Associated Papers
Genetics of Thyroid Function: Relevance for Biology and Disease Management.
Sterenborg RBTM et al.
The Journal of Clinical Endocrinology and Metabolism, 2025
Advances in genetic and molecular insights into thyroid disorders: Implications for diagnosis, prognosis, and personalized treatment.
Alshehri FF
Saudi Medical Journal, 2025
Whole-Genome Sequencing Reveals a Novel GATA2 Mutation in Lower-Grade Glioma: Bioinformatics Analysis of Functional and Therapeutic Implications.
Handoko et al.
Cancers, 2025
Personalized Approaches to Hypothyroidism: The Role of Triiodothyronine (T3) in Thyroid Hormone Replacement.
Mazza AD
Cureus, 2025
Thyroid Hormone Dynamics and DIO2 Variants in Schizophrenia: Exploring Genetic Links to Neuroendocrine Imbalance.
Akan G et al.
Journal of Cellular and Molecular Medicine, 2025
FVB But Not B6 Mice Carrying the Thr92Ala-Dio2 Polymorphism Have Impaired Thyroid Hormonogenesis and Goiter.
Batistuzzo A et al.
Endocrinology, 2025
Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma.
Villa M et al.
British Journal of Cancer, 2024
Thr92Ala-DIO2 heterozygosity is associated with skeletal muscle mass and myosteatosis in patients with COVID-19.
Beltrão FEL et al.
European Thyroid Journal, 2024
The Outcome of Metabolic and Bariatric Surgery in Morbidly Obese Patients with Different Genetic Variants Associated with Obesity: A Systematic Review.
Zafirovska M et al.
Nutrients, 2024
Mapping Thyroid Hormone Action in the Human Brain.
Salas-Lucia F
Thyroid : Official Journal of the American Thyroid Association, 2024
A DIO2 missense mutation and its impact on fetal response to PRRSV infection.
Ko H et al.
Bmc Veterinary Research, 2024
Genetic Background Strongly Influences the Impact of Carrying the Thr92Ala-DIO2 Polymorphism in the Male Mouse.
Gabriel de Almeida G et al.
Endocrinology, 2024
Gene polymorphisms and thyroid hormone signaling: implication for the treatment of hypothyroidism.
Penna GC et al.
Endocrine, 2024
Effect of DIO2 Gene Polymorphism on Thyroid Hormone Levels and Its Correlation with the Severity of Schizophrenia in a Pakistani Population.
Hanif F et al.
International Journal of Molecular Sciences, 2024
Current Understanding of Human Polymorphism in Selenoprotein Genes: A Review of Its Significance as a Risk Biomarker.
Ferreira RR et al.
International Journal of Molecular Sciences, 2024
Association of DIO2 and MCT10 Polymorphisms With Persistent Symptoms in LT4-Treated Patients in the UK Biobank.
Jensen CZ et al.
The Journal of Clinical Endocrinology and Metabolism, 2024
The Thr92Ala polymorphism in the type 2 deiodinase gene is linked to depression in patients with COVID-19 after hospital discharge.
Beltrão DCA et al.
Frontiers in Endocrinology, 2024
Polymorphisms within DIO2 and GADD45A genes increase the risk of liver disease progression in chronic hepatitis b carriers.
Rybicka M et al.
Scientific Reports, 2023
Association between Genotype and the Glycemic Response to an Oral Glucose Tolerance Test: A Systematic Review.
Bayer S et al.
Nutrients, 2023
Association between DIO2 Thr92Ala polymorphism and hypertension in patients with hypothyroidism: Korean Genome and Epidemiology Study.
Kang YM et al.
The Korean Journal of Internal Medicine, 2023
Type 2 Deiodinase Thr92Ala Polymorphism and Aging Are Associated with a Decreased Pituitary Sensitivity to Thyroid Hormone.
Luongo C et al.
Thyroid : Official Journal of the American Thyroid Association, 2023
Polymorphisms of Placental Iodothyronine Deiodinase Genes in a Rural Area of Northern China with High Prevalence of Neural Tube Defects.
Wang F et al.
Human Heredity, 2023
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
Association of Type 2 Deiodinase Thr92Ala Polymorphism with Pediatric Obesity in Japanese Children: A Case-Control Study.
Ota T et al.
Children (basel, Switzerland), 2022
Age Worsens the Cognitive Phenotype in Mice Carrying the Thr92Ala-DIO2 Polymorphism.
Lorena FB et al.
Metabolites, 2022
Type 2 deiodinase p.Thr92Ala polymorphism does not affect the severity of obesity and weight loss after bariatric surgery.
Benenati N et al.
Scientific Reports, 2022
Identification of polymorphic loci in the deiodinase 2 gene and their associations with head dimensions in geese.
Deng Y et al.
Animal Bioscience, 2022
Folate Related Pathway Gene Analysis Reveals a Novel Metabolic Variant Associated with Alzheimer's Disease with a Change in Metabolic Profile.
Miyan J et al.
Metabolites, 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
Type 2 Deiodinase Thr92Ala Polymorphism Is Not Associated with Cognitive Impairment in Older Adults: A Cross-Sectional Study.
Schwengber WK et al.
Metabolites, 2022
Improvement of depression in a patient with hypothyroidism and deiodinase polymorphism with LT3 Therapy.
Ahmed ZS et al.
Clinical Case Reports, 2022
A single nucleotide mutation in the dual-oxidase 2 (DUOX2) gene causes some of the panda's unique metabolic phenotypes.
Rudolf AM et al.
National Science Review, 2022
An Assessment of GPX1 (rs1050450), DIO2 (rs225014) and SEPP1 (rs7579) Gene Polymorphisms in Women with Endometrial Cancer.
Janowska M et al.
Genes, 2022
Pathophysiological Role of Genetic Factors Associated With Gestational Diabetes Mellitus.
Ortega-Contreras B et al.
Frontiers in Physiology, 2022
A Re-evaluation of Candidate Gene Studies for Well-Being in Light of Genome-Wide Evidence.
van de Weijer MP et al.
Journal of Happiness Studies, 2022
The Role of Thyroid in Renovascular Function: Independent Association of Serum TSH With Renal Plasma Flow.
Pappa T et al.
The Journal of Clinical Endocrinology and Metabolism, 2021
Assessment of children in the autistic spectrum disorder that carry the Thr92Ala-DIO2 polymorphism.
E Marcondes AA et al.
Journal of Endocrinological Investigation, 2021
Thyroid hormone, gene expression, and Central Nervous System: Where we are.
Giannocco G et al.
Seminars in Cell & Developmental Biology, 2021
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
Thyroid function, renal events and mortality in chronic kidney disease patients: the German Chronic Kidney Disease study.
Schultheiss UT et al.
Clinical Kidney Journal, 2021
Accelerating functional gene discovery in osteoarthritis.
Butterfield NC et al.
Nature Communications, 2021
Inherited Disorders of Thyroid Hormone Metabolism Defect Caused by the Dysregulation of Selenoprotein Expression.
Lee KW et al.
Frontiers in Endocrinology, 2021
Thr92Ala polymorphism in the type 2 deiodinase gene: an evolutionary perspective.
Ricci C et al.
Journal of Endocrinological Investigation, 2020
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
Type 2 deiodinase Thr92Ala polymorphism is associated with a reduction in bone mineral density: A community-based korean genome and epidemiology study.
Kang YE et al.
Clinical Endocrinology, 2020