The different approaches to the genetic analysis of autoimmune thyroid disease.

No abstract is available for this paper.

• Publication year

  1999

• Venue

  Journal of Endocrinology

• Publication date

  1999-10-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1677/JOE.0.1630007PMID 10495401
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Lack of Association Between Polymorphism of the Thyrotropin Receptor Gene and Graves' Disease in United Kingdom and Hong Kong Chinese Patients: Case Control and Family-Based Studies

  1998cited by this paper
• Linkage analysis of candidate genes in autoimmune thyroid disease: 1. Selected immunoregulatory genes. International Consortium for the Genetics of Autoimmune Thyroid Disease.

  1998influential reference
• Linkage disequilibrium between the human leukocyte antigen class II region of the major histocompatibility complex and Graves' disease: replication using a population case control and family-based study.

  1998cited by this paper
• A population‐based study of Graves' disease in Danish twins

  1998cited by this paper
• Is CTLA-4 a master switch for peripheral T cell tolerance?

  1997cited by this paper
• Genetic susceptibility to the development of autoimmune disease.

  1997cited by this paper
• A CTLA‐4 gene polymorphism is associated with both Graves' disease and autoimmune hypothyroidism

  1997cited by this paper
• Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31.

  1997influential reference
• CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus.

  1997cited by this paper
• No Association between a Thyrotropin Receptor Gene Polymorphism and Graves' Disease in the Female Population

  1997cited by this paper
• Association of HLA‐DQA1*0501 with Graves’ disease in English Caucasian men and women

  1996cited by this paper
• A full genome search in multiple sclerosis

  1996cited by this paper
• The Future of Genetic Studies of Complex Human Diseases

  1996cited by this paper
• Analysis of the thyrotropin receptor as a candidate gene in familial Graves' disease.

  1996influential reference
• A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex

  1996cited by this paper
• Lack of an association between alleles of interleukin-1 alpha and interleukin-1 receptor antagonist genes and Graves' disease in a North American Caucasian population.

  1996cited by this paper
• The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry.

  1996cited by this paper
• The interaction of a type A retroviral particle and class II human leukocyte antigen susceptibility genes in the pathogenesis of Graves' disease.

  1996cited by this paper
• A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

  1996cited by this paper
• The incidence of thyroid disorders in the community: a twenty‐year follow‐up of the Whickham Survey

  1995influential reference
• Genetic analysis of type 1 diabetes using whole genome approaches.

  1995influential reference
• A Polymorphism in the Extracellular Domain of the Thyrotropin Receptor Is Highly Associated with Autoimmune Thyroid Disease in Females

  1995cited by this paper
• CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population.

  1995cited by this paper
• Mutation of the glucagon receptor gene and diabetes mellitus in the UK: association or founder effect?

  1995cited by this paper
• Association of Graves' disease with an allele of the interleukin-1 receptor antagonist gene.

  1995cited by this paper
• Susceptibility and resistance alleles of human leukocyte antigen (HLA) DQA1 and HLA DQB1 are shared in endocrine autoimmune disease.

  1995cited by this paper
• Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31–q33

  1995cited by this paper
• Combined segregation and linkage analysis of Graves disease with a thyroid autoantibody diathesis.

  1994cited by this paper
• A genome-wide search for human type 1 diabetes susceptibility genes

  1994cited by this paper
• HLA‐DPB1 polymorphisms on the MHC‐extended haplotypes of families of patients with Graves' disease: two distinct HLA‐DR17 haplotypes

  1994cited by this paper
• Human histocompatibility leukocyte antigen-DQA1*0501 allele associated with genetic susceptibility to Graves' disease in a Caucasian population.

  1993influential reference
• Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

  1993cited by this paper
• Genetics of autoimmune thyroid disease: lack of evidence for linkage to HLA within families.

  1992influential reference
• HLA-DRB3 gene alleles in Caucasian patients with Graves' disease

  1992cited by this paper
• HLA Associations with Hashimoto's thyroiditis

  1991cited by this paper
• Autoimmune thyroid disease in type I diabetic families

  1989cited by this paper
• The genetics of Graves' disease: HLA and disease susceptibility.

  1985cited by this paper
• Type 1 (insulin-dependent) diabetes and a highly variable locus close to the insulin gene on chromosome 11

  1985cited by this paper
• A Polymorphic Locus Near the Human Insulin Gene Is Associated with Insulin-dependent Diabetes Melliitus

  1984cited by this paper
• [Human histocompatibility].

  1969cited by this paper
• Antibodies in the families of thyrotoxic patients.

  1967cited by this paper

• Association pernicious anemia and autoimmune polyendocrinopathy: a retrospective study

  2017cites this paper
• Differences between older and young patients with autoimmune gastritis

  2017cites this paper
• The Prevalence, Incidence and Natural Course of Positive Antithyroperoxidase Antibodies in a Population-Based Study: Tehran Thyroid Study

  2017cites this paper
• Genetics of Thyroid-Stimulating Hormone Receptor—Relevance for Autoimmune Thyroid Disease

  2017cites this paper
• Polyautoimmunity in autoimmune gastritis.

  2016cites this paper
• How Far Are We from Understanding the Genetic Basis of Hashimoto's Thyroiditis?

  2013cites this paper
• Genetics of Graves' Disease

  2013cites this paper
• Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population

  2013cites this paper
• Frequency, Pathogenesis, Prevention and Treatment of Iodine-Induced Hyperthyroidism

  2009cites this paper
• Occurrence and risk factors for autoimmune thyroid disease in patients with atrophic body gastritis.

  2008cites this paper
• Influences of age, gender, smoking, and family history on autoimmune thyroid disease phenotype.

  2006cites this paper
• The association and linkage of the HLA-A2 class I allele with autism.

  2006cites this paper
• A candidate gene approach to identify genes predisposing for the autoimmune disease canine lymphocytic thyroiditis (CTL)

  2006cites this paper
• Immunogenetics of Hashimoto's thyroiditis

  2005cites this paper
• Unravelling the genetic complexity of autoimmune thyroid disease: HLA, CTLA‐4 and beyond

  2004cites this paper
• Familial Juvenile Autoimmune Hypothyroidism, Pituitary Enlargement, Obesity, and Insulin Resistance

  2004cites this paper
• The genetics of autoimmune endocrine disease

  2003cites this paper
• Prevalence and clinico-epidemiology of familial Graves' disease in Japan based on nationwide epidemiologic survey in 2001.

  2003cites this paper
• Autoimmune thyroid diseases: etiology, pathogenesis, and dermatologic manifestations.

  2003cites this paper
• Autoimmune thyroid disease: propagation and progression.

  2003cites this paper
• Searching for the autoimmune thyroid disease susceptibility genes: from gene mapping to gene function.

  2003cites this paper
• Preliminary Evidence of Genetic Anticipation in Graves' Disease

  2003cites this paper
• Association of Graves' Disease with Intragenic Polymorphism of the Thyrotropin Receptor Gene in a Cohort of Singapore Patients of Multi-Ethnic Origins

  2003cites this paper
• Mapping to Gene Function Searching for the Autoimmune Thyroid Disease Susceptibility Genes: From Gene

  2003cites this paper
• Autoimmune Thyroid Diseases

  2003cites this paper
• The Involvement of the HLA Region in Genetic susceptibility to Graves’ disease

  2002cites this paper
• Polymorphism of the CTLA-4 Gene Is Associated with Autoimmune Hypothyroidism in the United Kingdom

  2002cites this paper
• Autoimmunity in thyroid disease

  2002cites this paper
• Evidence for a major role of heredity in Graves' disease: a population-based study of two Danish twin cohorts.

  2001cites this paper
• Postpartum thyroiditis and autoimmune thyroiditis in women of childbearing age: recent insights and consequences for antenatal and postnatal care.

  2001cites this paper
• Prevalence of thyroid disease, thyroid dysfunction and thyroid peroxidase antibodies in a large, unselected population. The Health Study of Nord-Trondelag (HUNT).

  2000cites this paper