A citation-based method for searching scientific literature

M G Dunlop, S M Farrington, I Nicholl, L Aaltonen, G Petersen, M Porteous, A Carothers. Br J Cancer 2000
Times Cited: 48







List of co-cited articles
421 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
920
37

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
37

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
33

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
31

Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer.
Melissa C Southey, Mark A Jenkins, Leeanne Mead, Jonathan Whitty, Melanie Trivett, Andrea A Tesoriero, Letitia D Smith, Kim Jennings, Garry Grubb, Simon G Royce,[...]. J Clin Oncol 2005
171
31

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
29

Cancer risk associated with germline DNA mismatch repair gene mutations.
M G Dunlop, S M Farrington, A D Carothers, A H Wyllie, L Sharp, J Burn, B Liu, K W Kinzler, B Vogelstein. Hum Mol Genet 1997
494
27

The search for unaffected individuals with Lynch syndrome: do the ends justify the means?
Heather Hampel, Albert de la Chapelle. Cancer Prev Res (Phila) 2011
95
27

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
25

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
25

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
25

Population-based molecular detection of hereditary nonpolyposis colorectal cancer.
R Salovaara, A Loukola, P Kristo, H Kääriäinen, H Ahtola, M Eskelinen, N Härkönen, R Julkunen, E Kangas, S Ojala,[...]. J Clin Oncol 2000
393
22

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
22

Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer.
Polly A Newcomb, John Baron, Michelle Cotterchio, Steve Gallinger, John Grove, Robert Haile, David Hall, John L Hopper, Jeremy Jass, Loïc Le Marchand,[...]. Cancer Epidemiol Biomarkers Prev 2007
275
22

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.
H F Vasen, J T Wijnen, F H Menko, J H Kleibeuker, B G Taal, G Griffioen, F M Nagengast, E H Meijers-Heijboer, L Bertario, L Varesco,[...]. Gastroenterology 1996
610
20

Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome.
M Aarnio, J P Mecklin, L A Aaltonen, M Nyström-Lahti, H J Järvinen. Int J Cancer 1995
434
20

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
20


MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.
H F Vasen, A Stormorken, F H Menko, F M Nagengast, J H Kleibeuker, G Griffioen, B G Taal, P Moller, J T Wijnen. J Clin Oncol 2001
267
16

The incidence of Lynch syndrome.
Albert de la Chapelle. Fam Cancer 2005
117
16

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
16

Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.
Aung Ko Win, Joanne P Young, Noralane M Lindor, Katherine M Tucker, Dennis J Ahnen, Graeme P Young, Daniel D Buchanan, Mark Clendenning, Graham G Giles, Ingrid Winship,[...]. J Clin Oncol 2012
206
16

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.
J T Wijnen, H F Vasen, P M Khan, A H Zwinderman, H van der Klift, A Mulder, C Tops, P Møller, R Fodde. N Engl J Med 1998
309
14

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
14

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
14

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
14

Explaining the familial colorectal cancer risk associated with mismatch repair (MMR)-deficient and MMR-stable tumors.
Lauri Aaltonen, Louise Johns, Heikki Järvinen, Jukka-Pekka Mecklin, Richard Houlston. Clin Cancer Res 2007
143
14

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
14


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
14



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
12


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
12

Surveillance for hereditary nonpolyposis colorectal cancer: a long-term study on 114 families.
Wouter H de Vos tot Nederveen Cappel, Fokko M Nagengast, Gerrit Griffioen, Fred H Menko, Babs G Taal, Jan H Kleibeuker, Hans F Vasen. Dis Colon Rectum 2002
148
12

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
12

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
12

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
12


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
12

Cancer risks for MLH1 and MSH2 mutation carriers.
James G Dowty, Aung K Win, Daniel D Buchanan, Noralane M Lindor, Finlay A Macrae, Mark Clendenning, Yoland C Antill, Stephen N Thibodeau, Graham Casey, Steve Gallinger,[...]. Hum Mutat 2013
149
12

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial.
John Burn, Anne-Marie Gerdes, Finlay Macrae, Jukka-Pekka Mecklin, Gabriela Moeslein, Sylviane Olschwang, Diane Eccles, D Gareth Evans, Eamonn R Maher, Lucio Bertario,[...]. Lancet 2011
585
12

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.
J Wijnen, P M Khan, H Vasen, H van der Klift, A Mulder, I van Leeuwen-Cornelisse, B Bakker, M Losekoot, P Møller, R Fodde. Am J Hum Genet 1997
179
10

Genetic instability occurs in the majority of young patients with colorectal cancer.
B Liu, S M Farrington, G M Petersen, S R Hamilton, R Parsons, N Papadopoulos, T Fujiwara, J Jen, K W Kinzler, A H Wyllie,[...]. Nat Med 1995
322
10

Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis.
M P de Leon, M Pedroni, P Benatti, A Percesepe, C Di Gregorio, M Foroni, G Rossi, M Genuardi, G Neri, F Leonardi,[...]. Gut 1999
47
10

Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
S M Farrington, J Lin-Goerke, J Ling, Y Wang, J D Burczak, D J Robbins, M G Dunlop. Am J Hum Genet 1998
146
10

The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis.
G Steinbach, P M Lynch, R K Phillips, M H Wallace, E Hawk, G B Gordon, N Wakabayashi, B Saunders, Y Shen, T Fujimura,[...]. N Engl J Med 2000
10

Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer.
G Moslein, D J Tester, N M Lindor, R Honchel, J M Cunningham, A J French, K C Halling, M Schwab, P Goretzki, S N Thibodeau. Hum Mol Genet 1996
215
10


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.