연구동향 분석

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

황보율 박영주 2018년

논문상세정보
    • 저자 황보율 박영주
    • 제어번호 105908467
    • 학술지명 Endocrinology and metabolism
    • 권호사항 Vol. 33 No. 2 [ 2018 ]
    • 발행처 대한내분비학회
    • 발행처 URL http://www.endocrinology.or.kr
    • 자료유형 학술저널
    • 수록면 175-184
    • 언어 English
    • 출판년도 2018
    • 등재정보 KCI등재
    • 소장기관 경북대학교 도서관 의학분관 부산대학교 중앙도서관 영남대학교 의료원 의학도서관
    • 판매처
    유사주제 논문( 0)
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' Genome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer' 의 참고문헌

  • Whole-genome sequence-based analysis of thyroid function
    Taylor PN [2015]
  • Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies
    Denny JC [2011]
  • Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations
    Mancikova V [2015]
  • The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors
    Landa I [2009]
  • The role of NRG1 in the predisposition to papillary thyroid carcinoma
    He H [2018]
  • The long-term outcomes of the second generation of familial nonmedullary thyroid carcinoma are more aggressive than sporadic cases
    Park YJ [2012]
  • The genetics of autoimmune thyroid disease
    Vaidya B [2002]
  • The epidemiology of Graves' disease: evidence of a genetic and an environmental contribution
    Hemminki K [2010]
  • The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease
    Velaga MR [2004]
  • The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl
    Takahashi M [2010]
  • Sibling recurrence risk in autoimmune thyroid disease
  • Seven newly identified loci for autoimmune thyroid disease
    Cooper JD [2012]
  • Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis
    Zhao SX [2013]
  • Relief of feedback inhibition of HER3 transcription by RAF and MEK inhibitors attenuates their antitumor effects in BRAF-mutant thyroid carcinomas
  • Regression mapping of association between the human leukocyte antigen region and Graves disease
    Simmonds MJ [2005]
  • Quantitative assessment of common genetic variants on FOXE1 and differentiated thyroid cancer risk
    Zhu H [2014]
  • Papillary thyroid carcinoma: association between germline DNA variant markers and clinical parameters
  • Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk
    Figlioli G [2014]
  • Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk
    Figlioli G [2015]
  • Novel associations for hypothyroidism include known autoimmune risk loci
    Eriksson N [2012]
  • Narrow individual variations in serum T(4) and T(3) in normal subjects: a clue to the understanding of subclinical thyroid disease
    Andersen S [2002]
  • Molecular pathways: targeting NRG1 fusions in lung cancer
  • Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function
    Rawal R [2012]
  • Major genetic influence on the regulation of the pituitary-thyroid axis: a study of healthy Danish twins
    Hansen PS [2004]
  • Increased familial clustering of autoimmune thyroid diseases
    Dittmar M [2011]
  • Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
    Medici M [2014]
  • Identification of a Hashimoto thyroiditis susceptibility locus via a genome-wide comparison with Graves' disease
    Oryoji D [2015]
  • Heritability of serum TSH, free T4 and free T3 concentrations: a study of a large UK twin cohort
    Panicker V [2008]
  • Genome-wide meta-analysis identifies novel gender specific loci associated with thyroid antibodies level in Croatians
    Matana A [2018]
  • Genome-wide association study on differentiated thyroid cancer
    Kohler A [2013]
  • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
  • Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations
    Zhan M [2014]
  • Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer
    Son HY [2017]
  • Genetics of thyroid function and disease
    Panicker V [2011]
  • Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network
  • Genetic and environmental influences on thyroid hormone variation in Mexican Americans
    Samollow PB [2004]
  • GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis
    Simmonds MJ [2013]
  • Familial nonmedullary thyroid carcinoma: a meta-review of case series
    Loh KC [1997]
  • Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population
    Uchino S [2002]
  • Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entity
    Capezzone M [2008]
  • Familial non-medullary thyroid cancer: unraveling the genetic maze
  • FOXE1 association with differentiated thyroid cancer and its progression
  • Evidence for a major role of heredity in Graves' disease: a population-based study of two Danish twin cohorts
    Brix TH [2001]
  • Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish Family-Cancer Database
    Czene K [2002]
  • Discovery of common variants associated with low TSH levels and thyroid cancer risk
  • Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations
  • Changes in thyroid function in euthyroid subjects with a family history of Graves' disease: a follow-up study of 69 patients
    Tamai H [1980]
  • Biological behavior and prognosis of familial papillary thyroid carcinoma
    Ito Y [2009]
  • Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
  • Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease
    Brand OJ [2009]
  • Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
    Ueda H [2003]
  • An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease
    Chu X [2013]
  • A population-based study of chronic autoimmune hypothyroidism in Danish twins
    Brix TH [2000]
  • A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect
    Simmonds MJ [2007]
  • A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
    Porcu E [2013]
  • A genome-wide association study yields five novel thyroid cancer risk loci
  • A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans
    Kwak SH [2014]
  • A genome-wide association study identifies two new risk loci for Graves' disease
    Chu X [2011]