Estimation of Copy Number Alterations from Exome Sequencing Data

Por Valdés-Mas, Rafael, Bea, Silvia, Puente, Diana A., López-Otín, Carlos, Puente, Xose S.
Publicado em 2012

Knowledge and attitudes of primary health care physicians and nurses with regard to population screening for colorectal cancer in Balearic Islands and Barcelona

Por Puente Diana, Cabeza Elena, Almeda Jesús, Esteva Magdalena, Ramos Maria, Saladich Rosa, Boada Albert, Llagostera Maria
Publicado em 2010-09-01

Knowledge and attitudes of primary health care physicians and nurses with regard to population screening for colorectal cancer in Balearic Islands and Barcelona

Por Ramos, Maria, Esteva, Magdalena, Almeda, Jesús, Cabeza, Elena, Puente, Diana, Saladich, Rosa, Boada, Albert, Llagostera, Maria
Publicado em 2010

The role of gender in a smoking cessation intervention: a cluster randomized clinical trial

Por Torrecilla Miguel, Cebrian Tránsito, Fernández-Alonso Carmen, Rodriguez-Blanco Teresa, Cabezas Carmen, Puente Diana, Clemente Lourdes, Martín Carlos
Publicado em 2011-05-01

The role of gender in a smoking cessation intervention: a cluster randomized clinical trial

Por Puente, Diana, Cabezas, Carmen, Rodriguez-Blanco, Teresa, Fernández-Alonso, Carmen, Cebrian, Tránsito, Torrecilla, Miguel, Clemente, Lourdes, Martín, Carlos
Publicado em 2011

Effectiveness of a stepped primary care smoking cessation intervention (ISTAPS study): design of a cluster randomised trial

Por Cabezas, Carmen, Martin, Carlos, Granollers, Silvia, Morera, Concepció, Ballve, Josep Lluis, Zarza, Elvira, Blade, Jordi, Borras, Margarida, Serra, Antoni, Puente, Diana
Publicado em 2009

A cross-sectional study of the appropriateness of colonoscopy requests in the Spanish region of Catalonia

Por Puente, Diana, Cantero, Francesc Xavier, Llagostera, Maria, Piñeiro, Pilar, Nieto, Raquel, Saladich, Rosa, Mascort, Juanjo, Marzo, Mercè, Almeda, Jesús, Segarra, Manel
Publicado em 2012

Impact of Glucose-Lowering Agents on the Risk of Cancer in Type 2 Diabetic Patients. The Barcelona Case-Control Study

Por Simó, Rafael, Plana-Ripoll, Oleguer, Puente, Diana, Morros, Rosa, Mundet, Xavier, Vilca, Luz M., Hernández, Cristina, Fuentes, Inmaculada, Procupet, Adriana, Tabernero, Josep M., Violán, Concepción
Publicado em 2013

Exome sequencing identifies a novel mutation in PIK3R1 as the cause of SHORT syndrome

Por Bárcena, Clea, Quesada, Víctor, De Sandre-Giovannoli, Annachiara, Puente, Diana A, Fernández-Toral, Joaquín, Sigaudy, Sabine, Baban, Anwar, Lévy, Nicolas, Velasco, Gloria, López-Otín, Carlos
Publicado em 2014

Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

Por Puente, Xose S., Quesada, Victor, Osorio, Fernando G., Cabanillas, Rubén, Cadiñanos, Juan, Fraile, Julia M., Ordóñez, Gonzalo R., Puente, Diana A., Gutiérrez-Fernández, Ana, Fanjul-Fernández, Miriam, Lévy, Nicolas, Freije, José M.P., López-Otín, Carlos
Publicado em 2011

POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance

Por Bellido, Fernando, Pineda, Marta, Aiza, Gemma, Valdés-Mas, Rafael, Navarro, Matilde, Puente, Diana A., Pons, Tirso, González, Sara, Iglesias, Silvia, Darder, Esther, Piñol, Virginia, Soto, José Luís, Valencia, Alfonso, Blanco, Ignacio, Urioste, Miguel, Brunet, Joan, Lázaro, Conxi, Capellá, Gabriel, Puente, Xose S., Valle, Laura
Publicado no Genet Med (2016)

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma

Por Beà, Sílvia, Valdés-Mas, Rafael, Navarro, Alba, Salaverria, Itziar, Martín-Garcia, David, Jares, Pedro, Giné, Eva, Pinyol, Magda, Royo, Cristina, Nadeu, Ferran, Conde, Laura, Juan, Manel, Clot, Guillem, Vizán, Pedro, Di Croce, Luciano, Puente, Diana A., López-Guerra, Mónica, Moros, Alexandra, Roue, Gael, Aymerich, Marta, Villamor, Neus, Colomo, Lluís, Martínez, Antonio, Valera, Alexandra, Martín-Subero, José I., Amador, Virginia, Hernández, Luis, Rozman, Maria, Enjuanes, Anna, Forcada, Pilar, Muntañola, Ana, Hartmann, Elena M., Calasanz, María J., Rosenwald, Andreas, Ott, German, Hernández-Rivas, Jesús M., Klapper, Wolfram, Siebert, Reiner, Wiestner, Adrian, Wilson, Wyndham H., Colomer, Dolors, López-Guillermo, Armando, López-Otín, Carlos, Puente, Xose S., Campo, Elías
Publicado em 2013

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

Por Puente, Xose S., Pinyol, Magda, Quesada, Víctor, Conde, Laura, Ordóñez, Gonzalo R., Villamor, Neus, Escaramis, Georgia, Jares, Pedro, Beà, Sílvia, González-Díaz, Marcos, Bassaganyas, Laia, Baumann, Tycho, Juan, Manel, López-Guerra, Mónica, Colomer, Dolors, Tubío, José M. C., López, Cristina, Navarro, Alba, Tornador, Cristian, Aymerich, Marta, Rozman, María, Hernández, Jesús M., Puente, Diana A., Freije, José M. P., Velasco, Gloria, Gutiérrez-Fernández, Ana, Costa, Dolors, Carrió, Anna, Guijarro, Sara, Enjuanes, Anna, Hernández, Lluís, Yagüe, Jordi, Nicolás, Pilar, Romeo-Casabona, Carlos M., Himmelbauer, Heinz, Castillo, Ester, Dohm, Juliane C., de Sanjosé, Silvia, Piris, Miguel A., de Alava, Enrique, Miguel, Jesús San, Royo, Romina, Gelpí, Josep L., Torrents, David, Orozco, Modesto, Pisano, David G., Valencia, Alfonso, Guigó, Roderic, Bayés, Mónica, Heath, Simon, Gut, Marta, Klatt, Peter, Marshall, John, Raine, Keiran, Stebbings, Lucy A., Futreal, P. Andrew, Stratton, Michael R., Campbell, Peter J., Gut, Ivo, López-Guillermo, Armando, Estivill, Xavier, Montserrat, Emili, López-Otín, Carlos, Campo, Elías
Publicado em 2011