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For: Sakai K, Shirasawa S, Ishikawa N, Ito K, Tamai H, Kuma K, Akamizu T, Tanimura M, Furugaki K, Yamamoto K. Identification of susceptibility loci for autoimmune thyroid disease to 5q31-q33 and Hashimoto's thyroiditis to 8q23-q24 by multipoint affected sib-pair linkage analysis in Japanese. Hum Mol Genet. 2001;10:1379-1386. [PMID: 11440990 DOI: 10.1093/hmg/10.13.1379] [Cited by in Crossref: 135] [Cited by in F6Publishing: 114] [Article Influence: 6.8] [Reference Citation Analysis]
Number Citing Articles
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2 Simmonds MJ, Gough SC. Unravelling the genetic complexity of autoimmune thyroid disease: HLA, CTLA-4 and beyond. Clin Exp Immunol 2004;136:1-10. [PMID: 15030506 DOI: 10.1111/j.1365-2249.2004.02424.x] [Cited by in Crossref: 56] [Cited by in F6Publishing: 46] [Article Influence: 3.3] [Reference Citation Analysis]
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4 Bednarczuk T, Placha G, Jazdzewski K, Kurylowicz A, Kloza M, Makowska U, Hiromatsu Y, Nauman J. Interleukin-13 gene polymorphisms in patients with Graves' disease. Clin Endocrinol (Oxf) 2003;59:519-25. [PMID: 14510917 DOI: 10.1046/j.1365-2265.2003.01880.x] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 0.7] [Reference Citation Analysis]
5 Tait KF, Gough SC. The genetics of autoimmune endocrine disease. Clin Endocrinol (Oxf) 2003;59:1-11. [PMID: 12807496 DOI: 10.1046/j.1365-2265.2003.01723.x] [Cited by in Crossref: 27] [Cited by in F6Publishing: 17] [Article Influence: 1.5] [Reference Citation Analysis]
6 Chu X, Dong Y, Shen M, Sun L, Dong C, Wang Y, Wang B, Zhang K, Hua Q, Xu S, Huang W. Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence. BMC Med Genet 2009;10:26. [PMID: 19284637 DOI: 10.1186/1471-2350-10-26] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 0.9] [Reference Citation Analysis]
7 Zettinig G, Tanew A, Fischer G, Mayr W, Dudczak R, Weissel M. Autoimmune diseases in vitiligo: do anti-nuclear antibodies decrease thyroid volume? Clin Exp Immunol 2003;131:347-54. [PMID: 12562399 DOI: 10.1046/j.1365-2249.2003.02089.x] [Cited by in Crossref: 43] [Cited by in F6Publishing: 37] [Article Influence: 2.4] [Reference Citation Analysis]
8 Stefan M, Jacobson EM, Huber AK, Greenberg DA, Li CW, Skrabanek L, Conception E, Fadlalla M, Ho K, Tomer Y. Novel variant of thyroglobulin promoter triggers thyroid autoimmunity through an epigenetic interferon alpha-modulated mechanism. J Biol Chem. 2011;286:31168-31179. [PMID: 21757724 DOI: 10.1074/jbc.m111.247510] [Cited by in Crossref: 42] [Cited by in F6Publishing: 30] [Article Influence: 4.2] [Reference Citation Analysis]
9 Hu Z, Li W, Li M, Wei H, Hu Z, Chen Y, Luo A, Li W. Screening of Graves' disease susceptibility genes by whole exome sequencing in a three-generation family. BMC Med Genomics 2021;14:46. [PMID: 33568133 DOI: 10.1186/s12920-020-00865-z] [Reference Citation Analysis]
10 Alaez C, Arellanes L, Vazquez A, Flores H, Navarro P, Vazquez-garcía M, Gorodezky C. Classic pars planitis: strong correlation of class II genes with gender and some clinical features in Mexican mestizos. Human Immunology 2003;64:965-72. [DOI: 10.1016/s0198-8859(03)00185-x] [Cited by in Crossref: 11] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
11 Nawata H, Shirasawa S, Nakashima N, Araki E, Hashiguchi J, Miyake S, Yamauchi T, Hamaguchi K, Yoshimatsu H, Takeda H, Fukushima H, Sasahara T, Yamaguchi K, Sonoda N, Sonoda T, Matsumoto M, Tanaka Y, Sugimoto H, Tsubouchi H, Inoguchi T, Yanase T, Wake N, Narazaki K, Eto T, Umeda F, Nakazaki M, Ono J, Asano T, Ito Y, Akazawa S, Hazegawa I, Takasu N, Shinohara M, Nishikawa T, Nagafuchi S, Okeda T, Eguchi K, Iwase M, Ishikawa M, Aoki M, Keicho N, Kato N, Yasuda K, Yamamoto K, Sasazuki T. Genome-wide linkage analysis of type 2 diabetes mellitus reconfirms the susceptibility locus on 11p13–p12 in Japanese. J Hum Genet 2004;49:629-34. [DOI: 10.1007/s10038-004-0199-3] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 0.9] [Reference Citation Analysis]
12 Tomer Y, Ban Y, Concepcion E, Barbesino G, Villanueva R, Greenberg DA, Davies TF. Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families. Am J Hum Genet 2003;73:736-47. [PMID: 12973666 DOI: 10.1086/378588] [Cited by in Crossref: 150] [Cited by in F6Publishing: 124] [Article Influence: 8.3] [Reference Citation Analysis]
13 Ban Y, Davies TF, Greenberg DA, Concepcion ES, Tomer Y. The influence of human leucocyte antigen (HLA) genes on autoimmune thyroid disease (AITD): results of studies in HLA-DR3 positive AITD families: HLA and AITD. Clinical Endocrinology 2002;57:81-8. [DOI: 10.1046/j.1365-2265.2002.01566.x] [Cited by in Crossref: 61] [Cited by in F6Publishing: 47] [Article Influence: 3.2] [Reference Citation Analysis]
14 Ban Y, Tozaki T, Taniyama M, Tomita M, Ban Y. Association of a CTLA-4 3' untranslated region (CT60) single nucleotide polymorphism with autoimmune thyroid disease in the Japanese population. Autoimmunity 2005;38:151-3. [PMID: 16040335 DOI: 10.1080/08916930500050319] [Cited by in Crossref: 44] [Cited by in F6Publishing: 39] [Article Influence: 2.8] [Reference Citation Analysis]
15 Hadj Kacem H, Rebai A, Kaffel N, Masmoudi S, Abid M, Ayadi H. PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study. J Clin Endocrinol Metab 2003;88:2274-80. [PMID: 12727986 DOI: 10.1210/jc.2002-021460] [Cited by in Crossref: 26] [Cited by in F6Publishing: 15] [Article Influence: 1.4] [Reference Citation Analysis]
16 Jang JP, Cho WK, Baek IC, Choi EJ, Shin DH, Suh BK, Kim TG. Comprehensive analysis of cytokine gene polymorphisms defines the association of IL-12 gene with ophthalmopthy in Korean children with autoimmune thyroid disease. Mol Cell Endocrinol 2016;426:43-9. [PMID: 26850223 DOI: 10.1016/j.mce.2016.02.002] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
17 Maierhaba M, Zhang J, Yu Z, Wang Y, Xiao W, Quan Y, Dong B. Association of the thyroglobulin gene polymorphism with autoimmune thyroid disease in Chinese population. Endocr 2008;33:294-9. [DOI: 10.1007/s12020-008-9082-x] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 1.9] [Reference Citation Analysis]
18 Fujimoto T, Doi K, Koyanagi M, Tsunoda T, Takashima Y, Yoshida Y, Sasazuki T, Shirasawa S. ZFAT is an antiapoptotic molecule and critical for cell survival in MOLT‐4 cells. FEBS Letters 2009;583:568-72. [DOI: 10.1016/j.febslet.2008.12.063] [Cited by in Crossref: 30] [Cited by in F6Publishing: 24] [Article Influence: 2.5] [Reference Citation Analysis]
19 Yin X, Latif R, Bahn R, Tomer Y, Davies TF. Influence of the TSH receptor gene on susceptibility to Graves’ disease and Graves’ ophthalmopathy. Thyroid. 2008;18:1201-1206. [PMID: 18925838 DOI: 10.1089/thy.2008.0098] [Cited by in Crossref: 40] [Cited by in F6Publishing: 26] [Article Influence: 3.3] [Reference Citation Analysis]
20 Brenner M, Meng H, Yarlett NC, Joe B, Griffiths MM, Remmers EF, Wilder RL, Gulko PS. The Non-MHC Quantitative Trait Locus Cia5 Contains Three Major Arthritis Genes That Differentially Regulate Disease Severity, Pannus Formation, and Joint Damage in Collagen- and Pristane-Induced Arthritis. J Immunol 2005;174:7894-903. [DOI: 10.4049/jimmunol.174.12.7894] [Cited by in Crossref: 40] [Cited by in F6Publishing: 36] [Article Influence: 2.5] [Reference Citation Analysis]
21 Tomer Y. Genetic dissection of familial autoimmune thyroid diseases using whole genome screening. Autoimmunity Reviews 2002;1:198-204. [DOI: 10.1016/s1568-9972(02)00053-8] [Cited by in Crossref: 22] [Cited by in F6Publishing: 4] [Article Influence: 1.2] [Reference Citation Analysis]
22 Zaletel K, Gaberšček S. Hashimoto's Thyroiditis: From Genes to the Disease. Curr Genomics 2011;12:576-88. [PMID: 22654557 DOI: 10.2174/138920211798120763] [Cited by in Crossref: 83] [Cited by in F6Publishing: 55] [Article Influence: 9.2] [Reference Citation Analysis]
23 Furugaki K, Shirasawa S, Ishikawa N, Ito K, Ito K, Kubota S, Kuma K, Tamai H, Akamizu T, Hiratani H, Tanaka M, Sasazuki T. Association of the T-cell regulatory gene CTLA4 with Graves' disease and autoimmune thyroid disease in the Japanese. J Hum Genet 2004;49:166-8. [PMID: 14986169 DOI: 10.1007/s10038-003-0120-5] [Cited by in Crossref: 52] [Cited by in F6Publishing: 45] [Article Influence: 3.1] [Reference Citation Analysis]
24 Namjou B, Kelly JA, Kilpatrick J, Kaufman KM, Nath SK, Scofield RH, Harley JB. Linkage at 5q14.3-15 in multiplex systemic lupus erythematosus pedigrees stratified by autoimmune thyroid disease. Arthritis Rheum 2005;52:3646-50. [DOI: 10.1002/art.21413] [Cited by in Crossref: 24] [Cited by in F6Publishing: 18] [Article Influence: 1.5] [Reference Citation Analysis]
25 Simmonds MJ, Heward JM, Franklyn JA, Gough SC. IL-13 and chromosome 5q31-q33: problems of identifying association within regions of linkage to Graves' disease. Clin Endocrinol (Oxf) 2005;63:695-7. [PMID: 16343107 DOI: 10.1111/j.1365-2265.2005.02385.x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 0.5] [Reference Citation Analysis]
26 Bourguiba-Hachemi S, Ashkanani TK, Kadhem FJ, Almawi WY, Alroughani R, Fathallah MD. ZFAT gene variant association with multiple sclerosis in the Arabian Gulf population: A genetic basis for gender-associated susceptibility. Mol Med Rep 2016;14:3543-50. [PMID: 27572828 DOI: 10.3892/mmr.2016.5692] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 1.8] [Reference Citation Analysis]
27 Osorio y Fortéa J, Bukulmez H, Petit-teixeira E, Michou L, Pierlot C, Cailleau-moindrault S, Lemaire I, Lasbleiz S, Alibert O, Quillet P, Bardin T, Prum B, Olson JM, Cornélis F. Dense genome-wide linkage analysis of rheumatoid arthritis, including covariates: Dense RA Genome Scan. Arthritis & Rheumatism 2004;50:2757-65. [DOI: 10.1002/art.20458] [Cited by in Crossref: 64] [Cited by in F6Publishing: 55] [Article Influence: 3.8] [Reference Citation Analysis]
28 Li N, Zhou Z, Liu X, Liu Y, Zhang J, Du L, Wei M, Chen X. Association of tumour necrosis factor alpha (TNF-alpha) polymorphisms with Graves' disease: A meta-analysis. Clin Biochem 2008;41:881-6. [PMID: 18472000 DOI: 10.1016/j.clinbiochem.2008.04.014] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 1.5] [Reference Citation Analysis]
29 Hall RJ, Merriman ME, Green RA, Markham VH, Smyth DJ, Heward JM, Jennings CE, Braithwaite AW, Cundy T, Darlow BA, Gow PJ, Harrison AA, Highton J, Hunt PJ, Manning P, Pokorny V, Scott RS, Taylor BJ, Willis JA, Yeoman S, Mclean L, Gough SC, Pearce SH, Merriman TR. The deleted in colorectal carcinoma (DCC) gene 201 R → G polymorphism: no evidence for genetic association with autoimmune disease. Eur J Hum Genet 2003;11:840-4. [DOI: 10.1038/sj.ejhg.5201059] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
30 Cai Y, Xu X, Zhang Z, Wang P, Hu Q, Jin Y, Wang Z, Liu X, Yang T. Identification of novel HLA-A0201-restricted T-cell epitopes against thyroid antigens in autoimmune thyroid diseases. Endocrine 2020;69:562-70. [PMID: 32198668 DOI: 10.1007/s12020-020-02264-x] [Reference Citation Analysis]
31 Heo S, Jang JH, Yu J. Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene. Ann Pediatr Endocrinol Metab 2019;24:199-202. [PMID: 31607114 DOI: 10.6065/apem.2019.24.3.199] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
32 Li Wang, Zeng Chan Wang, Cui Xie, Xiao Feng Liu, Mao Sheng Yang. Genome-Wide Screening for Risk Loci of Idiopathic Recurrent Miscarriage in a Han Chinese Population: A Pilot Study. Reprod Sci 2010;17:578-84. [DOI: 10.1177/1933719110364248] [Cited by in Crossref: 19] [Cited by in F6Publishing: 11] [Article Influence: 1.7] [Reference Citation Analysis]
33 Yang Y, Lingling S, Ying J, Yushu L, Zhongyan S, Wei H, Weiping T. Association study between the IL4, IL13, IRF1 and UGRP1 genes in chromosomal 5q31 region and Chinese Graves' disease. J Hum Genet 2005;50:574-82. [PMID: 16195814 DOI: 10.1007/s10038-005-0297-x] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 1.3] [Reference Citation Analysis]
34 Gough S. The thyroglobulin gene: the third locus for autoimmune thyroid disease or a false dawn? Trends in Molecular Medicine 2004;10:302-5. [DOI: 10.1016/j.molmed.2004.05.001] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]
35 Levin L, Ban Y, Concepcion E, Davies TF, Greenberg DA, Tomer Y. Analysis of HLA genes in families with autoimmune diabetes and thyroiditis. Hum Immunol. 2004;65:640-647. [PMID: 15219384 DOI: 10.1016/j.humimm.2004.02.026] [Cited by in Crossref: 55] [Cited by in F6Publishing: 41] [Article Influence: 3.4] [Reference Citation Analysis]
36 Zhu W, Liu N, Zhao Y, Jia H, Cui B, Ning G. Association analysis of polymorphisms in IL-3, IL-4, IL-5, IL-9, and IL-13 with Graves' disease. J Endocrinol Invest 2010;33:751-5. [PMID: 20332709 DOI: 10.1007/BF03346682] [Cited by in Crossref: 19] [Cited by in F6Publishing: 11] [Article Influence: 1.7] [Reference Citation Analysis]
37 Davies TF, Latif R, Yin X. Inheriting autoimmune thyroid disease. Endocr Pract 2009;15:63-6. [PMID: 19211403 DOI: 10.4158/EP.15.1.63] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
38 Davies TF, Yin X, Latif R. The genetics of the thyroid stimulating hormone receptor: history and relevance. Thyroid 2010;20:727-36. [PMID: 20578897 DOI: 10.1089/thy.2010.1638] [Cited by in Crossref: 43] [Cited by in F6Publishing: 28] [Article Influence: 3.9] [Reference Citation Analysis]
39 Gough SC, Walker LS, Sansom DM. CTLA4 gene polymorphism and autoimmunity. Immunol Rev. 2005;204:102-115. [PMID: 15790353 DOI: 10.1111/j.0105-2896.2005.00249.x] [Cited by in Crossref: 198] [Cited by in F6Publishing: 177] [Article Influence: 12.4] [Reference Citation Analysis]
40 Huber A, Menconi F, Corathers S, Jacobson EM, Tomer Y. Joint genetic susceptibility to type 1 diabetes and autoimmune thyroiditis: from epidemiology to mechanisms. Endocr Rev 2008;29:697-725. [PMID: 18776148 DOI: 10.1210/er.2008-0015] [Cited by in Crossref: 134] [Cited by in F6Publishing: 102] [Article Influence: 10.3] [Reference Citation Analysis]
41 Zeitlin AA, Simmonds MJ, Gough SCL. Genetic developments in autoimmune thyroid disease: an evolutionary process. Clin Endocrinol 2008;68:671-82. [DOI: 10.1111/j.1365-2265.2007.03075.x] [Cited by in Crossref: 33] [Cited by in F6Publishing: 22] [Article Influence: 2.5] [Reference Citation Analysis]
42 Davies TF. Really Significant Genes for Autoimmune Thyroid Disease Do Not Exist—So How Can We Predict Disease? Thyroid 2007;17:1027-9. [DOI: 10.1089/thy.2007.1526] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 1.3] [Reference Citation Analysis]
43 Serrano NC, Millan P, Páez MC. Non-HLA associations with autoimmune diseases. Autoimmun Rev 2006;5:209-14. [PMID: 16483921 DOI: 10.1016/j.autrev.2005.06.009] [Cited by in Crossref: 39] [Cited by in F6Publishing: 32] [Article Influence: 2.4] [Reference Citation Analysis]
44 Stefan M, Faustino LC. Genetics of Thyroid-Stimulating Hormone Receptor-Relevance for Autoimmune Thyroid Disease. Front Endocrinol (Lausanne) 2017;8:57. [PMID: 28421036 DOI: 10.3389/fendo.2017.00057] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
45 Jacobson EM, Tomer Y. The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity: back to the future. J Autoimmun 2007;28:85-98. [PMID: 17369021 DOI: 10.1016/j.jaut.2007.02.006] [Cited by in Crossref: 130] [Cited by in F6Publishing: 108] [Article Influence: 9.3] [Reference Citation Analysis]
46 Dechairo BM, Zabaneh D, Collins J, Brand O, Dawson GJ, Green AP, Mackay I, Franklyn JA, Connell JM, Wass JA, Wiersinga WM, Hegedus L, Brix T, Robinson BG, Hunt PJ, Weetman AP, Carey AH, Gough SC. Association of the TSHR gene with Graves' disease: the first disease specific locus. Eur J Hum Genet 2005;13:1223-30. [PMID: 16106256 DOI: 10.1038/sj.ejhg.5201485] [Cited by in Crossref: 122] [Cited by in F6Publishing: 92] [Article Influence: 8.1] [Reference Citation Analysis]
47 Brown RS. Autoimmune thyroid disease: unlocking a complex puzzle. Curr Opin Pediatr 2009;21:523-8. [PMID: 19474733 DOI: 10.1097/MOP.0b013e32832cf824] [Cited by in Crossref: 57] [Cited by in F6Publishing: 18] [Article Influence: 4.8] [Reference Citation Analysis]
48 Farra C, Awwad J, Fadlallah A, Sebaly G, Hage G, Souaid M, Ashkar H, Medlej R, Gannageh MH, Halaby G. Genetics of autoimmune thyroid disease in the Lebanese population. J Community Genet 2012;3:259-64. [PMID: 22392440 DOI: 10.1007/s12687-012-0085-1] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
49 Tomer Y, Davies TF. Searching for the autoimmune thyroid disease susceptibility genes: from gene mapping to gene function. Endocr Rev. 2003;24:694-717. [PMID: 14570752 DOI: 10.1210/er.2002-0030] [Cited by in Crossref: 269] [Cited by in F6Publishing: 216] [Article Influence: 15.8] [Reference Citation Analysis]
50 Ban Y, Tomer Y. The contribution of immune regulatory and thyroid specific genes to the etiology of Graves' and Hashimoto's diseases. Autoimmunity 2003;36:367-79. [PMID: 14669944 DOI: 10.1080/08916930310001603037] [Cited by in Crossref: 36] [Cited by in F6Publishing: 32] [Article Influence: 2.1] [Reference Citation Analysis]
51 Vono-toniolo J, Kopp P. Thyroglobulin gene mutations and other genetic defects associated with congenital hypothyroidism. Arq Bras Endocrinol Metab 2004;48:70-82. [DOI: 10.1590/s0004-27302004000100009] [Cited by in Crossref: 13] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
52 Tomer Y, Greenberg D. The thyroglobulin gene as the first thyroid-specific susceptibility gene for autoimmune thyroid disease. Trends Mol Med 2004;10:306-8. [PMID: 15242677 DOI: 10.1016/j.molmed.2004.05.002] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 0.8] [Reference Citation Analysis]
53 Atkinson TP, Schäffer AA, Grimbacher B, Schroeder HW Jr, Woellner C, Zerbe CS, Puck JM. An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family. Am J Hum Genet 2001;69:791-803. [PMID: 11517424 DOI: 10.1086/323611] [Cited by in Crossref: 30] [Cited by in F6Publishing: 24] [Article Influence: 1.5] [Reference Citation Analysis]
54 Simmonds MJ, Gough SCL. The search for the genetic contribution to autoimmune thyroid disease: the never ending story? Briefings in Functional Genomics 2011;10:77-90. [DOI: 10.1093/bfgp/elq036] [Cited by in Crossref: 20] [Cited by in F6Publishing: 17] [Article Influence: 2.0] [Reference Citation Analysis]
55 Płoski R, Szymański K, Bednarczuk T. The genetic basis of graves' disease. Curr Genomics 2011;12:542-63. [PMID: 22654555 DOI: 10.2174/138920211798120772] [Cited by in Crossref: 31] [Cited by in F6Publishing: 20] [Article Influence: 3.4] [Reference Citation Analysis]
56 Zhou Z, Zuo CL, Li XS, Ye XP, Zhang QY, Wang P, Zhang RX, Chen G, Yang JL, Chen Y, Ma QY, Song HD. Uterus globulin associated protein 1 (UGRP1) is a potential marker of progression of Graves' disease into hypothyroidism. Mol Cell Endocrinol 2019;494:110492. [PMID: 31255731 DOI: 10.1016/j.mce.2019.110492] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
57 Chistiakov DA, Voronova NV, Turakulov RI, Savost'anov KV. 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. J Appl Genet 2011;52:201-7. [PMID: 21170691 DOI: 10.1007/s13353-010-0022-0] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 0.5] [Reference Citation Analysis]
58 Simmonds MJ, Howson JM, Heward JM, Cordell HJ, Foxall H, Carr-Smith J, Gibson SM, Walker N, Tomer Y, Franklyn JA, Todd JA, Gough SC. Regression mapping of association between the human leukocyte antigen region and Graves disease. Am J Hum Genet 2005;76:157-63. [PMID: 15558498 DOI: 10.1086/426947] [Cited by in Crossref: 104] [Cited by in F6Publishing: 88] [Article Influence: 6.1] [Reference Citation Analysis]
59 Nolan DK, Sutton B, Haynes C, Johnson J, Sebek J, Dowdy E, Crosslin D, Crossman D, Sketch MH Jr, Granger CB, Seo D, Goldschmidt-Clermont P, Kraus WE, Gregory SG, Hauser ER, Shah SH. Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5. BMC Genet 2012;13:12. [PMID: 22369142 DOI: 10.1186/1471-2156-13-12] [Cited by in Crossref: 16] [Cited by in F6Publishing: 12] [Article Influence: 1.8] [Reference Citation Analysis]
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