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A
Abulí A, Fernández-Rozadilla C, Alonso-Espinaco V, Muñoz J, Gonzalo V, Bessa X, et al. Case-control study for colorectal cancer genetic susceptibility in EPICOLON: previously identified variants and mucins. BMC cancer. 2011;11:339. Abstract
Aguado A, Guinó E, Mukherjee B, Sicras A, Serrat J, Acedo M, et al. Variability in prescription drug expenditures explained by adjusted clinical groups (ACG) case-mix: a cross-sectional study of patient electronic records in primary care. BMC health services research. 2008;8:53. Abstract
Alazzouzi H, Suriano G, Guerra A, Plaja A, Espín E, Armengol M, et al. Tumour selection advantage of non-dominant negative P53 mutations in homozygotic MDM2-SNP309 colorectal cancer cells. Journal of medical genetics. 2007;44(1):75-80.
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
Azuara D, Rodriguez-Moranta F, de Oca J, Sanjuan X, Guardiola J, Lobaton T, et al. Novel methylation panel for the early detection of neoplasia in high-risk ulcerative colitis and Crohn's colitis patients. Inflammatory bowel diseases. 2012. Abstract
Azuara D, Rodriguez-Moranta F, de Oca J, Soriano-Izquierdo A, Mora J, Guardiola J, et al. Novel methylation panel for the early detection of colorectal tumors in stool DNA. Clinical colorectal cancer. 2010;9(3):168-76. Abstract
B
Babel I, Barderas R, Diaz-Uriarte R, Moreno V, Suarez A, Fernandez-Aceñero MJ, et al. 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. 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
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
Bonifaci N, Berenguer A, Díez J, Reina O, Medina I, Dopazo J, et al. Biological processes, properties and molecular wiring diagrams of candidate low-penetrance breast cancer susceptibility genes. BMC medical genomics. 2008;1:62.
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
Boonstra PS, Mukherjee B, Taylor JM, Nilbert M, Moreno V, Gruber SB. Bayesian modeling for genetic anticipation in presence of mutational heterogeneity: a case study in Lynch syndrome. Biometrics. 2011;67(4):1627-37. Abstract
Borràs E, Pineda M, Blanco I, Jewett EM, Wang F, Teulé A, et al. MLH1 founder mutations with moderate penetrance in Spanish Lynch syndrome families. Cancer research. 2010;70(19):7379-91. Abstract
C
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
Castaño-Vinyals G, Nieuwenhuijsen MJ, Moreno V, Carrasco E, Guinó E, Kogevinas M, et al. Participation rates in the selection of population controls in a case-control study of colorectal cancer using two recruitment methods. Gaceta sanitaria / S.E.S.P.A.S. 2011;25(5):353-6. Abstract
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
Clèries R, Valls J, Esteban L, Gálvez J, Pareja L, Sanz X, et al. WAERS: an application for Web-assisted estimation of relative survival. Medical informatics and the Internet in medicine. 2007;32(3):169-75.
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
D
Dolores Perea M, Castaño-Vinyals G, Altzibar JM, Ascunce N, Moreno V, Tardon A, et al. Cancer screening practices and associated lifestyles in population controls of the Spanish multi-case control study. . Gaceta sanitaria / S.E.S.P.A.S. 2012. Abstract
F
Feliubadaló L, Lopez-Doriga A, Castellsagué E, Del Valle J, Menéndez M, Tornero E, et al. 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. 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
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
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-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
de la Fuente JS, Granja V, Escobar I, de la Fuente EC, Moreno V, Rubio R. Study of the gastrointestinal tolerance of a new tablet formulation of the lopinavir/ritonavir antiretroviral in HIV-infected patients. Journal of acquired immune deficiency syndromes (1999). 2009;50(3):294-8.