Association of the TSHR gene with Graves' disease: the first disease specific locus (Q50758182)

18 March 2018

title

Association of the TSHR gene with Graves' disease: the first disease specific locus (English)

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18 March 2018

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12

Laszlo Hegedus

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18 March 2018

Thomas Heiberg Brix

13

Thomas Brix

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18 March 2018

Penny Hunt

15

Penny J Hunt

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18 March 2018

Tony Weetman

16

Anthony P Weetman

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18 March 2018

Bruce Robinson

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Bruce G Robinson

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18 March 2018

author name string

Bryan M Dechairo

1

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Delilah Zabaneh

2

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18 March 2018

Joanne Collins

3

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Oliver Brand

4

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Gary J Dawson

5

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Angie P Green

6

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Ian Mackay

7

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Jayne A Franklyn

8

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John M Connell

9

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John A H Wass

10

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Wilmar M Wiersinga

11

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Alisoun H Carey

17

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Stephen C Gough

18

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18 March 2018

publication date

1 November 2005

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18 March 2018

European Journal of Human Genetics

published in

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18 March 2018

volume

13

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18 March 2018

issue

11

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18 March 2018

page(s)

1223-1230

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18 March 2018

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

Complex association analysis of graves disease using a set of polymorphic markers

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

Association of Graves' disease with intragenic polymorphism of the thyrotropin receptor gene in a cohort of Singapore patients of multi-ethnic origins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

High-resolution haplotype structure in the human genome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

Replication validity of genetic association studies

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

The TSH receptor and its role in thyroid disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

Haplotype tagging for the identification of common disease genes

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

The spectrum of thyroid disease in a community: the Whickham survey

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

Natural history of autoimmune thyroiditis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

Identification of susceptibility loci for autoimmune thyroid disease to 5q31-q33 and Hashimoto's thyroiditis to 8q23-q24 by multipoint affected sib-pair linkage analysis in Japanese

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

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://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

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://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

No association between a thyrotropin receptor gene polymorphism and Graves' disease in the female population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

Common allelic variants of exons 10, 12, and 33 of the thyroglobulin gene are not associated with autoimmune thyroid disease in the United Kingdom

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

GOLD--graphical overview of linkage disequilibrium

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201485

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201485

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18 March 2018

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18 March 2018