A citation-based method for searching scientific literature

Hardeep Singh, Rachel Schiesser, Gobind Anand, Peter A Richardson, Hashem B El-Serag. Clin Gastroenterol Hepatol 2010
Times Cited: 49







List of co-cited articles
219 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
40



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
899
24

Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients.
Shilpa Grover, Elena M Stoffel, Laoti Bussone, Elizabeth Tschoegl, Sapna Syngal. Clin Gastroenterol Hepatol 2004
120
22

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
919
22

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
465
20

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
319
20

Hereditary colorectal cancer.
Henry T Lynch, Albert de la Chapelle. N Engl J Med 2003
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
529
18

Value of database linkage: are patients at risk of familial colorectal cancer being referred for genetic counselling and testing?
C Wong, P Gibbs, J Johns, I Jones, I Faragher, E Lynch, F Macrae, L Lipton. Intern Med J 2008
30
26

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
418
16

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
16

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
484
14

Family history is neglected in the work-up of patients with colorectal cancer: a quality assessment using cancer registry data.
D A van Dijk, M J Oostindiër, W M Kloosterman-Boele, P Krijnen, H F A Vasen. Fam Cancer 2007
41
17

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
94
14

Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population.
Tuan A Dinh, Benjamin I Rosner, James C Atwood, C Richard Boland, Sapna Syngal, Hans F A Vasen, Stephen B Gruber, Randall W Burt. Cancer Prev Res (Phila) 2011
121
14

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
144
14

ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Sapna Syngal, Randall E Brand, James M Church, Francis M Giardiello, Heather L Hampel, Randall W Burt. Am J Gastroenterol 2015
624
14

Most patients with colorectal tumors at young age do not visit a cancer genetics clinic.
Lucia I H Overbeek, Nicoline Hoogerbrugge, Joannes H J M van Krieken, Fokko M Nagengast, Theo J M Ruers, Marjolijn J L Ligtenberg, Rosella P M G Hermens. Dis Colon Rectum 2008
28
21

One to 2-year surveillance intervals reduce risk of colorectal cancer in families with Lynch syndrome.
Hans F A Vasen, Mohamed Abdirahman, Richard Brohet, Alexandra M J Langers, Jan H Kleibeuker, Mariette van Kouwen, Jan Jacob Koornstra, Henk Boot, Annemieke Cats, Evelien Dekker,[...]. Gastroenterology 2010
160
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
290
12

Barriers to and motivations for physician referral of patients to cancer genetics clinics.
Carrie F Prochniak, Lisa J Martin, Erin M Miller, Sara C Knapke. J Genet Couns 2012
24
25

Improving identification of lynch syndrome patients: a comparison of research data with clinical records.
Yen Y Tan, Julie McGaughran, Kaltin Ferguson, Michael D Walsh, Daniel D Buchanan, Joanne P Young, Penelope M Webb, Andreas Obermair, Amanda B Spurdle. Int J Cancer 2013
23
26

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
415
12

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).
H F A Vasen, G Möslein, A Alonso, I Bernstein, L Bertario, I Blanco, J Burn, G Capella, C Engel, I Frayling,[...]. J Med Genet 2007
357
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
243
10

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
880
10

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
10

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
10


Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.
H F A Vasen, G Möslein, A Alonso, S Aretz, I Bernstein, L Bertario, I Blanco, S Bulow, J Burn, G Capella,[...]. Fam Cancer 2010
81
10

Accuracy of reporting of family history of colorectal cancer.
R J Mitchell, D Brewster, H Campbell, M E M Porteous, A H Wyllie, C C Bird, M G Dunlop. Gut 2004
147
8

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
231
8

Endometrial cancer and Lynch syndrome: clinical and pathologic considerations.
Larissa A Meyer, Russell R Broaddus, Karen H Lu. Cancer Control 2009
116
8

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
804
8

US physicians' attitudes toward genetic testing for cancer susceptibility.
A N Freedman, L Wideroff, L Olson, W Davis, C Klabunde, K P Srinath, B B Reeve, R T Croyle, R Ballard-Barbash. Am J Med Genet A 2003
134
8

Errors in delivery of cancer genetics services: implications for practice.
Karina L Brierley, Danielle Campfield, Whitney Ducaine, Lindsay Dohany, Talia Donenberg, Kristen Shannon, Robin C Schwartz, Ellen T Matloff. Conn Med 2010
65
8

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
8

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
381
8

Mismatch repair status in the prediction of benefit from adjuvant fluorouracil chemotherapy in colorectal cancer.
R Jover, P Zapater, A Castells, X Llor, M Andreu, J Cubiella, V Piñol, R M Xicola, L Bujanda, J M Reñé,[...]. Gut 2006
160
8

Identification in daily practice of patients with Lynch syndrome (hereditary nonpolyposis colorectal cancer): revised Bethesda guidelines-based approach versus molecular screening.
Catherine Julié, Christophe Trésallet, Antoine Brouquet, Céline Vallot, Ute Zimmermann, Emmanuel Mitry, François Radvanyi, Etienne Rouleau, Rosette Lidereau, Florence Coulet,[...]. Am J Gastroenterol 2008
91
8

Underutilization of microsatellite instability analysis in colorectal cancer patients at high risk for Lynch syndrome.
Margot G F Van Lier, Johannes H W De Wilt, Jessie J M F Wagemakers, Winand N M Dinjens, Ronald A M Damhuis, Anja Wagner, Ernst J Kuipers, Monique E Van Leerdam. Scand J Gastroenterol 2009
24
16

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
8

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
179
8

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
8

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer.
Lucía Pérez-Carbonell, Clara Ruiz-Ponte, Carla Guarinos, Cristina Alenda, Artemio Payá, Alejandro Brea, Cecilia M Egoavil, Adela Castillejo, Victor M Barberá, Xavier Bessa,[...]. Gut 2012
131
8

Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels.
Katarina Domanska, Christina Carlsson, Pär-Ola Bendahl, Mef Nilbert. BMC Med Genet 2009
23
17

Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians.
L Wideroff, S T Vadaparampil, M H Greene, S Taplin, L Olson, A N Freedman. J Med Genet 2005
109
8


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.