Genética de Enfermedades Complejas
GENOME
Hospital Universitario Central de Asturias
Oviedo, EspañaPublikationen in Zusammenarbeit mit Forschern von Hospital Universitario Central de Asturias (9)
2012
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Lack of association of ACP1 gene with inflammatory bowel disease: A case-control study
Tissue Antigens, Vol. 80, Núm. 1, pp. 61-64
2011
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Analysis of the influence of two CD24 genetic variants in Crohn's disease and ulcerative colitis
Human Immunology, Vol. 72, Núm. 10, pp. 969-972
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Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis
Inflammatory Bowel Diseases, Vol. 17, Núm. 11, pp. 2287-2294
2010
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Association of FcgR2a, but not FcgR3a, with inflammatory bowel diseases across three Caucasian populations
Inflammatory Bowel Diseases, Vol. 16, Núm. 12, pp. 2080-2089
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CD40: Novel association with crohn's disease and replication in multiple sclerosis susceptibility
PLoS ONE, Vol. 5, Núm. 7, pp. 1-4
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STAT4 gene influences genetic predisposition to ulcerative colitis but not Crohn's disease in the Spanish population: A replication study
Human Immunology, Vol. 71, Núm. 5, pp. 515-519
2009
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Association of ATG16L1 and IRGM genes polymorphisms with inflammatory bowel disease: A meta-analysis approach
Genes and Immunity, Vol. 10, Núm. 4, pp. 356-364
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STAT4 associates with systemic lupus erythematosus through two independent effects that correlate with gene expression and act additively with IRF5 to increase risk
Annals of the Rheumatic Diseases, Vol. 68, Núm. 11, pp. 1746-1753
2007
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Structural insertion/deletion variation in IRF5 is associated with a risk haplotype and defines the precise IRF5 isoforms expressed in systemic lupus erythematosus
Arthritis and Rheumatism, Vol. 56, Núm. 4, pp. 1234-1241