A citation-based method for searching scientific literature

R Salovaara, A Loukola, P Kristo, H Kääriäinen, H Ahtola, M Eskelinen, N Härkönen, R Julkunen, E Kangas, S Ojala, J Tulikoura, E Valkamo, H Järvinen, J P Mecklin, L A Aaltonen, A de la Chapelle. J Clin Oncol 2000
Times Cited: 393







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



Times Cited
  Times     Co-cited
Similarity


Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease.
L A Aaltonen, R Salovaara, P Kristo, F Canzian, A Hemminki, P Peltomäki, R B Chadwick, H Kääriäinen, M Eskelinen, H Järvinen,[...]. N Engl J Med 1998
882
67

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
910
44

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
34

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
536
31

Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer.
Rebecca A Barnetson, Albert Tenesa, Susan M Farrington, Iain D Nicholl, Roseanne Cetnarskyj, Mary E Porteous, Harry Campbell, Malcolm G Dunlop. N Engl J Med 2006
311
23

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
23


Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer.
Virgínia Piñol, Antoni Castells, Montserrat Andreu, Sergi Castellví-Bel, Cristina Alenda, Xavier Llor, Rosa M Xicola, Francisco Rodríguez-Moranta, Artemio Payá, Rodrigo Jover,[...]. JAMA 2005
382
22

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
584
22


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
475
19


EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.
Glenn E Palomaki, Monica R McClain, Stephanie Melillo, Heather L Hampel, Stephen N Thibodeau. Genet Med 2009
322
18

Microsatellite instability in colorectal cancer.
C Richard Boland, Ajay Goel. Gastroenterology 2010
17

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

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
920
16

Hereditary colorectal cancer.
Henry T Lynch, Albert de la Chapelle. N Engl J Med 2003
15

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
15


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
234
14

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
231
13


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
421
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
251
12

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
384
12

Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome.
Kathleen M Schmeler, Henry T Lynch, Lee-may Chen, Mark F Munsell, Pamela T Soliman, Mary Beth Clark, Molly S Daniels, Kristin G White, Stephanie G Boyd-Rogers, Peggy G Conrad,[...]. N Engl J Med 2006
469
12

Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review.
Noralane M Lindor, Gloria M Petersen, Donald W Hadley, Anita Y Kinney, Susan Miesfeldt, Karen H Lu, Patrick Lynch, Wylie Burke, Nancy Press. JAMA 2006
419
12

Identification of Lynch syndrome among patients with colorectal cancer.
Leticia Moreira, Francesc Balaguer, Noralane Lindor, Albert de la Chapelle, Heather Hampel, Lauri A Aaltonen, John L Hopper, Loic Le Marchand, Steven Gallinger, Polly A Newcomb,[...]. JAMA 2012
295
12

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
264
12

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.
J M Cunningham, C Y Kim, E R Christensen, D J Tester, Y Parc, L J Burgart, K C Halling, S K McDonnell, D J Schaid, C Walsh Vockley,[...]. Am J Hum Genet 2001
259
11

Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer.
Christine M Ribic, Daniel J Sargent, Malcolm J Moore, Stephen N Thibodeau, Amy J French, Richard M Goldberg, Stanley R Hamilton, Pierre Laurent-Puig, Robert Gryfe, Lois E Shepherd,[...]. N Engl J Med 2003
11

Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members.
Heikki J Järvinen, Laura Renkonen-Sinisalo, Katja Aktán-Collán, Päivi Peltomäki, Lauri A Aaltonen, Jukka-Pekka Mecklin. J Clin Oncol 2009
177
11

Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset.
Heather Hampel, Julie A Stephens, Eero Pukkala, Risto Sankila, Lauri A Aaltonen, Jukka-Pekka Mecklin, Albert de la Chapelle. Gastroenterology 2005
283
11

Efficient detection of hereditary nonpolyposis colorectal cancer gene carriers by screening for tumor microsatellite instability before germline genetic testing.
J P Terdiman, J R Gum, P G Conrad, G A Miller, V Weinberg, S C Crawley, T R Levin, C Reeves, A Schmitt, M Hepburn,[...]. Gastroenterology 2001
129
11

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
11

Cancer risk in mutation carriers of DNA-mismatch-repair genes.
M Aarnio, R Sankila, E Pukkala, R Salovaara, L A Aaltonen, A de la Chapelle, P Peltomäki, J P Mecklin, H J Järvinen. Int J Cancer 1999
808
10

Prediction of germline mutations and cancer risk in the Lynch syndrome.
Sining Chen, Wenyi Wang, Shing Lee, Khedoudja Nafa, Johanna Lee, Kathy Romans, Patrice Watson, Stephen B Gruber, David Euhus, Kenneth W Kinzler,[...]. JAMA 2006
245
10

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
486
10

Calculation of risk of colorectal and endometrial cancer among patients with Lynch syndrome.
Elena Stoffel, Bhramar Mukherjee, Victoria M Raymond, Nabihah Tayob, Fay Kastrinos, Jennifer Sparr, Fei Wang, Prathap Bandipalliam, Sapna Syngal, Stephen B Gruber. Gastroenterology 2009
234
10

Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma.
J G Herman, A Umar, K Polyak, J R Graff, N Ahuja, J P Issa, S Markowitz, J K Willson, S R Hamilton, K W Kinzler,[...]. Proc Natl Acad Sci U S A 1998
10

Genetic susceptibility to non-polyposis colorectal cancer.
H T Lynch, A de la Chapelle. J Med Genet 1999
583
10

Mutation of a mutL homolog in hereditary colon cancer.
N Papadopoulos, N C Nicolaides, Y F Wei, S M Ruben, K C Carter, C A Rosen, W A Haseltine, R D Fleischmann, C M Fraser, M D Adams. Science 1994
10

Cancer risks for mismatch repair gene mutation carriers: a population-based early onset case-family study.
Mark A Jenkins, Laura Baglietto, James G Dowty, Christine M Van Vliet, Letitia Smith, Leeanne J Mead, Finlay A Macrae, D James B St John, Jeremy R Jass, Graham G Giles,[...]. Clin Gastroenterol Hepatol 2006
120
10

BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair.
Liang Wang, Julie M Cunningham, Jennifer L Winters, Jennifer C Guenther, Amy J French, Lisa A Boardman, Lawrence J Burgart, Shannon K McDonnell, Daniel J Schaid, Stephen N Thibodeau. Cancer Res 2003
216
9

Decrease in mortality in Lynch syndrome families because of surveillance.
Andrea E de Jong, Yvonne M C Hendriks, Jan H Kleibeuker, Sybrand Y de Boer, Annemieke Cats, Gerrit Griffioen, Fokko M Nagengast, Frits G Nelis, Matti A Rookus, Hans F A Vasen. Gastroenterology 2006
180
9

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
9

Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study.
Mark A Jenkins, Shinichi Hayashi, Anne-Marie O'Shea, Lawrence J Burgart, Tom C Smyrk, David Shimizu, Paul M Waring, Andrew R Ruszkiewicz, Aaron F Pollett, Mark Redston,[...]. Gastroenterology 2007
221
9

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
787
9

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
876
9

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
301
9


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.