Associated Papers
Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa.
Boukhalfa W et al.
Frontiers in Aging Neuroscience, 2023
A New Treatment Protocol of Combined High-Dose Levothyroxine and Repetitive Transcranial Magnetic Stimulation for the Treatment of Rapid-Cycling Bipolar Spectrum Disorders: A Cohort Evaluation of 55 Patients.
Zamar AC et al.
Journal of Clinical Medicine, 2022
Heterozygote Advantage of the Type II Deiodinase Thr92Ala Polymorphism on Intrahospital Mortality of COVID-19.
de Lima Beltrão FE et al.
The Journal of Clinical Endocrinology and Metabolism, 2022
Genetics of primary congenital hypothyroidism-a review.
Kostopoulou E et al.
Hormones (athens, Greece), 2021
Cholinesterase homozygous genotype as susceptible biomarker of hypertriglyceridaemia for pesticide-exposed agricultural workers.
Zhou X et al.
Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals, 2021
Inherited Disorders of Thyroid Hormone Metabolism Defect Caused by the Dysregulation of Selenoprotein Expression.
Lee KW et al.
Frontiers in Endocrinology, 2021
Single Nucleotide Polymorphisms in Thyroid Hormone Transporter Genes MCT8, MCT10 and Deiodinase DIO2 Contribute to Inter-Individual Variance of Executive Functions and Personality Traits.
Uter JC et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association, 2020
The Genetic Basis of Thyroid Function: Novel Findings and New Approaches.
Kuś A et al.
The Journal of Clinical Endocrinology and Metabolism, 2020
Concurrent TSHR mutations and DIO2 T92A polymorphism result in abnormal thyroid hormone metabolism.
Park E et al.
Scientific Reports, 2018
Treatment-associated TP53 DNA-binding domain missense mutations in the pathogenesis of secondary gliosarcoma.
Pain M et al.
Oncotarget, 2018
Genetics of thyroid function.
Medici M et al.
Best Practice & Research. Clinical Endocrinology & Metabolism, 2017
Role of Thyroid Hormones in Skeletal Development and Bone Maintenance.
Bassett JH et al.
Endocrine Reviews, 2016
Association of Type II 5' Monodeiodinase Thr92Ala Single Nucleotide Gene Polymorphism and Circulating Thyroid Hormones Among Type 2 Diabetes Mellitus Patients.
Yalakanti D et al.
Indian Journal of Clinical Biochemistry : Ijcb, 2016
Genetic determination of the hypothalamic-pituitary-thyroid axis: where do we stand?
Medici M et al.
Endocrine Reviews, 2015
Prevalent polymorphism in thyroid hormone-activating enzyme leaves a genetic fingerprint that underlies associated clinical syndromes.
McAninch EA et al.
The Journal of Clinical Endocrinology and Metabolism, 2015
Functional analysis of novel genetic variation in the thyroid hormone activating type 2 deiodinase.
Zevenbergen C et al.
The Journal of Clinical Endocrinology and Metabolism, 2014
Genetics in endocrinology: genetic variation in deiodinases: a systematic review of potential clinical effects in humans.
Verloop H et al.
European Journal of Endocrinology, 2014
Genetic variants and the metabolic syndrome: a systematic review.
Povel CM et al.
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity, 2011
Association of the type 2 deiodinase Thr92Ala polymorphism with type 2 diabetes: case-control study and meta-analysis.
Dora JM et al.
European Journal of Endocrinology, 2010
Pro12Ala polymorphism of the peroxisome proliferatoractivated receptor-gamma gene is associated with metabolic syndrome and surrogate measures of insulin resistance in healthy men: interaction with smoking status.
Tellechea ML et al.
Circulation Journal : Official Journal of the Japanese Circulation Society, 2009
Novel insights into thyroid hormones from the study of common genetic variation.
Dayan CM et al.
Nature Reviews. Endocrinology, 2009
Interaction of DIO2 T92A and PPARgamma2 P12A polymorphisms in the modulation of metabolic syndrome.
Fiorito M et al.
Obesity (silver Spring, Md.), 2007
[Chimpanzee genome sequencing and comparative analysis with the human genome].
Watanabe H et al.
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme, 2006
Association of PPAR-γ gene polymorphisms with obesity and obesity-associated phenotypes in North Indian population.
Prakash J et al.
American Journal of Human Biology : the Official Journal of the Human Biology Council, 0
Congenital Hypothyroidism Patients With Thyroid Hormone Receptor Variants Are Not Rare: A Systematic Review.
Da DZ et al.
Inquiry : a Journal of Medical Care Organization, Provision and Financing, 0
Determination of Frequency of Type 2 Deiodinase Thr92Ala Polymorphism (rs225014) in 131I-treated Differentiated Thyroid Cancer Patients Undertaking L-thyroxine (L-T4) Suppression Therapy.
Gawandi S et al.
Indian Journal of Nuclear Medicine : Ijnm : the Official Journal of the Society of Nuclear Medicine, India, 0