Helen E Stevens
occupation: researcher
Articles 28
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Capturing the systemic immune signature of a norovirus infection: an n-of-1 case study within a clinical trial.
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Neonatal and adult recent thymic emigrants produce IL-8 and express complement receptors CR1 and CR2.
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Regulatory T Cell Responses in Participants with Type 1 Diabetes after a Single Dose of Interleukin-2: A Non-Randomised, Open Label, Adaptive Dose-Finding Trial
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Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
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Postthymic expansion in human CD4 naive T cells defined by expression of functional high-affinity IL-2 receptors
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Plasma concentrations of soluble IL-2 receptor α (CD25) are increased in type 1 diabetes and associated with reduced C-peptide levels in young patients.
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Evidence of gene-gene interaction and age-at-diagnosis effects in type 1 diabetes
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Seven newly identified loci for autoimmune thyroid disease
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Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.
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Evidence of association with type 1 diabetes in the SLC11A1 gene region.
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Evidence that HLA class I and II associations with type 1 diabetes, autoantibodies to GAD and autoantibodies to IA-2, are distinct.
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FUT2 nonsecretor status links type 1 diabetes susceptibility and resistance to infection
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Inherited variation in vitamin D genes is associated with predisposition to autoimmune disease type 1 diabetes
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Genetic association analyses of atopic illness and proinflammatory cytokine genes with type 1 diabetes
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Common Genetic Determinants of Vitamin D Insufficiency: A Genome-Wide Association Study
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Common genetic determinants of vitamin D insufficiency: a genome-wide association study
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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
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Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
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Shared and distinct genetic variants in type 1 diabetes and celiac disease
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PTPN22 Trp620 explains the association of chromosome 1p13 with type 1 diabetes and shows a statistical interaction with HLA class II genotypes.
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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
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Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.
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Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
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Interaction analysis of the CBLB and CTLA4 genes in type 1 diabetes
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Analysis of Polymorphisms of the Interleukin-18 Gene in Type 1 Diabetes and Hardy-Weinberg Equilibrium Testing
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Parameters for reliable results in genetic association studies in common disease
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A Comprehensive, Statistically Powered Analysis of GAD2 in Type 1 Diabetes
Human - wd:Q63869281