about
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsGenome-wide association analysis of autoantibody positivity in type 1 diabetes cases.Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes riskA hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples.Confirmation of novel type 1 diabetes risk loci in families.Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity.Evidence of association with type 1 diabetes in the SLC11A1 gene region.No evidence of association or interaction between the IL4RA, IL4, and IL13 genes in type 1 diabetesEvidence that HLA class I and II associations with type 1 diabetes, autoantibodies to GAD and autoantibodies to IA-2, are distinct.Genetic analysis of adult-onset autoimmune diabetesFUT2 nonsecretor status links type 1 diabetes susceptibility and resistance to infectionEvidence for association of OCTN genes and IBD5 with ulcerative colitisA type 1 diabetes subgroup with a female bias is characterised by failure in tolerance to thyroid peroxidase at an early age and a strong association with the cytotoxic T-lymphocyte-associated antigen-4 geneNKG2D-RAE-1 receptor-ligand variation does not account for the NK cell defect in nonobese diabetic mice.HLA class II gene associations in African American type 1 diabetes reveal a protective HLA-DRB1*03 haplotype.Confirmation of HLA class II independent type 1 diabetes associations in the major histocompatibility complex including HLA-B and HLA-A.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.A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design.Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.Genetic and functional association of the immune signaling molecule 4-1BB (CD137/TNFRSF9) with type 1 diabetes.Fine mapping, gene content, comparative sequencing, and expression analyses support Ctla4 and Nramp1 as candidates for Idd5.1 and Idd5.2 in the nonobese diabetic mouse.Haplotype structure, LD blocks, and uneven recombination within the LRP5 gene.SLC11A1 (formerly NRAMP1) and susceptibility to visceral leishmaniasis in The Sudan.New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals.Testing the possible negative association of type 1 diabetes and atopic disease by analysis of the interleukin 4 receptor gene.A systematic approach to the assessment of known TNF-alpha polymorphisms in Graves' disease.Genetic susceptibility to visceral leishmaniasis in The Sudan: linkage and association with IL4 and IFNGR1.Comparison of population- and family-based methods for genetic association analysis in the presence of interacting loci.Sequencing-based genotyping and association analysis of the MICA and MICB genes in type 1 diabetes.Analysis of 17 autoimmune disease-associated variants in type 1 diabetes identifies 6q23/TNFAIP3 as a susceptibility locusGenetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traitsAnalysis of Polymorphisms of the Interleukin-18 Gene in Type 1 Diabetes and Hardy-Weinberg Equilibrium TestingTrans-ethnic association study of blood pressure determinants in over 750,000 individualsInterleukin‐10, Polymorphism inSLC11A1(formerlyNRAMP1), and Susceptibility to TuberculosisMeta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic lociIdentification of a Structurally Distinct CD101 Molecule Encoded in the 950-kb Idd10 Region of NOD MiceAssessing the causal association of glycine with risk of cardio-metabolic diseasesA novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effectCommon allelic variants of exons 10, 12, and 33 of the thyroglobulin gene are not associated with autoimmune thyroid disease in the United Kingdom
P50
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P50
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հետազոտող
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Joanna Howson
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Joanna Howson
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Joanna Howson
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Joanna Howson
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Joanna Howson
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Joanna Howson
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Joanna Howson
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Joanna M Howson
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Joanna M M Howson
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Joanna Howson
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Joanna Howson
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Joanna Howson
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Joanna Howson
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Joanna Howson
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P106
P1153
54935789800
P21
P31
P496
0000-0001-7618-0050