Browsing by Author Navarro, Matilde

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Issue DateTitleAuthor(s)
4-Jan-2017A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscapeCastellanos, Elisabeth; Gel, Bernat; Rosas, Inma; Tornero, Eva; Santín, Sheila; Pluvinet Ortega, Raquel; Velasco, Juan; Sumoy, Lauro; Valle Domínguez, Jesús del; Perucho, Manuel; Blanco Guillermo, Ignacio; Navarro, Matilde; Brunet, Joan; Pineda Riu, Marta; Feliubadaló i Elorza, Maria Lídia; Capellá, G. (Gabriel); Lázaro García, Conxi; Serra Arenas, Eduard
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
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
10-Oct-2017Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a prospective lynch syndrome databaseSeppälä, Toni; Pylvänäinen, Kirsi; Evans, D. Gareth; Järvinen, Heikki; Renkonen-Sinisalo, Laura; Bernstein, Inge; Holinski-Feder, Elke; Sala, Paola; Lindblom, Annika; Macrae, Finlay; Blanco, Inlay; Sijmons, Rolf; Jeffries, Jacqueline; Vasen, Hans F. A.; Burn, John; Nakken, Sigve; Hovig, Eivind; Rødland, Einar Andreas; Tharmaratnam, Kukatharmini; De Vos Tot Nederveen Cappel, Wouter H.; Hill, James; Wijnen, Juul; Jenkins, Mark A.; Genuardi, Maurizio; Green, Kate; Lalloo, Fiona; Sunde, Lone; Mints, Miriam; Bertario, Lucio; Pineda Riu, Marta; Navarro, Matilde; Morak, Monika; Frayling, Ian M.; Plazzer, John-Paul; Sampson, Julian R.; Capellá, G. (Gabriel); Möslein, Gabriela; Mecklin, Jukka-Pekka; Møller, Pål; Mallorca Group
10-Jul-2009Colorectal cancer screening: strategies to select populations with moderate risk for diseaseNavarro, Matilde; Binefa i Rodríguez, Gemma; Peris, Mercè; Blanco Guillermo, Ignacio; Guardiola, Jordi; Espinàs Piñol, Josep Alfons; Borràs Andrés, Josep Maria; Catalan Colorectal Cancer Screening Pilot Program Group
29-Sep-2020Complete Loss of EPCAM Immunoexpression Identifies EPCAM Deletion Carriers in MSH2-Negative Colorectal NeoplasiaCuatrecasas Freixas, Miriam; Gorostiaga, Iñigo; Riera, Cristina; Saperas, Esteban; Llort, Gemma; Costa, Irmgard; Matias-Guiu, Xavier; Carrato, Cristina; Navarro, Matilde; Pineda Riu, Marta; Dueñas, Núria; Brunet, Joan; Marco, Vicente; Trias, Isabel; Busteros, José Ignacio; Mateu, Gemma; Balaguer Prunés, Francesc; Fernández Figueras, María Teresa; Esteller, Manel; Musulén, Eva
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)
22-Dec-2018Does multilocus inherited neoplasia alleles syndrome have severe clinical expression?Stradella, Agostina; Valle, Jesús del; Rofes, Paula; Feliubadaló i Elorza, Maria Lídia; Grau Garcés, Èlia; Velasco, Àngela; González, Sara; Vargas Parra, Gardenía María; Izquierdo, Ángel; Campos, Olga; Tornero, Eva; Navarro, Matilde; Balmaña, Judith; Capellá, G. (Gabriel); Pineda Riu, Marta; Brunet, Joan; Lázaro García, Conxi
15-Feb-2018Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposisMur, 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
10-Apr-2019Germline variation in O6-methylguanine-DNA methyltransferase (MGMT) as cause of hereditary colorectal cancerBelhadj, Sami; Moutinho, Cátia; Mur, Pilar; Llinàs-Arias, Pere; Pérez Salvia, Montserrat; Pons, Tirso; Pineda Riu, Marta; Brunet, Joan; Navarro, Matilde; Esteller, Manel; Valle Velasco, Laura
1-Jun-2008Hallazgos colonoscópicos del estudio piloto de cribado de cáncer colorrectal realizado en CataluñaNavarro, Matilde; Peris, Mercè; Binefa i Rodríguez, Gemma; Nogueira, José Miguel; Miquel Collell, Josep M.; Espinàs Piñol, Josep Alfons; Borràs Andrés, Josep Maria
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, Maribel; Marín, Fátima; Puliafito, Benjamin; Bonifaci Cano, Núria; Fernández, Anna; Navarro, Matilde; Salvador, Hector; Balaguer Prunés, Francesc; Iglesias, Silvia; Velasco, Àngela; Grau Garces, Elia; 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-Sep-2019Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classificationParsons, Michael T.; Tudini, Emma; Li, Hongyan; Hahnen, Eric; Wappenschmidt, Barbara; Feliubadaló i Elorza, Maria Lídia; Aalfs, Cora M.; Agata, Simona; Aittomäki, Kristiina; Alducci, Elisa; Alonso Cerezo, María Concepción; Cops, Elisa J.; Cortesi, Laura; Couch, Fergus J.; Darder, Esther; Hoya, Miguel; Montagna, Marco; Toss, Angela; Dean, Michael; Debatin, Irmgard; Harris, Marion; Salinas, Monica; Rhiem, Kerstin; Marabelli, Monica; Del Valle, Jesús; Lalloo, Fiona; Pfeifer, Katharina; Delnatte, Capucine; Toland, Amanda E.; Viel, Alessandra; Derive, Nicolas; Diez, Orland; Sánchez de Abajo, Ana María; Monteiro, Alvaro N.; Ditsch, Nina; Maass, Nicolai; Riboli, Barbara; Domchek, Susan M.; Varon, Raymonda; Dutrannoy, Véronique; Eccles, Diana M.; Ehrencrona, Hans; Trainer, Alison H.; Schmidt, Gunnar; Enders, Ute; Walker, Logan C.; Pineda Riu, Marta; Evans, D. Gareth; Larsen, Mirjam; Gerdes, Anne Marie; Ritter, Julia; Farra, Chantal; Manoukian, Siranoush; Tornero, Eva; Schoenwiese, Ulrike; Germani, Aldo; Montalban, Gemma; Vega, Ana; Lautrup, Charlotte; Quante, Anne S.; Hauke, Jan; Heinrich, Tilman; Törngren, Therese; Hellebrand, Heide; Arnold, Norbert; Seggewiß, Jochen; Caldés, Trinidad; Herold, Karen N.; Honisch, Ellen; Walters, Rhiannon J.; Rump, Andreas; Horvath, Judit; Poplawski, Nicola K.; Velasco, Àngela; Houdayer, Claude; Brunet, Joan; Cini, Giulia; Hübbel, Verena; Iglesias, Silvia; Izquierdo, Angel; Barbieri, Elena; Wang Gohrke, Shan; James, Paul A.; Carnevali, Ileana; Torres Esquius, Sara; Janssen, Linda A.M.; Jeschke, Udo; Kruse, Torben A.; Ledig, Susanne; Vesper, Anne Sophie; Kaulfuß, Silke; Porfirio, Berardino; Auber, Bernd; Weber, Bernhard H. F.; Leinert, Elena; Rofes, Paula; Bruzzone, Carla; Matricardi, Laura; Solanes, Ares; Mackelenbergh, Marion T.; Montes, Eva; Mori, Luigi; Austin, Rachel; Moserle, Lidia; Müller, Clemens R.; Weichert, Wilko; Foulkes, William D.; Mundhenke, Christoph; Naldi, Nadia; Steinemann, Doris; Carrasco, Estela; Waha, Anke; Nathanson, Katherine L.; Tucker, Katherine M.; Bucksch, Karolin; Navarro, Matilde; Faust, Ulrike; González, Sara; Nevanlinna, Heli; Nichols, Cassandra B.; Wiesmüller, Lisa; Niederacher, Dieter; Vreeswijk, Maaike P. G.; Caux Moncoutier, Virginie; Nielsen, Henriette R.; Giesecke, Jutta; Azzollini, Jacopo; Ong, Kai Ren; Pachter, Nicholas; Galvao, Henrique C.R.; Palmero, Edenir I.; Guerrieri Gonzaga, Aliana; Cagnoli, Giulia; Papi, Laura; Asperen, Christi J.; Ramser, Juliane; Cavalli, Pietro; Pedersen, Inge Søkilde; Wagner, Sebastian A.; Felbor, Ute; Reis, Rui M.; Wieland, Kerstin; Gismondi, Viviana; Blümcke, Britta; Calvello, Mariarosaria; Stiller, Mathias; Bartram, Claus R.; Feroce, Irene; Stoppa Lyonnet, Dominique; Keupp, Katharina; Lucci Cordisco, Emanuela; Sullivan, Kelly J.; Susman, Rachel; Guillaud Bataille, Marine; Concolino, Paola; Sutter, Christian; Caliebe, Almuth; Gómez, Carolina; Tavtigian, Sean V.; Lewis, Alexandra L.; Teo, Soo H.; Teulé, Alex; Thomassen, Mads; Kvist, Anders; Gutiérrez Enríquez, Sara; Tibiletti, Maria Grazia; Meindl, Alfons; Fine, Miriam; Tischkowitz, Marc; Blanco, Ana; Varesco, Liliana; Garcia, Encarna B.; Tognazzo, Silvia; Caligo, Maria A.; Kiechle, Marion; Haaf, Thomas; Vargas Parra, Gardenia; Clarke, Edward M.; Lim, Joanna; Bonache, Sandra; Gensini, Francesca; Witzel, Isabell; Wöckel, Achim; Kölbl, Alexandra; Woodward, Emma R.; Bonanni, Bernardo; Hackmann, Karl; Pohl Rescigno, Esther; Zachariae, Silke; Zampiga, Valentina; Michelli, Rodrigo D.; Gross, Eva; Zeder Göß, Christine; Gambino, Gaetana; Loeffler, Markus; Investigators, Kconfab; Peissel, Bernard; Rivera, Daniela; Lázaro García, Conxi; Nicolo, Arcangela; Radice, Paolo; Grau Garcés, Èlia; Moghadasi, Setareh; Engel, Christoph; Revillion, Françoise; Krieger, Sophie; Schmutzler, Rita K.; Goldgar, David E.; Balmaña, Judith; Borg, Åke; López Fernández, Adrià; Spurdle, Amanda B.; Gehrig, Andrea; Capone, Gabriele L.; Moles Fernández, Alejandro; Bortesi, Beatrice; Grill, Sabine; Pérez Segura, Pedro; Caputo, Sandrine M.; Hansen, Thomas V.O.; Lattimore, Vanessa L.
3-Feb-2014Longer telomeres are associated with cancer risk in MMR-proficient hereditary non-polyposis colorectal cancerSeguí 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
28-Jun-2021No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database StudyDominguez Valentin, Mev; Plazzer, John Paul; Sampson, Julian R.; Engel, Christoph; Aretz, Stefan; Jenkins, Mark A.; Sunde, Lone; Bernstein, Inge; Capellá, G. (Gabriel); Balaguer Prunés, Francesc; Macrae, Finlay; Winship, Ingrid M.; Thomas, Huw; Evans, Dafydd Gareth; Burn, John; Greenblatt, Marc; de Vos Tot Nederveen Cappel, Wouter H.; Sijmons, Rolf H.; Nielsen, Maartje; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria Grazia; Cavestro, Giulia Martina; Lindblom, Annika; Valle, Adriana Della; Lopez Kostner, Francisco; Alvarez, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans F. A.; Perne, Claudia; Büttner, Reinhard; Görgens, Heike; Holinski Feder, Elke; Morak, Monika; Holzapfel, Stefanie; Hüneburg, Robert; von Knebel Doeberitz, Magnus; Loeffler, Markus; Rahner, Nils; Weitz, Jürgen; Steinke Lange, Verena; Schmiegel, Wolff; Vangala, Deepak; Crosbie, Emma J.; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Moreira, Leticia; Sánchez, Ariadna; Serra Burriel, Miquel; Mints, Miriam; Kariv, Revital; Rosner, Guy; Piñero, Tamara Alejandra; Pavicic, Walter Hernán; Kalfayan, Pablo; ten Broeke, Sanne W.; Mecklin, Jukka-Pekka; Pylvänäinen, Kirsi; Renkonen Sinisalo, Laura; Lepistö, Anna; Peltomäki, Päivi; Hopper, John L.; Ko Win, Aung; Buchanan, Daniel D.; Lindor, Noralane M.; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A.; Figueiredo, Jane C.; Thibodeau, Stephen N.; Therkildsen, Christina; Hansen, Thomas V. O.; Lindberg, Lars; Rødland, Einar Andreas; Neffa, Florencia; Esperon, Patricia; Tjandra, Douglas; Möslein, Gabriela; Seppälä, Toni T.; Møller, Pål
21-Jun-2019NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomasBelhadj, Sami; Quintana, Isabel; Mur, Pilar; Munoz-Torres, Pau M.; Alonso Aguado, Maria Henar; Navarro, Matilde; Terradas, Mariona; Pinol, Virginia; Brunet, Joan; Moreno Aguado, Víctor; Lázaro García, Conxi; Capellá, G. (Gabriel); Valle Velasco, Laura
Nov-2004Organochlorine exposure and colorectal cancer riskHowsam, Mike; Grimalt, Joan O.; Guinó, Elisabet; Navarro, Matilde; Martí Ragué, Joan; Peinado Morales, Miguel Á. (Miguel Ángel); Capellá, G. (Gabriel); Moreno Aguado, Víctor; Bellvitge Colorectal Cancer Group
17-Jan-2012Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriersLázaro García, Conxi; Blanco Guillermo, Ignacio; Tornero, Eva; Navarro, Matilde; CIMBA Consortium
3-Jun-2004Oxaliplatin, Fluorouracil, and Leucovorin as Adjuvant Treatment for Colon CancerAndré, Thierry; Boni, Corrado; Mounedji-Boudiaf, Lamia; Navarro, Matilde; Tabernero Caturla, Josep; Hickish, Tamas; Topham, Clare; Zaninelli, Marta; Clingan, Philip; Bridgewater, John; Tabah-Fisch, Isabelle; Gramont, Aimery de; Adjuvant Treatment of Colon Cancer (MOSAIC) Investigators
19-Jul-2004Polymorphisms in prostaglandin synthase 2/cyclooxygenase 2 (PTGS2/COX2) and risk of colorectal cancerCox, David G.; Pontes García, Caridad; Guinó, Elisabet; Navarro, Matilde; Osorio, Ana; Canzian, Federico; Moreno Aguado, Víctor; Bellvitge Colorectal Cancer Study Group