, K Gruenthal, M F Leppert, M L Slattery. Gastroenterology 2001
189
20

Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Mark Clendenning, Kaisa Sotamaa, Thomas Prior, Judith A Westman,[...]. J Clin Oncol 2008
547
20

Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia.
Aparna Raval, Stephan M Tanner, John C Byrd, Elizabeth B Angerman, James D Perko, Shih-Shih Chen, Björn Hackanson, Michael R Grever, David M Lucas, Jennifer J Matkovic,[...]. Cell 2007
271
13


Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
F S Leach, N C Nicolaides, N Papadopoulos, B Liu, J Jen, R Parsons, P Peltomäki, P Sistonen, L A Aaltonen, M Nyström-Lahti. Cell 1993
13

De novo constitutional MLH1 epimutations confer early-onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one.
Ajay Goel, Thuy-Phuong Nguyen, Hon-Chiu E Leung, Takeshi Nagasaka, Jennifer Rhees, Erin Hotchkiss, Mildred Arnold, Pia Banerji, Minoru Koi, Chau-To Kwok,[...]. Int J Cancer 2011
58
13


Somatic hypermethylation of MSH2 is a frequent event in Lynch Syndrome colorectal cancers.
Takeshi Nagasaka, Jennifer Rhees, Matthias Kloor, Johannes Gebert, Yoshio Naomoto, C Richard Boland, Ajay Goel. Cancer Res 2010
69
13


BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer.
Guoren Deng, Ian Bell, Suzanne Crawley, James Gum, Jonathan P Terdiman, Brian A Allen, Brindusa Truta, Marvin H Sleisenger, Young S Kim. Clin Cancer Res 2004
302
13

BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing.
E Domingo, P Laiho, M Ollikainen, M Pinto, L Wang, A J French, J Westra, T Frebourg, E Espín, M Armengol,[...]. J Med Genet 2004
252
13

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
129
13

The MLH1 c.-27C>A and c.85G>T variants are linked to dominantly inherited MLH1 epimutation and are borne on a European ancestral haplotype.
Chau-To Kwok, Ingrid P Vogelaar, Wendy A van Zelst-Stams, Arjen R Mensenkamp, Marjolijn J Ligtenberg, Robert W Rapkins, Robyn L Ward, Nicolette Chun, James M Ford, Uri Ladabaum,[...]. Eur J Hum Genet 2014
27
13

Utility of MLH1 methylation analysis in the clinical evaluation of Lynch Syndrome in women with endometrial cancer.
Amanda S Bruegl, Bojana Djordjevic, Diana L Urbauer, Shannon N Westin, Pamela T Soliman, Karen H Lu, Rajyalakshmi Luthra, Russell R Broaddus. Curr Pharm Des 2014
25
13



Clinical features and mismatch repair genes analyses of Chinese suspected hereditary non-polyposis colorectal cancer: a cost-effective screening strategy proposal.
Hong-Li Yan, Li-Qiang Hao, Hei-Ying Jin, Qing-He Xing, Geng Xue, Qian Mei, Jin He, Lin He, Shu-Han Sun. Cancer Sci 2008
19
13

Defective mismatch repair as a predictive marker for lack of efficacy of fluorouracil-based adjuvant therapy in colon cancer.
Daniel J Sargent, Silvia Marsoni, Genevieve Monges, Stephen N Thibodeau, Roberto Labianca, Stanley R Hamilton, Amy J French, Brian Kabat, Nathan R Foster, Valter Torri,[...]. J Clin Oncol 2010
901
13

The molecular basis of EPCAM expression loss in Lynch syndrome-associated tumors.
Cathrin Huth, Matthias Kloor, Anita Y Voigt, Gergana Bozukova, Christina Evers, Harald Gaspar, Mirjam Tariverdian, Peter Schirmacher, Magnus von Knebel Doeberitz, Hendrik Bläker. Mod Pathol 2012
35
13

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
13

Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family Registry.
Robyn L Ward, Timothy Dobbins, Noralane M Lindor, Robert W Rapkins, Megan P Hitchins. Genet Med 2013
51
13

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.
J M Cunningham, E R Christensen, D J Tester, C Y Kim, P C Roche, L J Burgart, S N Thibodeau. Cancer Res 1998
689
13

Performance of different microsatellite marker panels for detection of mismatch repair-deficient colorectal tumors.
Rosa M Xicola, Xavier Llor, Elisenda Pons, Antoni Castells, Cristina Alenda, Virgínia Piñol, Montserrat Andreu, Sergi Castellví-Bel, Artemio Payá, Rodrigo Jover,[...]. J Natl Cancer Inst 2007
132
13


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
215
13

The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.
Patrice Watson, Hans F A Vasen, Jukka-Pekka Mecklin, Inge Bernstein, Markku Aarnio, Heikki J Järvinen, Torben Myrhøj, Lone Sunde, Juul T Wijnen, Henry T Lynch. Int J Cancer 2008
371
13


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.