Analysis of immune regulatory genes' copy number variants in Graves' disease. (Q39635304)

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15 January 2020

title

Analysis of immune regulatory genes' copy number variants in Graves' disease (English)

1 reference

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15 January 2020

1

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15 January 2020

author name string

Erlinda S Concepcion

2

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15 January 2020

Alisha Gandhi

3

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15 January 2020

Francesca Menconi

4

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15 January 2020

Eric P Smith

5

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15 January 2020

Mehdi Keddache

6

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15 January 2020

Yaron Tomer

7

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15 January 2020

publication date

8 November 2010

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15 January 2020

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15 January 2020

volume

21

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15 January 2020

issue

1

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15 January 2020

page(s)

69-74

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

15 January 2020

cites work

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Copy number variation in the human genome and its implication in autoimmunity

14 September 2017

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14 September 2017

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Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake

14 September 2017

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The HLA gene complex in thyroid autoimmunity: from epidemiology to etiology

14 September 2017

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14 September 2017

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CCL3L1 gene-containing segmental duplications and polymorphisms in CCR5 affect risk of systemic lupus erythaematosus

14 September 2017

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FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

14 September 2017

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Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

14 September 2017

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The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity: back to the future

14 September 2017

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Global variation in copy number in the human genome

14 September 2017

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Bias of selection on human copy-number variants

14 September 2017

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Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

14 September 2017

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Structural variation in the human genome

14 September 2017

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A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

14 September 2017

1 reference

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Current perspective on the pathogenesis of Graves' disease and ophthalmopathy.

14 September 2017

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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

14 September 2017

1 reference

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Recent segmental duplications in the human genome

14 September 2017

1 reference

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Genetic instabilities in human cancers

14 September 2017

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

14 September 2017

1 reference

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The thyrotropin (TSH) receptor: interaction with TSH and autoantibodies

21 August 2018

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Analysis of immune regulatory genes in familial and sporadic Graves' disease

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3012451

Evidence for an influence of chemokine ligand 3-like 1 (CCL3L1) gene copy number on susceptibility to rheumatoid arthritis

4 November 2018

1 reference

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Primary role of the HLA class II DRB1*0301 allele in Graves disease

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21054240

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A Graves' disease-associated Kozak sequence single-nucleotide polymorphism enhances the efficiency of CD40 gene translation: a case for translational pathophysiology

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21054240

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1089/THY.2010.0262

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21054240%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

1 reference

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15 January 2020

PubMed publication ID

21054240

1 reference