Novel associations for hypothyroidism include known autoimmune risk loci
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Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic populationNew developments in the genetics, pathogenesis, and therapy of IgA nephropathyVav family exchange factors: an integrated regulatory and functional viewGenetic variants associated with breast size also influence breast cancer risk12q24 locus association with type 1 diabetes: SH2B3 or ATXN2?Surveying Recent Themes in Translational Bioinformatics: Big Data in EHRs, Omics for Drugs, and Personal GenomicsSystematic identification of trans eQTLs as putative drivers of known disease associationsApplying semantic web technologies for phenome-wide scan using an electronic health record linked BiobankGenetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion responseGWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition lociGenome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease).In silico pathway analysis and tissue specific cis-eQTL for colorectal cancer GWAS risk variants.eMERGEing progress in genomics-the first seven years.Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancerA genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.Polymorphisms in the TNFA and IL6 genes represent risk factors for autoimmune thyroid diseaseDiscovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens.A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid functionGenetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia.Common single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer.The genetic ancestry of African Americans, Latinos, and European Americans across the United States.Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.Convergent evolution of the genomes of marine mammals.A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal CancerA genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents.Genome-wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A, and Identification of ZBTB10 and Three Distinct HLA Associations.Association of three SNPs in the PARP-1 gene with Hashimoto's thyroiditis.Identifying genetically driven clinical phenotypes using linear mixed modelsA genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants.Signatures of natural selection on genetic variants affecting complex human traits.Additive, epistatic, and environmental effects through the lens of expression variability QTL in a twin cohortAssociation of VAV2 and VAV3 polymorphisms with cardiovascular risk factors.Role of the adaptor protein LNK in normal and malignant hematopoiesis.GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis.A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease.Bayesian analysis of genetic association across tree-structured routine healthcare data in the UK Biobank.
P2860
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P2860
Novel associations for hypothyroidism include known autoimmune risk loci
description
2012 nî lūn-bûn
@nan
2012 թուականին հրատարակուած գիտական յօդուած
@hyw
2012 թվականին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Novel associations for hypothyroidism include known autoimmune risk loci
@ast
Novel associations for hypothyroidism include known autoimmune risk loci
@en
Novel associations for hypothyroidism include known autoimmune risk loci
@nl
type
label
Novel associations for hypothyroidism include known autoimmune risk loci
@ast
Novel associations for hypothyroidism include known autoimmune risk loci
@en
Novel associations for hypothyroidism include known autoimmune risk loci
@nl
prefLabel
Novel associations for hypothyroidism include known autoimmune risk loci
@ast
Novel associations for hypothyroidism include known autoimmune risk loci
@en
Novel associations for hypothyroidism include known autoimmune risk loci
@nl
P2093
P2860
P3181
P1433
P1476
Novel associations for hypothyroidism include known autoimmune risk loci
@en
P2093
Amy K Kiefer
Chuong B Do
Joanna L Mountain
Joyce Y Tung
Nicholas Eriksson
Uta Francke
P2860
P304
P3181
P356
10.1371/JOURNAL.PONE.0034442
P407
P577
2012-01-01T00:00:00Z