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| Issue Date | Title | Author(s) |
|---|---|---|
| 3-Feb-2014 | Longer telomeres are associated with cancer risk in MMR-proficient hereditary non-polyposis colorectal cancer | Seguí Gracia, Nuria; Guinó, Elisabet; Pineda Riu, Marta; Navarro, Matilde; Bellido Molías, Fernando; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Moreno Aguado, Víctor; Capellá, G. (Gabriel); Valle Velasco, Laura |
| 17-Apr-2013 | Telomere length and genetic anticipation in lynch syndrome | Seguí Gracia, Nuria; Pineda Riu, Marta; Guinó, Elisabet; Borràs Flores, Ester; Navarro, Matilde; Bellido Molías, Fernando; Moreno Aguado, Víctor; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Valle Velasco, Laura |
| 8-Feb-2016 | Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis | Mur, Pilar; Sánchez Cuartielles, Elena; Aussó, Susanna; Aiza, Gemma; Valdés Mas, Rafael; Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Urioste, Miguel; Lázaro García, Conxi; Moreno Aguado, Víctor; Capellá, G. (Gabriel); Puente, Xose S.; Valle Velasco, Laura |
| 15-Feb-2018 | Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis | Mur, Pilar; de Voer, Richarda M.; Olivera-Salguero, Rubén; Rodriguez Perales, Sandra; Pons, Tirso; Setién, Fernando; Aiza, Gemma; Valdés Mas, Rafael; Bertini, Angelo; Pineda Riu, Marta; Vreede, Lilian; Navarro, Matilde; Iglesias Casals, Sílvia; González, Sara; Brunet, Joan; Valencia, Alfonso; Esteller, Manel; Lázaro García, Conxi; Kops, Geert J. P. L.; Urioste, Miguel; Puente, Xose S.; Capellá, G. (Gabriel); Valle Velasco, Laura |
| 1-Oct-2019 | Approaches to functionally validate candidate genetic variants involved in colorectal cancer predisposition | Bonjoch Gassol, Laia; Mur, Pilar; Arnau Collell, Coral; Vargas Parra, Gardenía María; Shamloo, Bahar; Franch Expósito, Sebastià; Pineda Riu, Marta; Capellá, G. (Gabriel); Erman, Batu; Castellví Bel, Sergi |
| 20-Dec-2013 | Application of a 5-tiered scheme for standardized classification of 2,360 Unique mismatch repair gene variants in the InSiGHT locus-specific database | Thompson, Bryony A.; Spurdle, Amanda B.; Plazzer, John-Paul; Greenblatt, Marc S.; Akagi, Kiwamu; Al-Mulla, Fahd; Bapat, Bharati; Bernstein, Inge; Capellá, G. (Gabriel); Dunnen, Johan T. den; Sart, Desiree du; Fabre, Aurelie; Farrell, Michael P.; Farrington, Susan M.; Frayling, Ian M.; Frebourg, Thierry; Goldgar, David E.; Heinen, Christopher D.; Holinski-Feder, Elke; Kohonen-Corish, Maija; Lagerstedt Robinson, Kristina; Leung, Suet Yi; Martins, Alexandra; Møller, Pål; Morak, Monika; Nystrom, Minna; Peltomäki, Päivi; Pineda Riu, Marta; Qi, Ming; Ramesar, Rajkumar; Rasmussen, Lene Juel; Royer-Pokora, Brigitte; Scott, Rodney J.; Sijmons, Rolf; Tavtigian, Sean V.; Tops, Carli M.; Weber, Thomas; Wijnen, Juul; Woods, Michael O.; Macrae, Finlay; Genuardi, Maurizio; InSiGHT |
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