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DOCAMPO E, GIARDINA E, RIVEIRA-MUÑOZ E, et al. "Delection of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis". Arthritis Rheum. 2011 Jul; 63(7): 1860-5.
FERNÁNDEZ-MORENO M, TAMAYO M, SOTO-HERMIDA A, et al. "mtDNA haplogroup J Modulates telomere length and Nitric Oxide production". BMC Musculoskelet Disord. 2011 Dec 15; 12:283.
DANECEK P, AUTON A, ABECASIS G, et al; 1000 GENOMES PROJECT ANALYSIS GROUP. "The variant call format and VCFtools". Bioinformatics. 2011 Aug 1;27(15):2156-8.
MACKINTOSH C, ORDOÑEZ JL, GARCÍA-DOMÍNGUEZ DJ, et al. "1q gain and CDT2 overexpression underlie an aggressive and highly proliferative form of Ewing sarcoma". 2011. Oncogene. 2011 Aug 8. doi: 10.1038/onc.2011.317.
FORTIER I, DOIRON A, LITTLE J, et al; International Harmonization Initiative. "Is rigorous retrospective harmonization possible? Application of the DataSHaPER approach across 53 large studies". Int J Epidemiol. 2011 Oct; 40(5): 1314-28.
SZCZYPIORSKA M, SÁNCHEZ A, BARTOLOMÉ N, et al. "ERAP1 polymorphisms and haplotypes are associated with ankylosing spondylitis susceptibility and functional severity in a Spanish population". 2011. Rheumatology (Oxford). 2011 Nov; 50(11): 1969-75.
PINO-YANES M, CORRALES A, BASALDÚA S, et al. "North African influences and potential bias in case-control association studies in the Spanish population". PLoS One. 2011 Mar 30; 6(3):e18389.
BENITO-SANZ S, ARAGONES A, GRACIA R, et al. "A non-pathogenic pseudoautosomal region 1 copy number variant downstream of SHOX". Am J Med Genet A. 2011 Apr; 155A(4): 935-7.
CHINCILLA A, DAIMI H, LOZANO-VELASCO E, et al. "PITX2 insufficiency leads to atrial electrical and structural remodeling linked to arrhythmogenesis". Cir Cardiovasc Genet. 2011 Jun;4(3):269-79.
ANDERSON CA, BOUCHER G, LEES CW et al. "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47". Nature Genetics. 2011 Mar; 43(3): 246-52.
BENITO-SANZ S, BARROSO E, HEINE-SUÑER D, et al. "Clinical and molecular evaluation of SHOX/PAR1 duplications in Lèri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS)". J Clin Endocrinol Metab. 2011 Feb; 96(2): E404-12.
SÁNCHEZ A, SZCZYPIORSKA M, JUANOLA X, et al. "Association of the intergenic single-nucleotide polymorphism rs10865331 (2p15) with ankylosing spondylitis in a Spanish population". 2010. J Rheumatol; 2010 Nov; 37(11):2345-7.
GARCÍA MONTERO AC, REGALADO AM. "Políticas de calidad de un biobanco". Viure en Salut, n. 83, año 2010. pp 12-13.
FRANKE A, McGOVERN DP, BARRETT JC et al. "Genome-wide meta-analysis increases to 71 the number of confirmed Crohn’s disease susceptibility loci". Nature Genetics. 2010 Dec; 42(12):1118-25.
FORTIER I, BURTON PR, ROBSON PJ et al. "Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies". Int J Epidemiol. 2010 Oct; 39(5):1383-93.
LAAYOUNI H, CALAFELL F, BERTRANPETIT J. "A genome-wide survey does not show the genetic distinctiveness of Basques". Hum Genet. 2010 Apr;127(4):455-8
VARGAS-ALARCÓN G, FRAGOSO JM, CRUZ-ROBLES D, et al. "Association of adrenergic receptor gene polymorphisms with different fibromyalgia syndrome domains". Arthritis Rheum. 2009 Jul;60(7):2169-73.
VILLAMÓN E, PIQUERAS M, MACKINTOSH C, et al. "Comparison of different techniques for the detection of genetic risk-identifying chromosomal gains and losses in neuroblastoma". Virchows Archiv. 2008 Jul;453(1):47-55.
RUBIO-CABEZAS O, DIAZ GONZALEZ F, ARAGONES A, et al. "Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene". Pediatr Diabetes. 2008 Jun; 9(3 Pt 1):245-9.
ESPINOSA AB, MACKINTOSH C, MAÍLLO A, et al. "Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningioma"s. Eur J Hum Genet. 2008 Dec; 16(12):1450-8.
LAVARINO C, GARCIA I, MACKINTOSH C, et al. "Differential expression of genes mapping to recurrently abnormal chromosomal regions characterize neuroblastic tumours with distinct ploidy status". BMC Med Genomics. 2008 Aug 13;1:36.
JULIÀ A, BALLINA J, CAÑETE JD, et al. "Genome-wide association study of rheumatoid arthritis in the Spanish population. KLF12 as a risk locus for rheumatoid arthritis susceptibility". Arthritis and Rheumatism. 2008 Aug; 58(8):2275-86.
HEATH KE, ARGENTE J, BARRIOS V, et al. "Primary acid-labile subunit deficiency due to recessive IGFALS mutations results in postnatal growth deficit associated to low circulating insulin growth factor (IGF)-I, IGF binding protein-3 levels, and hyperinsulinemia". J Clin Endocrinol Metab. 2008; May; 93(5):1616-24
VARGAS-ALARCON G, FRAGOSO JM, CRUZ-ROBLES D, et al. "Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromialgia". Artritis Res Ther. 2007; 9(5):R110.
DOCAMPO E, RABIONET R, RIVEIRA-MUÑOZ E, ET AL. Deletion of the late cornified envelope genes, LCE3C and LCE3B, is associated with rheumatoid arthritis. Arthritis Rheum. 2010 May; 62(5):1246-51.
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Edificio Multiusos I+D+i (Universidad de Salamanca)
C/ Espejo s/n. 37007 Salamanca
Teléfono de contacto: 923294500. Ext. 5473
