Publications
Filters: First Letter Of Last Name is H [Clear All Filters]
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. Abstract
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. Abstract
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. Abstract
COGENT (COlorectal cancer GENeTics) revisited. Mutagenesis. 2012;27(2):143-51. Abstract
Smoke-free legislation: global reach, impact and remaining challenges. Public health. 2012;126(3):227-9. Abstract
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
A DNA methylation fingerprint of 1628 human samples. Genome research. 2012;22(2):407-19. Abstract
Meta-analysis of new genome-wide association studies of colorectal cancer risk. Human genetics. 2012;131(2):217-34. Abstract
Evidence for a link between TNFRSF11A and risk of breast cancer. Breast cancer research and treatment. 2011;129(3):947-54. Abstract
Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer. PLoS biology. 2011;9(11):e1001199. Abstract
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. Abstract
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). Abstract
Exploring the link between MORF4L1 and risk of breast cancer. Breast cancer research : BCR. 2011;13(2):R40. Abstract
The TLX1 oncogene drives aneuploidy in T cell transformation. Nature medicine. 2010;16(11):1321-7. Abstract
Common variation in ISL1 confers genetic susceptibility for human congenital heart disease. PloS one. 2010;5(5):e10855. Abstract
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. Abstract
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. Abstract
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
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. Abstract
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. Abstract
