(Q44532167)

3 December 2017

title

Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population (English)

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3 December 2017

Asem Alkhateeb

1

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3 December 2017

Nour Al-Dain Marzouka

series ordinal

2

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3 December 2017

Reema Tashtoush

series ordinal

3

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3 December 2017

publication date

6 March 2013

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3 December 2017

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3 December 2017

volume

44

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3 December 2017

issue

3

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3 December 2017

page(s)

702-709

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Epidemiology and estimated population burden of selected autoimmune diseases in the United States

3 December 2017

cites work

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https://api.crossref.org/works/10.1007%2FS12020-013-9908-Z

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New genetic insights from autoimmune thyroid disease

21 January 2018

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Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12020-013-9908-Z

Novel associations for hypothyroidism include known autoimmune risk loci

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12020-013-9908-Z

Association of Protein Tyrosine Phosphatase Nonreceptor 22 (PTPN22) C1858T gene polymorphism with susceptibility to autoimmune thyroid diseases: a meta-analysis

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12020-013-9908-Z

Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population.

21 January 2018

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The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12020-013-9908-Z

The protein tyrosine phosphatase non-receptor type 22 C1858T polymorphism is a joint susceptibility locus for immunthyroiditis and autoimmune diabetes

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12020-013-9908-Z

Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12020-013-9908-Z

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12020-013-9908-Z

Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant

21 January 2018

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Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population

21 January 2018

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The codon 620 single nucleotide polymorphism of the protein tyrosine phosphatase-22 gene does not contribute to autoimmune thyroid disease susceptibility in the Japanese

21 January 2018

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Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families

21 January 2018

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Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8

21 January 2018

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The novel SPARC family member SMOC-2 potentiates angiogenic growth factor activity

21 January 2018

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The developmentally-regulated Smoc2 gene is repressed by Aryl-hydrocarbon receptor (Ahr) signaling.

21 January 2018

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The different approaches to the genetic analysis of autoimmune thyroid disease

21 January 2018

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Risk factors for and prevalence of thyroid disorders in a cross-sectional study among healthy female relatives of patients with autoimmune thyroid disease

21 January 2018

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PTPN22 allele polymorphisms in 15 Chinese populations

21 January 2018

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PTPN22 1858C>T polymorphism distribution in Europe and association with rheumatoid arthritis: case-control study and meta-analysis

21 January 2018

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Role of PTPN22 in type 1 diabetes and other autoimmune diseases

21 January 2018

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Association of the protein tyrosine phosphatase nonreceptor 22 haplotypes with autoimmune thyroid disease in the Japanese population.

21 January 2018

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Immunization with thyroglobulin induces Graves'-like disease in mice

21 January 2018

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Autoimmunity and atherosclerosis: functional polymorphism of PTPN22 is associated with phenotypes related to the risk of atherosclerosis. The Cardiovascular Risk in Young Finns Study

21 January 2018

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Affected-sib-pair mapping of a novel susceptibility gene to insulin-dependent diabetes mellitus (IDDM8) on chromosome 6q25-q27

21 January 2018

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12 December 2020

Saturation multipoint linkage mapping of chromosome 6q in type 1 diabetes

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12 December 2020

Associations between autoimmune thyroid disease prognosis and functional polymorphisms of susceptibility genes, CTLA4, PTPN22, CD40, FCRL3, and ZFAT, previously revealed in genome-wide association studies

1 reference

12 December 2020

Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31

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12 December 2020

SMOC2 gene variant and the risk of vitiligo in Jordanian Arabs

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12 December 2020

Association of PTPN22 haplotypes with Graves' disease

1 reference

12 December 2020

Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease

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12 December 2020

Linkage of rheumatoid arthritis to insulin-dependent diabetes mellitus loci: Evidence supporting a hypothesis for the existence of common autoimmune susceptibility loci

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12 December 2020

Physical and genetic mapping of IDDM8 on chromosome 6q27

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12 December 2020

10.1007/S12020-013-9908-Z

Identifiers

DOI

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3 December 2017

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