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Publicaciones relacionadas con el BNADN
DIAZ-GALLO LM, SIMEON CP, BROEN JC, et al; SPANISH SCLERODERMA GROUP. "Implication of IL-2/IL-21 region in systemic sclerosis genetic susceptibility". Ann Rheum Dis. 2013 Jul;72(7):1233-8. doi: 10.1136/annrheumdis-2012-202357
RODRÍGUEZ-CABALLERO A, HENRIQUES A, CRIADO I, et al. "Subjects with chronic lymphocytic leukaemia-like B-cell clones with stereotyped B-cell receptors frequently show MDS-associated phenotypes on myeloid cells". Br J Haematol. 2014 Sep 24. doi: 10.1111/bjh.13127
COLONNA V, AYUB Q, CHEN Y, et al. "Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences". Genome Biol. 2014 Jun 30;15(6):R88
LOPEZ-LOPEZ A, GAMEZ J, SYRIANI E, et al. "CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis". PLoS One. 2014 May 7;9(5):e96528. doi: 10.1371/journal.pone.0096528. eCollection
PINO-YANES M, CORRALES A, ACOSTA-HERRERA M, et al. "HLA-DRB1*15:01 allele protects from asthma susceptibility". J Allergy Clin Immunol. 2014 Jul 14. pii: S0091-6749(14)00770-2. doi: 10.1016/j.jaci.2014.05.031.
ARGENTE J, FLORES R, GUTIÉRREZ-ARUMÍ A, et al. "Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency". EMBO Mol Med. 2014 Mar;6(3):299-306. doi: 10.1002/emmm.201303573. Epub 2014 Jan 30
MAYES MD, BOSSINI-CASTILLO L, GORLOVA O, et al. "Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis". Am J Hum Genet. 2014 Jan 2;94(1):47-61. doi: 10.1016/j.ajhg.2013.12.002.
DOCAMPO E, ESCARAMÍS G, GRATACÒS M, et al. "Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system". Pain. 2014 Jun;155(6):1102-9. doi: 10.1016/j.pain. 2014.02.016. Epub 2014 Feb 26.
FERRÁN A, ALEGRET JM, SUBIRANA I, et al. "Association between rs2200733 and rs7193343 genetic variants and atrial fibrillation in a Spanish population, and meta-analysis of previous studies. Rev Esp Cardiol". 2014 May 19. pii: S0300-8932(14)00156-0. doi: 10.1016/j.recesp.2013.12.021.
AZA-CARMONA M, BARCA-TIERNO V, HISADO-OLIVA A, et al. "NPPB and ACAN, two novel SHOX2 transcription targets implicated in skeletal development". PLoS One. 2014 Jan 8;9(1):e83104. doi: 10.1371/journal.pone.0083104. eCollection 2014.
LÓPEZ-ISAC E, BOSSINI-CASTILLO L, SIMEON CP, et al; SPANISH SCLERODERMA GROUP. "A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility". Arthritis Res Ther. 2014 Jan 9;16(1):R6.
ABULÍ A, BUJANDA L, MUÑOZ J, et al; EPICOLON CONSORTIUM. "The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals". PLoS One. 2014 Apr 17;9(4):e95022. doi: 10.1371/journal.pone.0095022. eCollection 2014.
PARDINI B, VERDERIO P, PIZZAMIGLIO S, et al; EPICOLON Consortium. "Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: results from a multi-centric stud"y. PLoS One. 2014 Jan 21;9(1):e85538. doi: 10.1371/journal.pone.0085538. eCollection 2014.
FERNANDEZ-ROZADILLA C, CAZIER JB, TOMLINSON I, et al; EPICOLON CONSORTIUM. "A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cáncer". Hum Genet. 2014 May;133(5):525-34
REAL LM, RUIZ A, GAYÁN J, et al. "A colorectal cancer susceptibility new variant at 4q26 in the spanish population identified by genome-wide association analysis". PLoS One. 2014 Jun 30;9(6):e101178. doi: 10.1371/journal.pone. 0101178. eCollection 2014.
HENRIQUES A, RODRÍGUEZ-CABALLERO A, NIETO WG, et al. "Combined patterns of IGHV repertoire and cytogenetic/molecular alterations in monoclonal B lymphocytosis versus chronic lymphocytic leukemia". PLoS One. 2013 Jul 3;8(7)
ALMEIDA J, NIETO WG, TEODOSIO C, et al; Primary Health Care Group of Salamanca for the Study of MBL. "CLL-like B-lymphocytes are systematically present at very low numbers in peripheral blood of healthy adults". Leukemia. 2011 Apr;25(4):718-22
CASABONNE D, ALMEIDA J, NIETO WG, ; the Primary Health Care Group of Salamanca for the Study of MBL. "Correction: Common Infectious Agents and Monoclonal B-Cell Lymphocytosis: A Cross-Sectional Epidemiological Study among Healthy Adults". PLoS One. 2013 Oct 11;8(10)
CASABONNE D, ALMEIDA J, NIETO WG, et al; Primary Health Care Group of Salamanca for the Study of MBL. "Common infectious agents and monoclonal B-cell lymphocytosis: a cross-sectional epidemiological study among healthy adults". PLoS One. 2012; 7(12)
PARDINI B, VERDERIO P, PIZZAMIGLIO S, et al; EPICOLON Consortium. "Association between CASP8 -652 6N Del Polymorphism (rs3834129) and Colorectal Cancer Risk: Results from a Multi-Centric Study". PLoS One. 2014 Jan 21;9(1):e85538.
FERNÁNDEZ-CAGGIANO M, BARALLOBRE-BARREIRO J, REGO-PÉREZ I, et al. "Mitochondrial DNA haplogroup H as a risk factor for idiopathic dilated cardiomyopathy in Spanish population". Mitochondrion. 2013 Jul;13(4):263-8.
LIU JZ, HOV JR, FOLSERAAS T, et al; INTERNATIONAL PSC STUDY GROUP, FRANKE A, ANDERSON CA, KARLSEN TH. "Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing colangitis". Nat Genet. 2013 Jun;45(6):670-5.
SERRANO A, CARMONA FD, CASTAÑEDA S, et al. "A case-control study suggests that the CCR6 locus is not involved in the susceptibility to giant cell arteritis". Clin Exp Rheumatol. 2013 Jan 7
KHURANA E et al. 1000 GENOMES PROJECT CONSORTIUM. "Integrative annotation of variants from 1092 humans: application to cancer genomics". Science. 2013 Oct 4;342(6154):1235587
FERNANDEZ-ROZADILLA C, CAZIER JB, et al. "A Colorectal Cancer Genome-Wide Association Study in a Spanish cohort identifies two new candidate colorectal cancer susceptibility variants at 1p33 and 8p12". BMC Genomics. 2013 Jan 26;14(1):55.
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Universidad de Salamanca
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