| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1093/BFGP/ELQ036 |
| P698 | PubMed publication ID | 21436304 |
| P50 | author | Matt Simmonds | Q64513679 |
| P2093 | author name string | Stephen C L Gough | |
| P2860 | cites work | Finding the missing heritability of complex diseases | Q22122198 |
| A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities | Q24537702 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study | Q24597671 | ||
| Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls | Q24628710 | ||
| Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes | Q24632382 | ||
| Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants | Q24646663 | ||
| Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes | Q24651119 | ||
| Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes | Q24652324 | ||
| A haplotype map of the human genome | Q24679827 | ||
| Sequencing technologies - the next generation | Q27860568 | ||
| The International HapMap Project | Q27860695 | ||
| Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease | Q28201947 | ||
| Proteasome subunits, low-molecular-mass polypeptides 2 and 7 are hyperexpressed by target cells in autoimmune thyroid disease but not in insulin-dependent diabetes mellitus: implications for autoimmunity | Q28247370 | ||
| 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 | Q28289699 | ||
| Origins and functional impact of copy number variation in the human genome | Q28730507 | ||
| The HapMap and genome-wide association studies in diagnosis and therapy | Q28752130 | ||
| The gut microbiota shapes intestinal immune responses during health and disease | Q29547727 | ||
| Missing heritability and strategies for finding the underlying causes of complex disease | Q29614586 | ||
| Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families | Q33188524 | ||
| Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population | Q33253558 | ||
| Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence. | Q33417956 | ||
| Autoimmune disease classification by inverse association with SNP alleles | Q33521311 | ||
| Association of the large multifunctional proteasome (LMP2) gene with Graves' disease is a result of linkage disequilibrium with the HLA haplotype DRB1*0304-DQB1*02-DQA1*0501. | Q33872663 | ||
| How to interpret a genome-wide association study | Q34010528 | ||
| The immune system and the gut microbiota: friends or foes? | Q34024073 | ||
| Evidence for a new Graves disease susceptibility locus at chromosome 18q21. | Q34390493 | ||
| Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease. | Q34480522 | ||
| The association between HLA class II haplotype with Graves' disease in Thai population | Q34490400 | ||
| Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association | Q34596989 | ||
| Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility. | Q34632596 | ||
| A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene | Q34651283 | ||
| Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3. | Q35822169 | ||
| The thyroglobulin gene as the first thyroid-specific susceptibility gene for autoimmune thyroid disease | Q35830654 | ||
| Genetic insights into disease mechanisms of autoimmunity | Q36035381 | ||
| Interleukin (IL)-23 receptor is a major susceptibility gene for Graves' ophthalmopathy: the IL-23/T-helper 17 axis extends to thyroid autoimmunity. | Q36494390 | ||
| The Molecular Genetics of Three Thyroid Autoantigens: Thyroglobulin, Thyroid Peroxidase and the Thyrotropin Receptor | Q36681946 | ||
| Genetic developments in autoimmune thyroid disease: an evolutionary process | Q37032887 | ||
| Parental origin of sequence variants associated with complex diseases | Q37102209 | ||
| Human QTL linkage mapping | Q37230950 | ||
| Type 2 diabetes: new genes, new understanding | Q37308665 | ||
| Cis-regulatory mutations in human disease | Q37343922 | ||
| DNA variations in human and medical genetics: 25 years of my experience | Q37374228 | ||
| Transgenerational genetic effects on phenotypic variation and disease risk | Q37379485 | ||
| Genetics of thyroid autoimmunity and the role of the TSHR. | Q37677258 | ||
| Uncovering the roles of rare variants in common disease through whole-genome sequencing | Q37755970 | ||
| A CD40 Kozak sequence polymorphism and susceptibility to antibody-mediated autoimmune conditions: the role of CD40 tissue-specific expression. | Q38303947 | ||
| The HLA Region and Autoimmune Disease: Associations and Mechanisms of Action | Q40159351 | ||
| Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population | Q42641028 | ||
| Regression mapping of association between the human leukocyte antigen region and Graves disease | Q42949415 | ||
| Confirmation of association of chromosome 5q31-33 with United Kingdom Caucasian Graves' disease. | Q43530520 | ||
| Polymorphisms in the interleukin 3 gene show strong association with susceptibility to Graves' disease in Chinese population. | Q43701467 | ||
| Arginine at position 74 of the HLA-DR beta1 chain is associated with Graves' disease | Q44804359 | ||
| Lack of association of the vitamin D receptor gene with Graves' disease in UK Caucasians | Q44856216 | ||
| The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease | Q45142894 | ||
| Evaluating coverage of genome-wide association studies | Q46423138 | ||
| Vitamin D receptor polymorphisms are associated with Graves' disease in German and Polish but not in Serbian patients | Q46798189 | ||
| Association of a rare thyroglobulin gene microsatellite variant with autoimmune thyroid disease | Q47444459 | ||
| Lack of association of Graves' disease with the A2 allele of the interleukin-1 receptor antagonist gene in a white European population | Q47789514 | ||
| Drinking from the fire hose--statistical issues in genomewide association studies | Q47838945 | ||
| A systematic approach to the assessment of known TNF-alpha polymorphisms in Graves' disease. | Q47840935 | ||
| Association of the T-cell regulatory gene CTLA4 with Graves' disease and autoimmune thyroid disease in the Japanese | Q48032200 | ||
| Association of the TSHR gene with Graves' disease: the first disease specific locus. | Q50758182 | ||
| The regulatory T cell gene FOXP3 and genetic susceptibility to thyroid autoimmunity: an association analysis in Caucasian and Japanese cohorts. | Q51757534 | ||
| Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease. | Q51798434 | ||
| Betting odds and genetic associations. | Q52001328 | ||
| Evaluating and improving power in whole-genome association studies using fixed marker sets. | Q53255191 | ||
| Tag SNP screening of the PDCD1 gene for association with Graves' disease. | Q53554417 | ||
| A genome-wide screen in 1119 relative pairs with autoimmune thyroid disease. | Q53610166 | ||
| The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus. | Q54000430 | ||
| Role of the CD40 locus in Graves' disease. | Q54445221 | ||
| Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease. | Q54500126 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 77-90 | |
| P577 | publication date | 2011-03-01 | |
| P1433 | published in | Briefings in functional genomics | Q26841935 |
| P1476 | title | The search for the genetic contribution to autoimmune thyroid disease: the never ending story? | |
| P478 | volume | 10 |
| Q34878612 | A 20 year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction. |
| Q36421188 | Autoimmune thyroid disease in rheumatoid arthritis: a global perspective |
| Q56888768 | Correlation between CTLA-4 and CD40 gene polymorphisms and their interaction in graves' disease in a Chinese Han population |
| Q38093041 | GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis. |
| Q34476631 | Hashimoto's thyroiditis: celebrating the centennial through the lens of the Johns Hopkins hospital surgical pathology records |
| Q34311459 | Hürthle cells predict hypothyroidism in interferon-γ transgenic mice of different genetic backgrounds |
| Q28730714 | Novel associations for hypothyroidism include known autoimmune risk loci |
| Q34770032 | Replication of association of nine susceptibility loci with Graves' disease in the Chinese Han population |
| Q35730994 | The genetic basis of graves' disease |
| Q39675819 | Twin studies as a model for exploring the aetiology of autoimmune thyroid disease |
Search more.