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GARCÍA-BERMÚDEZ M, LÓPEZ-MEJÍAS R, GONZÁLEZ-JUANATEY C, et al. "CARD8 rs2043211 (p.C10X) polymorphism is not associated with disease susceptibility or cardiovascular events in Spanish rheumatoid arthritis patients". DNA Cell Biol. 2013 Jan;32(1):28-33.
JOSTINS L, RIPKE S, WEERSMA RK, et al. "Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease". Nature. 2012 Nov 1;491(7422):119-24.
BARCA-TIERNO V, AZA-CARMONA M, BARROSO E, et al. "Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic displasia". Eur J Hum Genet. 2011 Dec;19(12):1218-25.
FERNANDEZ-ROZADILLA C, PALLES C, CARVAJAL-CARMONA LG, et al. The EPICOLON Consortium. "BMP2/BMP4 colorectal cancer susceptibility loci in Northern and Souther European populations". Carconogenesis. 2012 Nov 25
ARREDONDO M, HACKETT J JR, DE BETHENCOURT FR, et al. "Prevalence of xenotropic murine leukemia virus-related virus infection in different risk populations in Spain". AIDS Res Hum Retroviruses. 2012 Sep;28(9):1089-94
ARREDONDO M, DE BETHENCOURT F, TREVIÑO A, et al. "Short communication: RNASEL alleles and susceptibility to infection by human retroviruses and hepatitis viruses". AIDS Res Hum Retroviruses. 2012 Oct;28(10):1259-61
RODRIGUEZ-REVENGA L, MADRIGAL I, BLANCH-RUBIÓ J, et al. "Screening for the presence of FMR1 premutation alleles in women with fibromialgia". Gene. 2012 Oct 27
CHANDA P, YUHKI N, LI M, et al. "Comprehensive evaluation of imputation performance in African Americans". J Hum Genet. 2012 Jul;57(7):411-21.
ROCCA RA, MAGOON G, REYNOLDS DF, et al. "Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach". PLoS One. 2012;
CARBONELL J, ALLOZA E, ARCE P, et al. "A map of human microRNA variation uncovers unexpectedly high levels of variability". Genome Med. 2012 Aug 20;4(8):62.
ZHENG HX, YAN S, QIN ZD, JIN L. "MtDNA analysis of global populations support that major population expansions began before Neolithic Time". Sci Rep. Oct 2012; 2:745.
GARCÍA-BERMÚDEZ M, LÓPEZ-MEJÍAS R, GONZÁLEZ-JUANATEY C, et al. "CARD8 rs2043211 (p.C10X) Polymorphism is not associated with disease susceptibility or cardiovascular events in Spanish rheumatoid arthritis patients". DNA Cell Biol. 2012 Oct 22.
ABECASIS GR, AUTON A, BROOKS LD, et al. 1000 GENOMES PROJECT CONSORTIUM. "An integrated map of genetic variation from 1,092 human genomes". Nature. 2012 Nov 1;491(7422):56-65. November 2012.
FERNÁNDEZ-CAGGIANO M, BARALLOBRE-BARREIRO J, REGO-PÉREZ I, et al. "Mitochondrial haplogroups H and J: risk and protective factors for ischemic cardiomyopathy". PLoS One. 2012;7(8):
LÓPEZ-MEJÍAS R, GARCÍA-BERMÚDEZ M, GONZÁLEZ-JUANATEY C, et al. "Lack of association between IL6 single nucleotide polymorphisms and cardiovascular disease in Spanish patients with rheumatoid arthritis". Atherosclerosis. 2011 Dec;219(2):655-8.
JULIA A, DOMÈNECH E, RICART E, et al. "A genome-wide association study on a Southern European population identifies a new Crohn’s Disease susceptibilitylocus at RBX1-EP300". Gut. 2012 Oct 9.
ORDOÑANA JR, REBOLLO-MESA I, CARRILLO E, et al. "The Murcia twin registry: a population-based registry of adult multiples in Spain". Twin Res Hum Genet. 2012 Oct 9:1-5.
CÉNIT MC, SIMEÓN CP, FONOLLOSA V, et al ; SPANISH SCLERODERMA GROUP. "No evidence of association between functional polymorphisms located within IL6R and IL6ST genes and systemic sclerosis". Tissue Antigens. 2012 Sep; 80(3):254-8.
ILLESCAS MJ, AZNAR JM, CARDOSO S, et al. "Genetic characterization of ten X-STRs in a population from the Spanish Levant". Forensic Sci Int Genet. 2012 Jul 5.
VAN DONGEN J, SLAGBOOM PE, DRAISMA HH, et al. "The continuing value of twin studies in the omics era". Nat Rev Genet. 2012 Aug 14;13(9):640-53.
SANCHEZ-JIMENO C, CUADRADO-CORRALES N, ALLER E, et al. "Recessive Dystrophic Epidermolysis Bullosa: The origin of the c.6527insC mutation in the Spanish population". Br J Dermatol. 2012 Jul 3.
JULIÀ A, TORTOSA R, HERNANZ JM, et al. "Risk variants for psoriasis vulgaris in a large case-control collection and association with clinical subphenotypes". Human Molecular Genetics. (in press, doi: 10.1093/hmg/dds295).
BENITO-SANZ S, AZA-CARMONA M, RODRÍGUEZ-ESTEVEZ A, et al. "Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short stature". Eur J Hum Genet. 2012 Jan; 20(1):125-7.
CELORRIO D, BUJANDA L, CASO C, et al. "A comparison of Val81Met and other polymorphisms of alcohol metabolising genes in patients and controls in Northern Spain". Alcohol. 2012 May 2.
BOSSINI-CASTILLO L, SIMEON CP, BERETTA L, et al; THE SPANISH SCLERODERMA GROUP. "A multicenter study confirms CD226 gene association with systemic sclerosis-related pulmonary fibrosis". Arthritis Res Ther. 2012 Apr 24; 14(2):R85.
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Universidad de Salamanca
Nucleus
PRB2
Red de biobancos
Instituto Carlos III
Junta de Castilla y León
Union Europea
Banco Nacional de ADN
Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
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