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Publications

Filtros: Autor es Blanco, I  [Restablecer todos los filtros]
2012
Bellido F, Guinó E, Jagmohan-Changur S, Seguí N, Pineda M, Navarro M, et al. Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome. European journal of human genetics : EJHG. 2012. Abstract
Saunders IW, Ross J, Macrae F, Young GP, Blanco I, Brohede J, et al. Evidence of linkage to chromosomes 10p15.3-p15.1, 14q24.3-q31.1 and 9q33.3-q34.3 in non-syndromic colorectal cancer families. European journal of human genetics : EJHG. 2012;20(1):91-6. Abstract
Feliubadaló L, Lopez-Doriga A, Castellsagué E, Del Valle J, Menéndez M, Tornero E, et al. Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes. European journal of human genetics : EJHG. 2012. Abstract
2011
Bonifaci N, Palafox M, Pellegrini P, Osorio A, Benítez J, Peterlongo P, et al. Evidence for a link between TNFRSF11A and risk of breast cancer. Breast cancer research and treatment. 2011;129(3):947-54. Abstract
Maxwell CA, Benítez J, Gómez-Baldó L, Osorio A, Bonifaci N, Fernández-Ramires R, et al. Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer. PLoS biology. 2011;9(11):e1001199. Abstract
Martrat G, Maxwell CA, Tominaga E, Porta M, Bonifaci N, Gomez-Baldo L, et al. Exploring the link between MORF4L1 and risk of breast cancer. Breast cancer research : BCR. 2011;13(2):R40. Abstract
2010
Borràs E, Pineda M, Blanco I, Jewett EM, Wang F, Teulé A, et al. MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families. Cancer research. 2010;70(19):7379-91. Abstract
Azuara D, Rodriguez-Moranta F, de Oca J, Soriano-Izquierdo A, Mora J, Guardiola J, et al. Novel methylation panel for the early detection of colorectal tumors in stool DNA. Clinical colorectal cancer. 2010;9(3):168-76. Abstract
Theodoratou E, Campbell H, Tenesa A, Houlston R, Webb E, Lubbe S, et al. A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants. British journal of cancer. 2010;103(12):1875-84. Abstract
Castellsagué E, González S, Guinó E, Stevens KN, Borràs E, Raymond VM, et al. Allele-specific expression of APC in adenomatous polyposis families. Gastroenterology. 2010;139(2):439-7, 447.e1. Abstract
2009
Fernández-Ramires R, Solé X, De Cecco L, Llort G, Cazorla A, Bonifaci N, et al. Gene expression profiling integrated into network modelling reveals heterogeneity in the mechanisms of BRCA1 tumorigenesis. British journal of cancer. 2009;101(8):1469-80.
Navarro M, Binefa G, Blanco I, Guardiola J, Rodríguez-Moranta F, Peris M, et al. Colorectal cancer screening: strategies to select populations with moderate risk for disease. Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva. 2009;101(12):855-60. Abstract
2008
Castellsagué E, González S, Nadal M, Campos O, Guinó E, Urioste M, et al. Detection of APC gene deletions using quantitative multiplex PCR of short fluorescent fragments. Clinical chemistry. 2008;54(7):1132-40. Abstract
Menéndez M, González S, Obrador-Hevia A, Domínguez A, Pujol MJ, Valls J, et al. Functional characterization of the novel APC N1026S variant associated with attenuated familial adenomatous polyposis. Gastroenterology. 2008;134(1):56-64.