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CÉNIT MC, MÁRQUEZ A, CORDERO-COMA M, et al. "Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveítis". Mol Vis. 2013;19:638-43.
CÉNIT MC, MÁRQUEZ A, CORDERO-COMA M, et al. "Evaluation of the IL2/IL21, IL2RA and IL2RB genetic variants influence on the endogenous non-anterior uveitis genetic predisposition". BMC Med Genet. 2013 May 15;14:52
TERUEL M, MCKINNEY C, BALSA A, et al. "Association of CD247 polymorphisms with rheumatoid arthritis: a replication study and a meta-analysis". PLoS One. 2013 Jul 5;8(7):e68295
MARTIN JE, ASSASSI S, DIAZ-GALLO LM, et al. "A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci". Hum Mol Genet. 2013 Oct 1;22(19):4021-9
CARMONA FD, CÉNIT MC, DIAZ-GALLO LM, et al; SPANISH SCLERODERMA GROUP. "New insight on the Xq28 association with systemic sclerosis". Ann Rheum Dis. 2013 Dec;72(12):2032-8
BOSSINI-CASTILLO L, MARTIN JE, BROEN J, et al; SPANISH SCLERODERMA GROUP. "Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study". Ann Rheum Dis. 2013 Apr;72(4):602-7
SERRANO A, MÁRQUEZ A, MACKIE SL, et al; UK GCA CONSORTIUM SPANISH GCA CONSORTIUM. "Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis". Ann Rheum Dis. 2013 Nov 1;72(11):1882-6
TERUEL M, SIMEON CP, BROEN J, et al; SPANISH SCLERODERMA GROUP. "The role of the NLRP1 gene in systemic sclerosis: a replication study". Clin Exp Rheumatol. 2013 Mar-Apr;31(2 Suppl 76):187-8.
BOSSINI-CASTILLO L, SIMEON CP, BERETTA L, et al. "KCNA5 gene is not confirmed as a systemic sclerosis-related pulmonary arterial hypertension genetic susceptibility factor". Arthritis Res Ther. 2012 Dec 27;14(6):R273
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.
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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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