-
1
-
-
19944422075
-
Regression mapping of association between the human leukocyte antigen region and Graves' disease
-
Simmonds MJ, Howson JM, Heward JM, Cordell HJ, Foxall H, et al. (2005) Regression mapping of association between the human leukocyte antigen region and Graves' disease. Am J Hum Genet 76: 157-163.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 157-163
-
-
Simmonds, M.J.1
Howson, J.M.2
Heward, J.M.3
Cordell, H.J.4
Foxall, H.5
-
2
-
-
34548447535
-
A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect
-
Simmonds MJ, Howson JM, Heward JM, Carr-Smith J, Franklyn JA, et al. (2007) A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect. Hum Mol Genet 16: 2149-2153.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 2149-2153
-
-
Simmonds, M.J.1
Howson, J.M.2
Heward, J.M.3
Carr-Smith, J.4
Franklyn, J.A.5
-
3
-
-
0037648405
-
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
-
Ueda H, Howson JM, Esposito L, Heward J, Snook H, et al. (2003) Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature 423: 506-511.
-
(2003)
Nature
, vol.423
, pp. 506-511
-
-
Ueda, H.1
Howson, J.M.2
Esposito, L.3
Heward, J.4
Snook, H.5
-
4
-
-
79952117074
-
Association of the CTLA4 gene with Graves' disease in the Chinese Han population
-
Zhao SX, Pan CM, Cao HM, Han B, Shi JY, et al. (2010) Association of the CTLA4 gene with Graves' disease in the Chinese Han population. PloS one 5: e9821.
-
(2010)
PloS One
, vol.5
-
-
Zhao, S.X.1
Pan, C.M.2
Cao, H.M.3
Han, B.4
Shi, J.Y.5
-
5
-
-
34249309946
-
The regulatory T cell gene FOXP3 and genetic susceptibility to thyroid autoimmunity: an association analysis in Caucasian and Japanese cohorts
-
Ban Y, Tozaki T, Tobe T, Jacobson EM, Concepcion ES, et al. (2007) The regulatory T cell gene FOXP3 and genetic susceptibility to thyroid autoimmunity: an association analysis in Caucasian and Japanese cohorts. J Autoimmun 28: 201-207.
-
(2007)
J Autoimmun
, vol.28
, pp. 201-207
-
-
Ban, Y.1
Tozaki, T.2
Tobe, T.3
Jacobson, E.M.4
Concepcion, E.S.5
-
6
-
-
18844421908
-
A Graves' disease-associated Kozak sequence single-nucleotide polymorphism enhances the efficiency of CD40 gene translation: a case for translational pathophysiology
-
Jacobson EM, Concepcion E, Oashi T, Tomer Y, (2005) A Graves' disease-associated Kozak sequence single-nucleotide polymorphism enhances the efficiency of CD40 gene translation: a case for translational pathophysiology. Endocrinology 146: 2684-2691.
-
(2005)
Endocrinology
, vol.146
, pp. 2684-2691
-
-
Jacobson, E.M.1
Concepcion, E.2
Oashi, T.3
Tomer, Y.4
-
7
-
-
33748367018
-
A proposed classification of the immunological diseases
-
McGonagle D, McDermott MF, (2006) A proposed classification of the immunological diseases. PLoS Med 3: e297.
-
(2006)
PLoS Med
, vol.3
-
-
McGonagle, D.1
McDermott, M.F.2
-
8
-
-
7844227331
-
Linkage analysis of candidate genes in autoimmune thyroid disease. II. Selected gender-related genes and the X-chromosome
-
Barbesino G, Tomer Y, Concepcion ES, Davies TF, Greenberg DA, (1998) Linkage analysis of candidate genes in autoimmune thyroid disease. II. Selected gender-related genes and the X-chromosome. J Clin Endocrinol Metab 83: 3290-3295.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 3290-3295
-
-
Barbesino, G.1
Tomer, Y.2
Concepcion, E.S.3
Davies, T.F.4
Greenberg, D.A.5
-
9
-
-
0035092635
-
Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population
-
Imrie H, Vaidya B, Perros P, Kelly WF, Toft AD, et al. (2001) Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population. J Clin Endocrinol Metab 86: 626-630.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 626-630
-
-
Imrie, H.1
Vaidya, B.2
Perros, P.3
Kelly, W.F.4
Toft, A.D.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. Human Molecular Genetics 18: 1156-1170.
-
(2009)
Human Molecular Genetics
, vol.18
, pp. 1156-1170
-
-
Song, H.D.1
Liang, J.2
Shi, J.Y.3
Zhao, S.X.4
Liu, Z.5
-
11
-
-
84874673513
-
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 (2010) 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. Journal of Applied Genetics: 1-7.
-
(2010)
Journal of Applied Genetics
, pp. 1-7
-
-
Chistiakov, D.A.1
Voronova, N.V.2
Turakulov, R.I.3
Savost'anov, K.V.4
-
12
-
-
77952411922
-
Confirmation of Association of Chromosome 5q31-33 with United Kingdom Caucasian Graves' Disease
-
Simmonds MJ, Yesmin K, Newby PR, Brand OJ, Franklyn JA, et al. (2010) Confirmation of Association of Chromosome 5q31-33 with United Kingdom Caucasian Graves' Disease. Thyroid 20: 413-417.
-
(2010)
Thyroid
, vol.20
, pp. 413-417
-
-
Simmonds, M.J.1
Yesmin, K.2
Newby, P.R.3
Brand, O.J.4
Franklyn, J.A.5
-
13
-
-
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
-
14
-
-
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
-
15
-
-
12144289140
-
Insulin autoimmunity: prediction/precipitation/prevention type 1A diabetes
-
Eisenbarth GS, Moriyama H, Robles DT, Liu E, Yu L, et al. (2002) Insulin autoimmunity: prediction/precipitation/prevention type 1A diabetes. Autoimmun Rev 1: 139-145.
-
(2002)
Autoimmun Rev
, vol.1
, pp. 139-145
-
-
Eisenbarth, G.S.1
Moriyama, H.2
Robles, D.T.3
Liu, E.4
Yu, L.5
-
16
-
-
20944434679
-
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities
-
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. Nat Genet 37: 478-485.
-
(2005)
Nat Genet
, vol.37
, pp. 478-485
-
-
Kochi, Y.1
Yamada, R.2
Suzuki, A.3
Harley, J.B.4
Shirasawa, S.5
-
17
-
-
34247213251
-
Is FCRL3 a new general autoimmunity gene?
-
Chistiakov DA, Chistiakov AP, (2007) Is FCRL3 a new general autoimmunity gene? Hum Immunol 68: 375-383.
-
(2007)
Hum Immunol
, vol.68
, pp. 375-383
-
-
Chistiakov, D.A.1
Chistiakov, A.P.2
-
18
-
-
77949268368
-
Association between Fc receptor-like 3 C169T polymorphism and risk of systemic lupus erythematosus: a meta-analysis
-
Mao C, Pan H, Chen Q, Wang X, Ye D, et al. (2010) Association between Fc receptor-like 3 C169T polymorphism and risk of systemic lupus erythematosus: a meta-analysis. Molecular biology reports 37: 191-196.
-
(2010)
Molecular Biology Reports
, vol.37
, pp. 191-196
-
-
Mao, C.1
Pan, H.2
Chen, Q.3
Wang, X.4
Ye, D.5
-
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
-
-
77958573366
-
Development of a new sensitive ELISA for the determination of uteroglobin-related protein 1, a new potential biomarker
-
Van De Velde V, Courtens W, Bernard A, (2010) Development of a new sensitive ELISA for the determination of uteroglobin-related protein 1, a new potential biomarker. Biomarkers 15: 619-624.
-
(2010)
Biomarkers
, vol.15
, pp. 619-624
-
-
Van De Velde, V.1
Courtens, W.2
Bernard, A.3
-
21
-
-
0033826638
-
Changes in Th1/Th2 cytokine balance in Graves' desease
-
Kocjan T, Wraber B, Repnik U, Hojker S, (2000) Changes in Th1/Th2 cytokine balance in Graves' desease. Pflugers Arch 440: 94-95.
-
(2000)
Pflugers Arch
, vol.440
, pp. 94-95
-
-
Kocjan, T.1
Wraber, B.2
Repnik, U.3
Hojker, S.4
-
22
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
-
23
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie BN, Donnelly P, Marchini J, (2009) A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 5: e1000529.
-
(2009)
PLoS Genet
, vol.5
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
24
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini J, Howie B, Myers S, McVean G, Donnelly P, (2007) A new multipoint method for genome-wide association studies by imputation of genotypes. Nat Genet 39: 906-913.
-
(2007)
Nat Genet
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
25
-
-
34548805282
-
A genome-wide association study of global gene expression
-
Dixon AL, Liang L, Moffatt MF, Chen W, Heath S, et al. (2007) A genome-wide association study of global gene expression. Nat Genet 39: 1202-1207.
-
(2007)
Nat Genet
, vol.39
, pp. 1202-1207
-
-
Dixon, A.L.1
Liang, L.2
Moffatt, M.F.3
Chen, W.4
Heath, S.5
-
26
-
-
77956637896
-
Genetics and beyond-the transcriptome of human monocytes and disease susceptibility
-
Zeller T, Wild P, Szymczak S, Rotival M, Schillert A, et al. (2010) Genetics and beyond-the transcriptome of human monocytes and disease susceptibility. PloS one 5: e10693.
-
(2010)
PloS One
, vol.5
-
-
Zeller, T.1
Wild, P.2
Szymczak, S.3
Rotival, M.4
Schillert, A.5
-
27
-
-
84860317030
-
Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles
-
Fairfax BP, Makino S, Radhakrishnan J, Plant K, Leslie S, et al. (2012) Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles. Nature genetics 44: 502-510.
-
(2012)
Nature Genetics
, vol.44
, pp. 502-510
-
-
Fairfax, B.P.1
Makino, S.2
Radhakrishnan, J.3
Plant, K.4
Leslie, S.5
-
28
-
-
0019267555
-
Statistical methods in cancer research. Volume I- The analysis of case-control studies
-
Breslow NE, Day NE (1980) Statistical methods in cancer research. Volume I- The analysis of case-control studies. IARC Sci Publ: 5-338.
-
(1980)
IARC Sci Publ
, pp. 5-338
-
-
Breslow, N.E.1
Day, N.E.2
-
29
-
-
84869021173
-
Seven newly identified loci for autoimmune thyroid disease
-
Cooper JD, Simmonds MJ, Walker NM, Burren O, Brand OJ, et al. (2012) Seven newly identified loci for autoimmune thyroid disease. Hum Mol Genet 21: 5202-5208.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 5202-5208
-
-
Cooper, J.D.1
Simmonds, M.J.2
Walker, N.M.3
Burren, O.4
Brand, O.J.5
-
30
-
-
0031860393
-
Databases on transcriptional regulation: TRANSFAC, TRRD and COMPEL
-
Heinemeyer T, Wingender E, Reuter I, Hermjakob H, Kel AE, et al. (1998) Databases on transcriptional regulation: TRANSFAC, TRRD and COMPEL. Nucleic Acids Res 26: 362-367.
-
(1998)
Nucleic Acids Res
, vol.26
, pp. 362-367
-
-
Heinemeyer, T.1
Wingender, E.2
Reuter, I.3
Hermjakob, H.4
Kel, A.E.5
-
31
-
-
40649108591
-
Prognostic value of thyrotropin receptor antibodies (TRAb) in Graves' disease: a 120 months prospective study
-
Cappelli C, Gandossi E, Castellano M, Pizzocaro C, Agosti B, et al. (2007) Prognostic value of thyrotropin receptor antibodies (TRAb) in Graves' disease: a 120 months prospective study. Endocr J 54: 713-720.
-
(2007)
Endocr J
, vol.54
, pp. 713-720
-
-
Cappelli, C.1
Gandossi, E.2
Castellano, M.3
Pizzocaro, C.4
Agosti, B.5
-
32
-
-
77957907024
-
Parity Is not related to autoimmune thyroid disease in a population-based study of Japanese-Brazilians
-
Sgarbi JA, Kasamatsu TS, Matsumura LK, Maciel RMB, (2010) Parity Is not related to autoimmune thyroid disease in a population-based study of Japanese-Brazilians. Thyroid 20: 1151-1156.
-
(2010)
Thyroid
, vol.20
, pp. 1151-1156
-
-
Sgarbi, J.A.1
Kasamatsu, T.S.2
Matsumura, L.K.3
Maciel, R.M.B.4
-
33
-
-
33947546815
-
Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association
-
Owen CJ, Kelly H, Eden JA, Merriman ME, Pearce SH, et al. (2007) Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association. J Clin Endocrinol Metab 92: 1106-1111.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 1106-1111
-
-
Owen, C.J.1
Kelly, H.2
Eden, J.A.3
Merriman, M.E.4
Pearce, S.H.5
-
34
-
-
84870502629
-
Bayesian refinement of association signals for 14 loci in 3 common diseases
-
Maller JB, McVean G, Byrnes J, Vukcevic D, Palin K, et al. (2012) Bayesian refinement of association signals for 14 loci in 3 common diseases. Nat Genet 44: 1294-1301.
-
(2012)
Nat Genet
, vol.44
, pp. 1294-1301
-
-
Maller, J.B.1
McVean, G.2
Byrnes, J.3
Vukcevic, D.4
Palin, K.5
-
35
-
-
0037089218
-
IRTAs: a new family of immunoglobulinlike receptors differentially expressed in B cells
-
Miller I, Hatzivassiliou G, Cattoretti G, Mendelsohn C, Dalla-Favera R, (2002) IRTAs: a new family of immunoglobulinlike receptors differentially expressed in B cells. Blood 99: 2662-2669.
-
(2002)
Blood
, vol.99
, pp. 2662-2669
-
-
Miller, I.1
Hatzivassiliou, G.2
Cattoretti, G.3
Mendelsohn, C.4
Dalla-Favera, R.5
-
36
-
-
34247895443
-
Fc receptor-like molecules
-
Davis RS, (2007) Fc receptor-like molecules. Annual Review of Immunology 25: 525-560.
-
(2007)
Annual Review of Immunology
, vol.25
, pp. 525-560
-
-
Davis, R.S.1
-
37
-
-
78650294948
-
New B-cell CD molecules
-
Matesanz-Isabel J, Sintes J, Llinàs L, de Salort J, Lázaro A, et al. (2011) New B-cell CD molecules. Immunology letters 134: 104-112.
-
(2011)
Immunology Letters
, vol.134
, pp. 104-112
-
-
Matesanz-Isabel, J.1
Sintes, J.2
Llinàs, L.3
de Salort, J.4
Lázaro, A.5
-
38
-
-
77951956004
-
FCRL3, an autoimmune susceptibility gene, has inhibitory potential on B-cell receptor-mediated signaling
-
Kochi Y, Myouzen K, Yamada R, Suzuki A, Kurosaki T, et al. (2009) FCRL3, an autoimmune susceptibility gene, has inhibitory potential on B-cell receptor-mediated signaling. The Journal of Immunology 183: 5502-5510.
-
(2009)
The Journal of Immunology
, vol.183
, pp. 5502-5510
-
-
Kochi, Y.1
Myouzen, K.2
Yamada, R.3
Suzuki, A.4
Kurosaki, T.5
-
39
-
-
77951627133
-
Expression of the autoimmune susceptibility gene FcRL3 on human regulatory T cells is associated with dysfunction and high levels of programmed cell death-1
-
Swainson LA, Mold JE, Bajpai UD, McCune JM, (2010) Expression of the autoimmune susceptibility gene FcRL3 on human regulatory T cells is associated with dysfunction and high levels of programmed cell death-1. J Immunol 184: 3639-3647.
-
(2010)
J Immunol
, vol.184
, pp. 3639-3647
-
-
Swainson, L.A.1
Mold, J.E.2
Bajpai, U.D.3
McCune, J.M.4
|