150 related articles for article (PubMed ID: 27304844)
1. Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy.
Khong JJ; Burdon KP; Lu Y; Leonardos L; Laurie KJ; Walsh JP; Gajdatsy AD; Ebeling PR; McNab AA; Hardy TG; Stawell RJ; Davis GJ; Selva D; Tsirbas A; Montgomery GW; Macgregor S; Craig JE
Invest Ophthalmol Vis Sci; 2016 Jun; 57(7):3129-37. PubMed ID: 27304844
[TBL] [Abstract][Full Text] [Related]
2. Pooled genome wide association detects association upstream of FCRL3 with Graves' disease.
Khong JJ; Burdon KP; Lu Y; Laurie K; Leonardos L; Baird PN; Sahebjada S; Walsh JP; Gajdatsy A; Ebeling PR; Hamblin PS; Wong R; Forehan SP; Fourlanos S; Roberts AP; Doogue M; Selva D; Montgomery GW; Macgregor S; Craig JE
BMC Genomics; 2016 Nov; 17(1):939. PubMed ID: 27863461
[TBL] [Abstract][Full Text] [Related]
3. CD28/CTLA-4/ICOS haplotypes confers susceptibility to Graves' disease and modulates clinical phenotype of disease.
Pawlak-Adamska E; Frydecka I; Bolanowski M; Tomkiewicz A; Jonkisz A; Karabon L; Partyka A; Nowak O; Szalinski M; Daroszewski J
Endocrine; 2017 Jan; 55(1):186-199. PubMed ID: 27638540
[TBL] [Abstract][Full Text] [Related]
4. Influence of the TSH receptor gene on susceptibility to Graves' disease and Graves' ophthalmopathy.
Yin X; Latif R; Bahn R; Tomer Y; Davies TF
Thyroid; 2008 Nov; 18(11):1201-6. PubMed ID: 18925838
[TBL] [Abstract][Full Text] [Related]
5. Gender-dependent and age-of-onset-specific association of the rs11675434 single-nucleotide polymorphism near TPO with susceptibility to Graves' ophthalmopathy.
Kuś A; Szymański K; Jurecka-Lubieniecka B; Pawlak-Adamska E; Kula D; Miśkiewicz P; Bolanowski M; Płoski R; Bossowski A; Daroszewski J; Jarząb B; Bednarczuk T
J Hum Genet; 2017 Mar; 62(3):373-377. PubMed ID: 27829681
[TBL] [Abstract][Full Text] [Related]
6. Polymorphisms of endothelin 1 (G5665T and T-1370G) and endothelin receptor type A (C+70G and G-231A) in Graves' disease.
Aydın AF; Develi-İş S; Doğru-Abbasoğlu S; Vural P; Ozderya A; Karadağ B; Uysal M
Int Immunopharmacol; 2014 Jan; 18(1):198-202. PubMed ID: 24291390
[TBL] [Abstract][Full Text] [Related]
7. TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves' disease and Graves' ophthalmopathy.
Bufalo NE; Dos Santos RB; Marcello MA; Piai RP; Secolin R; Romaldini JH; Ward LS
J Endocrinol Invest; 2015 May; 38(5):555-61. PubMed ID: 25543543
[TBL] [Abstract][Full Text] [Related]
8. Association of CTLA-4 gene polymorphism with Graves' disease and ophthalmopathy in Iranian patients.
Esteghamati A; Khalilzadeh O; Mobarra Z; Anvari M; Tahvildari M; Amiri HM; Rashidi A; Solgi G; Parivar K; Nikbin B; Amirzargar A
Eur J Intern Med; 2009 Jul; 20(4):424-8. PubMed ID: 19524188
[TBL] [Abstract][Full Text] [Related]
9. The association of thyroid peroxidase antibody risk loci with susceptibility to and phenotype of Graves' disease.
Kuś A; Szymański K; Peeters RP; Miśkiewicz P; Porcu E; Pistis G; Sanna S; Naitza S; Płoski R; Medici M; Bednarczuk T
Clin Endocrinol (Oxf); 2015 Oct; 83(4):556-62. PubMed ID: 25345847
[TBL] [Abstract][Full Text] [Related]
10. The Role of Vitamin D Receptor Gene Polymorphisms in Thyroid-Associated Orbitopathy.
Maciejewski A; Kowalczyk MJ; Gasińska T; Szeliga A; Prendecki M; Dorszewska J; Żaba R; Łącka K
Ocul Immunol Inflamm; 2020 Apr; 28(3):354-361. PubMed ID: 31424978
[No Abstract] [Full Text] [Related]
11. The VDR gene confers a genetic predisposition to Graves' disease and Graves' ophthalmopathy in the Southwest Chinese Han population.
Zhou F; Liang Z; Wang X; Tan G; Wei W; Zheng G; Ma X; Tian D; Li H; Yu H
Gene; 2021 Aug; 793():145750. PubMed ID: 34077777
[TBL] [Abstract][Full Text] [Related]
12. Pretibial myxedema is associated with polymorphism in exon 1 of CTLA-4 gene in patients with Graves' ophthalmopathy.
Khalilzadeh O; Mojazi Amiri H; Tahvildari M; Anvari M; Esteghamati A; Mobarra Z; Tehranchinia Z; Rashidi A; Amirzargar A
Arch Dermatol Res; 2009 Oct; 301(10):719-23. PubMed ID: 19037649
[TBL] [Abstract][Full Text] [Related]
13. Graves' ophthalmopathy and gene polymorphisms in interleukin-1alpha, interleukin-1beta, interleukin-1 receptor and interleukin-1 receptor antagonist.
Khalilzadeh O; Anvari M; Esteghamati A; Mahmoudi M; Tahvildari M; Rashidi A; Khosravi F; Amirzargar A
Clin Exp Ophthalmol; 2009 Aug; 37(6):614-9. PubMed ID: 19702713
[TBL] [Abstract][Full Text] [Related]
14. Association analysis of polymorphisms in IL-3, IL-4, IL-5, IL-9, and IL-13 with Graves' disease.
Zhu W; Liu N; Zhao Y; Jia H; Cui B; Ning G
J Endocrinol Invest; 2010 Nov; 33(10):751-5. PubMed ID: 20332709
[TBL] [Abstract][Full Text] [Related]
15. Association of Graves' disease and Graves' ophthalmopathy with the polymorphisms in promoter and exon 1 of cytotoxic T lymphocyte associated antigen-4 gene.
Zhang Q; Yang YM; Lv XY
J Zhejiang Univ Sci B; 2006 Nov; 7(11):887-91. PubMed ID: 17048303
[TBL] [Abstract][Full Text] [Related]
16. Association between methylenetetrahydrofolate reductase (MTHFR) polymorphisms and susceptibility to Graves' ophthalmopathy.
Lee JY; Kim NK; Cho YW; Lew H
Mol Med Rep; 2016 Sep; 14(3):2276-82. PubMed ID: 27430300
[TBL] [Abstract][Full Text] [Related]
17. Soluble CTLA-4 receptor an immunological marker of Graves' disease and severity of ophthalmopathy is associated with CTLA-4 Jo31 and CT60 gene polymorphisms.
Daroszewski J; Pawlak E; Karabon L; Frydecka I; Jonkisz A; Slowik M; Bolanowski M
Eur J Endocrinol; 2009 Nov; 161(5):787-93. PubMed ID: 19734241
[TBL] [Abstract][Full Text] [Related]
18. Risk Factors for Graves' Orbitopathy; the Australian Thyroid-Associated Orbitopathy Research (ATOR) Study.
Khong JJ; Finch S; De Silva C; Rylander S; Craig JE; Selva D; Ebeling PR
J Clin Endocrinol Metab; 2016 Jul; 101(7):2711-20. PubMed ID: 27055083
[TBL] [Abstract][Full Text] [Related]
19. 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.
Liu YH; Chen YJ; Wu HH; Wang TY; Tsai FJ
Ophthalmology; 2014 Oct; 121(10):2033-9. PubMed ID: 24908204
[TBL] [Abstract][Full Text] [Related]
20. Genetic variants of BANK1 gene in autoimmune thyroid diseases: a case-control association study.
Muhali FS; Song RH; Wang X; Shi XH; Jiang WJ; Xiao L; Li DF; He ST; Xu J; Zhang JA
Exp Clin Endocrinol Diabetes; 2013 Oct; 121(9):556-60. PubMed ID: 24127308
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
