Genome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer.

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Genome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer. is …
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scholarly articleQ13442814

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P356DOI10.3803/ENM.2018.33.2.175
P932PMC publication ID6021314
P698PubMed publication ID29947174

P50authorYul HwangboQ61121483
Young Joo ParkQ37370841
P2860cites workThe variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factorsQ21092455
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Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populationsQ57083774
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A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effectQ80539372
Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entityQ82192474
The epidemiology of Graves' disease: evidence of a genetic and an environmental contributionQ82429098
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Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid diseaseQ35105700
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative riskQ35160562
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesQ35286565
The long-term outcomes of the second generation of familial nonmedullary thyroid carcinoma are more aggressive than sporadic casesQ35860194
Relief of feedback inhibition of HER3 transcription by RAF and MEK inhibitors attenuates their antitumor effects in BRAF-mutant thyroid carcinomas.Q36836677
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsQ36878530
An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.Q36939412
Quantitative assessment of common genetic variants on FOXE1 and differentiated thyroid cancer riskQ37529666
A genome-wide association study yields five novel thyroid cancer risk lociQ37652005
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Molecular Pathways: Targeting NRG1 Fusions in Lung CancerQ38287017
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid functionQ39386768
A genome-wide association study identifies two new risk loci for Graves' disease.Q39671701
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysisQ39672021
Papillary Thyroid Carcinoma: Association Between Germline DNA Variant Markers and Clinical ParametersQ41180944
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Evidence for a major role of heredity in Graves' disease: a population-based study of two Danish twin cohortsQ42641036
Regression mapping of association between the human leukocyte antigen region and Graves diseaseQ42949415
Increased familial clustering of autoimmune thyroid diseasesQ44765275
Major genetic influence on the regulation of the pituitary-thyroid axis: a study of healthy Danish twinsQ44786958
Genetic and environmental influences on thyroid hormone variation in Mexican AmericansQ44968748
The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' diseaseQ45142894
Heritability of serum TSH, free T4 and free T3 concentrations: a study of a large UK twin cohortQ46923557
Sibling Recurrence Risk in Autoimmune Thyroid DiseaseQ47443163
The role of NRG1 in the predisposition to papillary thyroid carcinomaQ47625240
Novel genome-wide association study-based candidate loci for differentiated thyroid cancer riskQ48657228
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.Q48850972
P275copyright licenseCreative Commons Attribution-NonCommercial 4.0 InternationalQ34179348
P6216copyright statuscopyrightedQ50423863
P433issue2
P921main subjectgenome-wide association studyQ1098876
P304page(s)175-184
P577publication date2018-06-01
P1433published inEndocrinology and metabolism : EnMQ26841897
P1476titleGenome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer.
P478volume33

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cites work (P2860)
Q91902151A Case of Papillary Thyroid Carcinoma and Kostmann Syndrome: A Genomic Theranostic Approach for Comprehensive Treatment
Q89908815Association of rs944289, rs965513, and rs1443434 in TITF1/TITF2 with Risks of Papillary Thyroid Carcinoma and with Nodular Goiter in Northern Chinese Han Populations
Q93081074Current Knowledge of Germline Genetic Risk Factors for the Development of Non-Medullary Thyroid Cancer
Q61812749Development of a prognostic index based on an immunogenomic landscape analysis of papillary thyroid cancer
Q96683905FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Q103804804Familial risks between giant cell arteritis and Takayasu arteritis and other autoimmune diseases in the population of Sweden
Q57026318Selenium and Selenoproteins in Immune Mediated Thyroid Disorders
Q59807548Sex-specific genetic influence on thyroid-stimulating hormone and free thyroxine levels, and interactions between measurements: KNHANES 2013-2015
Q64071123The Risk of Recurrence of Subacute Thyroiditis Is HLA-Dependent
Q92372843Thyroid Cancer: The Quest for Genetic Susceptibility Involving DNA Repair Genes

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