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A
Buckland G, González CA, Agudo A, Vilardell M, Berenguer A, Amiano P, et al. 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
Fernandez-Navarro P, Pita G, Santamariña C, Moreno MP, Vidal C, Miranda-García J, et al. 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
B
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.
Ferrari P, Roddam A, Fahey MT, Jenab M, Bamia C, Ocké M, et al. 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
C
de Oca J, Azuara D, Sanchez-Santos R, Navarro M, Capella G, Moreno V, et al. Caspase-3 activity, response to chemotherapy and clinical outcome in patients with colon cancer. International journal of colorectal disease. 2008;23(1):21-7.
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.
Parker LA, Porta M, Lumbreras B, López T, Guarner L, Hernández-Aguado I, et al. 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
Houlston RS, members of CO, Moreno V. COGENT (COlorectal cancer GENeTics) revisited. Mutagenesis. 2012;27(2):143-51. Abstract
Tomlinson IP, Dunlop M, Campbell H, Zanke B, Gallinger S, Hudson T, et al. 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
Stevens KN, Hakonarson H, Kim CE, Doevendans PA, Koeleman BP, Mital S, et al. Common variation in ISL1 confers genetic susceptibility for human congenital heart disease. PloS one. 2010;5(5):e10855. Abstract
Crous-Bou M, De Vivo I, Porta M, Pumarega JA, López T, Alguacil J, et al. CYP1B1 polymorphisms and k-ras mutations in patients with pancreatic ductal adenocarcinoma. Digestive diseases and sciences. 2008;53(5):1417-21. Abstract
D
Bamia C, Trichopoulos D, Ferrari P, Overvad K, Bjerregaard L, Tjønneland A, et al. Dietary patterns and survival of older Europeans: the EPIC-Elderly Study (European Prospective Investigation into Cancer and Nutrition). Public health nutrition. 2007;10(6):590-8. Abstract
Fernandez AF, Assenov Y, Martin-Subero JI, Balint B, Siebert R, Taniguchi H, et al. A DNA methylation fingerprint of 1628 human samples. Genome research. 2012;22(2):407-19. Abstract
E
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
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.
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
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
López MJ, Fernández E, Gorini G, Moshammer H, Polanska K, Clancy L, et al. Exposure to secondhand smoke in terraces and other outdoor areas of hospitality venues in eight European countries. PloS one. 2012;7(8):e42130. Abstract
F
Hartmann E, Fernàndez V, Moreno V, Valls J, Hernández L, Bosch F, et al. Five-gene model to predict survival in mantle-cell lymphoma using frozen or formalin-fixed, paraffin-embedded tissue. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2008;26(30):4966-72.
Leich E, Salaverria I, Bea S, Zettl A, Wright G, Moreno V, et al. Follicular lymphomas with and without translocation t(14;18) differ in gene expression profiles and genetic alterations. Blood. 2009;114(4):826-34. Abstract
G
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.
Maxwell CA, Moreno V, Solé X, Gómez L, Hernández P, Urruticoechea A, et al. Genetic interactions: the missing links for a better understanding of cancer susceptibility, progression and treatment. Molecular cancer. 2008;7:4.
Tenesa A, Farrington SM, Prendergast JG, Porteous ME, Walker M, Haq N, et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nature genetics. 2008;40(5):631-7.
I
Moreira L, Balaguer F, Lindor N, de la Chapelle A, Hampel H, Aaltonen LA, et al. Identification of Lynch syndrome among patients with colorectal cancer. JAMA : the journal of the American Medical Association. 2012;308(15):1555-65. Abstract
Martino A, Campa D, Jamroziak K, Reis RM, Sainz J, Buda G, et al. 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.