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Novel MLH1 duplication identified in Colombian families with Lynch syndrome ‌ Alonso-Espinaco, V, Giráldez, MD, Trujillo, C, Van Der Klift, H, Muñoz, J, Balaguer, F, Ocaña, T, Madrigal, I, Jones, A, Echeverry, M, Velez, A, Tomlinson, I, Milà, M, Wijnen, J, Carvajal-Carmona, L, Castells, A, Castellví-Bel, S

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. ‌ Tomlinson, I, Dunlop, M, Campbell, H, Zanke, B, Gallinger, S, Hudson, T, Koessler, T, Pharoah, P, Niittymäki, I, Niittymäkix, I, Tuupanen, S, Tuupanenx, S, Aaltonen, L, Hemminki, K, Lindblom, A, Försti, A, Sieber, O, Lipton, L, van Wezel, T, Morreau, H, Wijnen, J, Devilee, P, Matsuda, K, Nakamura, Y, Castellví-Bel, S

Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome. ‌ Wijnen, J, Brohet, R, van Eijk, R, Jagmohan-Changur, S, Middeldorp, A, Tops, C, van Puijenbroek, M, Ausems, MG, Gómez García, E, Hes, F, Hoogerbrugge, N, Menko, F, van Os, T, Sijmons, R, Verhoef, S, Wagner, A, Nagengast, F, Kleibeuker, J, Devilee, P, Morreau, H, Goldgar, D, Tomlinson, I, Houlston, R, van Wezel, T, Vasen, H

Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility ‌ Picelli, S, Lorenzo Bermejo, J, Chang-Claude, J, Hoffmeister, M, Fernández-Rozadilla, C, Carracedo, A, Castells, A, Castellví-Bel, S, Naccarati, A, Pardini, B, Vodickova, L, Müller, H, Talseth-Palmer, B, Stibbard, G, Peterlongo, P, Nici, C, Veneroni, S, Li, L, Casey, G, Tenesa, A, Farrington, S, Tomlinson, I, Moreno, V, Van Wezel, T, Wijnen, J, Dunlop, M, Radice, P, Scott, R, Vodicka, P, Ruiz-Ponte, C, Brenner, H, Buch, S, Völzke, H, Hampe, J, Schafmayer, C, Lindblom, A