Browsing by Author Capellá, G. (Gabriel)
Showing results 20 to 39 of 108
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| Issue Date | Title | Author(s) |
|---|---|---|
| 20-Feb-2009 | Biological convergence of cancer signatures | Solé 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-2014 | Biomarcadors en càncer colorectal hereditari: aplicacions clíniques i estudi de la dinàmica tumoral | Gausachs Romero, Mireia |
| 28-Jul-2017 | Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database | Møller, 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-2020 | Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database | Dominguez 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-2016 | Carcinoma-associated fibroblasts affect sensitivity to oxaliplatin and 5FU in colorectal cancer cells | Gonçalves-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. |
| 29-Sep-2009 | Càncer colorectal hereditari: Aplicacions diagnòstiques de l'estudi de la dosi dels gens APC, MLH1 i MSH2 | Castellsagué Torrents, Ester |
| 7-Nov-2012 | Clinical value of prognosis gene expression signatures in colorectal cancer: a systematic review | Sanz Pamplona, Rebeca; Berenguer, Antoni; Cordero Romera, David; Riccadonna, Samantha; Solé Acha, Xavier; Crous Bou, Marta; Guinó, Elisabet; Sanjuan, Xavier; Biondo, Sebastián; Soriano Izquierdo, Antonio; Jurman, Giuseppe; Capellá, G. (Gabriel); Furlanello, Cesare; Moreno Aguado, Víctor |
| 13-May-2021 | CNVfilteR: an R/bioconductor package to identify false positives produced by germline NGS CNV detection tools. | Moreno Cabrera, José Marcos; Valle, Jesús del; Castellanos, Elisabeth; Feliubadaló i Elorza, Maria Lídia; Pineda Riu, Marta; Serra Arenas, Eduard; Capellá, G. (Gabriel); Lázaro, Conxi; Gel, Bernat |
| 13-Mar-2020 | Colorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibility | Arnau 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 |
| 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 |
| 1-Oct-2022 | Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium | Møller, Pål; Seppälä, Toni T.; Dowty, James G.; Haupt, Saskia; Dominguez Valentin, Mev; Sunde, Lone; Bernstein, Inge; Engel, Christoph; Aretz, Stefan; Nielsen, Maartje; Capellá, G. (Gabriel); Lindblom, Annika; Gluck, Nathan; Kalfayan, Pablo; Torrezan, Giovana Tardin; Winship, Ingrid; Plazzer, John Paul; Sijmons, Rolf; Backman, Ann Sofie; De Vargas, Aída Falcón; Vangala, Deepak; Lautrup, Charlotte K.; Laghi, Luigi; Valle, Adriana Della; Abu Freha, Naim; Winter, Des; Bohorquez, Mabel; Horisberger, Karoline; Heinimann, Karl; Half, Elizabeth; Lopez Koestner, Francisco; Alvarez Valenzuela, Karin; Van Hest, Liselotte P.; Scott, Rodney J.; Ligtenberg, Marjolijn J. L.; Katz, Lior; Da Silva, Leandro Apolinário; Zahary, Mohd N.; Laish, Ido; Rossi, Norma Teresa; Morrison, Patrick J.; Vainer, Elez; Nascimento, Ivana; Steinke Lange, Verena; Vaccaro, Carlos Alberto; Carraro, Dirce Maria; Thomas, Huw; Zaránd, Attila; Poplawski, Nicola; Aronson, Melyssa; Kohonen Corish, Maija R. J.; Lee, Grant; Mecklin, Jukka Pekka; Pylvänäinen, Kirsi; Schmiegel, Wolff; Hüneburg, Robert; Gerdes, Anne Marie; Snyder, Carrie; Renkonen Sinisalo, Laura; Lepisto, Anna; Peltomäki, Päivi; Therkildsen, Christina; Lindberg, Lars Joachim; Lindor, Noralane; Thorlacius Ussing, Ole; Stoffel, Elena; Newcomb, Polly A.; Von Knebel Doeberitz, Magnus; Palmero, Edenir; Thibodeau, Stephen N.; Loeffler, Markus; Amor, David; Hoogerbrugge, Nicoline; Rahner, Nils; Duijkers, Floor; Hall, Michael J.; Buchanan, Daniel D.; Le Marchand, Loïc; Win, Aung Ko; Hovig, Eivind; Hampel, Heather; Williams, Heinric; Ricciardiello, Luigi; Southey, Melissa; Samadder, N. Jewel; James, Paul; Okkels, Henrik; Lubiński, Jan; Reece, Jeanette; Ngeow, Joanne; Bassaneze, Thiago; Guillem, Jose G.; Ahadova, Aysel; Arnold, Julie; Pai, Rish; Jenkins, Mark A.; Wadt, Karin; Ankathil, Ravindran; Holinski Feder, Elke; Monahan, Kevin; Chen Shtoyerman, Rakefet; Heuveline, Vincent; Senter, Leigha; Rasmussen, Lene J.; Ward, Robyn; Parry, Susan; Evans, D. Gareth; Sampson, Julian R.; Moslein, Gabriela; Bonanni, Bernardo; Dębniak, Tadeusz; John, Thomas; Hopper, John L.; Gallinger, Steven; Figueiredo, Jane; Ten Broeke, Sanne W.; Van Overeem Hansen, Thomas; Caldés, Trinidad; Yamaguchi, Tatsuro; Barca Tierno, Verónica; Garre, Pilar; Kennelly, Rory; Cavestro, Giulia Martina; Dueñas, Nuria; Greenblatt, Marc; Weitz, Jürgen; Pineda, Marta; Lino Silva, Leonardo S.; Redler, Silke; Nakken, Sigve; Burn, John; Büttner, Reinhard; Brunet, Joan; Green, Kate; Sheth, Harsh; Rossi, Benedito Mauro; Stakelum, Aine; Portenkirchner, Carmen; Lalloo, Fiona; Newton, Katie; Martin, Claudia; Kloor, Matthias; The European Hereditary Tumour Group (ehtg) And The International Mismatch Repair Consortium (imrc); Bertario, Lucio; Crosbie, Emma J.; Mints, Miriam; Tjandra, Douglas; Neffa, Florencia; Perne, Claudia; Esperon, Patricia; Latchford, Andrew; Kariv, Revital; Macrae, Finlay; Guillén Ponce, Carmen; Rosner, Guy; Levi, Zohar; Tibiletti, Maria Grazia; Pavicic, Walter Hernán |
| 25-Jul-2017 | Comprehensive analysis of copy number aberrations in microsatellite stable colon cancer in view of stromal component | Alonso Aguado, Maria Henar; Aussó, Susanna; López Dóriga Guerra, Adriana; Cordero Romera, David; Guinó, Elisabet; Solé Acha, Xavier; Barenys de Lacha, Mercé; Oca Burguete, Javier de; Capellá, G. (Gabriel); Salazar Soler, Ramón; Sanz Pamplona, Rebeca; Moreno Aguado, Víctor |
| 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) |
| 25-Mar-2015 | Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine | Castellsagué, Joan; Gel, Bernat; Fernández Rodríguez, Juana; Llatjós, Roger; Blanco Guillermo, Ignacio; Benavente, Yolanda; Pérez Sidelnikova, Diana; García del Muro Solans, Xavier; Viñals, Joan Maria; Vidal-Bel, August; Valdés Mas, Rafael; Terribas Pérez, Ernest; López Dóriga Guerra, Adriana; Pujana Genestar, M. Ángel; Capellá, G. (Gabriel); Puente, Xose S.; Serra Arenas, Eduard; Villanueva Garatachea, Alberto; Lázaro García, Conxi |
| 5-Sep-2018 | Computational tools for splicing defect prediction in breast/ovarian cancer genes: how efficient are they at predicting RNA alterations? | Moles-Fernández, Alejandro; Duran-Lozano, Laura; Montalban, Gemma; Bonache, Sandra; López-Perolio, Irene; Menéndez Vilà, Mireia; Santamariña-Pena, Marta; Behar, Raquel; Blanco, Ana; Carrasco, Estela; López-Fernández, Adrià; Stjepanovic, Neda; Balmaña, Judith; Capellá, G. (Gabriel); Pineda Riu, Marta; Vega, Ana; Lázaro García, Conxi; Hoya, Miguel de la; Díez Gibert, Orland; Gutiérrez Enríquez, Sara |
| 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 |
| 13-Dec-2019 | Desarrollo de nuevas aproximaciones para el diagnóstico molecular de los síndromes de predisposición hereditaria al cáncer asociados a deficiencia del sistema de reparación de apareamientos erróneos | González Acosta, María Isabel |
| Feb-2012 | A DNA methylation fingerprint of 1628 human samples | Fernández, Agustín F.; Martín-Subero, José Ignacio; Hidalgo, Manuel; Ferrer, Isidro (Ferrer Abizanda); Sánchez Céspedes, Montserrat; Villanueva Garatachea, Alberto; Carmona, F. Javier; Sanchez-Mut, Jose Vicente; Berdasco, María; Moreno Aguado, Víctor; Capellá, G. (Gabriel); Ballestar Tarín, Esteban; Pérez Jurado, Luis; Mora Graupera, Jaume; Puig i Sardà, Susana; Prat, Jaime; Badimón, Lina, 1953-; Esteller, Manel |
| 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 |
| 1-Jun-2020 | Dominantly inherited hereditary nonpolyposis colorectal cancer not caused by MMR genes | Terradas, Mariona; Capellá, G. (Gabriel); Valle, Laura |