Browsing by Author Navarro, Matilde
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| Issue Date | Title | Author(s) |
|---|---|---|
| 4-Jan-2017 | A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape | Castellanos, 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-2020 | Assessing effectiveness of colonic and gynecological risk reducing surgery in lynch syndrome individuals | Dueñas, 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-2017 | Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer | Feliubadaló 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-2017 | Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a prospective lynch syndrome database | Seppälä, Toni T.; 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; 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-2009 | Colorectal cancer screening: strategies to select populations with moderate risk for disease | Navarro, 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-2020 | Complete Loss of EPCAM Immunoexpression Identifies EPCAM Deletion Carriers in MSH2-Negative Colorectal Neoplasia | Cuatrecasas Freixas, Miriam; Gorostiaga, Iñigo; Riera, Cristina; Saperas, Esteban; Llort, Gemma; Costa, Irmgard; Matias-Guiu, Xavier; Carrato, Cristina; Navarro, Matilde; Pineda Riu, Marta; Dueñas, Nuria; Brunet, Joan; Marco, Vicente; Trias, Isabel; Busteros, José Ignacio; Mateu, Gemma; Balaguer Prunés, Francesc; Fernández Figueras, María Teresa; Esteller, Manel; Musulén, Eva |
| 1-Jul-2020 | Comprehensive Constitutional Genetic and Epigenetic Characterization of Lynch-Like Individuals | Dámaso, 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-Jun-2021 | Correction: Dueñas et al. Assessing effectiveness of colonic and gynecological risk reducing surgery in Lynch syndrome individuals. Cancers 2020, 12, 3419. | Dueñas, 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 |
| 22-Dec-2018 | Does 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-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 |
| 10-Apr-2019 | Germline variation in O6-methylguanine-DNA methyltransferase (MGMT) as cause of hereditary colorectal cancer | Belhadj, 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-2008 | Hallazgos colonoscópicos del estudio piloto de cribado de cáncer colorrectal realizado en Cataluña | Navarro, Matilde; Peris, Mercè; Binefa i Rodríguez, Gemma; Nogueira, José Miguel; Miquel Collell, Josep M.; Espinàs Piñol, Josep Alfons; Borràs Andrés, Josep Maria |
| 16-Jul-2020 | High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers | González 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 |
| 28-Feb-2019 | Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report | Seppälä, Toni T.; Ahadova, Aysel; Dominguez Valentin, Mev; Macrae, Finlay; Evans, D. Gareth; Therkildsen, Christina; Sampson, Julian R.; Scott, RodneyJ.; Burn, John; Moslein, Gabriela; Bernstein, Inge; Holinski-Feder, Elke; Pylvanainen, Kirsi; Renkonen Sinisalo; Lepisto, Anna; Lautrup, Charlotte K.; Lindblom, Annika; Plazzer, John Paul; Winship, Ingrid; Tjandra, Douglas; Katz, Lior; Aretz, Stefan; Hüneburg, Robert; Holzapfel, Stefanie; Heinimann, Karl; Della Valle, Adriana; Neffa, Florencia; Gluck, Nathan; De Vos Tot Nederveen Cappel, Wouter H. WH.; Vasen, Hans; Morak, Monika; Steinke-Lange, Verena; Engel, Christoph; Rahner, Nils; Schmiegel, Wolff; Vangala, Deepak; Thomas, Huw; Green, Kate; Lalloo, Fiona; Crosbie, Emma J.; Hill, James; Capellá, G. (Gabriel); Pineda Riu, Marta; Navarro, Matilde; Blanco Guillermo, Ignacio; ten Broeke, Sanne W.; Nielsen, Maartje; Ljungmann, Ken; Nakken, Sigve; Lindor, Noralane; Frayling, Ian M.; Hovig, Eivind; Sunde, Lone; Kloor, Matthias; Mecklin, Jukka-Pekka; Kalager, Mette; Møller, Pål |
| 1-Sep-2019 | Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification | Parsons, 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; Hauke, Jan; Heinrich, Tilman; Törngren, Therese; Hellebrand, Heide; Arnold, Norbert; Seggewiß, Jochen; Caldés, Trinidad; Herold, Karen N.; Honisch, Ellen; Naldi, Nadia; Witzel, Isabell; Walters, Rhiannon J.; Rump, Andreas; Horvath, Judit; Poplawski, Nicola K.; Velasco, Àngela; Houdayer, Claude; Brunet, Joan; Cini, Giulia; Hübbel, Verena; Iglesias, Silvia; Wöckel, Achim; Steinemann, Doris; Izquierdo, Angel; Barbieri, Elena; Wang Gohrke, Shan; James, Paul A.; Carnevali, Ileana; Torres Esquius, Sara; Janssen, Linda A.M.; Jeschke, Udo; Kruse, Torben A.; Kölbl, Alexandra; Ledig, Susanne; Cops, Elisa J.; Vesper, Anne Sophie; Kaulfuß, Silke; Porfirio, Berardino; Auber, Bernd; Weber, Bernhard H. F.; Leinert, Elena; Rofes, Paula; Bruzzone, Carla; Woodward, Emma R.; Matricardi, Laura; Solanes, Ares; Carrasco, Estela; Mackelenbergh, Marion T.; Waha, Anke; Nathanson, Katherine L.; Tucker, Katherine M.; Bucksch, Karolin; Navarro, Matilde; Faust, Ulrike; Bonanni, Bernardo; González, Sara; Nevanlinna, Heli; Nichols, Cassandra B.; Cortesi, Laura; Wiesmüller, Lisa; Niederacher, Dieter; Vreeswijk, Maaike P. G.; Caux Moncoutier, Virginie; Nielsen, Henriette R.; Giesecke, Jutta; Hackmann, Karl; Azzollini, Jacopo; Ong, Kai Ren; Pachter, Nicholas; Galvao, Henrique C.R.; Couch, Fergus J.; Palmero, Edenir I.; Guerrieri Gonzaga, Aliana; Cagnoli, Giulia; Papi, Laura; Asperen, Christi J.; Pohl Rescigno, Esther; Ramser, Juliane; Cavalli, Pietro; Pedersen, Inge Søkilde; Wagner, Sebastian A.; Felbor, Ute; Darder, Esther; Reis, Rui M.; Wieland, Kerstin; Gismondi, Viviana; Blümcke, Britta; Zachariae, Silke; Calvello, Mariarosaria; Stiller, Mathias; Bartram, Claus R.; Feroce, Irene; Stoppa Lyonnet, Dominique; Keupp, Katharina; Hoya, Miguel; Lucci Cordisco, Emanuela; Sullivan, Kelly J.; Susman, Rachel; Zampiga, Valentina; Guillaud Bataille, Marine; Concolino, Paola; Sutter, Christian; Caliebe, Almuth; Gómez, Carolina; Tavtigian, Sean V.; Lewis, Alexandra L.; Montagna, Marco; Teo, Soo H.; Teulé, Alex; Debatin, Irmgard; Thomassen, Mads; Kvist, Anders; Gutiérrez Enríquez, Sara; Tibiletti, Maria Grazia; Meindl, Alfons; Fine, Miriam; Tischkowitz, Marc; Blanco, Ana; Toss, Angela; Varesco, Liliana; Montes, Eva; Garcia, Encarna B.; Tognazzo, Silvia; Caligo, Maria A.; Kiechle, Marion; Haaf, Thomas; Vargas Parra, Gardenía María; Clarke, Edward M.; Lim, Joanna; Bonache, Sandra; Dean, Michael; Michelli, Rodrigo D.; Gensini, Francesca; Gross, Eva; Zeder Göß, Christine; Gambino, Gaetana; Loeffler, Markus; Investigators, Kconfab; Peissel, Bernard; Rivera, Daniela; Lázaro García, Conxi; Nicolo, Arcangela; Mori, Luigi; Harris, Marion; Radice, Paolo; Grau Garcés, Èlia; Moghadasi, Setareh; Engel, Christoph; Revillion, Françoise; Krieger, Sophie; Schmutzler, Rita K.; Goldgar, David E.; Balmaña, Judith; Austin, Rachel; Borg, Åke; Salinas, Monica; López Fernández, Adrià; Spurdle, Amanda B.; Gehrig, Andrea; Capone, Gabriele L.; Moles Fernández, Alejandro; Bortesi, Beatrice; Grill, Sabine; Pérez Segura, Pedro; Moserle, Lidia; Caputo, Sandrine M.; Hansen, Thomas V.O.; Rhiem, Kerstin; Lattimore, Vanessa L.; Marabelli, Monica; Del Valle, Jesús; Lalloo, Fiona; Pfeifer, Katharina; Delnatte, Capucine; Toland, Amanda E.; Müller, Clemens R.; Viel, Alessandra; Derive, Nicolas; Diez, Orland; Sánchez de Abajo, Ana María; Monteiro, Alvaro N.; Ditsch, Nina; Maass, Nicolai; Riboli, Barbara; Domchek, Susan M.; Varon-Mateeva, Raymonda; Weichert, Wilko; Dutrannoy, Véronique; Eccles, Diana; Ehrencrona, Hans; Trainer, Alison H.; Schmidt, Gunnar; Enders, Ute; Walker, Logan C.; Pineda Riu, Marta; Evans, D. Gareth; Larsen, Mirjam; Foulkes, William D.; Gerdes, Anne Marie; Ritter, Julia; Farra, Chantal; Manoukian, Siranoush; Tornero, Eva; Schoenwiese, Ulrike; Germani, Aldo; Montalban, Gemma; Vega, Ana; Lautrup, Charlotte; Mundhenke, Christoph; Quante, Anne S. |
| 1-Nov-2022 | Lessons learnt from the implementation of a colorectal cancer screening programme for lynch syndrome in a tertiary public hospital. | Dueñas, Nuria; Navarro, Matilde; Sanjuán, Xavier; Ruiz, Núria; Iglesias, Silvia; Matias Guiu, Xavier; Guardiola, Jordi; Kreisler, Esther; Biondo, Sebastiano; González, Sara; Legido, Raquel; Blanco, Ana; Navarro, Silvia; Asiain, Leyre; Santos, Cristina; Capellá, G. (Gabriel); Pineda, Marta; Brunet, Joan |
| 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 |
| 28-Jun-2021 | No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study | Dominguez 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, D. 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 Valenzuela, Karin; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Nakken, Sigve; Hovig, Eivind; Green, Kate; Lalloo, Fiona; Hill, James; Vasen, Hans; 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-2019 | NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas | Belhadj, 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-2004 | Organochlorine exposure and colorectal cancer risk | Howsam, 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 |