The search for the genetic contribution to autoimmune thyroid disease: the never ending story? (Q37857568)

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scientific article published on March 2011

Language	Label	Description	Also known as
English	The search for the genetic contribution to autoimmune thyroid disease: the never ending story?	scientific article published on March 2011

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

1 reference

Europe PubMed Central

The search for the genetic contribution to autoimmune thyroid disease: the never ending story? (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

author name string

Stephen C L Gough

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

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based on heuristic

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publication date

1 March 2011

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

Briefings in functional genomics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

77-90

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

DNA variations in human and medical genetics: 25 years of my experience

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Evidence for a new Graves disease susceptibility locus at chromosome 18q21.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

A genome-wide screen in 1119 relative pairs with autoimmune thyroid disease.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The HLA Region and Autoimmune Disease: Associations and Mechanisms of Action

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Genetic developments in autoimmune thyroid disease: an evolutionary process

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Confirmation of association of chromosome 5q31-33 with United Kingdom Caucasian Graves' disease.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The HapMap and genome-wide association studies in diagnosis and therapy

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Human QTL linkage mapping

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Genetics of thyroid autoimmunity and the role of the TSHR.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The International HapMap Project

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Evaluating coverage of genome-wide association studies

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Evaluating and improving power in whole-genome association studies using fixed marker sets.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

How to interpret a genome-wide association study

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Drinking from the fire hose--statistical issues in genomewide association studies

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Betting odds and genetic associations.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Genetic insights into disease mechanisms of autoimmunity

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Autoimmune disease classification by inverse association with SNP alleles

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Finding the missing heritability of complex diseases

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Type 2 diabetes: new genes, new understanding

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Origins and functional impact of copy number variation in the human genome

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Uncovering the roles of rare variants in common disease through whole-genome sequencing

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Missing heritability and strategies for finding the underlying causes of complex disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Sequencing technologies - the next generation

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Cis-regulatory mutations in human disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Transgenerational genetic effects on phenotypic variation and disease risk

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Parental origin of sequence variants associated with complex diseases

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The gut microbiota shapes intestinal immune responses during health and disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The immune system and the gut microbiota: friends or foes?

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Arginine at position 74 of the HLA-DR beta1 chain is associated with Graves' disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Regression mapping of association between the human leukocyte antigen region and Graves disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The association between HLA class II haplotype with Graves' disease in Thai population

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Association of the T-cell regulatory gene CTLA4 with Graves' disease and autoimmune thyroid disease in the Japanese

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The cytotoxic T lymphocyte antigen-4 is a major Graves' disease locus.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Association of the TSHR gene with Graves' disease: the first disease specific locus.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Role of the CD40 locus in Graves' disease.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

A CD40 Kozak sequence polymorphism and susceptibility to antibody-mediated autoimmune conditions: the role of CD40 tissue-specific expression.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Interleukin (IL)-23 receptor is a major susceptibility gene for Graves' ophthalmopathy: the IL-23/T-helper 17 axis extends to thyroid autoimmunity.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Polymorphisms in the interleukin 3 gene show strong association with susceptibility to Graves' disease in Chinese population.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

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.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Tag SNP screening of the PDCD1 gene for association with Graves' disease.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

A systematic approach to the assessment of known TNF-alpha polymorphisms in Graves' disease.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The Molecular Genetics of Three Thyroid Autoantigens: Thyroglobulin, Thyroid Peroxidase and the Thyrotropin Receptor

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The regulatory T cell gene FOXP3 and genetic susceptibility to thyroid autoimmunity: an association analysis in Caucasian and Japanese cohorts.

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Lack of association of Graves' disease with the A2 allele of the interleukin-1 receptor antagonist gene in a white European population

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Association of a rare thyroglobulin gene microsatellite variant with autoimmune thyroid disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

The thyroglobulin gene as the first thyroid-specific susceptibility gene for autoimmune thyroid disease

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Lack of association of the vitamin D receptor gene with Graves' disease in UK Caucasians

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Vitamin D receptor polymorphisms are associated with Graves' disease in German and Polish but not in Serbian patients

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELQ036

21 January 2018

Identifiers

10.1093/BFGP/ELQ036

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21436304%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

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