Filters: Author is Capellá, G [Clear All Filters]
Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome. European journal of human genetics : EJHG. 2012.
Nanofluidic Digital PCR for KRAS Mutation Detection and Quantification in Gastrointestinal Cancer. Clinical chemistry. 2012;58(9):1332-41.
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.
Novel methylation panel for the early detection of neoplasia in high-risk ulcerative colitis and Crohn's colitis patients. Inflammatory bowel diseases. 2012.
Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer. PLoS biology. 2011;9(11):e1001199.
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.
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.
MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families. Cancer research. 2010;70(19):7379-91.
Oncogenic KRAS is not necessary for Wnt signalling activation in APC-associated FAP adenomas. The Journal of pathology. 2010;221(1):57-67.
TACC3-TSC2 maintains nuclear envelope structure and controls cell division. Cell cycle (Georgetown, Tex.). 2010;9(6):1143-55.
Novel methylation panel for the early detection of colorectal tumors in stool DNA. Clinical colorectal cancer. 2010;9(3):168-76.
Allele-specific expression of APC in adenomatous polyposis families. Gastroenterology. 2010;139(2):439-7, 447.e1.
Detection of APC gene deletions using quantitative multiplex PCR of short fluorescent fragments. Clinical chemistry. 2008;54(7):1132-40.
Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility. BMC genomics. 2008;9:12.
Functional characterization of the novel APC N1026S variant associated with attenuated familial adenomatous polyposis. Gastroenterology. 2008;134(1):56-64.
CLEAR-test: combining inference for differential expression and variability in microarray data analysis. Journal of biomedical informatics. 2008;41(1):33-45.
Evidence for systems-level molecular mechanisms of tumorigenesis. BMC genomics. 2007;8:185.
Integrative analysis of a cancer somatic mutome. Molecular cancer. 2007;6:13.
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.