GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis. - Wikidata - awgldk - TriplyDB

GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.

GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.

http://www.wikidata.org/entity/Q38093041

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Peroxisome Proliferator-Activated Receptor- γ in Thyroid Autoimmunity Rituximab in the Treatment of Thyroid Eye Disease: A Review Guidelines for the treatment of childhood-onset Graves' disease in Japan, 2016 A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.mRNA-Seq reveals novel molecular mechanisms and a robust fingerprint in Graves' disease.Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.Myeloid-derived suppressor cells regulate T cell and B cell responses during autoimmune disease A genetic risk score for thyroid peroxidase antibodies associates with clinical thyroid disease in community-based populations.Pooled genome wide association detects association upstream of FCRL3 with Graves' disease.Genetic associations of the thyroid stimulating hormone receptor gene with Graves diseases and Graves ophthalmopathy: A meta-analysis TNFSF4 Gene Variations Are Related to Early-Onset Autoimmune Thyroid Diseases and Hypothyroidism of Hashimoto's Thyroiditis.Copy number variations exploration of multiple genes in Graves' disease.Environmental Issues in Thyroid Diseases Novel Therapies for Thyroid Autoimmune Diseases.Association of Established Thyroid-stimulating Hormone and Free Thyroxine Genetic Variants with Hashimoto's Thyroiditis.Association of established hypothyroidism-associated genetic variants with Hashimoto's thyroiditis.Autoimmune Thyroiditis and Myasthenia Gravis.Variants of Interleukin-22 Gene Confer Predisposition to Autoimmune Thyroid Disease.Vitiligo and Autoimmune Thyroid Disorders.Single nucleotide polymorphisms in the STAT3 gene influence AITD susceptibility, thyroid autoantibody levels, and IL6 and IL17 secretion.The Footprints of Poly-Autoimmunity: Evidence for Common Biological Factors Involved in Multiple Sclerosis and Hashimoto's Thyroiditis.Meta-Analysis of the Association between Vitamin D Receptor Polymorphisms and the Risk of Autoimmune Thyroid Disease.Genome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer.Correlation between CTLA-4 and CD40 gene polymorphisms and their interaction in graves' disease in a Chinese Han population

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GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.

http://www.wikidata.org/entity/Q38093041

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GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.

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GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.

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GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.

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Nature Reviews Endocrinology

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GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis

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Matthew J Simmonds

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Initial sequencing and analysis of the human genome

The Sequence of the Human Genome

Finding the missing heritability of complex diseases

Human tribbles, a protein family controlling mitogen-activated protein kinase cascades

A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome

Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defects

TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study

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277-287

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10.1038/NRENDO.2013.56

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genome-wide association study