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A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn’s disease
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GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
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Implication of IL-2/IL-21 region in systemic sclerosis genetic susceptibility
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A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci
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A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci
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Analysis of Class II human leucocyte antigens in Italian and Spanish systemic sclerosis
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Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up
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Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up
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Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up
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Analysis of Class II human leucocyte antigens in Italian and Spanish systemic sclerosis
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Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up
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Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
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In: PLoS genetics, vol 7, iss 7 (2011)
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Association of a non-synonymous functional variant of the ITGAM gene with systemic sclerosis
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Association of a non-synonymous functional variant of the ITGAM gene with systemic sclerosis
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A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort
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Association of a non-synonymous functional variant of the ITGAM gene with systemic sclerosis
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Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy
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Correction: Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy
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Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy
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A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort
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