Genome-wide association study reveals distinct genetic susceptibility of thyroid nodules from thyroid cancer

Y Hwangbo, EK Lee, HY Son, SW Im… - The Journal of …, 2018 - academic.oup.com
Context Thyroid nodules are very common, and 7% to 15% of them are diagnosed as thyroid
cancer. However, the inherited genetic risk factors for thyroid nodules and their associations …

A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study

V Panicker, SG Wilson, JP Walsh, JB Richards… - The American Journal of …, 2010 - cell.com
Thyroid hormones are key regulators of cellular growth, development, and metabolism, and
thyroid disorders are a common cause of ill health in the community. Circulating …

Causal relationship between type 1 diabetes and hypothyroidism: A Mendelian randomization study

Y Zhao, S Si, K Zhang, J Yuan, J Li… - Clinical …, 2022 - Wiley Online Library
Objectives Although an association between type 1 diabetes (T1D) and hypothyroidism has
been found in multiple observational studies, whether T1D plays a causal role in the …

Contribution of Single Nucleotide Polymorphisms within FCRL3 and MAP3K7IP2 to the Pathogenesis of Graves' Disease

MJ Simmonds, JM Heward, J Carr-Smith… - The Journal of …, 2006 - academic.oup.com
Context: Recently six DNA variants, two of which (M55V and 001Msp) are present in nuclear
factor-κB inhibitors SUMO-4 and MAP3K7IP2 and four of which (fcrl3_3, fcrl3_4, fcrl3_5, and …

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

A Teumer, L Chaker, S Groeneweg, Y Li… - Nature …, 2018 - nature.com
Thyroid dysfunction is an important public health problem, which affects 10% of the general
population and increases the risk of cardiovascular morbidity and mortality. Many aspects of …

Transcriptome, methylome and genomic variations analysis of ectopic thyroid glands

R Abu-Khudir, J Paquette, A Lefort, F Libert… - PloS one, 2010 - journals.plos.org
Background Congenital hypothyroidism from thyroid dysgenesis (CHTD) is predominantly a
sporadic disease characterized by defects in the differentiation, migration or growth of …

Gene-gene and gene-sex epistatic interactions of DNMT1, DNMT3A and DNMT3B in autoimmune thyroid disease

T Cai, J Zhang, X Wang, R Song, Q Qin, F Muhali… - Endocrine …, 2016 - jstage.jst.go.jp
The aim of this study was to investigate the associations of DNA methyltransferases
(DNMTs) polymorphisms with susceptibility to autoimmune thyroid diseases (AITDs) and to …

The Role of NRG1 in the Predisposition to Papillary Thyroid Carcinoma

H He, W Li, S Liyanarachchi, Y Wang… - The Journal of …, 2018 - academic.oup.com
Context Previous genome-wide association studies have shown that single-nucleotide
polymorphism (SNP) rs2439302 in chromosome 8p12 is significantly associated with …

Exploring blood metabolites and thyroid disorders: a bidirectional mendelian randomization study

X Zhang, J Zhou, Z Xie, X Li, J Hu, H He… - Frontiers in …, 2023 - frontiersin.org
Background Human blood metabolites have demonstrated close associations with thyroid
disorders in observational studies. However, it's essential to determine whether these …

Associations between single nucleotide polymorphisms in thyroid hormone transporter genes (MCT8, MCT10 and OATP1C1) and circulating thyroid hormones

GL Roef, ER Rietzschel, T De Meyer, S Bekaert… - Clinica chimica acta, 2013 - Elsevier
Background Thyroid hormone (TH) action takes place intracellularly; therefore, transport
across the plasma membrane by specific TH transporters, such as MCT8, MCT10 and …