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Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
openAccess | | 2020 | Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes | Fachal, Laura; Aschard, Hugues; Beesley, Jonathan; Barnes, Daniel R.; Allen, Jamie; Kar, Siddhartha; Pooley, Karen A.; Dennis, Joe; Michailidou, Kyriaki; Turman, Constance; Soucy, Penny; Lemaçon, Audrey; Lush, Michael; Tyrer, Jonathan P.; Ghoussaini, Maya; Moradi Marjaneh, Mahdi; Jiang, Xia; Agata, Simona; Aittomäki, Kristiina; Alonso, M. Rosario; Andrulis, Irene L.; Anton-Culver, Hoda; Antonenkova, Natalia N.; Arason, Adalgeir; Arndt, Volker; Aronson, Kristan J.; Arun, Banu K.; Auber, Bernd; Auer, Paul L.; Azzollini, Jacopo; Balmaña, Judith; Barkardottir, Rosa B.; Barrowdale, Daniel; Beeghly-Fadiel, Alicia; Benitez, Javier; Bermisheva, Marina; Białkowska, Katarzyna; Blanco, Amie M.; Blomqvist, Carl; Blot, William; Bogdanova, Natalia V.; Bojesen, Stig E.; Bolla, Manjeet K.; Bonanni, Bernardo; Borg, Ake; Bosse, Kristin; Brauch, Hiltrud; Brenner, H.; Briceno, I.; Caldés, T.; Castelao, J. E.; Hoya, Miguel de la; Diez, Orland; Durán, Mercedes CSIC ORCID; Gago-Dominguez, Manuela; García-Saenz, José Ángel; González-Neira, Anna; Moreno, Fernando CSIC ORCID; Muñoz-Garzón, Víctor M.; Osorio, Ana; Pujana, Miguel Ángel; Romero, Atocha; Sánchez-Herrero, Estela; Santamariña, Marta; Teulé, Alex; Vega, Ana | artículo |
closedAccess | | 2012 | Frequency of germ line MUTYH mutations in patients diagnosed with colorectal cancer in Castilla y León (Spain) | Tascón, Mónica; Pérez-Cabornero, Lucía CSIC; Infante, Mar CSIC ORCID; Velasco, Eladio CSIC ORCID ; Lastra, Enrique; Marcos García, G.; Esteban Cardeñosa, Eva CSIC; Miner, Cristina CSIC; Durán, Mercedes CSIC ORCID | póster de congreso |
openAccess | | jul-2011 | Frequency of rearrangements in lynch syndrome cases associated with MSH2: Characterization of a new deletion involving both EPCAM and the 5′ part of MSH2 | Pérez-Cabornero, Lucía CSIC; Infante, Mar CSIC ORCID; Velasco, Eladio CSIC ORCID ; Lastra, Enrique; Acedo, Alberto CSIC ORCID; Miner, Cristina CSIC; Durán, Mercedes CSIC ORCID | artículo |
closedAccess | | 2016 | Functional characterization of DNA variants from exons 17 and 18 of the BRCA2 gene | Fraile-Bethencourt, Eugenia CSIC ORCID; Díez-Gómez, Beatriz CSIC; Velásquez-Zapata, Valeria; Acedo, Alberto CSIC ORCID; Sanz, David J. CSIC ORCID; Hernández-Moro, Cristina; Marcos García, G.; Infante, Mar CSIC ORCID; Durán, Mercedes CSIC ORCID; Velasco, Eladio CSIC ORCID | póster de congreso |
closedAccess | | 2014 | GALNT12 is not a major contributor of familial colorectal cancer type X | Infante, Mar CSIC ORCID; Durán, Mercedes CSIC ORCID; Blanco, Ignacio; Valle, Laura | artículo |
closedAccess | | 2018 | Genetic dissection of the BRCA2 promoter and transcriptional impact of DNA variants | Fraile-Bethencourt, Eugenia CSIC ORCID; Valenzuela-Palomo, Alberto CSIC; Díez-Gómez, Beatriz CSIC; Infante, Mar CSIC ORCID; Durán, Mercedes CSIC ORCID; Marcos García, G.; Lastra, Enrique; Gómez-Barrero, Susana; Velasco, Eladio CSIC ORCID | artículo |
closedAccess | | 2011 | Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers | Ramus, Susan J.; Durán, Mercedes CSIC ORCID; Tejada, María Isabel | artículo |
openAccess | | 2013 | Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk | Couch, Fergus J.; Durán, Mercedes CSIC ORCID; Antoniou, Antonis C. | artículo |
closedAccess | | 2013 | Genotype-phenotype correlation in MMR mutation-positive families with Lynch syndrome | Pérez-Cabornero, Lucía CSIC; Infante, Mar CSIC ORCID; Velasco, Eladio CSIC ORCID ; Lastra, Enrique; Miner, Cristina CSIC; Durán, Mercedes CSIC ORCID | artículo |
openAccess | | 3-ago-2020 | Germline genetic findings which may impact therapeutic decisions in families with a presumed predisposition for hereditary breast and ovarian cancer | Velázquez Pérez, Carolina; Leeneer, Kim de; Esteban Cardeñosa, Eva CSIC; Avila Cobos, Francisco; Lastra, Enrique; Abella Santos, Luis Enrique; Cruz, Virginia de la; Lobatón, Carmen D.; Claes, Kathleen B.; Durán, Mercedes CSIC ORCID; Infante, Mar CSIC ORCID | artículo |
openAccess | | 2015 | Germline mutations in FAN1 cause hereditary colorectal cancer by impairing DNA repair | Seguí, Nuria; Mina, Leonardo B.; Durán, Mercedes CSIC ORCID; Lastra, Enrique; Blanco, Ignacio; Valle, Laura | artículo |
closedAccess | | 2011 | Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers | Im, Kate M.; Durán, Mercedes CSIC ORCID | artículo |
openAccess | | 2016 | Hereditary breast and ovarian cancer syndrome: looking for mutations in ERCC4 when BRCAs are not the origin | Velázquez Pérez, Carolina; Esteban Cardeñosa, Eva CSIC; Durán, Mercedes CSIC ORCID; Tascón, Mónica; Lastra, Enrique; Marcos García, G.; Hernández, Lara CSIC ORCID; Martínez Martín, N.; Infante, Mar CSIC ORCID | póster de congreso |
closedAccess | | 2007 | Heteroduplex analysis by capillary array electrophoresis for rapid mutation detection in large multiexon genes | Velasco, Eladio CSIC ORCID ; Infante, Mar CSIC ORCID; Durán, Mercedes CSIC ORCID; Pérez-Cabornero, Lucía CSIC; Sanz, David J. CSIC ORCID; Esteban Cardeñosa, Eva CSIC; Miner, Cristina CSIC | artículo |
closedAccess | | jul-2006 | High proportion of novel mutations ofBRCA1 andBRCA2 in breast/ovarian cancer patients from Castilla-León (central Spain) | Infante, Mar CSIC ORCID; Durán, Mercedes CSIC ORCID; Esteban Cardeñosa, Eva CSIC; Miner, Cristina CSIC; Velasco, Eladio CSIC ORCID | artículo |
openAccess | | feb-2004 | High-throughput mutation detection method to scan BRCA1 and BRCA2 based on heteroduplex analysis by capillary array electrophoresis | Esteban Cardeñosa, Eva CSIC; Durán, Mercedes CSIC ORCID; Infante, Mar CSIC ORCID; Velasco, Eladio CSIC ORCID ; Miner, Cristina CSIC | artículo |
closedAccess | | 2017 | Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer | Phelan, Catherine; Durán, Mercedes CSIC ORCID; Pharoah, Paul D. P. | artículo |
closedAccess | | 2016 | Identification of novel causal genes of hereditary colorectal cancer by performing whole-exome sequencing in individual high-risk families | Seguí, Nuria; Mina, Leonardo B.; Durán, Mercedes CSIC ORCID; Blanco, Ignacio; Valle, Laura | póster de congreso |
openAccess | | 2015 | Identification of six new susceptibility loci for invasive epithelial ovarian cancer | Kuchenbaecker, Karoline B.; Ramus, Susan J.; Tyrer, Jonathan; Hoya, Miguel de la; Díez, Orland; Blanco, Ignacio; Durán, Mercedes CSIC ORCID; Tejada, María Isabel | artículo |
closedAccess | | 2013 | Incidence of -93 MLH1 promoter polymorphism in familial and sporadic colorectal cancer | Martínez-Urueña, N.; Macías, Laura; Pérez-Cabornero, Lucía CSIC; Infante, Mar CSIC ORCID; Lastra, Enrique; Cruz, Juan Jesús CSIC ORCID; Miner, Cristina CSIC; González-Sarmiento, Rogelio CSIC ORCID ; Durán, Mercedes CSIC ORCID | artículo |