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Journal Abstract Search

218 related items for PubMed ID: 30796769

  • 1. Linkage Analysis of the Chromosome 5q31-33 Region Identifies JAKMIP2 as a Risk Factor for Graves' Disease in the Chinese Han Population.
    Li J, Teng W, Yu Y, Hou X, Shan Z.
    Med Sci Monit; 2019 Feb 23; 25():1439-1451. PubMed ID: 30796769
    [Abstract] [Full Text] [Related]

  • 2. Association study between the IL4, IL13, IRF1 and UGRP1 genes in chromosomal 5q31 region and Chinese Graves' disease.
    Yang Y, Lingling S, Ying J, Yushu L, Zhongyan S, Wei H, Weiping T.
    J Hum Genet; 2005 Feb 23; 50(11):574-582. PubMed ID: 16195814
    [Abstract] [Full Text] [Related]

  • 3. Confirmation of association of chromosome 5q31-33 with United Kingdom Caucasian Graves' disease.
    Simmonds MJ, Yesmin K, Newby PR, Brand OJ, Franklyn JA, Gough SC.
    Thyroid; 2010 Apr 23; 20(4):413-7. PubMed ID: 20210668
    [Abstract] [Full Text] [Related]

  • 4. TNFSF15 Polymorphisms are Associated with Graves' Disease and Graves' Ophthalmopathy in a Han Chinese Population.
    Zhang M, Liu S, Xu J, Lv S, Fan Y, Zhang Y, Zhang Y, Wu Y, Su Y, Yu H, Song S, He J, Li H.
    Curr Eye Res; 2020 Jul 23; 45(7):888-895. PubMed ID: 31869260
    [Abstract] [Full Text] [Related]

  • 5. Genome-wide scan of Graves' disease: evidence for linkage on chromosome 5q31 in Chinese Han pedigrees.
    Jin Y, Teng W, Ben S, Xiong X, Zhang J, Xu S, Shugart YY, Jin L, Chen J, Huang W.
    J Clin Endocrinol Metab; 2003 Apr 23; 88(4):1798-803. PubMed ID: 12679476
    [Abstract] [Full Text] [Related]

  • 6. Association Analysis of Single Nucleotide Polymorphisms in C1QTNF6, RAC2, and an Intergenic Region at 14q32.2 with Graves' Disease in Chinese Han Population.
    Zhang XH, Shen M, Liu L, Li FM, Hu PC, Hua Q, Zhang J, Pang LN, Lu HW, Wang ZM, Chu X, Huang W.
    Genet Test Mol Biomarkers; 2017 Aug 23; 21(8):479-484. PubMed ID: 28665696
    [Abstract] [Full Text] [Related]

  • 7. Association of the large multifunctional proteasome (LMP2) gene with Graves' disease is a result of linkage disequilibrium with the HLA haplotype DRB1*0304-DQB1*02-DQA1*0501.
    Heward JM, Allahabadia A, Sheppard MC, Barnett AH, Franklyn JA, Gough SC.
    Clin Endocrinol (Oxf); 1999 Jul 23; 51(1):115-8. PubMed ID: 10468973
    [Abstract] [Full Text] [Related]

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  • 9. RNASET2 tag SNP but not CCR6 polymorphisms is associated with autoimmune thyroid diseases in the Chinese Han population.
    Chen XJ, Gong XH, Yan N, Meng S, Qin Q, Jiang YF, Zheng HY, Zhang JA.
    BMC Med Genet; 2015 Feb 26; 16():11. PubMed ID: 25928629
    [Abstract] [Full Text] [Related]

  • 10. Foxp3 gene polymorphisms and haplotypes associate with susceptibility of Graves' disease in Chinese Han population.
    Zheng L, Wang X, Xu L, Wang N, Cai P, Liang T, Hu L.
    Int Immunopharmacol; 2015 Apr 26; 25(2):425-31. PubMed ID: 25708657
    [Abstract] [Full Text] [Related]

  • 11. Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence.
    Chu X, Dong Y, Shen M, Sun L, Dong C, Wang Y, Wang B, Zhang K, Hua Q, Xu S, Huang W.
    BMC Med Genet; 2009 Mar 13; 10():26. PubMed ID: 19284637
    [Abstract] [Full Text] [Related]

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  • 13. Correlation between CTLA-4 and CD40 gene polymorphisms and their interaction in graves' disease in a Chinese Han population.
    Chen X, Hu Z, Liu M, Li H, Liang C, Li W, Bao L, Chen M, Wu G.
    BMC Med Genet; 2018 Sep 17; 19(1):171. PubMed ID: 30223781
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  • 15. Association of 4p14 and 6q27 variation with Graves disease: a case-control study and a meta-analysis of available evidence.
    Li FM, Liu L, Pang LN, Shen M, Lu HW, Zhang XH, Chu X, Song ZJ.
    BMC Med Genet; 2017 May 18; 18(1):56. PubMed ID: 28521825
    [Abstract] [Full Text] [Related]

  • 16. The -112G>A polymorphism of the secretoglobin 3A2 (SCGB3A2) gene encoding uteroglobin-related protein 1 (UGRP1) increases risk for the development of Graves' disease in subsets of patients with elevated levels of immunoglobulin E.
    Chistiakov DA, Voronova NV, Turakulov RI, Savost'anov KV.
    J Appl Genet; 2011 May 18; 52(2):201-7. PubMed ID: 21170691
    [Abstract] [Full Text] [Related]

  • 17. A dense mapping study of six European AITD susceptibility regions in a large Chinese Han Cohort of Graves' disease.
    Liu W, Zhang QY, Yuan FF, Wang HN, Zhang LL, Ma YR, Ye XP, Zhang MM, Song ZY, Li SX, Du WH, Liang J, Zhang XM, Gao GQ, Zhao SX, Chen FL, Song HD, China Consortium for the Genetics of Autoimmune Thyroid Disease.
    Clin Endocrinol (Oxf); 2018 Dec 18; 89(6):840-848. PubMed ID: 30176063
    [Abstract] [Full Text] [Related]

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  • 19. Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.
    Song HD, Liang J, Shi JY, Zhao SX, Liu Z, Zhao JJ, Peng YD, Gao GQ, Tao J, Pan CM, Shao L, Cheng F, Wang Y, Yuan GY, Xu C, Han B, Huang W, Chu X, Chen Y, Sheng Y, Li RY, Su Q, Gao L, Jia WP, Jin L, Chen MD, Chen SJ, Chen Z, Chen JL.
    Hum Mol Genet; 2009 Mar 15; 18(6):1156-70. PubMed ID: 19126779
    [Abstract] [Full Text] [Related]

  • 20. Screening of SNPs at 18 positional candidate genes, located within the GD-1 locus on chromosome 14q23-q32, for susceptibility to Graves' disease: a TDT study.
    Chistiakov DA, Savost'anov KV, Turakulov RI.
    Mol Genet Metab; 2004 Nov 15; 83(3):264-70. PubMed ID: 15542398
    [Abstract] [Full Text] [Related]

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