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Publicaciones relacionadas con el BNADN
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DELANEAU O, MARCHINI J. 1000 Genomes Project Consortium; "Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel"; Nat Commun. 2014 Jun 13;5:3934. doi: 10.1038/ncomms4934.
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 2014.
MÁRQUEZ A, SOLANS R, HERNÁNDEZ-RODRÍGUEZ J, et al. "A Candidate Gene Approach Identifies an IL33 Genetic Variant as a Novel Genetic Risk Factor for GCA". PLoS One. 2014 Nov 19;9(11):e113476.
LÓPEZ-MEJÍAS R, GENRE F, PÉREZ BS, et al. "HLA-DRB1 association with Henoch-Schonlein purpura". Arthritis Rheumatol. 2014 Dec 2. doi: 10.1002/art.38979
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 (Engl Ed). 2014 Oct;67(10):822-9. doi: 10.1016/j.rec.2013.12.019.
IVORRA JL, RIVERO O, COSTAS J, et al. "Replication of previous genome-wide association studies of psychiatric diseases in a large schizophrenia case-control sample from Spain". Schizophr Res. 2014 Oct;159(1):107-13. doi: 10.1016/j.schres.2014.07.004
CASH TP, PITA G, DOMÍNGUEZ O, et al. "Exome sequencing of three cases of familial exceptional longevity". Aging Cell. 2014 Aug 12. doi: 10.1111/acel.12261
CARRERAS-TORRES R, KUNDU S, ZANETTI D, et al. "Genetic risk score of NOS gene variants associated with myocardial infarction correlates with coronary incidence across Europe". PLoS One. 2014 May 7;9(5):e96504. doi: 10.1371/journal.pone.0096504.
LÓPEZ S, GARCÍA O, YURREBASO I, et al. "The interplay between natural selection and susceptibility to melanoma on allele 374F of SLC45A2 gene in a South European population". PLoS One. 2014 Aug 5;9(8):e104367. doi: 10.1371/journal.pone.0104367.
BOTIGUÉ LR, HENN BM, GRAVEL S, et al. "Gene flow from North Africa contributes to differential human genetic diversity in southern Europe". Proc Natl Acad Sci USA. 2013 Jul 16;110(29):11791-6. doi: 10.1073/pnas.1306223110
JULIÀ A, DOMÈNECH E, CHAPARRO M, et al. "A genome-wide association study identifies a novel locus at 6q22.1 associated with ulcerative colitis". Hum Mol Genet. 2014 Jul 31.
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
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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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