Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts. (Q30992731)

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English	Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.	scientific article

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17 January 2020

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21124799%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Graves' disease

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based on heuristic

inferred from title

1

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17 January 2020

Beata Jurecka-Lubieniecka

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17 January 2020

5

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17 January 2020

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17 January 2020

Barbara Jarząb

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17 January 2020

Tomasz Bednarczuk

12

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Tomasz Bednarczuk

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17 January 2020

Paweł Krajewski

6

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Paweł Krajewski

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17 January 2020

Maria Franaszczyk

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Maria Franaszczyk

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17 January 2020

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Oliver J Brand

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17 January 2020

Muhammad A Karamat

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17 January 2020

Jayne A Franklyn

9

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17 January 2020

Stephen C L Gough

10

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17 January 2020

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25 November 2010

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17 January 2020

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21124799%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

5

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Europe PubMed Central

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17 January 2020

11

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17 January 2020

e15512

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17 January 2020

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Creative Commons Attribution 4.0 International

25 November 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

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

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21 June 2018

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

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21 June 2018

TSH receptor antibodies

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21 June 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

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Cohort profile: 1958 British birth cohort (National Child Development Study).

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21 June 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

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21 June 2018

Haploview: analysis and visualization of LD and haplotype maps

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21 June 2018

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

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21 June 2018

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

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21 June 2018

The structure of haplotype blocks in the human genome

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21 June 2018

Association of autoimmune thyroid disease with microsatellite markers for the thyrotropin receptor gene and CTLA-4 in Japanese patients

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21 June 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0015512

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0015512

21 January 2018

Association of tumor necrosis factor and human leukocyte antigen DRB1 alleles with Graves' ophthalmopathy

1 reference

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21 January 2018

A germline single nucleotide polymorphism at the intracellular domain of the human thyrotropin receptor does not have a major effect on the development of Graves' disease

1 reference

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21 January 2018

Polymorphism of the oestrogen receptor beta gene (ESR2) is associated with susceptibility to Graves' disease

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21 January 2018

Interaction of HLA-DRB1 alleles with CTLA-4 in the predisposition to Graves' disease: the impact of DRB1*07

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21 January 2018

Association of autoimmune thyroid disease with a microsatellite marker for the thyrotropin receptor gene and CTLA-4 in a Japanese population.

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25 November 2018

Analysis of mutations in exon 1 of the human thyrotropin receptor gene: high frequency of the D36H and P52T polymorphic variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/21124799

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21124799

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the genetic variability of the 1st (CCC/ACC, P52T) and the 10th exons (bp 1012-1704) of the TSH receptor gene in Graves' disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21124799

12 December 2020

based on heuristic

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Influences of Age, Gender, Smoking, and Family History on Autoimmune Thyroid Disease Phenotype

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism in the extracellular domain of the thyrotropin receptor is highly associated with autoimmune thyroid disease in females

1 reference

https://pubmed.ncbi.nlm.nih.gov/21124799

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21124799

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0015512

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Europe PubMed Central

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17 January 2020

2010PLoSO...515512P

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17 January 2020

PubMed publication ID

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Europe PubMed Central

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17 January 2020

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