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Issue DateTitleAuthor(s)
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
1-Jul-2020Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like IndividualsDámaso, Estela; González Acosta, María Isabel; Vargas Parra, Gardenía María; Navarro, Matilde; Balmaña, Judith; Ramon y Cajal, Teresa; Tuset, Noemí; Thompson, Bryony A.; Marín, Fátima; Fernández, Anna; Gomez, Carolina; Velasco, Àngela; Solanes, Ares; Iglesias Casals, Sílvia; Urgel, Gisela; López, Consol; Valle, Jesús del; Campos, Olga; Santacana, Maria; Matias-Guiu, Xavier; Lázaro García, Conxi; Valle, Laura; Brunet, Joan; Pineda Riu, Marta; Capellá, G. (Gabriel)
Jul-2020Germline Mutations in FAF1 Are Associated With Hereditary Colorectal CancerBonjoch Gassol, Laia; Franch Expósito, Sebastià; Garre, Pilar; Belhadj, Sami; Muñoz, Jenifer; Arnau Collell, Coral; Díaz Gay, Marcos; Gratacós Mulleras, Anna; Raimondi, Giulia; Esteban Jurado, Clara; Soares de Lima, Yasmin; Herrera Pariente, Cristina; Cuatrecasas Freixas, Miriam; Ocaña, Teresa; Castells Garangou, Antoni; Fillat i Fonts, Cristina; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Caldés, Trinidad; Valle Velasco, Laura; Castellví Bel, Sergi
16-Jul-2020High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriersGonzález Acosta, María Isabel; Marín, Fátima; Puliafito, Benjamin; Bonifaci Cano, Núria; Fernández, Anna; Navarro, Matilde; Salvador, Hector; Balaguer Prunés, Francesc; Iglesias, Silvia; Velasco, Àngela; Grau Garcés, Èlia; Moreno Aguado, Víctor; González Granado, Luis Ignacio; Guerra García, Pilar; Ayala, Rosa; Florkin, Benoît; Kratz, Christian; Ripperger, Tim; Rosenbaum, Thorsten; Januszkiewicz-Lewandowska, Danuta; Azizi, Amedeo A.; Ragab, Iman; Nathrath, Michaela; Pander, Hans-Jürgen; Lobitz, Stephan; Suerink, Manon; Dahan, Karin; Imschweiler, thomas; Demirsoy, Ugur; Brunet, Joan; Lázaro García, Conxi; Rueda, Daniel; Wimmer, Katharina; Capellá, G. (Gabriel); Pineda, Marta
1-Jun-2020Dominantly inherited hereditary nonpolyposis colorectal cancer not caused by MMR genesTerradas, Mariona; Capellá, G. (Gabriel); Valle, Laura
1-Dec-2020Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.Dominguez Valentin, Mev; Crosbie, Emma J.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capellá, G. (Gabriel); Thomas, Huw; Nakken, Sigve; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauß, Hans Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda Riu, Marta; Navarro, Matilde; Brunet, Joan; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; González, María Laura; Kalfayan, Pablo; Ryan, Neil A. J.; Ten Broeke, Sanne W.; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Della Valle, Adriana; Lopez Kostner, Francisco; Alvarez Valenzuela, Karin; Büttner, Reinhard; Görgens, Heike; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Auranen, Annika; Hopper, John L.; Ko Win, Aung; Haile, Robert W.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Okkels, Henrik; Ketabi, Zohreh; Denton, Oliver G.; Rødland, Einar A.; Vasen, Hans; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Sampson, Julian R.; Evans, D. Gareth; Seppälä, Toni T.; Møller, Pål
13-Mar-2020Colorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibilityArnau Collell, Coral; Soares de Lima, Yasmin; Díaz Gay, Marcos; Muñoz, Jenifer; Carballal, Sabela; Bonjoch Gassol, Laia; Moreira, Leticia; Lozano Salvatella, Juan José; Ocaña, Teresa; Cuatrecasas Freixas, Miriam; Díaz de Bustamante, Aranzazu; Castells Garangou, Antoni; Capellá, G. (Gabriel); Bujanda, Luis; Cubiella, Joaquín; Rodríguez Alcalde, Daniel; Balaguer Prunés, Francesc; Ruiz Ponte, Clara; Valle, Laura; Moreno Aguado, Víctor; Castellví Bel, Sergi
14-Aug-2020Role of POLE and POLD1 in familial cancerMur, Pilar; García Mulero, Sandra; Valle, Jesús del; Magraner Pardo, Lorena; Vidal-Bel, August; Pineda Riu, Marta; Cinnirella, Giacomo; Martín Ramos, Edgar; Pons, Tirso; López Dóriga Guerra, Adriana; Belhadj, Sami; Feliubadaló i Elorza, Maria Lídia; Muñoz Torres, Pau M.; Navarro, Matilde; Grau Garcés, Èlia; Darder, Esther; Llort, Gemma; Sanz, Judit; Ramón y Cajal, Teresa; Balmaña, Judith; Brunet, Joan; Moreno Aguado, Víctor; Piulats, Josep M.; Matias-Guiu, Xavier; Sanz Pamplona, Rebeca; Aligué i Alemany, Rosa Maria; Capellá, G. (Gabriel); Lázaro García, Conxi; Valle, Laura