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COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.
Tomlinson IP, Dunlop M, Campbell H, Zanke B, Gallinger S, Hudson T, Koessler T, Pharoah PD, Niittymäki I, Tuupanen S, Aaltonen LA, Hemminki K, Lindblom A, Försti A, Sieber O, Lipton L, van Wezel T, Morreau H, Wijnen JT, Devilee P, Matsuda K, Nakamura Y, Castellví-Bel S, Ruiz-Ponte C, Castells A, Carracedo A, Ho JW, Sham P, Hofstra RM, Vodicka P, Brenner H, Hampe J, Schafmayer C, Tepel J, Schreiber S, Völzke H, Lerch MM, Schmidt CA, Buch S, Moreno V, Villanueva CM, Peterlongo P, Radice P, Echeverry MM, Velez A, Carvajal-Carmona L, Scott R, Penegar S, Broderick P, Tenesa A, Houlston RS. Tomlinson IP, et al. Among authors: van wezel t. Br J Cancer. 2010 Jan 19;102(2):447-54. doi: 10.1038/sj.bjc.6605338. Epub 2009 Nov 17. Br J Cancer. 2010. PMID: 19920828 Free PMC article.
Increased frequency of 20q gain and copy-neutral loss of heterozygosity in mismatch repair proficient familial colorectal carcinomas.
Middeldorp A, van Eijk R, Oosting J, Forte GI, van Puijenbroek M, van Nieuwenhuizen M, Corver WE, Ruano D, Caldes T, Wijnen J, Morreau H, van Wezel T. Middeldorp A, et al. Among authors: van puijenbroek m, van eijk r, van wezel t, van nieuwenhuizen m. Int J Cancer. 2012 Feb 15;130(4):837-46. doi: 10.1002/ijc.26093. Epub 2011 Jul 15. Int J Cancer. 2012. PMID: 21445971 Free article.
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.
Ghorbanoghli Z, Nieuwenhuis MH, Houwing-Duistermaat JJ, Jagmohan-Changur S, Hes FJ, Tops CM, Wagner A, Aalfs CM, Verhoef S, Gómez García EB, Sijmons RH, Menko FH, Letteboer TG, Hoogerbrugge N, van Wezel T, Vasen HF, Wijnen JT. Ghorbanoghli Z, et al. Among authors: van wezel t. Fam Cancer. 2016 Oct;15(4):563-70. doi: 10.1007/s10689-016-9877-5. Fam Cancer. 2016. PMID: 26880076 Free PMC article.
High frequency of copy-neutral LOH in MUTYH-associated polyposis carcinomas.
Middeldorp A, van Puijenbroek M, Nielsen M, Corver WE, Jordanova ES, ter Haar N, Tops CM, Vasen HF, Lips EH, van Eijk R, Hes FJ, Oosting J, Wijnen J, van Wezel T, Morreau H. Middeldorp A, et al. Among authors: van puijenbroek m, van eijk r, van wezel t. J Pathol. 2008 Sep;216(1):25-31. doi: 10.1002/path.2375. J Pathol. 2008. PMID: 18506705
A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature.
Aydemirli MD, van der Tuin K, Hes FJ, van den Ouweland AMW, van Wezel T, Kapiteijn E, Morreau H. Aydemirli MD, et al. Among authors: van der tuin k, van den ouweland amw, van wezel t. Fam Cancer. 2020 Jan;19(1):15-21. doi: 10.1007/s10689-019-00146-4. Fam Cancer. 2020. PMID: 31598872 Free PMC article. Review.
204 results