Browsing by Author Capellá, G. (Gabriel)

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Issue DateTitleAuthor(s)
31-May-2021A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variantsUnhjem Wiik, Mariann; Evans, Tiffany Jane; Belhadj, Sami; Bolton, Katherine A.; Dymerska, Dagmara; Jagmohan Changur, Shantie; Capellá, G. (Gabriel); Kurzawski, Grzegorz; Wijnen, Juul T.; Valle, Laura; Vasen, Hans; Lubinski, Jan; Scott, Rodney J.; Talseth-Palmer, Bente A.
7-Dec-2010A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variantsTheodoratou, Evropi; Campbell, Harry; Tenesa, Albert; Houlston, Richard S.; Webb Youdale, Susan; Lubbe, Steven; Broderick, Peter; Gallinger, Steven; Croitoru, Marina E.; Jenkins, Mark A.; Win, Aung K.; Cleary, Sean; Koessler, Thibaud; Pharoah, Paul D. P.; Küry, Sébastien; Bézieau, Stéphane; Buecher, Bruno; Ellis, Nathan A.; Peterlongo, Paolo; Offit, Kenneth; Aaltonen, Lauri A.; Enholm, Susa; Lindblom, Annika; Zhou, X.L.; Tomlinson, Ian P.; Moreno Aguado, Víctor; Blanco Guillermo, Ignacio; Capellá, G. (Gabriel); Barnetson, Rebecca; Porteous, Mary E.; Dunlop, Malcolm; Farrington, Susan M.
Jul-2011A mild neurofibromatosis type 1 phenotype produced by the combination of the benign nature of a leaky NF1-splice mutation and the presence of a complex mosaicismFernández-Rodríguez, Juana; Castellsagué, Joan; Benito-Aracil, Llúcia; Benavente, Yolanda; Capellá, G. (Gabriel); Blanco Guillermo, Ignacio; Serra Arenas, Eduard; Lázaro García, Conxi
29-Apr-2010Allele-Specific Expression of APC in Adenomatous Polyposis FamiliesCastellsagué Torrents, Ester; González, Sara; Guinó, Elisabet; Stevens, Kristen N.; Borràs, Ester; Raymond, Victoria M.; Lázaro García, Conxi; Blanco Guillermo, Ignacio; Gruber, Stephen B.; Capellá, G. (Gabriel)
29-Jun-2022An Integrated Approach for the Early Detection of Endometrial and Ovarian Cancers (Screenwide Study): Rationale, Study Design and Pilot StudyPeremiquel-Trillas, Paula; Paytubi Casabona, Sònia; Pelegrina, Beatriz; Frias Gomez, Jon; Carmona, Álvaro; Martínez Delgado, José Manuel; Francisco, Javier de; Benavente, Yolanda; Barahona, Marc; Briansó, Ferran; Canet Hermida, Júlia; Caño, Víctor; Vidal, Augusto, 1909-1976; Zanca, Alba; Baixeras, Núria; Rodríguez, Axel; Fernández Gonzalez, Sergi; Dueñas, Nuria; Càrdenas, Laura; Aytés Meneses, Álvaro; Bianchi, Ilaria; Pavón, Miquel Àngel; Reventós, Jaume; Capellá, G. (Gabriel); Gómez, David, 1968-; Diaz, Mireia; Ponce, Jordi; Brunet, Joan; Matias-Guiu, Xavier; Bosch Font, Francesc; Sanjosé, Silvia de; Alemany, Laia; Pineda, Marta; Marin, Fátima; Costas, Laura
11-Mar-2012Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer familiesFernández-Rodríguez, Juana; Quiles Vidal, Francisco de Asís; Blanco Guillermo, Ignacio; Teulé-Vega, Àlex; Feliubadaló i Elorza, Maria Lídia; Valle Domínguez, Jesús del; Salinas Masdeu, Mònica; Izquierdo i Font, Àngel Xavier; Darder, Esther; Schindler, Detlev; Capellá, G. (Gabriel); Brunet, Joan; Lázaro García, Conxi; Pujana Genestar, M. Ángel
18-Dec-2015Anàlisis [sic] de variants en els gens APC i UNC5C associats a càncer colorectalSánchez Cuartielles, Elena
Mar-2008Antiangiogenic effect of gemcitabine following metronomic administration in a pancreas cancer modelLaquente, Berta; Lacasa Salavert, Cristina; Ginestà, Mireia M.; Casanovas i Casanovas, Oriol; Figueras i Amat, Agnès; Galán, Maica; García Ribas, Ignacio; Germà Lluch, José Ramón; Capellá, G. (Gabriel); Viñals Canals, Francesc
20-Dec-2013Application of a 5-tiered scheme for standardized classification of 2,360 Unique mismatch repair gene variants in the InSiGHT locus-specific databaseThompson, 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
1-Oct-2019Approaches to functionally validate candidate genetic variants involved in colorectal cancer predispositionBonjoch 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
1-Aug-2019Are women with pathogenic variants in PMS2 and MSH6 really at high lifetime risk of breast cancer?Evans, D. Gareth; Woodward, E. R.; Lalloo, Fiona; Møller, Pål; Sampson, J.; Burn, John; Moeslein, Gabriela; Capellá, G. (Gabriel)
18-Nov-2020Assessing effectiveness of colonic and gynecological risk reducing surgery in lynch syndrome individualsDueñas, Nuria; Navarro, Matilde; Teulé-Vega, Àlex; Solanes, Ares; Salinas Masdeu, Mònica; Iglesias Casals, Sílvia; Munté, Elisabet; Ponce i Sebastià, Jordi; Guardiola, Jordi; Kreisler, Esther; Carballas, Elvira; Cuadrado, Marta; Matias-Guiu, Xavier; Ossa, Napoleón de la; Lop, Joan; Lázaro García, Conxi; Capellá, G. (Gabriel); Pineda Riu, Marta; Brunet, Joan
29-Jun-2005Avaluació de la utilitat com a marcadors pronòstics en càncer colorectal de P53, P21, P27 i ciclina EVilardell Villellas, Felip
23-Jan-2021BARD1 Pathogenic Variants are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer CohortRofes, Paula; Valle, Jesús del; Torres Esquius, Sara; Feliubadaló i Elorza, Maria Lídia; Stradella, Agostina; Moreno Cabrera, José Marcos; López Dóriga Guerra, Adriana; Munté, Elisabet; Cid, Rafael de; Campos, Olga; Cuesta, Raquel; Teulé-Vega, Àlex; Grau Garcés, Èlia; Sanz, Judit; Capellá, G. (Gabriel); Díez Gibert, Orland; Brunet, Joan; Balmaña, Judith; Lázaro García, Conxi
4-Jan-2017Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary CancerFeliubadaló i Elorza, Maria Lídia; Tonda, Raul; Gausachs Romero, Mireia; Trotta, Jean Rémi; Castellanos, Elisabeth; López Dóriga Guerra, Adriana; Teulé-Vega, Àlex; Tornero, Eva; Valle Domínguez, Jesús del; Gel, Bernat; Gut, Marta; Pineda Riu, Marta; González, Sara; Menéndez Vilà, Mireia; Navarro, Matilde; Capellá, G. (Gabriel); Gut, Ivo G.; Serra Arenas, Eduard; Brunet, Joan; Beltran i Agulló, Sergi; Lázaro García, Conxi
20-Feb-2009Biological convergence of cancer signaturesSolé Acha, Xavier; Bonifaci Cano, Núria; López Bigas, Núria; Berenguer, Antoni; Hernández, Pilar; Reina, Oscar; Maxwell, Christopher A.; Aguilar, Helena; Urruticoechea Ribate, Ander; Sanjosé Llongueras, Silvia de; Comellas, Francesc; Capellá, G. (Gabriel); Moreno Aguado, Víctor; Pujana Genestar, M. Ángel
30-May-2014Biomarcadors en càncer colorectal hereditari: aplicacions clíniques i estudi de la dinàmica tumoralGausachs Romero, Mireia
28-Jul-2017Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome DatabaseMøller, Pål; Seppälä, Toni T.; Bernstein, Inge; Holinski Feder, Elke; Sala, Paulo; Gareth Evans, D.; Lindblom, Annika; Macrae, Finlay; Blanco Guillermo, Ignacio; Sijmons, Rolf H.; Jeffries, Jacqueline; Vasen, Hans; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; de Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul T.; Jenkins, Mark A.; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro García, Matilde; Morak, Monika; Renkonen Sinisalo, Laura; Dominguez Valentin, Mev; Frayling, Ian M.; Plazzer, John Paul; Pylvanainen, Kirsi; Genuardi, Maurizio; Mecklin, Jukka-Pekka; Moeslein, Gabriela; Sampson, Julian R.; Capellá, G. (Gabriel); Mallorca Group
1-Jan-2020Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseDominguez Valentin, Mev; Sampson, Julian R.; Seppälä, Toni T.; ten Broeke, Sanne W.; Plazzer, John Paul; Nakken, Sigve; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Thomas, Huw; Evans, D. Gareth; Burn, John; Greenblatt, Marc; Hovig, Eivind; de Vos Tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Bertario, Lucio; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Della Valle, Adriana; Lopez Kostner, Francisco; Gluck, Nathan; Katz, Lior H.; Heinimann, Karl; Vaccaro, Carlos A.; Buettner, Reinhard; Goergens, Heike; Holinski Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hueneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Schackert, Hans K.
13-Sep-2016Carcinoma-associated fibroblasts affect sensitivity to oxaliplatin and 5FU in colorectal cancer cellsGonçalves-Ribeiro, Samuel; Guillén Díaz-Maroto, Natalia; Berdiel Acer, Mireia; Soriano Izquierdo, Antonio; Guardiola, Jordi; Martínez Villacampa, Mercedes; Salazar Soler, Ramón; Capellá, G. (Gabriel); Villanueva Garatachea, Alberto; Martínez Balibrea, Eva; Molleví, David G.