-
1
-
-
1842555649
-
Hypothyroidism and thyroiditis
-
Orlando, Fla, USA W.B. Saunders
-
Davies T., Wilson J., Foster D. W., Larsen P. R., Kronenberg H., Hypothyroidism and thyroiditis. Williams Textbook of Endocrinology 2002 Orlando, Fla, USA W.B. Saunders 423 456
-
(2002)
Williams Textbook of Endocrinology
, pp. 423-456
-
-
Davies, T.1
Wilson, J.2
Foster, D.W.3
Larsen, P.R.4
Kronenberg, H.5
-
2
-
-
0029046372
-
The incidence of thyroid disorders in the community: A twenty-year follow-up of the Whickham Survey
-
2-s2.0-0029046372
-
Vanderpump M. P. J., Tunbridge W. M. G., French J. M., Appleton D., Bates D., Clark F., Grimley Evans J., Hasan D. M., Rodgers H., Tunbridge F., Young E. T., The incidence of thyroid disorders in the community: a twenty-year follow-up of the Whickham Survey. Clinical Endocrinology 1995 43 1 55 68 2-s2.0-0029046372
-
(1995)
Clinical Endocrinology
, vol.43
, Issue.1
, pp. 55-68
-
-
Vanderpump, M.P.J.1
Tunbridge, W.M.G.2
French, J.M.3
Appleton, D.4
Bates, D.5
Clark, F.6
Grimley Evans, J.7
Hasan, D.M.8
Rodgers, H.9
Tunbridge, F.10
Young, E.T.11
-
3
-
-
0042144871
-
Familial studies of autoimmune thyroiditis
-
2-s2.0-0042144871
-
Hall R., Stanbury J. B., Familial studies of autoimmune thyroiditis. Clinical and Experimental Immunology 1967 2 719 725 2-s2.0-0042144871
-
(1967)
Clinical and Experimental Immunology
, vol.2
, pp. 719-725
-
-
Hall, R.1
Stanbury, J.B.2
-
4
-
-
0017686568
-
Abnormalities in thyroid function in relatives of patients with Graves' disease and Hashimoto's thyroiditis: Lack of correlation with inheritance of HLA B8
-
Chopra I. J., Solomon D. H., Chopra U., Abnormalities in thyroid function in relatives of patients with Graves' disease and Hashimoto's thyroiditis: lack of correlation with inheritance of HLA B8. Journal of Clinical Endocrinology and Metabolism 1977 45 1 45 54 (Pubitemid 8146688)
-
(1977)
Journal of Clinical Endocrinology and Metabolism
, vol.45
, Issue.1
, pp. 45-54
-
-
Chopra, I.J.1
Solomon, D.H.2
Chopra, U.3
-
5
-
-
0020444025
-
The presence of thyroid autoantibodies in children and adolescents with autoimmune thyroid disease and in their siblings and parents
-
DOI 10.1016/0090-1229(82)90204-5
-
Burek C. L., Hoffman W. H., Rose N. R., The presence of thyroid autoantibodies in children and adolescents with autoimmune thyroid disease and in their siblings and parents. Clinical Immunology and Immunopathology 1982 25 3 395 404 2-s2.0-0020444025 (Pubitemid 13167799)
-
(1982)
Clinical Immunology and Immunopathology
, vol.25
, Issue.3
, pp. 395-404
-
-
Burek, C.L.1
Hoffman, W.H.2
Rose, N.R.3
-
6
-
-
0017757504
-
The spectrum of thyroid disease in a community: The Whickham survey
-
Tunbridge W. M. G., Evered D. C., Hall R., The spectrum of thyroid disease in a community: the Whickham survey. Clinical Endocrinology 1977 7 6 481 493 (Pubitemid 8235965)
-
(1977)
Clinical Endocrinology
, vol.7
, Issue.6
, pp. 481-493
-
-
Tunbridge, W.M.G.1
Evered, D.C.2
Hall, R.3
-
7
-
-
0027225778
-
Complex segregation analysis of antibodies to thyroid peroxidase in Old Order Amish families
-
Pauls D. L., Zakarija M., McKenzie J. M., Egeland J. A., Complex segregation analysis of antibodies to thyroid peroxidase in Old Order Amish families. American Journal of Medical Genetics 1993 47 3 375 379 2-s2.0-0027225778 (Pubitemid 23263639)
-
(1993)
American Journal of Medical Genetics
, vol.47
, Issue.3
, pp. 375-379
-
-
Pauls, D.L.1
Zakarija, M.2
McKenzie, J.M.3
Egeland, J.A.4
-
8
-
-
0025904238
-
Autosomal dominant inheritance of autoantibodies to thyroid peroxidase and thyroglobulin - Studies in families not selected for autoimmune thyroid disease
-
Phillips D., Prentice L., Upadhyaya M., Lunt P., Chamberlain S., Roberts D. F., McLachlan S., Smith B. R., Autosomal dominant inheritance of autoantibodies to thyroid peroxidase and thyroglobulinstudies in families not selected for autoimmune thyroid disease. Journal of Clinical Endocrinology and Metabolism 1991 72 5 973 975 2-s2.0-0025904238 (Pubitemid 21921793)
-
(1991)
Journal of Clinical Endocrinology and Metabolism
, vol.72
, Issue.5
, pp. 973-975
-
-
Phillips, D.1
Prentice, L.2
Upadhyaya, M.3
Lunt, P.4
Chamberlain, S.5
Roberts, D.F.6
McLachlan, S.7
Smith, B.R.8
-
9
-
-
0033306925
-
Evidence for genetic transmission of thyroid peroxidase autoantibody epitopic 'fingerprints'
-
Jaume J. C., Guo J., Pauls D. L., Zakarija M., McKenzie J. M., Egeland J. A., Burek C. L., Rose N. R., Hoffman W. H., Rapoport B., McLachlan S. M., Evidence for genetic transmission of thyroid peroxidase autoantibody epitopic 'fingerprints'. Journal of Clinical Endocrinology and Metabolism 1999 84 4 1424 1431 2-s2.0-0033306925 (Pubitemid 30644410)
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, Issue.4
, pp. 1424-1431
-
-
Jaume, J.C.1
Guo, J.2
Pauls, D.L.3
Zakarija, M.4
McKenzie, J.M.5
Egeland, J.A.6
Burek, C.L.7
Rose, N.R.8
Hoffman, W.H.9
Rapoport, B.10
McLachlan, S.M.11
-
10
-
-
0019742917
-
The human major histocompatibility complex and endocrine disease
-
2-s2.0-0019742917
-
Farid N. R., Bear J. C., The human major histocompatibility complex and endocrine disease. Endocrine Reviews 1981 2 1 50 86 2-s2.0-0019742917
-
(1981)
Endocrine Reviews
, vol.2
, Issue.1
, pp. 50-86
-
-
Farid, N.R.1
Bear, J.C.2
-
11
-
-
0031834892
-
A population-based study of graves' disease in danish twins
-
DOI 10.1046/j.1365-2265.1998.00450.x
-
Brix T. H., Christensen K., Holm N. V., Harvald B., Hegedüs L., A population-based study of graves' disease in danish twins. Clinical Endocrinology 1998 48 4 397 400 2-s2.0-0031834892 10.1046/j.1365-2265.1998. 00450.x (Pubitemid 28258810)
-
(1998)
Clinical Endocrinology
, vol.48
, Issue.4
, pp. 397-400
-
-
Brix, T.H.1
Christensen, K.2
Holm, N.V.3
Harvald, B.4
Hegedus, L.5
-
12
-
-
3242784051
-
Arginine at position 74 of the HLA-DR β1 chain is associated with Graves' disease
-
DOI 10.1038/sj.gene.6364059
-
Ban Y., Davies T. F., Greenberg D. A., Concepcion E. S., Osman R., Oashi T., Tomer Y., Arginine at position 74 of the HLA-DR β 1 chain is associated with Graves' disease. Genes and Immunity 2004 5 3 203 208 2-s2.0-3242784051 10.1038/sj.gene.6364059 (Pubitemid 38967653)
-
(2004)
Genes and Immunity
, vol.5
, Issue.3
, pp. 203-208
-
-
Ban, Y.1
Davies, T.F.2
Greenberg, D.A.3
Concepcion, E.S.4
Osman, R.5
Oashi, T.6
Tomer, Y.7
-
13
-
-
0030023292
-
Complex traits on the map
-
DOI 10.1038/379772a0
-
Ott J., Complex traits on the map. Nature 1996 379 6568 772 773 2-s2.0-0030023292 10.1038/379772a0 (Pubitemid 26067713)
-
(1996)
Nature
, vol.379
, Issue.6568
, pp. 772-773
-
-
Ott, J.1
-
14
-
-
0026518634
-
Genetics of autoimmune thyroid disease: Lack of evidence for linkage to HLA within families
-
2-s2.0-0026518634 10.1210/jc.74.3.496
-
Roman S. H., Greenberg D., Rubinstein P., Wallenstein S., Davies T. F., Genetics of autoimmune thyroid disease: lack of evidence for linkage to HLA within families. Journal of Clinical Endocrinology and Metabolism 1992 74 3 496 503 2-s2.0-0026518634 10.1210/jc.74.3.496
-
(1992)
Journal of Clinical Endocrinology and Metabolism
, vol.74
, Issue.3
, pp. 496-503
-
-
Roman, S.H.1
Greenberg, D.2
Rubinstein, P.3
Wallenstein, S.4
Davies, T.F.5
-
15
-
-
0025525784
-
Human DNA polymorphisms and methods of analysis
-
Weber J. L., Human DNA polymorphisms and methods of analysis. Current Opinion in Biotechnology 1990 1 2 166 171 2-s2.0-0025525784 (Pubitemid 120036510)
-
(1990)
Current Opinion in Biotechnology
, vol.1
, Issue.2
, pp. 166-171
-
-
Weber, J.L.1
-
16
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
DOI 10.1038/nature06258, PII NATURE06258
-
Frazer K. A., Ballinger D. G., Cox D. R., Hinds D. A., Stuve L. L., Gibbs R. A., Belmont J. W., Boudreau A., Hardenbol P., Leal S. M., Pasternak S., Wheeler D. A., Willis T. D., Yu F., Yang H., Zeng C., Gao Y., Hu H., Hu W., Li C., Lin W., Liu S., Pan H., Tang X., Wang J., Wang W., Yu J., Zhang B., Zhang Q., Zhao H., Zhao H., Zhou J., Gabriel S. B., Barry R., Blumenstiel B., Camargo A., Defelice M., Faggart M., Goyette M., Gupta S., Moore J., Nguyen H., Onofrio R. C., Parkin M., Roy J., Stahl E., Winchester E., Ziaugra L., Altshuler D., Shen Y., Yao Z., Huang W., Chu X., He Y., Jin L., Liu Y., Shen Y., Sun W., Wang H., Wang Y., Wang Y., Xiong X., Xu L., Waye M. M. Y., Tsui S. K. W., Xue H., Wong J. T. F., Galver L. M., Fan J. B., Gunderson K., Murray S. S., Oliphant A. R., Chee M. S., Montpetit A., Chagnon F., Ferretti V., Leboeuf M., Olivier J. F., Phillips M. S., Roumy S., Sallée C., Verner A., Hudson T. J., Kwok P. Y., Cai D., Koboldt D. C., Miller R. D., Pawlikowska L., Taillon-Miller P., Xiao M., Tsui L. C., Mak W., You Q. S., Tam P. K. H., Nakamura Y., Kawaguchi T., Kitamoto T., Morizono T., Nagashima A., Ohnishi Y., Sekine A., Tanaka T., Tsunoda T., Deloukas P., Bird C. P., Delgado M., Dermitzakis E. T., Gwilliam R., Hunt S., Morrison J., Powell D., Stranger B. E., Whittaker P., Bentley D. R., Daly M. J., De Bakker P. I. W., Barrett J., Chretien Y. R., Maller J., McCarroll S., Patterson N., Pe'Er I., Price A., Purcell S., Richter D. J., Sabeti P., Saxena R., Schaffner S. F., Sham P. C., Varilly P., Stein L. D., Krishnan L., Smith A. V., Tello-Ruiz M. K., Thorisson G. A., Chakravarti A., Chen P. E., Cutler D. J., Kashuk C. S., Lin S., Abecasis G. R., Guan W., Li Y., Munro H. M., Qin Z. S., Thomas D. J., McVean G., Auton A., Bottolo L., Cardin N., Eyheramendy S., Freeman C., Marchini J., Myers S., Spencer C., Stephens M., Donnelly P., Cardon L. R., Clarke G., Evans D. M., Morris A. P., Weir B. S., Johnson T. A., Mullikin J. C., Sherry S. T., Feolo M., Skol A., Zhang H., Matsuda I., Fukushima Y., MacEr D. R., Suda E., Rotimi C. N., Adebamowo C. A., Ajayi I., Aniagwu T., Marshall P. A., Nkwodimmah C., Royal C. D. M., Leppert M. F., Dixon M., Peiffer A., Qiu R., Kent A., Kato K., Niikawa N., Adewole I. F., Knoppers B. M., Foster M. W., Clayton E. W., Watkin J., Muzny D., Nazareth L., Sodergren E., Weinstock G. M., Yakub I., Birren B. W., Wilson R. K., Fulton L. L., Rogers J., Burton J., Carter N. P., Clee C. M., Griffiths M., Jones M. C., McLay K., Plumb R. W., Ross M. T., Sims S. K., Willey D. L., Chen Z., Han H., Kang L., Godbout M., Wallenburg J. C., L'Archevêque P., Bellemare G., Saeki K., Wang H., An D., Fu H., Li Q., Wang Z., Wang R., Holden A. L., Brooks L. D., McEwen J. E., Guyer M. S., Wang V. O., Peterson J. L., Shi M., Spiegel J., Sung L. M., Zacharia L. F., Collins F. S., Kennedy K., Jamieson R., Stewart J., A second generation human haplotype map of over 3.1 million SNPs. Nature 2007 449 7164 851 861 2-s2.0-35348983887 10.1038/nature06258 (Pubitemid 47598626)
-
(2007)
Nature
, vol.449
, Issue.7164
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
Pasternak, S.11
Wheeler, D.A.12
Willis, T.D.13
Yu, F.14
Yang, H.15
Zeng, C.16
Gao, Y.17
Hu, H.18
Hu, W.19
Li, C.20
Lin, W.21
Liu, S.22
Pan, H.23
Tang, X.24
Wang, J.25
Wang, W.26
Yu, J.27
Zhang, B.28
Zhang, Q.29
Zhao, H.30
Zhao, H.31
Zhou, J.32
Gabriel, S.B.33
Barry, R.34
Blumenstiel, B.35
Camargo, A.36
Defelice, M.37
Faggart, M.38
Goyette, M.39
Gupta, S.40
Moore, J.41
Nguyen, H.42
Onofrio, R.C.43
Parkin, M.44
Roy, J.45
Stahl, E.46
Winchester, E.47
Ziaugra, L.48
Altshuler, D.49
Shen, Y.50
Yao, Z.51
Huang, W.52
Chu, X.53
He, Y.54
Jin, L.55
Liu, Y.56
Shen, Y.57
Sun, W.58
Wang, H.59
Wang, Y.60
Wang, Y.61
Xiong, X.62
Xu, L.63
Waye, M.M.Y.64
Tsui, S.K.W.65
Xue, H.66
Wong, J.T.-F.67
Galver, L.M.68
Fan, J.-B.69
Gunderson, K.70
Murray, S.S.71
Oliphant, A.R.72
Chee, M.S.73
Montpetit, A.74
Chagnon, F.75
Ferretti, V.76
Leboeuf, M.77
Olivier, J.-F.78
Phillips, M.S.79
Roumy, S.80
Sallee, C.81
Verner, A.82
Hudson, T.J.83
Kwok, P.-Y.84
Cai, D.85
Koboldt, D.C.86
Miller, R.D.87
Pawlikowska, L.88
Taillon-Miller, P.89
Xiao, M.90
Tsui, L.-C.91
Mak, W.92
You, Q.S.93
Tam, P.K.H.94
Nakamura, Y.95
more..
-
17
-
-
33947285368
-
Focus on research: What genome-wide association studies can do for medicine
-
DOI 10.1056/NEJMp068126
-
Christensen K., Murray J. C., Focus on research: what genome-wide association studies can do for medicine. New England Journal of Medicine 2007 356 11 1094 1097 2-s2.0-33947285368 10.1056/NEJMp068126 (Pubitemid 46425594)
-
(2007)
New England Journal of Medicine
, vol.356
, Issue.11
, pp. 1094-1097
-
-
Christensen, K.1
Murray, J.C.2
-
18
-
-
43049146524
-
A HapMap harvest of insights into the genetics of common disease
-
DOI 10.1172/JCI34772
-
Manolio T. A., Brooks L. D., Collins F. S., A HapMap harvest of insights into the genetics of common disease. Journal of Clinical Investigation 2008 118 5 1590 1605 2-s2.0-43049146524 10.1172/JCI34772 (Pubitemid 351632361)
-
(2008)
Journal of Clinical Investigation
, vol.118
, Issue.5
, pp. 1590-1605
-
-
Manolio, T.A.1
Brooks, L.D.2
Collins, F.S.3
-
19
-
-
80052260527
-
A genome-wide association study identifies two new risk loci for Graves' disease
-
guangning@medmail.com.cn zchen@stn.sh.cn J.-L.C.xuyanrr@yahoo.com.cn sjchen@stn.sh.cn huangwei@chgc.sh.cn huaidongs1966@163.com 10.1038/ng.898
-
Chu X., Pan C.-M., Zhao S.-X., Liang J., Gao G. -Q., Zhang X. -M., Yuan G. -Y., Li C. -G., Xue L. -Q., Shen M., Liu W., Xie F., Yang S. -Y., Wang H. -F., Shi J. -Y., Sun W. -W., Du W. -H., Zuo C. -L., Shi J. -X., Liu B. -L., Guo C. -C., Zhan M., Gu Z. -H., Zhang X. -N., Sun F., Wang Z. -Q., Song Z. -Y., Zou C. -Y., Sun W. -H., Guo T., Cao H. -M., Ma J. -H., Han B., Li P., Jiang H., Huang Q. -H., Liang L., Liu L. -B., Chen G., Su Q., Peng Y. -D., Zhao J. -J., Ning G., guangning@medmail.com.cn Chen Z., zchen@stn.sh.cn Chen J. -L., J.-L.C.xuyanrr@yahoo.com.cn Chen S. -J., sjchen@stn.sh.cn Huang W., huangwei@chgc.sh.cn Song H. -D., huaidongs1966@163.com A genome-wide association study identifies two new risk loci for Graves' disease. Nature Genetics 2011 43 9 897 901 10.1038/ng.898
-
(2011)
Nature Genetics
, vol.43
, Issue.9
, pp. 897-901
-
-
Chu, X.1
Pan, C.-M.2
Zhao, S.-X.3
Liang, J.4
Gao, G.-Q.5
Zhang, X.-M.6
Yuan, G.-Y.7
Li, C.-G.8
Xue, L.-Q.9
Shen, M.10
Liu, W.11
Xie, F.12
Yang, S.-Y.13
Wang, H.-F.14
Shi, J.-Y.15
Sun, W.-W.16
Du, W.-H.17
Zuo, C.-L.18
Shi, J.-X.19
Liu, B.-L.20
Guo, C.-C.21
Zhan, M.22
Gu, Z.-H.23
Zhang, X.-N.24
Sun, F.25
Wang, Z.-Q.26
Song, Z.-Y.27
Zou, C.-Y.28
Sun, W.-H.29
Guo, T.30
Cao, H.-M.31
Ma, J.-H.32
Han, B.33
Li, P.34
Jiang, H.35
Huang, Q.-H.36
Liang, L.37
Liu, L.-B.38
Chen, G.39
Su, Q.40
Peng, Y.-D.41
Zhao, J.-J.42
Ning, G.43
Chen, Z.44
Chen, J.-L.45
Chen, S.-J.46
Huang, W.47
Song, H.-D.48
more..
-
20
-
-
34547618083
-
Drinking from the fire hose - Statistical issues in genomewide association studies
-
DOI 10.1056/NEJMp078120
-
Hunter D. J., Kraft P., Drinking from the fire hosestatistical issues in genomewide association studies. New England Journal of Medicine 2007 357 5 436 439 2-s2.0-34547618083 10.1056/NEJMp078120 (Pubitemid 47204871)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.5
, pp. 436-439
-
-
Hunter, D.J.1
Kraft, P.2
-
21
-
-
34347408099
-
Problems with genome-wide association studies
-
2-s2.0-34347408099
-
Shriner D., Vaughan L. K., Padilla M. A., Tiwari H. K., Problems with genome-wide association studies. Science 2007 316 5833 1840 1841 2-s2.0-34347408099
-
(2007)
Science
, vol.316
, Issue.5833
, pp. 1840-1841
-
-
Shriner, D.1
Vaughan, L.K.2
Padilla, M.A.3
Tiwari, H.K.4
-
22
-
-
0028873470
-
CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population
-
2-s2.0-0028873470
-
Yanagawa T., Hidaka Y., Guimaraes V., Soliman M., DeGroot L. J., CTLA-4 gene polymorphism associated with Graves' disease in a Caucasian population. Journal of Clinical Endocrinology and Metabolism 1995 80 1 41 45 2-s2.0-0028873470
-
(1995)
Journal of Clinical Endocrinology and Metabolism
, vol.80
, Issue.1
, pp. 41-45
-
-
Yanagawa, T.1
Hidaka, Y.2
Guimaraes, V.3
Soliman, M.4
Degroot, L.J.5
-
23
-
-
0023553685
-
Immunogenetics of autoimmune thyroid disorders
-
Farid N. R., Immunogenetics of autoimmune thyroid disorders. Endocrinology and Metabolism Clinics of North America 1987 16 2 229 245 2-s2.0-0023553685 (Pubitemid 18088076)
-
(1987)
Endocrinology and Metabolism Clinics of North America
, vol.16
, Issue.2
, pp. 229-245
-
-
Farid, N.R.1
-
24
-
-
80052239824
-
The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness
-
ksimin@mshri.on.ca 10.1038/ng.904
-
Zhang J., Zahir N., Jiang Q., Miliotis H., Heyraud S., Meng X., Dong B., Xie G., Qiu F., Hao Z., McCulloch C. A., Keystone E. C., Peterson A. C., Siminovitch K. A., ksimin@mshri.on.ca The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness. Nature Genetics 2011 43 9 902 907 10.1038/ng.904
-
(2011)
Nature Genetics
, vol.43
, Issue.9
, pp. 902-907
-
-
Zhang, J.1
Zahir, N.2
Jiang, Q.3
Miliotis, H.4
Heyraud, S.5
Meng, X.6
Dong, B.7
Xie, G.8
Qiu, F.9
Hao, Z.10
McCulloch, C.A.11
Keystone, E.C.12
Peterson, A.C.13
Siminovitch, K.A.14
-
25
-
-
78349272440
-
Genetic susceptibility to autoimmune thyroid disease: Past, present, and future
-
2-s2.0-78349272440
-
Tomer Y., Genetic susceptibility to autoimmune thyroid disease: past, present, and future. Thyroid 2010 20 7 715 725 2-s2.0-78349272440
-
(2010)
Thyroid
, vol.20
, Issue.7
, pp. 715-725
-
-
Tomer, Y.1
-
26
-
-
0036149916
-
Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases
-
DOI 10.1210/jc.87.1.404
-
Tomer Y., Greenberg D. A., Concepcion E., Ban Y., Davies T. F., Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases. Journal of Clinical Endocrinology and Metabolism 2002 87 1 404 407 2-s2.0-0036149916 10.1210/jc.87.1.404 (Pubitemid 34084722)
-
(2002)
Journal of Clinical Endocrinology and Metabolism
, vol.87
, Issue.1
, pp. 404-407
-
-
Tomer, Y.1
Greenberg, D.A.2
Concepcion, E.3
Ban, Y.4
Davies, T.F.5
-
27
-
-
56549107801
-
Influence of the TSH receptor gene on susceptibility to Graves' disease and Graves' ophthalmopathy
-
2-s2.0-56549107801 10.1089/thy.2008.0098
-
Yin X., Latif R., Bahn R., Tomer Y., Davies T. F., Influence of the TSH receptor gene on susceptibility to Graves' disease and Graves' ophthalmopathy. Thyroid 2008 18 11 1201 1206 2-s2.0-56549107801 10.1089/thy.2008.0098
-
(2008)
Thyroid
, vol.18
, Issue.11
, pp. 1201-1206
-
-
Yin, X.1
Latif, R.2
Bahn, R.3
Tomer, Y.4
Davies, T.F.5
-
28
-
-
33644790167
-
Association of the TSHR gene with Graves' disease: The first disease specific locus
-
2-s2.0-33644790167 10.1038/sj.ejhg.5201485
-
Dechairo B. M., Zabaneh D., Collins J., Brand O., Dawson G. J., Green A. P., Mackay I., Franklyn J. A., Connell J. M., Wass J. A. H., Wiersinga W. M., Hegedus L., Brix T., Robinson B. G., Hunt P. J., Weetman A. P., Carey A. H., Gough S. C., Association of the TSHR gene with Graves' disease: the first disease specific locus. European Journal of Human Genetics 2005 13 11 1223 1230 2-s2.0-33644790167 10.1038/sj.ejhg.5201485
-
(2005)
European Journal of Human Genetics
, vol.13
, Issue.11
, pp. 1223-1230
-
-
Dechairo, B.M.1
Zabaneh, D.2
Collins, J.3
Brand, O.4
Dawson, G.J.5
Green, A.P.6
MacKay, I.7
Franklyn, J.A.8
Connell, J.M.9
Wass, J.A.H.10
Wiersinga, W.M.11
Hegedus, L.12
Brix, T.13
Robinson, B.G.14
Hunt, P.J.15
Weetman, A.P.16
Carey, A.H.17
Gough, S.C.18
-
29
-
-
80052425160
-
Novel variant of thyroglobulin promoter triggers thyroid autoimmunity through an epigenetic interferon α -modulated mechanism
-
mihaela.stefan@mssm.edu yaron.tomer@mssm.edu 10.1074/jbc.M111.247510
-
Stefan M., mihaela.stefan@mssm.edu Jacobson E. M., Huber A. K., Greenberg D. A., Li C. W., Skrabanek L., Conception E., Fadlalla M., Ho K., Tomer Y., yaron.tomer@mssm.edu Novel variant of thyroglobulin promoter triggers thyroid autoimmunity through an epigenetic interferon α -modulated mechanism. Journal of Biological Chemistry 2011 286 36 31168 31179 10.1074/jbc.M111.247510
-
(2011)
Journal of Biological Chemistry
, vol.286
, Issue.36
, pp. 31168-31179
-
-
Stefan, M.1
Jacobson, E.M.2
Huber, A.K.3
Greenberg, D.A.4
Li, C.W.5
Skrabanek, L.6
Conception, E.7
Fadlalla, M.8
Ho, K.9
Tomer, Y.10
-
30
-
-
18844366115
-
Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease
-
DOI 10.1210/jc.2004-2148
-
Hiratani H., Bowden D. W., Ikegami S., Shirasawa S., Shimizu A., Iwatani Y., Akamizu T., Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease. Journal of Clinical Endocrinology and Metabolism 2005 90 5 2898 2903 2-s2.0-18844366115 10.1210/jc.2004-2148 (Pubitemid 40686341)
-
(2005)
Journal of Clinical Endocrinology and Metabolism
, vol.90
, Issue.5
, pp. 2898-2903
-
-
Hiratani, H.1
Bowden, D.W.2
Ikegami, S.3
Shirasawa, S.4
Shimizu, A.5
Iwatani, Y.6
Akamizu, T.7
-
31
-
-
80051705017
-
Association of an SNP with intrathymic transcription of TSHR and graves' disease: A role for defective thymic tolerance
-
ricardo.pujol@uab.cat 10.1093/hmg/ddr247
-
Colobran R., Armengol M. d. P., Faner R., Gärtner M., Tykocinski L., Lucas A., Ruiz M., Juan M., Kyewski B., Pujol-Borrell R., ricardo.pujol@uab.cat Association of an SNP with intrathymic transcription of TSHR and graves' disease: a role for defective thymic tolerance. Human Molecular Genetics 2011 20 17 3415 3423 10.1093/hmg/ddr247
-
(2011)
Human Molecular Genetics
, vol.20
, Issue.17
, pp. 3415-3423
-
-
Colobran, R.1
Armengol D. M, P.2
Faner, R.3
Gärtner, M.4
Tykocinski, L.5
Lucas, A.6
Ruiz, M.7
Juan, M.8
Kyewski, B.9
Pujol-Borrell, R.10
-
32
-
-
0033304849
-
Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: Evidence for genetic heterogeneity and gene interactions
-
2-s2.0-0033304849
-
Tomer Y., Barbesino G., Greenberg D. A., Concepcion E., Davies T. F., Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: evidence for genetic heterogeneity and gene interactions. Journal of Clinical Endocrinology and Metabolism 1999 84 12 4656 4664 2-s2.0-0033304849
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, Issue.12
, pp. 4656-4664
-
-
Tomer, Y.1
Barbesino, G.2
Greenberg, D.A.3
Concepcion, E.4
Davies, T.F.5
-
33
-
-
0142059659
-
Common and Unique Susceptibility Loci in Graves and Hashimoto Diseases: Results of Whole-Genome Screening in a Data Set of 102 Multiplex Families
-
DOI 10.1086/378588
-
Tomer Y., Ban Y., Conception E., Barbesino G., Villanueva R., Greenberg D. A., Davies T. F., Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families. American Journal of Human Genetics 2003 73 4 736 747 2-s2.0-0142059659 10.1086/378588 (Pubitemid 37271879)
-
(2003)
American Journal of Human Genetics
, vol.73
, Issue.4
, pp. 736-747
-
-
Tomer, Y.1
Ban, Y.2
Conception, E.3
Barbesino, G.4
Villanueva, R.5
Greenberg, D.A.6
Davies, T.F.7
-
34
-
-
34548524948
-
Dissecting genetic heterogeneity in autoimmune thyroid diseases by subset analysis
-
DOI 10.1016/j.jaut.2007.05.006, PII S0896841107000698
-
Tomer Y., Menconi F., Davies T. F., Barbesino G., Rocchi R., Pinchera A., Concepcion E., Greenberg D. A., Dissecting genetic heterogeneity in autoimmune thyroid diseases by subset analysis. Journal of Autoimmunity 2007 29 2-3 69 77 2-s2.0-34548524948 10.1016/j.jaut.2007.05.006 (Pubitemid 47385112)
-
(2007)
Journal of Autoimmunity
, vol.29
, Issue.2-3
, pp. 69-77
-
-
Tomer, Y.1
Menconi, F.2
Davies, T.F.3
Barbesino, G.4
Rocchi, R.5
Pinchera, A.6
Concepcion, E.7
Greenberg, D.A.8
-
35
-
-
32544442160
-
A genome-wide screen in 1119 relative pairs with autoimmune thyroid disease
-
DOI 10.1210/jc.2005-0686
-
Taylor J. C., Gough S. C., Hunt P. J., Brix T. H., Chatterjee K., Connell J. M., Franklyn J. A., Hegedus L., Robinson B. G., Wiersinga W. M., Wass J. A. H., Zabaneh D., Mackay I., Weetman A. P., A genome-wide screen in 1119 relative pairs with autoimmune thyroid disease. Journal of Clinical Endocrinology and Metabolism 2006 91 2 646 653 2-s2.0-32544442160 10.1210/jc.2005-0686 (Pubitemid 43236938)
-
(2006)
Journal of Clinical Endocrinology and Metabolism
, vol.91
, Issue.2
, pp. 646-653
-
-
Taylor, J.C.1
Gough, S.C.2
Hunt, P.J.3
Brix, T.H.4
Chatterjee, K.5
Connell, J.M.6
Franklyn, J.A.7
Hegedus, L.8
Robinson, B.G.9
Wiersinga, W.M.10
Wass, J.A.H.11
Zabaneh, D.12
Mackay, I.13
Weetman, A.P.14
-
36
-
-
0035875097
-
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
-
Sakai K., Shirasawa S., Ishikawa N., Ito K., Tamai H., Kuma K., Akamizu T., Tanimura M., Furugaki K., Yamamoto K., Sasazuki T., 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. Human Molecular Genetics 2001 10 13 1379 1386 2-s2.0-0035875097 (Pubitemid 32640666)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.13
, pp. 1379-1386
-
-
Sakai, K.1
Shirasawa, S.2
Ishikawa, N.3
Ito, K.4
Tamai, H.5
Kuma, K.6
Akamizu, T.7
Tanimura, M.8
Furugaki, K.9
Yamamoto, K.10
Sasazuki, T.11
-
37
-
-
35748981184
-
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
-
DOI 10.1038/ng.2007.17, PII NG200717
-
Burton P. R., Clayton D. G., Cardon L. R., Craddock N., Deloukas P., Duncanson A., Kwiatkowski D. P., McCarthy M. I., Ouwehand W. H., Samani N. J., Todd J. A., Donnelly P., Barrett J. C., Davison D., Easton D., Evans D. M., Leung H. T., Marchini J. L., Morris A. P., Spencer C. C. A., Tobin M. D., Attwood A. P., Boorman J. P., Cant B., Everson U., Hussey J. M., Jolley J. D., Knight A. S., Koch K., Meech E., Nutland S., Prowse C. V., Stevens H. E., Taylor N. C., Walters G. R., Walker N. M., Watkins N. A., Winzer T., Jones R. W., McArdle W. L., Ring S. M., Strachan D. P., Pembrey M., Breen G., Clair D. S., Caesar S., Gordon-Smith K., Jones L., Fraser C., Green E. K., Grozeva D., Hamshere M. L., Holmans P. A., Jones I. R., Kirov G., Moskivina V., Nikolov I., O'Donovan M. C., Owen M. J., Collier D. A., Elkin A., Farmer A., Williamson R., McGuffin P., Young A. H., Ferrier I. N., Ball S. G., Balmforth A. J., Barrett J. H., Bishop T. D., Iles M. M., Maqbool A., Yuldasheva N., Hall A. S., Braund P. S., Dixon R. J., Mangino M., Stevens S., Thompson J. R., Bredin F., Tremelling M., Parkes M., Drummond H., Lees C. W., Nimmo E. R., Satsangi J., Fisher S. A., Forbes A., Lewis C. M., Onnie C. M., Prescott N. J., Sanderson J., Matthew C. G., Barbour J., Mohiuddin M. K., Todhunter C. E., Mansfield J. C., Ahmad T., Cummings F. R., Jewell D. P., Webster J., Brown M. J., Lathrop M. G., Connell J., Dominiczak A., Marcano C. A. B., Burke B., Dobson R., Gungadoo J., Lee K. L., Munroe P. B., Newhouse S. J., Onipinla A., Wallace C., Xue M., Caulfield M., Farrall M., Barton A., Bruce I. N., Donovan H., Eyre S., Gilbert P. D., Hilder S. L., Hinks A. M., John S. L., Potter C., Silman A. J., Symmons D. P. M., Thomson W., Worthington J., Dunger D. B., Widmer B., Frayling T. M., Freathy R. M., Lango H., Perry J. R. B., Shields B. M., Weedon M. N., Hattersley A. T., Hitman G. A., Walker M., Elliott K. S., Groves C. J., Lindgren C. M., Rayner N. W., Timpson N. J., Zeggini E., Newport M., Sirugo G., Lyons E., Vannberg F., Hill A. V. S., Bradbury L. A., Farrar C., Pointon J. J., Wordsworth P., Brown M. A., Franklyn J. A., Heward J. M., Simmonds M. J., Gough S. C. L., Seal S., Stratton M. R., Rahman N., Ban M., Goris A., Sawcer S. J., Compston A., Conway D., Jallow M., Rockett K. A., Bumpstead S. J., Chaney A., Downes K., Ghori M. J. R., Gwilliam R., Hunt S. E., Inouye M., Keniry A., King E., McGinnis R., Potter S., Ravindrarajah R., Whittaker P., Widden C., Withers D., Cardin N. J., Ferreira T., Pereira-Gale J., Hallgrimsdóttir I. B., Howie B. N., Su Z., Teo Y. Y., Vukcevic D., Bentley D., Mitchell S. L., Newby P. R., Brand O. J., Carr-Smith J., Pearce S. H. S., Gough S. C. L., McGinnis R., Keniry A., Deloukas P., Reveille J. D., Zhou X., Sims A. M., Dowling A., Taylor J., Doan T., Davis J. C., Savage L., Ward M. M., Learch T. L., Weisman M. H., Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nature Genetics 2007 39 11 1329 1337 2-s2.0-35748981184 10.1038/ng.2007.17 (Pubitemid 350041542)
-
(2007)
Nature Genetics
, vol.39
, Issue.11
, pp. 1329-1337
-
-
Burton, P.R.1
Clayton, D.G.2
Cardon, L.R.3
Craddock, N.4
Deloukas, P.5
Duncanson, A.6
Kwiatkowski, D.P.7
McCarthy, M.I.8
Ouwehand, W.H.9
Samani, N.J.10
Todd, J.A.11
Donnelly, P.12
Barrett, J.C.13
Davison, D.14
Easton, D.15
Evans, D.M.16
Leung, H.-T.17
Marchini, J.L.18
Morris, A.P.19
Spencer, C.C.A.20
Tobin, M.D.21
Attwood, A.P.22
Boorman, J.P.23
Cant, B.24
Everson, U.25
Hussey, J.M.26
Jolley, J.D.27
Knight, A.S.28
Koch, K.29
Meech, E.30
Nutland, S.31
Prowse, C.V.32
Stevens, H.E.33
Taylor, N.C.34
Walters, G.R.35
Walker, N.M.36
Watkins, N.A.37
Winzer, T.38
Jones, R.W.39
McArdle, W.L.40
Ring, S.M.41
Strachan, D.P.42
Pembrey, M.43
Breen, G.44
Clair, D.St.45
Caesar, S.46
Gordon-Smith, K.47
Jones, L.48
Fraser, C.49
Green, E.K.50
Grozeva, D.51
Hamshere, M.L.52
Holmans, P.A.53
Jones, I.R.54
Kirov, G.55
Moskivina, V.56
Nikolov, I.57
O'Donovan, M.C.58
Owen, M.J.59
Collier, D.A.60
Elkin, A.61
Farmer, A.62
Williamson, R.63
McGuffin, P.64
Young, A.H.65
Ferrier, I.N.66
Ball, S.G.67
Balmforth, A.J.68
Barrett, J.H.69
Bishop, T.D.70
Iles, M.M.71
Maqbool, A.72
Yuldasheva, N.73
Hall, A.S.74
Braund, P.S.75
Dixon, R.J.76
Mangino, M.77
Stevens, S.78
Thompson, J.R.79
Bredin, F.80
Tremelling, M.81
Parkes, M.82
Drummond, H.83
Lees, C.W.84
Nimmo, E.R.85
Satsangi, J.86
Fisher, S.A.87
Forbes, A.88
Lewis, C.M.89
Onnie, C.M.90
Prescott, N.J.91
Sanderson, J.92
Matthew, C.G.93
Barbour, J.94
more..
-
38
-
-
77955983679
-
Follow-up of potential novel graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study
-
2-s2.0-77955983679 10.1038/ejhg.2010.55
-
Newby P. R., Pickles O. J., Mazumdar S., Brand O. J., Carr-Smith J. D., Pearce S. H. S., Franklyn J. A., Evans D. M., Simmonds M. J., Gough S. C. L., Follow-up of potential novel graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. European Journal of Human Genetics 2010 18 9 1021 1026 2-s2.0-77955983679 10.1038/ejhg.2010.55
-
(2010)
European Journal of Human Genetics
, vol.18
, Issue.9
, pp. 1021-1026
-
-
Newby, P.R.1
Pickles, O.J.2
Mazumdar, S.3
Brand, O.J.4
Carr-Smith, J.D.5
Pearce, S.H.S.6
Franklyn, J.A.7
Evans, D.M.8
Simmonds, M.J.9
Gough, S.C.L.10
-
39
-
-
36749034777
-
Really significant genes for autoimmune thyroid disease do not exist - So how can we predict disease?
-
DOI 10.1089/thy.2007.1526
-
Davies T. F., Really significant genes for autoimmune thyroid disease do not existso how can we predict disease? Thyroid 2007 17 11 1027 1029 2-s2.0-36749034777 10.1089/thy.2007.1526 (Pubitemid 350207766)
-
(2007)
Thyroid
, vol.17
, Issue.11
, pp. 1027-1029
-
-
Davies, T.F.1
-
40
-
-
79955096234
-
Maternal diet and aging alter the epigenetic control of a promoter-enhancer interaction at the Hnf4a gene in rat pancreatic islets
-
jmasmc2@cam.ac.uk seo10@cam.ac.uk 10.1073/pnas.1019007108
-
Sandovici I., Smith N. H., Nitert M. D., Ackers-Johnson M., Uribe-Lewis S., Ito Y., Jones R. H., Marquez V. E., Cairns W., Tadayyon M., O'Neill L. P., Murrell A., Ling C., Constância M., jmasmc2@cam.ac.uk Ozanne S. E., seo10@cam.ac.uk Maternal diet and aging alter the epigenetic control of a promoter-enhancer interaction at the Hnf4a gene in rat pancreatic islets. Proceedings of the National Academy of Sciences of the United States of America 2011 108 13 5449 5454 10.1073/pnas.1019007108
-
(2011)
Proceedings of the National Academy of Sciences of the United States of America
, vol.108
, Issue.13
, pp. 5449-5454
-
-
Sandovici, I.1
Smith, N.H.2
Nitert, M.D.3
Ackers-Johnson, M.4
Uribe-Lewis, S.5
Ito, Y.6
Jones, R.H.7
Marquez, V.E.8
Cairns, W.9
Tadayyon, M.10
O'Neill, L.P.11
Murrell, A.12
Ling, C.13
Constância, M.14
Ozanne, S.E.15
-
41
-
-
77953904042
-
Virus-plus-susceptibility gene interaction determines Crohn's disease gene Atg16L1 phenotypes in intestine
-
2-s2.0-77953904042 10.1016/j.cell.2010.05.009
-
Cadwell K., Patel K. K., Maloney N. S., Liu T. C., Ng A. C. Y., Storer C. E., Head R. D., Xavier R., Stappenbeck T. S., Virgin H. W., Virus-plus-susceptibility gene interaction determines Crohn's disease gene Atg16L1 phenotypes in intestine. Cell 2010 141 7 1135 1145 2-s2.0-77953904042 10.1016/j.cell.2010.05.009
-
(2010)
Cell
, vol.141
, Issue.7
, pp. 1135-1145
-
-
Cadwell, K.1
Patel, K.K.2
Maloney, N.S.3
Liu, T.C.4
Ng, A.C.Y.5
Storer, C.E.6
Head, R.D.7
Xavier, R.8
Stappenbeck, T.S.9
Virgin, H.W.10
-
42
-
-
27744454481
-
High frequency of skewed x-chromosome inactivation in females with autoimmune thyroid disease: A possible explanation for the female predisposition to thyroid autoimmunity
-
DOI 10.1210/jc.2005-1366
-
Brix T. H., Knudsen G. P. S., Kristiansen M., Kyvik K. O., Orstavik K. H., Hegedüs L., High frequency of skewed x-chromosome inactivation in females with autoimmune thyroid disease: a possible explanation for the female predisposition to thyroid autoimmunity. Journal of Clinical Endocrinology and Metabolism 2005 90 11 5949 5953 2-s2.0-27744454481 10.1210/jc.2005-1366 (Pubitemid 41606510)
-
(2005)
Journal of Clinical Endocrinology and Metabolism
, vol.90
, Issue.11
, pp. 5949-5953
-
-
Brix, T.H.1
Knudsen, G.P.S.2
Kristiansen, M.3
Kyvik, K.O.4
Orstavik, K.H.5
Hegedus, L.6
-
43
-
-
35748941353
-
Thyroid epigenetics: X chromosome inactivation in patients with autoimmune thyroid disease
-
DOI 10.1196/annals.1423.021, Autoimmunity, Part B Novel Applications of Basic Research
-
Yin X., Latif R., Tomer Y., Davies T. F., Thyroid epigenetics: X chromosome inactivation in patients with autoimmune thyroid disease. Annals of the New York Academy of Sciences 2007 1110 193 200 2-s2.0-35748941353 10.1196/annals.1423.021 (Pubitemid 350043008)
-
(2007)
Annals of the New York Academy of Sciences
, vol.1110
, pp. 193-200
-
-
Yin, X.1
Latif, R.2
Tomer, Y.3
Davies, T.F.4
|