A citation-based method for searching scientific literature

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, Steven Gallinger, Encarna Gomez Garcia, Jane C Figueiredo, Robert Haile, Heather L Hampel, John L Hopper, Nicoline Hoogerbrugge, Magnus von Knebel Doeberitz, Loic Le Marchand, Tom G W Letteboer, Mark A Jenkins, Annika Lindblom, Noralane M Lindor, Arjen R Mensenkamp, Pål Møller, Polly A Newcomb, Theo A M van Os, Rachel Pearlman, Marta Pineda, Nils Rahner, Egbert J W Redeker, Maran J W Olderode-Berends, Christophe Rosty, Hans K Schackert, Rodney Scott, Leigha Senter, Liesbeth Spruijt, Verena Steinke-Lange, Manon Suerink, Stephen Thibodeau, Yvonne J Vos, Anja Wagner, Ingrid Winship, Frederik J Hes, Hans F A Vasen, Juul T Wijnen, Maartje Nielsen, Aung Ko Win. J Clin Oncol 2018
Times Cited: 89







List of shared articles



Times cited

Risk assessment and genetic counseling for Lynch syndrome - Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer.
Spring Holter, Michael J Hall, Heather Hampel, Kory Jasperson, Sonia S Kupfer, Joy Larsen Haidle, Maureen E Mork, Selvi Palaniapppan, Leigha Senter, Elena M Stoffel,[...]. J Genet Couns 2022
1

European guidelines from the EHTG and ESCP for Lynch syndrome: an updated third edition of the Mallorca guidelines based on gene and gender.
T T Seppälä, A Latchford, I Negoi, A Sampaio Soares, R Jimenez-Rodriguez, L Sánchez-Guillén, D G Evans, N Ryan, E J Crosbie, M Dominguez-Valentin,[...]. Br J Surg 2021
27

An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome.
Manon Suerink, Mar Rodríguez-Girondo, Heleen M van der Klift, Chrystelle Colas, Laurence Brugieres, Noémie Lavoine, Marjolijn Jongmans, Gabriel Capellá Munar, D Gareth Evans, Michael P Farrell,[...]. Genet Med 2019
5

The diverse molecular profiles of lynch syndrome-associated colorectal cancers are (highly) dependent on underlying germline mismatch repair mutations.
Noah C Helderman, Sanne W Bajwa-Ten Broeke, Hans Morreau, Manon Suerink, Diantha Terlouw, Anne-Sophie van der Werf-' T Lam, Tom van Wezel, Maartje Nielsen. Crit Rev Oncol Hematol 2021
0

Endoscopy to Diagnose and Prevent Digestive Cancers in Lynch Syndrome.
Raphael Olivier, Violaine Randrian, David Tougeron, Jean-Christophe Saurin. Cancers (Basel) 2021
3

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
94

Lynch Syndrome: Its Impact on Urothelial Carcinoma.
Andrea Katharina Lindner, Gert Schachtner, Gennadi Tulchiner, Martin Thurnher, Gerold Untergasser, Peter Obrist, Iris Pipp, Fabian Steinkohl, Wolfgang Horninger, Zoran Culig,[...]. Int J Mol Sci 2021
4

Hereditary gastrointestinal cancers: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†.
N Stjepanovic, L Moreira, F Carneiro, F Balaguer, A Cervantes, J Balmaña, E Martinelli. Ann Oncol 2019
54

Diagnosis of Lynch Syndrome and Strategies to Distinguish Lynch-Related Tumors from Sporadic MSI/dMMR Tumors.
Julie Leclerc, Catherine Vermaut, Marie-Pierre Buisine. Cancers (Basel) 2021
13

Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.
Adam S Gordon, Elisabeth A Rosenthal, David S Carrell, Laura M Amendola, Michael O Dorschner, Aaron Scrol, Ian B Stanaway, Shannon DeVange, James D Ralston, Hana Zouk,[...]. Am J Hum Genet 2019
1

From Genetics to Histomolecular Characterization: An Insight into Colorectal Carcinogenesis in Lynch Syndrome.
Martina Lepore Signorile, Vittoria Disciglio, Gabriella Di Carlo, Antonio Pisani, Cristiano Simone, Giuseppe Ingravallo. Int J Mol Sci 2021
2

Characterisation of heterozygous PMS2 variants in French patients with Lynch syndrome.
Qing Wang, Julie Leclerc, Gaëlle Bougeard, Sylviane Olschwang, Stéphanie Vasseur, Kévin Cassinari, Denis Boidin, Cédrick Lefol, Pierre Naïbo, Thierry Frébourg,[...]. J Med Genet 2020
3