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An inverse association between history of childhood eczema and subsequent risk of type 1 diabetes that is not likely to be explained by HLA-DQ, PTPN22, or CTLA4 polymorphisms
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Association of PTPN22 C1858T and CTLA-4 A49G polymorphisms with type 1 diabetes in Croatians
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PTPN22 Trp(620) explains the association of chromosome 1p13 with type 1 diabetes and shows a statistical interaction with HLA class II genotypes
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Sex-specific association of the human PTPN22 1858T-allele with type 1 diabetes
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Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population
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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
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No independent role of the -1123 G>C and +2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations
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PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits
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Association of the PTPN22/LYP gene with type 1 diabetes
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Lymphoid tyrosine phosphatase (LYP/PTPN22) Arg620Trp variant regulates insulin autoimmunity and progression to type 1 diabetes
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The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population
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Systematic search for single nucleotide polymorphisms in a lymphoid tyrosine phosphatase gene (PTPN22):: Association between a promoter polymorphism and type I diabetes in Asian populations
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Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population
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PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases
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Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population
A Zhernakova et al.
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Genetic association between a lymphoid tyrosine phosphatase (PTPN22) and type 1 diabetes
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A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes
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Genetics of type 1 diabetes
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Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus
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The genetics of complex autoimmune diseases: non-MHC susceptibility genes
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