A citation-based method for searching scientific literature

Christoph Engel, Aysel Ahadova, Toni T Seppälä, Stefan Aretz, Marloes Bigirwamungu-Bargeman, Hendrik Bläker, Karolin Bucksch, Reinhard Büttner, Wouter T de Vos Tot Nederveen Cappel, Volker Endris, Elke Holinski-Feder, Stefanie Holzapfel, Robert Hüneburg, Maarten A J M Jacobs, Jan J Koornstra, Alexandra M Langers, Anna Lepistö, Monika Morak, Gabriela Möslein, Päivi Peltomäki, Kirsi Pylvänäinen, Nils Rahner, Laura Renkonen-Sinisalo, Karsten Schulmann, Verena Steinke-Lange, Albrecht Stenzinger, Christian P Strassburg, Paul C van de Meeberg, Mariette van Kouwen, Monique van Leerdam, Deepak B Vangala, Juda Vecht, Marie-Louise Verhulst, Magnus von Knebel Doeberitz, Jürgen Weitz, Silke Zachariae, Markus Loeffler, Jukka-Pekka Mecklin, Matthias Kloor, Hans F Vasen. Gastroenterology 2020
Times Cited: 27







List of co-cited articles
297 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
265
51

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies.
Christoph Engel, Hans F Vasen, Toni Seppälä, Stefan Aretz, Marloes Bigirwamungu-Bargeman, Sybrand Y de Boer, Karolin Bucksch, Reinhard Büttner, Elke Holinski-Feder, Stefanie Holzapfel,[...]. Gastroenterology 2018
62
51

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.
Pål Møller, Toni T Seppälä, Inge Bernstein, Elke Holinski-Feder, Paulo Sala, D Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf H Sijmons,[...]. Gut 2018
241
51

Three molecular pathways model colorectal carcinogenesis in Lynch syndrome.
Aysel Ahadova, Richard Gallon, Johannes Gebert, Alexej Ballhausen, Volker Endris, Martina Kirchner, Albrecht Stenzinger, John Burn, Magnus von Knebel Doeberitz, Hendrik Bläker,[...]. Int J Cancer 2018
71
51

Prevalence of mismatch repair-deficient crypt foci in Lynch syndrome: a pathological study.
Matthias Kloor, Cathrin Huth, Anita Y Voigt, Axel Benner, Peter Schirmacher, Magnus von Knebel Doeberitz, Hendrik Bläker. Lancet Oncol 2012
90
48

CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome.
Aysel Ahadova, Magnus von Knebel Doeberitz, Hendrik Bläker, Matthias Kloor. Fam Cancer 2016
46
48

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
Mev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, Sanne W Ten Broeke, John-Paul Plazzer, Sigve Nakken, Christoph Engel, Stefan Aretz, Mark A Jenkins, Lone Sunde,[...]. Genet Med 2020
173
48

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
939
37

Cancer Risks for PMS2-Associated Lynch Syndrome.
Sanne W Ten Broeke, Heleen M van der Klift, Carli M J Tops, Stefan Aretz, Inge Bernstein, Daniel D Buchanan, Albert de la Chapelle, Gabriel Capella, Mark Clendenning, Christoph Engel,[...]. J Clin Oncol 2018
89
33

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
757
29

Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial.
John Burn, Harsh Sheth, Faye Elliott, Lynn Reed, Finlay Macrae, Jukka-Pekka Mecklin, Gabriela Möslein, Fiona E McRonald, Lucio Bertario, D Gareth Evans,[...]. Lancet 2020
86
29

The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillance.
Aysel Ahadova, Toni T Seppälä, Christoph Engel, Richard Gallon, John Burn, Elke Holinski-Feder, Verena Steinke-Lange, Gabriela Möslein, Maartje Nielsen, Sanne W Ten Broeke,[...]. Int J Cancer 2021
13
61

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report.
Toni T Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, Finlay Macrae, D Gareth Evans, Christina Therkildsen, Julian Sampson, Rodney Scott, John Burn, Gabriela Möslein,[...]. Hered Cancer Clin Pract 2019
25
28

Mismatch repair-deficient crypt foci in Lynch syndrome--molecular alterations and association with clinical parameters.
Laura Staffa, Fabian Echterdiek, Nina Nelius, Axel Benner, Wiebke Werft, Bernd Lahrmann, Niels Grabe, Martin Schneider, Mirjam Tariverdian, Magnus von Knebel Doeberitz,[...]. PLoS One 2015
38
25

PD-1 Blockade in Tumors with Mismatch-Repair Deficiency.
Dung T Le, Jennifer N Uram, Hao Wang, Bjarne R Bartlett, Holly Kemberling, Aleksandra D Eyring, Andrew D Skora, Brandon S Luber, Nilofer S Azad, Dan Laheru,[...]. N Engl J Med 2015
25

Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2.
Sanne W Ten Broeke, Tom C van Bavel, Anne M L Jansen, Encarnca Gómez-García, Frederik J Hes, Liselot P van Hest, Tom G W Letteboer, Maran J W Olderode-Berends, Dina Ruano, Liesbeth Spruijt,[...]. Gastroenterology 2018
18
38

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report.
Toni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, Heikki Järvinen, Laura Renkonen-Sinisalo, Inge Bernstein, Elke Holinski-Feder, Paola Sala, Annika Lindblom, Finlay Macrae,[...]. Hered Cancer Clin Pract 2017
27
25

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
164
25

The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC.
Andrea E De Jong, Hans Morreau, Marjo Van Puijenbroek, Paul H c Eilers, Juul Wijnen, Fokko M Nagengast, Gerrit Griffioen, Annemieke Cats, Fred H Menko, Jan H Kleibeuker,[...]. Gastroenterology 2004
133
25

Hereditary and familial colon cancer.
Kory W Jasperson, Thérèse M Tuohy, Deborah W Neklason, Randall W Burt. Gastroenterology 2010
663
25

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a 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
73
25

Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade.
Dung T Le, Jennifer N Durham, Kellie N Smith, Hao Wang, Bjarne R Bartlett, Laveet K Aulakh, Steve Lu, Holly Kemberling, Cara Wilt, Brandon S Luber,[...]. Science 2017
25

Mismatch repair deficiency commonly precedes adenoma formation in Lynch Syndrome-Associated colorectal tumorigenesis.
Shigeki Sekine, Taisuke Mori, Reiko Ogawa, Masahiro Tanaka, Hiroshi Yoshida, Hirokazu Taniguchi, Takeshi Nakajima, Kokichi Sugano, Teruhiko Yoshida, Mamoru Kato,[...]. Mod Pathol 2017
40
25

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
25

Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome.
Hans Binder, Lydia Hopp, Michal R Schweiger, Steve Hoffmann, Frank Jühling, Martin Kerick, Bernd Timmermann, Susann Siebert, Christina Grimm, Lilit Nersisyan,[...]. J Pathol 2017
39
22

Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)/United Kingdom Cancer Genetics Group (UKCGG).
Kevin J Monahan, Nicola Bradshaw, Sunil Dolwani, Bianca Desouza, Malcolm G Dunlop, James E East, Mohammad Ilyas, Asha Kaur, Fiona Lalloo, Andrew Latchford,[...]. Gut 2020
100
22


Endoscopic management of Lynch syndrome and of familial risk of colorectal cancer: European Society of Gastrointestinal Endoscopy (ESGE) Guideline.
Monique E van Leerdam, Victorine H Roos, Jeanin E van Hooft, Francesc Balaguer, Evelien Dekker, Michal F Kaminski, Andrew Latchford, Helmut Neumann, Luigi Ricciardiello, Maria Rupińska,[...]. Endoscopy 2019
34
22

White-Light Endoscopy Is Adequate for Lynch Syndrome Surveillance in a Randomized and Noninferiority Study.
Liseth Rivero-Sánchez, Coral Arnau-Collell, Jesús Herrero, David Remedios, Joaquín Cubiella, Marta García-Cougil, Victoria Alvarez, Eduardo Albéniz, Patricia Calvo, Jordi Gordillo,[...]. Gastroenterology 2020
13
46

Development of colorectal tumors in colonoscopic surveillance in Lynch syndrome.
Jukka-Pekka Mecklin, Markku Aarnio, Esa Läärä, Matti V Kairaluoma, Kirsi Pylvänäinen, Päivi Peltomäki, Lauri A Aaltonen, Heikki J Järvinen. Gastroenterology 2007
100
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
633
22

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer.
Aung Ko Win, Mark A Jenkins, James G Dowty, Antonis C Antoniou, Andrew Lee, Graham G Giles, Daniel D Buchanan, Mark Clendenning, Christophe Rosty, Dennis J Ahnen,[...]. Cancer Epidemiol Biomarkers Prev 2017
174
22


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
157
18

The Manchester International Consensus Group recommendations for the management of gynecological cancers in Lynch syndrome.
Emma J Crosbie, Neil A J Ryan, Mark J Arends, Tjalling Bosse, John Burn, Joanna M Cornes, Robin Crawford, Diana Eccles, Ian M Frayling, Sadaf Ghaem-Maghami,[...]. Genet Med 2019
77
18

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
453
18


Impact of chromoscopy on adenoma detection in patients with Lynch syndrome: a prospective, multicenter, blinded, tandem colonoscopy study.
Gabriel Rahmi, Thierry Lecomte, David Malka, Thibault Maniere, Marc Le Rhun, Rosine Guimbaud, Marie-Georges Lapalus, Anne Le Sidaner, Driffa Moussata, Olivier Caron,[...]. Am J Gastroenterol 2015
36
18

Effect of chromoendoscopy in the proximal colon on colorectal neoplasia detection in Lynch syndrome: a multicenter randomized controlled trial.
Jasmijn F Haanstra, Evelien Dekker, Annemieke Cats, Fokko M Nagengast, James C Hardwick, Steven A Vanhoutvin, Wouter H de Vos Tot Nederveen Cappel, Hans F Vasen, Jan H Kleibeuker, Jan J Koornstra. Gastrointest Endosc 2019
14
35

Impact of an optimized colonoscopic screening program for patients with Lynch syndrome: 6-year results of a specialized French network.
Guillaume Perrod, Elia Samaha, Gabriel Rahmi, Sherine Khater, Leila Abbes, Camille Savale, Geraldine Perkins, Aziz Zaanan, Gilles Chatellier, Georgia Malamut,[...]. Therap Adv Gastroenterol 2018
13
38

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
323
18

Nonpolypoid colorectal neoplasms: a challenge in endoscopic surveillance of patients with Lynch syndrome.
E J A Rondagh, S Gulikers, E B Gómez-García, Y Vanlingen, Y Detisch, B Winkens, H F A Vasen, A A M Masclee, S Sanduleanu. Endoscopy 2013
39
18

Incident colorectal cancer in Lynch syndrome is usually not preceded by compromised quality of colonoscopy.
Jutta Lappalainen, Darja Holmström, Anna Lepistö, Juha Saarnio, Jukka-Pekka Mecklin, Toni Seppälä. Scand J Gastroenterol 2019
5
100

The Immune Biology of Microsatellite-Unstable Cancer.
Matthias Kloor, Magnus von Knebel Doeberitz. Trends Cancer 2016
111
18

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
385
18

Colonoscopy screening compliance and outcomes in patients with Lynch syndrome.
K Newton, K Green, F Lalloo, D G Evans, J Hill. Colorectal Dis 2015
40
18

Yield of Lynch Syndrome Surveillance for Patients With Pathogenic Variants in DNA Mismatch Repair Genes.
Anne Goverde, Ellis L Eikenboom, Ellemieke L Viskil, Marco J Bruno, Michael Doukas, Winand N M Dinjens, Erik Jan Dubbink, Ans M W van den Ouweland, Robert M W Hofstra, Anja Wagner,[...]. Clin Gastroenterol Hepatol 2020
8
62

Mutation and cancer: statistical study of retinoblastoma.
A G Knudson. Proc Natl Acad Sci U S A 1971
18

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
610
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
491
14


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.