| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S12020-013-9908-Z |
| P698 | PubMed publication ID | 23463390 |
| P2093 | author name string | Asem Alkhateeb | |
| Nour Al-Dain Marzouka | |||
| Reema Tashtoush | |||
| P2860 | cites work | 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 | Q24538382 |
| Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families | Q28213015 | ||
| Role of PTPN22 in type 1 diabetes and other autoimmune diseases | Q28239964 | ||
| A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis | Q28267921 | ||
| Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant | Q28280659 | ||
| Novel associations for hypothyroidism include known autoimmune risk loci | Q28730714 | ||
| Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8 | Q28943256 | ||
| Epidemiology and estimated population burden of selected autoimmune diseases in the United States | Q33500191 | ||
| The different approaches to the genetic analysis of autoimmune thyroid disease | Q33737731 | ||
| PTPN22 1858C>T polymorphism distribution in Europe and association with rheumatoid arthritis: case-control study and meta-analysis | Q34031304 | ||
| The novel SPARC family member SMOC-2 potentiates angiogenic growth factor activity | Q34538166 | ||
| Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population. | Q35052064 | ||
| Affected-sib-pair mapping of a novel susceptibility gene to insulin-dependent diabetes mellitus (IDDM8) on chromosome 6q25-q27 | Q35644380 | ||
| New genetic insights from autoimmune thyroid disease | Q35864459 | ||
| The developmentally-regulated Smoc2 gene is repressed by Aryl-hydrocarbon receptor (Ahr) signaling. | Q37120603 | ||
| Immunization with thyroglobulin induces Graves'-like disease in mice | Q37262565 | ||
| The incidence and prevalence of thyroid autoimmunity | Q38014355 | ||
| Association of Protein Tyrosine Phosphatase Nonreceptor 22 (PTPN22) C1858T gene polymorphism with susceptibility to autoimmune thyroid diseases: a meta-analysis | Q38417781 | ||
| The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population | Q38936485 | ||
| Risk factors for and prevalence of thyroid disorders in a cross-sectional study among healthy female relatives of patients with autoimmune thyroid disease | Q40568360 | ||
| Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease | Q42171148 | ||
| Association of the protein tyrosine phosphatase nonreceptor 22 haplotypes with autoimmune thyroid disease in the Japanese population. | Q42976149 | ||
| Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease | Q43271595 | ||
| The protein tyrosine phosphatase non-receptor type 22 C1858T polymorphism is a joint susceptibility locus for immunthyroiditis and autoimmune diabetes | Q44905066 | ||
| PTPN22 allele polymorphisms in 15 Chinese populations | Q46221122 | ||
| The codon 620 single nucleotide polymorphism of the protein tyrosine phosphatase-22 gene does not contribute to autoimmune thyroid disease susceptibility in the Japanese | Q46798186 | ||
| Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population | Q46831303 | ||
| Linkage of rheumatoid arthritis to insulin-dependent diabetes mellitus loci: Evidence supporting a hypothesis for the existence of common autoimmune susceptibility loci | Q56446817 | ||
| 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 | Q56897699 | ||
| Mapping of a major susceptibility locus for Graves' disease (GD-1) to chromosome 14q31 | Q56908461 | ||
| Autoimmunity and atherosclerosis: functional polymorphism of PTPN22 is associated with phenotypes related to the risk of atherosclerosis. The Cardiovascular Risk in Young Finns Study | Q57417550 | ||
| Saturation multipoint linkage mapping of chromosome 6q in type 1 diabetes | Q71558362 | ||
| Physical and genetic mapping of IDDM8 on chromosome 6q27 | Q73929162 | ||
| Association of PTPN22 haplotypes with Graves' disease | Q79407766 | ||
| SMOC2 gene variant and the risk of vitiligo in Jordanian Arabs | Q85237906 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 702-709 | |
| P577 | publication date | 2013-03-06 | |
| P1433 | published in | Endocrine | Q15757048 |
| P1476 | title | Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population | |
| P478 | volume | 44 |
| Q99711793 | Autoimmune thyroid disease and type 1 diabetes mellitus: same pathogenesis; new perspective? |
| Q90408401 | Downregulation of SMOC2 expression in papillary thyroid carcinoma and its prognostic significance |
| Q26766384 | Genetic Susceptibility to Vitiligo: GWAS Approaches for Identifying Vitiligo Susceptibility Genes and Loci |
| Q39232393 | Heritability analysis of IgG4 antibodies in autoimmune thyroid disease |
| Q58544606 | Novel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto's thyroiditis |
| Q98945117 | SMOC2, an intestinal stem cell marker, is an independent prognostic marker associated with better survival in colorectal cancers |
| Q90716393 | Secreted modular calcium-binding proteins in pathophysiological processes and embryonic development |
| Q38724335 | Smoc2 potentiates proliferation of hepatocellular carcinoma cells via promotion of cell cycle progression |
| Q38788500 | The PTPN22 R263Q polymorphism confers protection against systemic lupus erythematosus and rheumatoid arthritis, while PTPN22 R620W confers susceptibility to Graves' disease in a Mexican population. |
| Q37722737 | The SPARC-related modular calcium binding protein 2 (SMOC2) gene polymorphism in primary glaucoma: a case-control study |
| Q34252769 | The association of PTPN22 rs2476601 polymorphism and CTLA-4 rs231775 polymorphism with LADA risks: a systematic review and meta-analysis |
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