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Publications

Filters: Author is Capellá, G  [Clear All Filters]
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
Azuara D, Ginesta MM, Gausachs M, Rodriguez-Moranta F, Fabregat J, Busquets J, et al. Nanofluidic Digital PCR for KRAS Mutation Detection and Quantification in Gastrointestinal Cancer. Clinical chemistry. 2012;58(9):1332-41. Abstract
Barderas R, Babel I, Díaz-Uriarte R, Moreno V, Suárez A, Bonilla F, et al. An optimized predictor panel for colorectal cancer diagnosis based on the combination of tumor-associated antigens obtained from protein and phage microarrays. Journal of proteomics. 2012. 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
Azuara D, Rodriguez-Moranta F, de Oca J, Sanjuan X, Guardiola J, Lobaton T, et al. Novel methylation panel for the early detection of neoplasia in high-risk ulcerative colitis and Crohn's colitis patients. Inflammatory bowel diseases. 2012. Abstract
2011
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
Babel I, Barderas R, Diaz-Uriarte R, Moreno V, Suarez A, Fernandez-Aceñero MJ, et al. Identification of MST1/STK4 and SULF1 proteins as autoantibody targets for the diagnosis of colorectal cancer by using phage microarrays. Molecular & cellular proteomics : MCP. 2011;10(3):M110.001784. Abstract
Seguí N, Stevens KN, Guinó E, Rozek LS, Moreno VR, Capellá G, et al. No association between germline allele-specific expression of TGFBR1 and colorectal cancer risk in Caucasian and Ashkenazi populations. British journal of cancer. 2011;104(4):735-40. 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
Obrador-Hevia A, Chin SF, González S, Rees J, Vilardell F, Greenson JK, et al. Oncogenic KRAS is not necessary for Wnt signalling activation in APC-associated FAP adenomas. The Journal of pathology. 2010;221(1):57-67. Abstract
Gómez-Baldó L, Schmidt S, Maxwell CA, Bonifaci N, Gabaldón T, Vidalain PO, et al. TACC3-TSC2 maintains nuclear envelope structure and controls cell division. Cell cycle (Georgetown, Tex.). 2010;9(6):1143-55. 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
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
Solé X, Bonifaci N, López-Bigas N, Berenguer A, Hernández P, Reina O, et al. Biological convergence of cancer signatures. PloS one. 2009;4(2):e4544.
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
Solé X, Hernández P, de Heredia ML, Armengol L, Rodríguez-Santiago B, Gómez L, et al. Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility. BMC genomics. 2008;9:12.
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.
Valls J, Grau M, Solé X, Hernández P, Montaner D, Dopazo J, et al. CLEAR-test: combining inference for differential expression and variability in microarray data analysis. Journal of biomedical informatics. 2008;41(1):33-45.
2007
Hernández P, Huerta-Cepas J, Montaner D, Al-Shahrour F, Valls J, Gómez L, et al. Evidence for systems-level molecular mechanisms of tumorigenesis. BMC genomics. 2007;8:185.
Hernández P, Solé X, Valls J, Moreno V, Capellá G, Urruticoechea A, et al. Integrative analysis of a cancer somatic mutome. Molecular cancer. 2007;6:13.
Pujana MA, Ruiz A, Badenas C, Puig-Butille JA, Nadal M, Stark M, et al. Molecular characterization of a t(9;12)(p21;q13) balanced chromosome translocation in combination with integrative genomics analysis identifies C9orf14 as a candidate tumor-suppressor. Genes, chromosomes & cancer. 2007;46(2):155-62. Abstract