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



McKinsey L Goodenberger, Brittany C Thomas, Douglas Riegert-Johnson, C Richard Boland, Sharon E Plon, Mark Clendenning, Aung Ko Win, Leigha Senter, Steven M Lipkin, Zsofia K Stadler, Finlay A Macrae, Henry T Lynch, Jeffrey N Weitzel, Albert de la Chapelle, Sapna Syngal, Patrick Lynch, Susan Parry, Mark A Jenkins, Steven Gallinger, Spring Holter, Melyssa Aronson, Polly A Newcomb, Terrilea Burnett, Loïc Le Marchand, Pavel Pichurin, Heather Hampel, Jonathan P Terdiman, Karen H Lu, Stephen Thibodeau, Noralane M Lindor. Genet Med 2016
Times Cited: 41




List of shared articles



Times cited

Characteristics of colorectal carcinoma patients with PMS2 defects detected by immunohistochemistry.
Zhijun Zeng, Qijia Yan, Guodong Chen, Xiaoli Zhang, Jia Huang, Kai Fu, Xiuda Peng, Shuai Xiao. Eur J Cancer Prev 2021
2

PMS2 expression decrease causes severe problems in mismatch repair.
Mariann Kasela, Minna Nyström, Minttu Kansikas. Hum Mutat 2019
8

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes.
Richard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, Harsh Sheth, Christine Hayes, Stefan Aretz, Karin Dahan, William Foulkes, Christian P Kratz, Tim Ripperger,[...]. Hum Mutat 2019
16

Up-Front Multigene Panel Testing for Cancer Susceptibility in Patients With Newly Diagnosed Endometrial Cancer: A Multicenter Prospective Study.
Monica D Levine, Rachel Pearlman, Heather Hampel, Casey Cosgrove, David Cohn, Alexis Chassen, Adrian Suarez, David A Barrington, Joseph P McElroy, Steven Waggoner,[...]. JCO Precis Oncol 2021
1


The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect.
Sanne W Ten Broeke, Mar Rodríguez-Girondo, Manon Suerink, Stefan Aretz, Inge Bernstein, Gabriel Capellá, Christoph Engel, Encarna B Gomez-Garcia, Liselot P van Hest, Magnus von Knebel Doeberitz,[...]. Cancer Epidemiol Biomarkers Prev 2019
3

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

The coding microsatellite mutation profile of PMS2-deficient colorectal cancer.
Sanne W Bajwa-Ten Broeke, Alexej Ballhausen, Aysel Ahadova, Manon Suerink, Lena Bohaumilitzky, Florian Seidler, Hans Morreau, Tom van Wezel, Julia Krzykalla, Axel Benner,[...]. Exp Mol Pathol 2021
2