Genotype-phenotype correlations in Graves' disease.
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[1] A. Lewiński,et al. Significance of HLA in the development of Graves’ orbitopathy , 2023, Genes & Immunity.
[2] A. Leung,et al. Management of thyroid eye disease: a Consensus Statement by the American Thyroid Association and the European Thyroid Association , 2022, European thyroid journal.
[3] H. Y. Ahn,et al. Predictive model for Graves' ophthalmopathy in patients with new-onset Graves' disease. , 2022, Thyroid : official journal of the American Thyroid Association.
[4] Jin-an Zhang,et al. Polymorphisms of ATG5 Gene Are Associated with Autoimmune Thyroid Diseases, Especially Thyroid Eye Disease , 2022, Journal of immunology research.
[5] Y. Tomer,et al. Genetics and epigenetics of autoimmune thyroid diseases: Translational implications. , 2022, Best practice & research. Clinical endocrinology & metabolism.
[6] J. Vrbíková,et al. Recurrence of Graves’ Disease: What Genetics of HLA and PTPN22 Can Tell Us , 2021, Frontiers in Endocrinology.
[7] P. Åsman,et al. Increased risk of Graves´ophthalmopathy in patients with increasing TRAb after radioiodine treatment and the impact of CTLA4 on TRAb titres , 2021, Endocrine.
[8] W. Wiersinga,et al. THE 2021 EUROPEAN GROUP ON GRAVES' ORBITOPATHY (EUGOGO) CLINICAL PRACTICE GUIDELINES FOR THE MEDICAL MANAGEMENT OF GRAVES' ORBITOPATHY. , 2021, European journal of endocrinology.
[9] Y. Tomer,et al. Precision Medicine in Graves’ Disease: CD40 Gene Variants Predict Clinical Response to an Anti-CD40 Monoclonal Antibody , 2021, Frontiers in Endocrinology.
[10] F. Gianfagna,et al. Change in newly diagnosed Graves’ disease phenotype between the twentieth and the twenty-first centuries: meta-analysis and meta-regression , 2020, Journal of Endocrinological Investigation.
[11] M. Mahmoudi,et al. Graves' disease: introducing new genetic and epigenetic contributors. , 2020, Journal of molecular endocrinology.
[12] G. Kahaly. Management of Graves Thyroidal and Extrathyroidal Disease: An Update , 2020, The Journal of clinical endocrinology and metabolism.
[13] S. Pearce,et al. New Therapeutic Horizons for Graves’ Hyperthyroidism , 2020, Endocrine reviews.
[14] C. Khoo,et al. Prevalence of thyroid eye disease in Graves’ disease: A meta‐analysis and systematic review , 2020, Clinical endocrinology.
[15] G. Barbesino,et al. Graves’ disease , 2020, Nature Reviews Disease Primers.
[16] H. Cordell,et al. An Intronic HCP5 Variant Is Associated With Age of Onset and Susceptibility to Graves Disease in UK and Polish Cohorts , 2020, The Journal of clinical endocrinology and metabolism.
[17] R. Murray,et al. Antigen-Specific Immunotherapy with Thyrotropin Receptor Peptides in Graves' Hyperthyroidism: A Phase I Study , 2019, Thyroid : official journal of the American Thyroid Association.
[18] W. Cho,et al. HLA alleles, especially amino-acid signatures of HLA-DPB1, might contribute to the molecular pathogenesis of early-onset autoimmune thyroid disease , 2019, PloS one.
[19] G. Novelli,et al. STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects , 2019, Journal of immunology research.
[20] R. Płoski,et al. Paediatric‐onset and adult‐onset Graves' disease share multiple genetic risk factors , 2018, Clinical endocrinology.
[21] D. Valverde,et al. Long-term remission following antithyroid drug withdrawal in patients with Graves’ hyperthyroidism: parameters with prognostic value , 2018, Endocrine.
[22] P. Taylor,et al. Global epidemiology of hyperthyroidism and hypothyroidism , 2018, Nature Reviews Endocrinology.
[23] S. Pearce,et al. 2018 European Thyroid Association Guideline for the Management of Graves’ Hyperthyroidism , 2018, European Thyroid Journal.
[24] W. Wiersinga,et al. Antithyroid drug treatment for Graves’ disease: baseline predictive models of relapse after treatment for a patient-tailored management , 2018, Journal of Endocrinological Investigation.
[25] L. Hegedüs,et al. Predictive score for the development or progression of Graves' orbitopathy in patients with newly diagnosed Graves' hyperthyroidism. , 2018, European journal of endocrinology.
[26] W. Teng,et al. Alterations of Global DNA Methylation and DNA Methyltransferase Expression in T and B Lymphocytes from Patients with Newly Diagnosed Autoimmune Thyroid Diseases After Treatment: A Follow-Up Study. , 2018, Thyroid : official journal of the American Thyroid Association.
[27] Wei Liu,et al. Genetic study of early‐onset Graves’ disease in the Chinese Han population , 2018, Clinical genetics.
[28] A. Krętowski,et al. Analysis of chosen polymorphisms rs2476601 a/G – PTPN22, rs1990760 C/T – IFIH1, rs179247 a/G – TSHR in pathogenesis of autoimmune thyroid diseases in children , 2018, Autoimmunity.
[29] Z. Xin,et al. A genome-wide DNA methylation analysis in peripheral blood from patients identifies risk loci associated with Graves’ orbitopathy , 2018, Journal of Endocrinological Investigation.
[30] Samsuridjal Djauzi,et al. The Role of Cytotoxic T-lymphocyte-associated Protein 4 (CTLA-4) Gene, Thyroid Stimulating Hormone Receptor (TSHR) Gene and Regulatory T-cells as Risk Factors for Relapse in Patients with Graves Disease. , 2017, Acta medica Indonesiana.
[31] Guang Wang,et al. Predictive Value of Gene Polymorphisms on Recurrence after the Withdrawal of Antithyroid Drugs in Patients with Graves’ Disease , 2017, Front. Endocrinol..
[32] W. Cho,et al. Association of Polymorphisms in Toll-Like Receptors 4 and 9 with Autoimmune Thyroid Disease in Korean Pediatric Patients , 2017, International journal of endocrinology.
[33] S. Balasubramanian,et al. Epidemiology, management and outcomes of Graves’ disease—real life data , 2017, Endocrine.
[34] R. Płoski,et al. Gender-dependent and age-of-onset-specific association of the rs11675434 single-nucleotide polymorphism near TPO with susceptibility to Graves’ ophthalmopathy , 2016, Journal of Human Genetics.
[35] P. White,et al. Graves' disease in children: long‐term outcomes of medical therapy , 2016, Clinical endocrinology.
[36] M. Bolanowski,et al. CD28/CTLA-4/ICOS haplotypes confers susceptibility to Graves’ disease and modulates clinical phenotype of disease , 2016, Endocrine.
[37] K. Badenhoop,et al. Relapse prediction in Graves´ disease: Towards mathematical modeling of clinical, immune and genetic markers , 2016, Reviews in Endocrine and Metabolic Disorders.
[38] E. J. Lee,et al. Role of miR-146a in the Regulation of Inflammation in an In Vitro Model of Graves' Orbitopathy. , 2016, Investigative ophthalmology & visual science.
[39] G. Montgomery,et al. Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy. , 2016, Investigative ophthalmology & visual science.
[40] F. Lo,et al. Association of Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA4) Gene Polymorphisms with Autoimmune Thyroid Disease in Children and Adults: Case-Control Study , 2016, PLoS ONE.
[41] A. Zwinderman,et al. Predicting the Risk of Recurrence Before the Start of Antithyroid Drug Therapy in Patients With Graves' Hyperthyroidism. , 2016, The Journal of clinical endocrinology and metabolism.
[42] Terry J. Smith,et al. Graves' Disease. , 2016, The New England journal of medicine.
[43] S. Sanna,et al. The association of thyroid peroxidase antibody risk loci with susceptibility to and phenotype of Graves' disease , 2015, Clinical endocrinology.
[44] D. Ye,et al. Emerging role of long noncoding RNAs in autoimmune diseases. , 2015, Autoimmunity reviews.
[45] Huaxi Xu,et al. MiR-346 regulates CD4+CXCR5+ T cells in the pathogenesis of Graves’ disease , 2015, Endocrine.
[46] R. Secolin,et al. TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves’ disease and Graves’ ophthalmopathy , 2015, Journal of Endocrinological Investigation.
[47] Weiqing Wang,et al. Circulating microRNA predicts insensitivity to glucocorticoid therapy in Graves’ ophthalmopathy , 2015, Endocrine.
[48] G. Novelli,et al. A Multilocus Genetic Study in a Cohort of Italian SLE Patients Confirms the Association with STAT4 Gene and Describes a New Association with HCP5 Gene , 2014, PloS one.
[49] F. Tsai,et al. Single nucleotide polymorphisms at the PRR3, ABCF1, and GNL1 genes in the HLA class I region are associated with Graves' ophthalmopathy in a gender-dependent manner. , 2014, Ophthalmology.
[50] P. Laurberg,et al. Relapse following antithyroid drug therapy for Graves’ hyperthyroidism , 2014, Current opinion in endocrinology, diabetes, and obesity.
[51] R. Płoski,et al. Association between Polymorphisms in the TSHR Gene and Graves' Orbitopathy , 2014, PloS one.
[52] Xiaojie Ma,et al. Associations of CTLA4 Gene Polymorphisms with Graves' Ophthalmopathy: A Meta-Analysis , 2014, International journal of genomics.
[53] W. Wiersinga,et al. Mechanisms in endocrinology: autoimmune thyroid disease: old and new players. , 2014, European journal of endocrinology.
[54] M. Szalecki,et al. Analysis of chosen polymorphisms in FoxP3 gene in children and adolescents with autoimmune thyroid diseases , 2014, Autoimmunity.
[55] Vaneet Lotay,et al. Genetic analysis in young-age-of-onset Graves' disease reveals new susceptibility loci. , 2014, The Journal of clinical endocrinology and metabolism.
[56] Yaoming Xue,et al. Circulating levels of miR-146a and IL-17 are significantly correlated with the clinical activity of Graves' ophthalmopathy. , 2014, Endocrine journal.
[57] A. Kucharska,et al. CTLA-4 polymorphisms (+49 A/G and -318 C/T) are important genetic determinants of AITD susceptibility and predisposition to high levels of thyroid autoantibodies in Polish children - preliminary study. , 2013, Acta biochimica Polonica.
[58] S. Jansson,et al. Incidence rate and clinical features of hyperthyroidism in a long‐term iodine sufficient area of Sweden (Gothenburg) 2003–2005 , 2013, Clinical endocrinology.
[59] M. Bolanowski,et al. PPARg2 Ala12 variant protects against Graves' orbitopathy and modulates the course of the disease , 2013, Immunogenetics.
[60] R. Płoski,et al. Association between Age at Diagnosis of Graves' Disease and Variants in Genes Involved in Immune Response , 2013, PloS one.
[61] M. Watanabe,et al. Association of polymorphisms in DNMT1, DNMT3A, DNMT3B, MTHFR and MTRR genes with global DNA methylation levels and prognosis of autoimmune thyroid disease , 2012, Clinical and experimental immunology.
[62] F. Lo,et al. The HLA-DRB1 gene and Graves disease in Taiwanese children: a case-control and family-based study. , 2012, Tissue antigens.
[63] R. Latif,et al. Genetic profiling in Graves' disease: further evidence for lack of a distinct genetic contribution to Graves' ophthalmopathy. , 2012, Thyroid : official journal of the American Thyroid Association.
[64] L. Seah,et al. Ethnic differences in the clinical presentation of Graves' ophthalmopathy. , 2012, Best practice & research. Clinical endocrinology & metabolism.
[65] S. Juo,et al. Genotype and Phenotype Predictors of Relapse of Graves’ Disease after Antithyroid Drug Withdrawal , 2012, European Thyroid Journal.
[66] W. Cho,et al. Association of HLA Alleles with Autoimmune Thyroid Disease in Korean Children , 2011, Hormone Research in Paediatrics.
[67] Yang Liu,et al. Genome-Wide Interaction-Based Association Analysis Identified Multiple New Susceptibility Loci for Common Diseases , 2011, PLoS genetics.
[68] A. Esteghamati,et al. Genetic susceptibility to Graves’ ophthalmopathy: the role of polymorphisms in proinflammatory cytokine genes , 2010, Eye.
[69] S. Greene,et al. Incidence of thyrotoxicosis in childhood: a national population based study in the UK and Ireland , 2010, Clinical endocrinology.
[70] R. Bahn. Graves' ophthalmopathy. , 2010, The New England journal of medicine.
[71] A. Esteghamati,et al. Graves' ophthalmopathy and gene polymorphisms in interleukin‐1α, interleukin‐1β, interleukin‐1 receptor and interleukin‐1 receptor antagonist , 2009, Clinical & experimental ophthalmology.
[72] N. Morgenthaler,et al. The T393C polymorphism of the Galphas gene (GNAS1) is associated with the course of Graves' disease. , 2009, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.
[73] P. Czernichow,et al. Predictors of autoimmune hyperthyroidism relapse in children after discontinuation of antithyroid drug treatment. , 2008, The Journal of clinical endocrinology and metabolism.
[74] Ya-Ting Chang,et al. Association of CT60 Polymorphism of the CTLA4 Gene with Graves' Disease in Taiwanese Children , 2008, Journal of pediatric endocrinology & metabolism : JPEM.
[75] K. Park,et al. Susceptible alleles of the CD40 and CTLA-4 genes are not associated with the relapse after antithyroid withdrawal in Graves' disease. , 2007, Thyroid : official journal of the American Thyroid Association.
[76] J. Franklyn,et al. Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves’ ophthalmopathy , 2007, Clinical endocrinology.
[77] M. Hsieh,et al. Association between a C/T polymorphism in exon 33 of the thyroglobulin gene is associated with relapse of Graves' hyperthyroidism after antithyroid withdrawal in Taiwanese. , 2007, The Journal of clinical endocrinology and metabolism.
[78] S. Juo,et al. Cytotoxic T lymphocyte-associated molecule-4 gene polymorphism and hyperthyroid Graves' disease relapse after antithyroid drug withdrawal: a follow-up study. , 2007, The Journal of clinical endocrinology and metabolism.
[79] R. Płoski,et al. Susceptibility genes in Graves’ ophthalmopathy: searching for a needle in a haystack? , 2007, Clinical endocrinology.
[80] H. Issever,et al. The predictive value of CTLA-4 and Tg polymorphisms in the recurrence of graves’ disease after antithyroid withdrawal , 2006, Endocrine.
[81] M. Erdoğan,et al. Cytotoxic T lymphocyte-associated molecule-4 polymorphisms in Turkish Graves' disease patients and association with probability of remission after antithyroid therapy. , 2005, European journal of internal medicine.
[82] R. Płoski,et al. Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves’ disease in a Polish population: association and gene dose‐dependent correlation with age of onset , 2005, Clinical endocrinology.
[83] K. Jażdżewski,et al. Association of tumor necrosis factor and human leukocyte antigen DRB1 alleles with Graves' ophthalmopathy. , 2004, Human immunology.
[84] A. Krętowski,et al. Intercellular adhesion molecule 1 gene polymorphisms in Graves' disease. , 2003, The Journal of clinical endocrinology and metabolism.
[85] F. Lo,et al. Polymorphism in the transmembrane region of the major histocompatibility complex class I chain-related gene A: association of five GCT repetitions with Graves' disease in children. , 2003, Thyroid : official journal of the American Thyroid Association.
[86] P. Perros,et al. CTLA4 gene and Graves’ disease: association of Graves’ disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphism , 2003, Clinical endocrinology.
[87] T. Kouki,et al. Remission of Graves' hyperthyroidism and A/G polymorphism at position 49 in exon 1 of cytotoxic T lymphocyte-associated molecule-4 gene. , 2002, The Journal of clinical endocrinology and metabolism.
[88] L. Hegedüs,et al. Evidence for a major role of heredity in Graves' disease: a population-based study of two Danish twin cohorts. , 2001, The Journal of clinical endocrinology and metabolism.
[89] T. Bednarczuk,et al. A polymorphism of the 5′ flanking region of tumour necrosis factor α gene is associated with thyroid‐associated ophthalmopathy in Japanese , 2000, Clinical endocrinology.
[90] J. Franklyn,et al. The development of Graves' disease and the CTLA-4 gene on chromosome 2q33. , 1999, The Journal of clinical endocrinology and metabolism.
[91] H. Perrild,et al. Incidence of juvenile thyrotoxicosis in Denmark, 1982-1988. A nationwide study. , 1994, European journal of endocrinology.
[92] R. Holle,et al. Prospective multicentre study on the prediction of relapse after antithyroid drug treatment in patients with Graves' disease. , 1989, Acta endocrinologica.