| Q34388225 | A new Graves disease-susceptibility locus maps to chromosome 20q11.2. International Consortium for the Genetics of Autoimmune Thyroid Disease |
| Q46231004 | A patient with stress-related onset and exacerbations of Graves disease |
| Q28076206 | A possible link between the Epstein-Barr virus infection and autoimmune thyroid disorders |
| Q51612155 | Association of polymorphisms of rs179247 and rs12101255 in thyroid stimulating hormone receptor intron 1 with an increased risk of Graves' disease: A meta-analysis. |
| Q36077116 | Association of the CTLA4 gene CT60/rs3087243 single-nucleotide polymorphisms with Graves' disease |
| Q67209937 | Autoimmune disease in a DFNA6/14/38 family carrying a novel missense mutation in WFS1. |
| Q27691806 | Current concepts in the molecular pathogenesis of thyroid-associated ophthalmopathy. |
| Q36660991 | Dissecting the Genetic Susceptibility to Graves' Disease in a Cohort of Patients of Italian Origin |
| Q57075123 | Editorial: The Association of Other Autoimmune Diseases in Patients With Thyroid Autoimmunity |
| Q35867015 | Epigenetics and autoimmune diseases. |
| Q38093041 | GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis. |
| Q58050337 | Gene polymorphisms of interleukin-4, interleukin-10 and transforming growth factor-beta in Graves’ disease |
| Q34739056 | Graves' disease in monozygotic twins - a case report |
| Q73661041 | HLA DQA1*0501 and DRB1*0301 antigens do not independently convey susceptibility to Graves' disease |
| Q40607323 | HLA-DRB1 the notorious gene in the mosaic of autoimmunity |
| Q35730981 | Immunogenetic mechanisms leading to thyroid autoimmunity: recent advances in identifying susceptibility genes and regions |
| Q36236762 | Immunogenetics of autoimmune thyroid diseases: A comprehensive review |
| Q33890792 | Insulin-like growth factor-I regulation of immune function: a potential therapeutic target in autoimmune diseases? |
| Q42225256 | Is Graves' disease a primary immunodeficiency? New immunological perspectives on an endocrine disease |
| Q36973929 | Joint genetic susceptibility to type 1 diabetes and autoimmune thyroiditis: from epidemiology to mechanisms. |
| Q39198547 | Lack of association of VDR gene polymorphisms with thyroid autoimmune disorders: familial and case/control studies |
| Q56904840 | Lack of linkage and association between autoimmune thyroid diseases and the CTLA-4 gene in a large Tunisian family |
| Q47232663 | Low birth weight is not associated with clinically overt thyroid disease: a population based twin case-control study |
| Q26827065 | Mechanisms of autoimmune thyroid diseases: from genetics to epigenetics |
| Q35864459 | New genetic insights from autoimmune thyroid disease |
| Q36198104 | Pooled genome wide association detects association upstream of FCRL3 with Graves' disease |
| Q47443163 | Sibling Recurrence Risk in Autoimmune Thyroid Disease |
| Q44211565 | Subacute thyroiditis with cell destruction and temporary hyperthyroidism in Graves'disease--case report |
| Q36239418 | The Prevalence, Incidence and Natural Course of Positive Antithyroperoxidase Antibodies in a Population-Based Study: Tehran Thyroid Study |
| Q47926898 | The aetiology of Graves' disease: what is the genetic contribution? |
| Q35605705 | The contribution of immune regulatory and thyroid specific genes to the etiology of Graves' and Hashimoto's diseases |
| Q35730994 | The genetic basis of graves' disease |
| Q34110141 | The genetics of the thyroid stimulating hormone receptor: history and relevance |
| Q33741165 | The role of genetic factors in autoimmune disease: implications for environmental research |
| Q37063551 | The role of genetics in Graves' disease and thyroid orbitopathy |
| Q39675819 | Twin studies as a model for exploring the aetiology of autoimmune thyroid disease |
| Q34715426 | Type 1A diabetes mellitus-associated autoimmunity |
| Q33735061 | Update on the medical treatment of Graves' ophthalmopathy |
| Q54513970 | rs3827440, a nonsynonymous single nucleotide polymorphism within GPR174 gene in X chromosome, is associated with Graves' disease in Polish Caucasian population. |