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Publications

Filtres: Autor és Moreno, V  [Clear All Filters]
2013
Clèries R, Martínez JM, Moreno V, Yasui Y, Ribes J, Borràs JM. Predicting the Change in Breast Cancer Deaths in Spain by 2019: A Bayesian Approach. Epidemiology (Cambridge, Mass.). 2013. Abstract
Martino A, Sainz J, Manuel Reis R, Moreno V, Buda G, Lesueur F, et al. Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case-control study in the context of the IMMEnSE consortium. Journal of human genetics. 2013;58(3):155-9. Abstract
Fernandez-Rozadilla C, Cazier JB, Tomlinson IP, Carvajal-Carmona LG, Palles C, Lamas MJ, et al. A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12. BMC genomics. 2013;14:55. Abstract
Santos C, López-Doriga A, Navarro M, Mateo J, Biondo S, Martínez Villacampa M, et al. Clinicopathological risk factors of Stage II colon cancer: results of a prospective study. Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland. 2013;15(4):414-22. Abstract
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
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.
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
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
Fernandez-Rozadilla C, Palles C, Carvajal-Carmona L, Peterlongo P, Nici C, Veneroni S, et al. BMP2/BMP4 colorectal cancer susceptibility loci in Northern and Southern European populations. Carcinogenesis. 2012. Abstract
Zamora-Ros R, Not C, Guinó E, Luján-Barroso L, García RM, Biondo S, et al. Association between habitual dietary flavonoid and lignan intake and colorectal cancer in a Spanish case-control study (the Bellvitge Colorectal Cancer Study). Cancer causes & control : CCC. 2012. Abstract
Sala N, Muñoz X, Travier N, Agudo A, Duell EJ, Moreno V, et al. 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
Milà N, García M, Binefa G, Borràs JM, Espinàs JA, Moreno V. Adherence to a population-based colorectal cancer screening program in Catalonia (Spain), 2000-2008 . Gaceta sanitaria / S.E.S.P.A.S. 2012;26(3):217-22. Abstract
Campa D, Martino A, Sainz J, Buda G, Jamroziak K, Weinhold N, et al. Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium. British journal of haematology. 2012;157(3):331-8. 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
Houlston RS, members of CO, Moreno V. COGENT (COlorectal cancer GENeTics) revisited. Mutagenesis. 2012;27(2):143-51. Abstract
Crous-Bou M, Rennert G, Salazar R, Rodriguez-Moranta F, Rennert HS, Lejbkowicz F, et al. Genetic polymorphisms in fatty acid metabolism genes and colorectal cancer. Mutagenesis. 2012;27(2):169-76. Abstract
Martino A, Sainz J, Buda G, Jamroziak K, Reis RM, García-Sanz R, et al. Genetics and molecular epidemiology of multiple myeloma: the rationale for the IMMEnSE consortium (review). International journal of oncology. 2012;40(3):625-38. Abstract
Giráldez MD, López-Dóriga A, Bujanda L, Abulí A, Bessa X, Fernández-Rozadilla C, et al. Susceptibility genetic variants associated with early-onset colorectal cancer. Carcinogenesis. 2012;33(3):613-9. Abstract
Tian S, Simon I, Moreno V, Roepman P, Tabernero J, Snel M, et al. A combined oncogenic pathway signature of BRAF, KRAS and PI3KCA mutation improves colorectal cancer classification and cetuximab treatment prediction. Gut. 2012. Abstract
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
Garcia M, Borràs JM, Binefa G, Milà N, Espinàs JA, Moreno V. Repeated screening for colorectal cancer with fecal occult blood test in Catalonia, Spain. European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP). 2012;21(1):42-5. Abstract
Sanz-Pamplona R, Berenguer A, Sole X, Cordero D, Crous-Bou M, Serra-Musach J, et al. Tools for protein-protein interaction network analysis in cancer research. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico. 2012;14(1):3-14. Abstract
Fernandez-Rozadilla C, Cazier JB, Moreno V, Crous-Bou M, Guinó E, Durán G, et al. Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration. The pharmacogenomics journal. 2012. 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
Peters U, Hutter CM, Hsu L, Schumacher FR, Conti DV, Carlson CS, et al. Meta-analysis of new genome-wide association studies of colorectal cancer risk. Human genetics. 2012;131(2):217-34. Abstract