-
1
-
-
0036173697
-
Serum TSH, T4, and Thyroid Antibodies in the United States Population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III)
-
Hollowell JG, Staehling NW, Flanders WD, Hannon WH, Gunter EW, et al. (2002) Serum TSH, T4, and Thyroid Antibodies in the United States Population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III). J Clin Endocrinol Metab 87: 489-499.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 489-499
-
-
Hollowell, J.G.1
Staehling, N.W.2
Flanders, W.D.3
Hannon, W.H.4
Gunter, E.W.5
-
2
-
-
61849149680
-
The effect of salt iodization for 10 years on the prevalences of endemic goiter and hyperthyroidism
-
Chen X, Wu WS, Chen GL, Zhang KZ, Zhang FL, et al. (2000) The effect of salt iodization for 10 years on the prevalences of endemic goiter and hyperthyroidism. Chin J Endocrinol Metab 18: 342-344.
-
(2000)
Chin J Endocrinol Metab
, vol.18
, pp. 342-344
-
-
Chen, X.1
Wu, W.S.2
Chen, G.L.3
Zhang, K.Z.4
Zhang, F.L.5
-
3
-
-
0025662985
-
Anti-thyroglobulin antibodies induced with recombinant reovirus infection in BALB/c mice
-
Onodera T, Awaya A (1990) Anti-thyroglobulin antibodies induced with recombinant reovirus infection in BALB/c mice. Immunology 71: 581-585.
-
(1990)
Immunology
, vol.71
, pp. 581-585
-
-
Onodera, T.1
Awaya, A.2
-
4
-
-
0035095887
-
Evidence for a Major Role of Heredity in Graves' Disease: A Population-Based Study of Two Danish Twin Cohorts 1
-
Brix TH, Kyvik KO, Christensen K, Hegedus L (2001) Evidence for a Major Role of Heredity in Graves' Disease: A Population-Based Study of Two Danish Twin Cohorts 1. Endocrine Soc. pp 930-934.
-
(2001)
Endocrine Soc
, pp. 930-934
-
-
Brix, T.H.1
Kyvik, K.O.2
Christensen, K.3
Hegedus, L.4
-
5
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Consortium WTCC (2007) Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447: 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
Consortium, W.T.C.C.1
-
6
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
Saxena R, Voight BF, Lyssenko V, Burtt NP, de Bakker PI, et al. (2007) Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science 316: 1331-1336.
-
(2007)
Science
, vol.316
, pp. 1331-1336
-
-
Saxena, R.1
Voight, B.F.2
Lyssenko, V.3
Burtt, N.P.4
de Bakker, P.I.5
-
7
-
-
34249885875
-
A genomewide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
Scott LJ, Mohlke KL, Bonnycastle LL, Willer CJ, Li Y, et al. (2007) A genomewide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 316: 1341-1345.
-
(2007)
Science
, vol.316
, pp. 1341-1345
-
-
Scott, L.J.1
Mohlke, K.L.2
Bonnycastle, L.L.3
Willer, C.J.4
Li, Y.5
-
8
-
-
33847176604
-
A genome-wide association study identifies novel risk loci for type 2 diabetes
-
Sladek R, Rocheleau G, Rung J, Dina C, Shen L, et al. (2007) A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature 445: 881-885.
-
(2007)
Nature
, vol.445
, pp. 881-885
-
-
Sladek, R.1
Rocheleau, G.2
Rung, J.3
Dina, C.4
Shen, L.5
-
9
-
-
34548524948
-
Dissecting genetic heterogeneity in autoimmune thyroid diseases by subset analysis
-
Tomer Y, Menconi F, Davies TF, Barbesino G, Rocchi R, et al. (2007) Dissecting genetic heterogeneity in autoimmune thyroid diseases by subset analysis. J Autoimmun 29: 69-77.
-
(2007)
J Autoimmun
, vol.29
, pp. 69-77
-
-
Tomer, Y.1
Menconi, F.2
Davies, T.F.3
Barbesino, G.4
Rocchi, R.5
-
10
-
-
61849168176
-
Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease
-
Song HD, Liang J, Shi JY, Zhao SX, Liu Z, et al. (2009) Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease. Hum Mol Genet 18: 1156-1170.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1156-1170
-
-
Song, H.D.1
Liang, J.2
Shi, J.Y.3
Zhao, S.X.4
Liu, Z.5
-
11
-
-
18844366115
-
Multiple SNPs in Intron 7 of Thyrotropin Receptor Are Associated with Graves' Disease
-
Hiratani H, Bowden DW, Ikegami S, Shirasawa S, Shimizu A, et al. (2005) Multiple SNPs in Intron 7 of Thyrotropin Receptor Are Associated with Graves' Disease. J Clin Endocrinol Metab 90: 2898-2903.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 2898-2903
-
-
Hiratani, H.1
Bowden, D.W.2
Ikegami, S.3
Shirasawa, S.4
Shimizu, A.5
-
12
-
-
20944434679
-
-
Nature Publishing Group
-
Kochi Y, Yamada R, Suzuki A, Harley JB, Shirasawa S, et al. (2005) A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities. Nature Publishing Group. pp 478-485.
-
(2005)
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities
, pp. 478-485
-
-
Kochi, Y.1
Yamada, R.2
Suzuki, A.3
Harley, J.B.4
Shirasawa, S.5
-
13
-
-
5444230036
-
SNPs in the promoter of aB cell-specific antisense transcript, SAS-ZFAT, determine susceptibility to autoimmune thyroid disease
-
Shirasawa S, Harada H, Furugaki K, Akamizu T, Ishikawa N, et al. (2004) SNPs in the promoter of aB cell-specific antisense transcript, SAS-ZFAT, determine susceptibility to autoimmune thyroid disease. Hum Mol Genet 13: 2221-2231.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2221-2231
-
-
Shirasawa, S.1
Harada, H.2
Furugaki, K.3
Akamizu, T.4
Ishikawa, N.5
-
14
-
-
0036959340
-
AC/T single-nucleotide polymorphism in the region of the CD40 gene is associated with Graves' disease
-
Tomer Y, Concepcion E, Greenberg DA (2002) AC/T single-nucleotide polymorphism in the region of the CD40 gene is associated with Graves' disease. Thyroid 12: 1129-1135.
-
(2002)
Thyroid
, vol.12
, pp. 1129-1135
-
-
Tomer, Y.1
Concepcion, E.2
Greenberg, D.A.3
-
15
-
-
0141801751
-
Searching for the Autoimmune Thyroid Disease Susceptibility Genes: From Gene Mapping to Gene Function
-
Tomer Y, Davies TF (2003) Searching for the Autoimmune Thyroid Disease Susceptibility Genes: From Gene Mapping to Gene Function. Endocr Rev 24: 694-717.
-
(2003)
Endocr Rev
, vol.24
, pp. 694-717
-
-
Tomer, Y.1
Davies, T.F.2
-
16
-
-
0037648405
-
Association of the T-cell regulatory gene CTLA 4 with susceptibility to autoimmune disease
-
Ueda H, Howson JMM, Esposito L, Heward J, Snook H, et al. (2003) Association of the T-cell regulatory gene CTLA 4 with susceptibility to autoimmune disease. Nature 423: 506-511.
-
(2003)
Nature
, vol.423
, pp. 506-511
-
-
Ueda, H.1
Howson, J.M.M.2
Esposito, L.3
Heward, J.4
Snook, H.5
-
17
-
-
8744266374
-
The Codon 620 Tryptophan Allele of the Lymphoid Tyrosine Phosphatase (LYP) Gene Is a Major Determinant of Graves' Disease
-
Velaga MR, Wilson V, Jennings CE, Owen CJ, Herington S, et al. (2004) The Codon 620 Tryptophan Allele of the Lymphoid Tyrosine Phosphatase (LYP) Gene Is a Major Determinant of Graves' Disease. J Clin Endocrinol Metab 89: 5862-5865.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5862-5865
-
-
Velaga, M.R.1
Wilson, V.2
Jennings, C.E.3
Owen, C.J.4
Herington, S.5
-
18
-
-
0028873470
-
CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population
-
Yanagawa T (1995) CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population. J Clin Endocrinol Metab 80: 41-45.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 41-45
-
-
Yanagawa, T.1
-
19
-
-
35748981184
-
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
-
Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, et al. (2007) Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 39: 1329-1337.
-
(2007)
Nat Genet
, vol.39
, pp. 1329-1337
-
-
Burton, P.R.1
Clayton, D.G.2
Cardon, L.R.3
Craddock, N.4
Deloukas, P.5
-
20
-
-
64549147052
-
Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease
-
Brand OJ, Barrett JC, Simmonds MJ, Newby PR, McCabe CJ, et al. (2009) Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease. Hum Mol Genet 18: 1704-1713.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1704-1713
-
-
Brand, O.J.1
Barrett, J.C.2
Simmonds, M.J.3
Newby, P.R.4
McCabe, C.J.5
-
21
-
-
8944259914
-
The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry
-
Nistico L, Buzzetti R, Pritchard LE, Van der Auwera B, Giovannini C, et al. (1996) The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry. Hum Mol Genet 5: 1075-1080.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1075-1080
-
-
Nistico, L.1
Buzzetti, R.2
Pritchard, L.E.3
van der Auwera, B.4
Giovannini, C.5
-
22
-
-
0031014716
-
CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus
-
Donner H, Rau H, Walfish PG, Braun J, Siegmund T, et al. (1997) CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus. J Clin Endocrinol Metab 82: 143-146.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 143-146
-
-
Donner, H.1
Rau, H.2
Walfish, P.G.3
Braun, J.4
Siegmund, T.5
-
23
-
-
0031434409
-
CTLA4 gene polymorphism confers susceptibility to Graves' disease in Japanese
-
Yanagawa T, Taniyama M, Enomoto S, Gomi K, Maruyama H, et al. (1997) CTLA4 gene polymorphism confers susceptibility to Graves' disease in Japanese. Thyroid 7: 843-846.
-
(1997)
Thyroid
, vol.7
, pp. 843-846
-
-
Yanagawa, T.1
Taniyama, M.2
Enomoto, S.3
Gomi, K.4
Maruyama, H.5
-
24
-
-
1642295096
-
Assessing the probability that a positive report is false: An approach for molecular epidemiology studies
-
Wacholder S, Chanock S, Garcia-Closas M, El Ghormli L, Rothman N (2004) Assessing the probability that a positive report is false: an approach for molecular epidemiology studies. J Natl Cancer Inst. pp 434-442.
-
(2004)
J Natl Cancer Inst
, pp. 434-442
-
-
Wacholder, S.1
Chanock, S.2
Garcia-Closas, M.3
El Ghormli, L.4
Rothman, N.5
-
25
-
-
20144363340
-
CT60 single nucleotide polymorphisms of the cytotoxic T-lymphocyte-associated antigen-4 gene region is associated with Graves' disease in an Italian population
-
Petrone A, Giorgi G, Galgani A, Alemanno I, Corsello SM, et al. (2005) CT60 single nucleotide polymorphisms of the cytotoxic T-lymphocyte-associated antigen-4 gene region is associated with Graves' disease in an Italian population. Thyroid 15: 232-238.
-
(2005)
Thyroid
, vol.15
, pp. 232-238
-
-
Petrone, A.1
Giorgi, G.2
Galgani, A.3
Alemanno, I.4
Corsello, S.M.5
-
26
-
-
34447118880
-
Cytotoxic T lymphocyte-associated molecule-4 gene polymorphism and hyperthyroid Graves' disease relapse after antithyroid drug withdrawal: A follow-up study
-
Wang PW, Chen IY, Liu RT, Hsieh CJ, Hsi E, et al. (2007) Cytotoxic T lymphocyte-associated molecule-4 gene polymorphism and hyperthyroid Graves' disease relapse after antithyroid drug withdrawal: a follow-up study. J Clin Endocrinol Metab 92: 2513-2518.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 2513-2518
-
-
Wang, P.W.1
Chen, I.Y.2
Liu, R.T.3
Hsieh, C.J.4
Hsi, E.5
-
27
-
-
51349123893
-
Association of CT60 polymorphism of the CTLA4 gene with Graves' disease in Taiwanese children
-
Tsai ST, Huang CY, Lo FS, Chang YT, Tanizawa T, et al. (2008) Association of CT60 polymorphism of the CTLA4 gene with Graves' disease in Taiwanese children. J Pediatr Endocrinol Metab 21: 665-672.
-
(2008)
J Pediatr Endocrinol Metab
, vol.21
, pp. 665-672
-
-
Tsai, S.T.1
Huang, C.Y.2
Lo, F.S.3
Chang, Y.T.4
Tanizawa, T.5
-
28
-
-
84873336888
-
Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease
-
In press
-
Gu LQ, Zhu W, Zhao SX, Zhao L, Zhang MJ, et al. (2009) Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease. Clin Endocrinol (Oxf). In press.
-
(2009)
Clin Endocrinol (Oxf)
-
-
Gu, L.Q.1
Zhu, W.2
Zhao, S.X.3
Zhao, L.4
Zhang, M.J.5
-
29
-
-
40049108936
-
Association of Systemic Lupus Erythematosus with C8orf13-BLK and ITGAMITGAX
-
Hom G, Graham RR, Modrek B, Taylor KE, Ortmann W, et al. (2008) Association of Systemic Lupus Erythematosus with C8orf13-BLK and ITGAMITGAX. N Engl J Med 358: 900-909.
-
(2008)
N Engl J Med
, vol.358
, pp. 900-909
-
-
Hom, G.1
Graham, R.R.2
Modrek, B.3
Taylor, K.E.4
Ortmann, W.5
-
30
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ (2005) Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21: 263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
31
-
-
0036137030
-
A Unified Stepwise Regression Procedure for Evaluating the Relative Effects of Polymorphisms within a Gene Using Case/ Control or Family Data: Application to[ITAL] HLA [/ITAL] in Type 1 Diabetes
-
Cordell HJ, Clayton DG (2002) A Unified Stepwise Regression Procedure for Evaluating the Relative Effects of Polymorphisms within a Gene Using Case/ Control or Family Data: Application to[ITAL] HLA [/ITAL] in Type 1 Diabetes. Am J Hum Genet 70: 124-141.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 124-141
-
-
Cordell, H.J.1
Clayton, D.G.2
-
32
-
-
0033903432
-
Complex association analysis of Graves disease using a set of polymorphic markers
-
Chistyakov DA, Savost'anov KV, Turakulov RI, Petunina NA, Trukhina LV, et al. (2000) Complex association analysis of Graves disease using a set of polymorphic markers. Mol Genet Metab 70: 214-218.
-
(2000)
Mol Genet Metab
, vol.70
, pp. 214-218
-
-
Chistyakov, D.A.1
Savost'anov, K.V.2
Turakulov, R.I.3
Petunina, N.A.4
Trukhina, L.V.5
-
33
-
-
71449083275
-
Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies
-
Xu S, Yin X, Li S, Jin W, Lou H, et al. (2009) Genomic Dissection of Population Substructure of Han Chinese and Its Implication in Association Studies. Am J Hum Genet 85: 762-774.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 762-774
-
-
Xu, S.1
Yin, X.2
Li, S.3
Jin, W.4
Lou, H.5
-
34
-
-
71149105110
-
Genetic Structure of the Han Chinese Population Revealed by Genome-wide SNP Variation
-
Chen J, Zheng H, Bei JX, Sun L, Jia WH, et al. (2009) Genetic Structure of the Han Chinese Population Revealed by Genome-wide SNP Variation. Am J Hum Genet 85: 775-785.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 775-785
-
-
Chen, J.1
Zheng, H.2
Bei, J.X.3
Sun, L.4
Jia, W.H.5
|