GENOMICA FUNCIONAL Y EVOLUTIVA
GENETICA DE MAMIFEROS
Radboud University Nijmegen Medical Centre
Nimega, HolandaPublicaciones en colaboración con investigadores/as de Radboud University Nijmegen Medical Centre (21)
2019
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GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
Nature Communications, Vol. 10, Núm. 1
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Low RUNX3 expression alters dendritic cell function in patients with systemic sclerosis and contributes to enhanced fibrosis
Annals of the Rheumatic Diseases, Vol. 78, Núm. 9, pp. 1249-1259
2017
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An MIF promoter polymorphism is associated with susceptibility to pulmonary arterial hypertension in diffuse cutaneous systemic sclerosis
Journal of Rheumatology, Vol. 44, Núm. 10, pp. 1453-1457
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Association of MicroRNA-618 Expression With Altered Frequency and Activation of Plasmacytoid Dendritic Cells in Patients With Systemic Sclerosis
Arthritis and Rheumatology, Vol. 69, Núm. 9, pp. 1891-1902
2015
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A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides
Annals of the Rheumatic Diseases, Vol. 74, Núm. 3
2014
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A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility
Arthritis Research and Therapy, Vol. 16, Núm. 1
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Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis
American Journal of Human Genetics, Vol. 94, Núm. 1, pp. 47-61
2013
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Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study
Annals of the Rheumatic Diseases, Vol. 72, Núm. 4, pp. 602-607
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The Systemic Lupus Erythematosus IRF5 Risk Haplotype Is Associated with Systemic Sclerosis
PLoS ONE, Vol. 8, Núm. 1
2012
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A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populations
Human Molecular Genetics, Vol. 21, Núm. 4, pp. 926-933
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A multicenter study confirms CD226 gene association with systemic sclerosis-related pulmonary fibrosis
Arthritis Research and Therapy, Vol. 14, Núm. 2
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A rare polymorphism in the gene for Toll-like receptor 2 is associated with systemic sclerosis phenotype and increases the production of inflammatory mediators
Arthritis and Rheumatism, Vol. 64, Núm. 1, pp. 264-271
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Independent replication and metaanalysis of association studies establish TNFSF4 as a susceptibility gene preferentially associated with the subset of anticentromere-positive patients with systemic sclerosis
Journal of Rheumatology, Vol. 39, Núm. 5, pp. 997-1003
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KCNA5 gene is not confirmed as a systemic sclerosis-related pulmonary arterial hypertension genetic susceptibility factor
Arthritis Research and Therapy, Vol. 14, Núm. 6
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Polymorphisms in the interleukin 4, interleukin 13, and corresponding receptor genes are not associated with systemic sclerosis and do not influence gene expression
Journal of Rheumatology, Vol. 39, Núm. 1, pp. 112-118
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The autoimmune disease-associated IL2RA locus is involved in the clinical manifestations of systemic sclerosis
Genes and Immunity, Vol. 13, Núm. 2, pp. 191-196
2011
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A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort
Annals of the Rheumatic Diseases, Vol. 70, Núm. 4, pp. 638-641
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Analysis of the rel polymorphism rs13031237 in autoimmune diseases
Annals of the Rheumatic Diseases
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Association of a non-synonymous functional variant of the ITGAM gene with systemic sclerosis
Annals of the Rheumatic Diseases
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