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Association analysis between breast cancer genetic variants and mammographic density in a large population-based study (Determinants of Density in Mammographies in Spain) identifies susceptibility loci in TOX3 gene. European journal of cancer (Oxford, England : 1990). 2012.
Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma. British journal of haematology. 2012;158(6):805-9.
Identification of Lynch syndrome among patients with colorectal cancer. JAMA : the journal of the American Medical Association. 2012;308(15):1555-65.
Prostate stem-cell antigen gene is associated with diffuse and intestinal gastric cancer in Caucasians: Results from the EPIC-EURGAST study. International journal of cancer. Journal international du cancer. 2012;130(10):2417-27.
COGENT (COlorectal cancer GENeTics) revisited. Mutagenesis. 2012;27(2):143-51.
Smoke-free legislation: global reach, impact and remaining challenges. Public health. 2012;126(3):227-9.
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.
A DNA methylation fingerprint of 1628 human samples. Genome research. 2012;22(2):407-19.
Meta-analysis of new genome-wide association studies of colorectal cancer risk. Human genetics. 2012;131(2):217-34.
Evidence for a link between TNFRSF11A and risk of breast cancer. Breast cancer research and treatment. 2011;129(3):947-54.
Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer. PLoS biology. 2011;9(11):e1001199.
Clinical validity of detecting K-ras mutations for the diagnosis of exocrine pancreatic cancer: a prospective study in a clinically-relevant spectrum of patients. European Journal of Epidemiology. 2011;26(3):229-36.
Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome. Epigenetics : official journal of the DNA Methylation Society. 2011;6(6).
Exploring the link between MORF4L1 and risk of breast cancer. Breast cancer research : BCR. 2011;13(2):R40.
The TLX1 oncogene drives aneuploidy in T cell transformation. Nature medicine. 2010;16(11):1321-7.
Common variation in ISL1 confers genetic susceptibility for human congenital heart disease. PloS one. 2010;5(5):e10855.
Smoking, gender, and ethnicity predict somatic BRAF mutations in colorectal cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2010;19(3):838-43.
COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. British journal of cancer. 2010;102(2):447-54.
A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants. British journal of cancer. 2010;103(12):1875-84.
A bivariate measurement error model for nitrogen and potassium intakes to evaluate the performance of regression calibration in the European Prospective Investigation into Cancer and Nutrition study. European journal of clinical nutrition. 2009;63 Suppl 4:S179-87.
Semiparametric Bayesian modeling of random genetic effects in family-based association studies. Statistics in medicine. 2009;28(1):113-39.
Pathologic predictors of microsatellite instability in colorectal cancer. The American journal of surgical pathology. 2009;33(1):126-33.
Adherence to the Mediterranean diet and risk of coronary heart disease in the Spanish EPIC Cohort Study. American journal of epidemiology. 2009;170(12):1518-29.