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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.
TERUEL M, MARTIN JE, GÓMEZ-GARCÍA M, et al. "Lack of association of ACP1 gene with inflammatory bowel disease: a case-control study". Tissue Antigens. 2012 Jul; 80(1):61-64.
TERUEL M, SIMEON CP, BROEN J, et al. "Analysis of the association between CD40 and CD40 ligand polymorphisms and systemic sclerosis". Arthritis Res Ther. 2012 Jun 25; 14(3):R154.
PINO-YANES M, SÁNCHEZ-MACHÍN I, CUMPLIDO J, et al. "IL-1 receptor-associated kinase 3 gene (IRAK3) variants associate with asthma in a replication study in the Spanish population". J Allergy Clin Immunol. 2012 Feb;129(2):573-5, 575.
MARTÍN JE, BROEN JC, CARMONA D, et al. "Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up". Hum Mol Genet. 2012 Mar 9.
GAZQUEZ I, LOPEZ-ESCAMEZ JA, MORENO A, et al. "Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Menière’s disease in a European Caucasian population". DNA Cell Biol 2011 30 (9): 699-708.
BALLANA E, GONZALO E, GRAU E, et al. "Rare LEDGF/p75 genetic variants in white long-term nonprogressor HIV+ individuals". AIDS. 2012 Feb 20; 26(4): 527-8.
BALLANA E, RUIZ-DE ANDRES A, MOTHE B, et al. "Differential prevalence of the HLA-C -35 CC genotype among viremic long term non-progressor and elite controller HIV+ individuals". Immunobiology. 2012 Jan 8.
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Teléfono de contacto: 923294500. Ext. 5473
Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
