-
2
-
-
0017757504
-
The spectrum of thyroid disease in a community: The Whickham survey
-
Tunbridge, W.M., Evered, D.C., Hall, R., Appleton, D., Brewis, M., Clark, F., Evans, J.G., Young, E., Bird, T. and Smith, P.A. (1977) The spectrum of thyroid disease in a community: The Whickham survey. Clin. Endocrinol. (Oxf), 7, 481-493.
-
(1977)
Clin. Endocrinol. (Oxf)
, vol.7
, pp. 481-493
-
-
Tunbridge, W.M.1
Evered, D.C.2
Hall, R.3
Appleton, D.4
Brewis, M.5
Clark, F.6
Evans, J.G.7
Young, E.8
Bird, T.9
Smith, P.A.10
-
3
-
-
19944422075
-
Regression mapping of association between the human leukocyte antigen region and Graves disease
-
Simmonds, M.J., Howson, J.M., Heward, J.M., Cordell, H.J., Foxall, H., Carr-Smith, J., Gibson, S.M., Walker, N., Tomer, Y., Franklyn, J.A. 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
Carr-Smith, J.6
Gibson, S.M.7
Walker, N.8
Tomer, Y.9
Franklyn, J.A.10
-
4
-
-
34548447535
-
A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect
-
Simmonds, M.J., Howson, J.M., Heward, J.M., Carr-Smith, J., Franklyn, J.A., Todd, J.A. and Gough, S.C. (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
Todd, J.A.6
Gough, S.C.7
-
5
-
-
0037648405
-
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
-
Ueda, H., Howson, J.M., Esposito, L., Heward, J., Snook, H., Chamberlain, G., Rainbow, D.B., Hunter, K.M., Smith, A.N., Di Genova, G. 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
Chamberlain, G.6
Rainbow, D.B.7
Hunter, K.M.8
Smith, A.N.9
Di Genova, G.10
-
6
-
-
7044253358
-
Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus
-
Smyth, D., Cooper, J.D., Collins, J.E., Heward, J.M., Franklyn, J.A., Howson, J.M., Vella, A., Nutland, S., Rance, H.E., Maier, L. et al. (2004) Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus. Diabetes, 53, 3020-3023.
-
(2004)
Diabetes
, vol.53
, pp. 3020-3023
-
-
Smyth, D.1
Cooper, J.D.2
Collins, J.E.3
Heward, J.M.4
Franklyn, J.A.5
Howson, J.M.6
Vella, A.7
Nutland, S.8
Rance, H.E.9
Maier, L.10
-
7
-
-
33947274768
-
Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs
-
Brand, O.J., Lowe, C.E., Heward, J.M., Franklyn, J.A., Cooper, J.D., Todd, J.A. and Gough, S.C. (2007) Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs. Clin. Endocrinol. (Oxf), 66, 508-512.
-
(2007)
Clin. Endocrinol. (Oxf)
, vol.66
, pp. 508-512
-
-
Brand, O.J.1
Lowe, C.E.2
Heward, J.M.3
Franklyn, J.A.4
Cooper, J.D.5
Todd, J.A.6
Gough, S.C.7
-
8
-
-
14744304660
-
Do autoantigens define autoimmunity or vice versa?
-
Eisenberg, R. (2005) Do autoantigens define autoimmunity or vice versa? Eur. J. Immunol., 35, 367-370.
-
(2005)
Eur. J. Immunol
, vol.35
, pp. 367-370
-
-
Eisenberg, R.1
-
9
-
-
0029062430
-
A polymorphism in the extracellular domain of the thyrotropin receptor is highly associated with autoimmune thyroid disease in females
-
Cuddihy, R.M., Dutton, C.M. and Bahn, R.S. (1995) A polymorphism in the extracellular domain of the thyrotropin receptor is highly associated with autoimmune thyroid disease in females. Thyroid, 5, 89-95.
-
(1995)
Thyroid
, vol.5
, pp. 89-95
-
-
Cuddihy, R.M.1
Dutton, C.M.2
Bahn, R.S.3
-
10
-
-
0030952262
-
No association between a thyrotropin receptor gene polymorphism and Graves' disease in the female population
-
Kotsa, K.D., Watson, P.F. and Weetman, A.P. (1997) No association between a thyrotropin receptor gene polymorphism and Graves' disease in the female population. Thyroid, 7, 31-33.
-
(1997)
Thyroid
, vol.7
, pp. 31-33
-
-
Kotsa, K.D.1
Watson, P.F.2
Weetman, A.P.3
-
11
-
-
13144305111
-
Lack of association between polymorphism of the thyrotropin receptor gene and Graves' disease in UK and Hong Kong Chinese patients: Case control and family-based studies
-
Allahabadia, A., Heward, J.M., Mijovic, C., Carr-Smith, J., Daykin, J., Cockram, C., Barnett, A.H., Sheppard, M.C., Franklyn, J.A. and Gough, S.C. (1998) Lack of association between polymorphism of the thyrotropin receptor gene and Graves' disease in UK and Hong Kong Chinese patients: case control and family-based studies. Thyroid, 8, 777-780.
-
(1998)
Thyroid
, vol.8
, pp. 777-780
-
-
Allahabadia, A.1
Heward, J.M.2
Mijovic, C.3
Carr-Smith, J.4
Daykin, J.5
Cockram, C.6
Barnett, A.H.7
Sheppard, M.C.8
Franklyn, J.A.9
Gough, S.C.10
-
12
-
-
0033305338
-
Germline polymorphism of codon 727 of human thyroid-stimulating hormone receptor is associated with toxic multinodular goiter
-
Gabriel, E.M., Bergert, E.R., Grant, C.S., van Heerden, J.A., Thompson, G.B. and Morris, J.C. (1999) Germline polymorphism of codon 727 of human thyroid-stimulating hormone receptor is associated with toxic multinodular goiter. J. Clin. Endocrinol. Metab., 84, 3328-3335.
-
(1999)
J. Clin. Endocrinol. Metab
, vol.84
, pp. 3328-3335
-
-
Gabriel, E.M.1
Bergert, E.R.2
Grant, C.S.3
van Heerden, J.A.4
Thompson, G.B.5
Morris, J.C.6
-
13
-
-
0033001342
-
Analysis of mutations in exon 1 of the human thyrotropin receptor gene: High frequency of the D36H and P52T polymorphic variants
-
Simanainen, J., Kinch, A., Westermark, K., Winsa, B., Bengtsson, M., Schuppert, F., Westermark, B. and Heldin, N.E. (1999) Analysis of mutations in exon 1 of the human thyrotropin receptor gene: High frequency of the D36H and P52T polymorphic variants. Thyroid, 9 7-11.
-
(1999)
Thyroid
, vol.9
, pp. 7-11
-
-
Simanainen, J.1
Kinch, A.2
Westermark, K.3
Winsa, B.4
Bengtsson, M.5
Schuppert, F.6
Westermark, B.7
Heldin, N.E.8
-
14
-
-
0033956268
-
Analysis of the genetic variability of the 1st (CCC/ACC, P52T) and the 10th exons (bp 1012-1704) of the TSH receptor gene in Graves' disease
-
Kaczur, V., Takacs, M., Szalai, C., Falus, A., Nagy, Z., Berencsi, G. and Balazs, C. (2000) Analysis of the genetic variability of the 1st (CCC/ACC, P52T) and the 10th exons (bp 1012-1704) of the TSH receptor gene in Graves' disease. Eur. J. Immunogenet., 27, 17-23.
-
(2000)
Eur. J. Immunogenet
, vol.27
, pp. 17-23
-
-
Kaczur, V.1
Takacs, M.2
Szalai, C.3
Falus, A.4
Nagy, Z.5
Berencsi, G.6
Balazs, C.7
-
15
-
-
0033903432
-
Complex association analysis of Graves' disease using a set of polymorphic markers
-
Chistyakov, D.A., Savost'anov, K.V., Turakulov, R.I., Petunina, N.A., Trukhina, L.V., Kudinova, A.V., Balabolkin, M.I. and Nosikov, V.V. (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
Kudinova, A.V.6
Balabolkin, M.I.7
Nosikov, V.V.8
-
16
-
-
0028948985
-
Lack of association between a polymorphism in the coding region of the thyrotropin receptor gene and Graves' disease
-
Watson, P.F., French, A., Pickerill, A.P., McIntosh, R.S. and Weetman, A.P. (1995) Lack of association between a polymorphism in the coding region of the thyrotropin receptor gene and Graves' disease. J. Clin. Endocrinol. Metab., 80, 1032-1035.
-
(1995)
J. Clin. Endocrinol. Metab
, vol.80
, pp. 1032-1035
-
-
Watson, P.F.1
French, A.2
Pickerill, A.P.3
McIntosh, R.S.4
Weetman, A.P.5
-
17
-
-
0038506972
-
Association of Graves' disease with intragenic polymorphism of the thyrotropin receptor gene in a cohort of Singapore patients of multi-ethnic origins
-
Ho, S.C., Goh, S.S. and Khoo, D.H. (2003) Association of Graves' disease with intragenic polymorphism of the thyrotropin receptor gene in a cohort of Singapore patients of multi-ethnic origins. Thyroid, 13, 523-528.
-
(2003)
Thyroid
, vol.13
, pp. 523-528
-
-
Ho, S.C.1
Goh, S.S.2
Khoo, D.H.3
-
18
-
-
12244262763
-
A germline single nucleotide polymorphism at the intracellular domain of the human thyrotropin receptor does not have a major effect on the development of Graves' disease
-
Ban, Y., Greenberg, D.A., Concepcion, E.S. and Tomer, Y. (2002) A germline single nucleotide polymorphism at the intracellular domain of the human thyrotropin receptor does not have a major effect on the development of Graves' disease. Thyroid, 12, 1079-1083.
-
(2002)
Thyroid
, vol.12
, pp. 1079-1083
-
-
Ban, Y.1
Greenberg, D.A.2
Concepcion, E.S.3
Tomer, Y.4
-
19
-
-
17944389189
-
Further studies of genetic susceptibility to Graves' disease in a Russian population
-
Chistiakov, D.A., Savost'anov, K.V., Turakulov, R.I., Petunina, N., Balabolkin, M.I. and Nosikov, V.V. (2002) Further studies of genetic susceptibility to Graves' disease in a Russian population. Med. Sci. Monit., 8, CR180-184.
-
(2002)
Med. Sci. Monit
, vol.8
-
-
Chistiakov, D.A.1
Savost'anov, K.V.2
Turakulov, R.I.3
Petunina, N.4
Balabolkin, M.I.5
Nosikov, V.V.6
-
20
-
-
0034457053
-
Lack of association of nonautoimmune hyperfunctioning thyroid disorders and a germline polymorphism of codon 727 of the human thyrotropin receptor in a European Caucasian population
-
Muhlberg, T., Herrmann, K., Joba, W., Kirchberger, M., Heberling, H.J. and Heufelder, A.E. (2000) Lack of association of nonautoimmune hyperfunctioning thyroid disorders and a germline polymorphism of codon 727 of the human thyrotropin receptor in a European Caucasian population. J. Clin. Endocrinol. Metab., 85, 2640-2643.
-
(2000)
J. Clin. Endocrinol. Metab
, vol.85
, pp. 2640-2643
-
-
Muhlberg, T.1
Herrmann, K.2
Joba, W.3
Kirchberger, M.4
Heberling, H.J.5
Heufelder, A.E.6
-
21
-
-
33644790167
-
Association of the TSHR gene with Graves' disease: The first disease specific locus
-
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. et al. (2005) Association of the TSHR gene with Graves' disease: the first disease specific locus. Eur. J. Hum. Genet., 13, 1223-1230.
-
(2005)
Eur. J. Hum. Genet
, vol.13
, 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.10
-
22
-
-
18844366115
-
Multiple SNPs in intron 7 of thyrotropin receptor are associated with Graves' disease
-
Hiratani, H., Bowden, D.W., Ikegami, S., Shirasawa, S., Shimizu, A., Iwatani, Y. and Akamizu, T. (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
Iwatani, Y.6
Akamizu, T.7
-
23
-
-
35748981184
-
-
Burton, P.R., Clayton, D.G., Cardon, L.R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D.P., McCarthy, M.I., Ouwehand, W.H. et al. WTCCC (2007) Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat. Genet., 39 1329-1337.
-
Burton, P.R., Clayton, D.G., Cardon, L.R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D.P., McCarthy, M.I., Ouwehand, W.H. et al. WTCCC (2007) Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat. Genet., 39 1329-1337.
-
-
-
-
24
-
-
33644824363
-
Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease
-
Simmonds, M.J., Heward, J.M., Carr-Smith, J., Foxall, H., Franklyn, J.A. and Gough, S.C. (2006) Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease. J. Clin. Endocrinol. Metab., 91, 1056-1061.
-
(2006)
J. Clin. Endocrinol. Metab
, vol.91
, pp. 1056-1061
-
-
Simmonds, M.J.1
Heward, J.M.2
Carr-Smith, J.3
Foxall, H.4
Franklyn, J.A.5
Gough, S.C.6
-
25
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel, S.B., Schaffner, S.F., Nguyen, H., Moore, J.M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M. et al. (2002) The structure of haplotype blocks in the human genome. Science, 296, 2225-2229.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
-
26
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M.A., Bender, D., Maller, J., Sklar, P., de Bakker, P.I., Daly, M.J. 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
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.9
Daly, M.J.10
-
27
-
-
0025054351
-
Isolation of TSH and LH/CG receptor cDNAs from human thyroid: Regulation by tissue specific splicing
-
Frazier, A.L., Robbins, L.S., Stork, P.J., Sprengel, R., Segaloff, D.L. and Cone, R.D. (1990) Isolation of TSH and LH/CG receptor cDNAs from human thyroid: Regulation by tissue specific splicing. Mol. Endocrinol., 4, 1264-1276.
-
(1990)
Mol. Endocrinol
, vol.4
, pp. 1264-1276
-
-
Frazier, A.L.1
Robbins, L.S.2
Stork, P.J.3
Sprengel, R.4
Segaloff, D.L.5
Cone, R.D.6
-
28
-
-
0036251484
-
Multiple messenger ribonucleic acid transcripts and revised gene organization of the human TSH receptor
-
Kakinuma, A. and Nagayama, Y. (2002) Multiple messenger ribonucleic acid transcripts and revised gene organization of the human TSH receptor. Endocr. J., 49, 175-180.
-
(2002)
Endocr. J
, vol.49
, pp. 175-180
-
-
Kakinuma, A.1
Nagayama, Y.2
-
29
-
-
0028847909
-
Novel splicing variants of the human thyrotropin receptor encode truncated polypeptides without a membrane-spanning domain
-
Hunt, N., Wiley, K.P., Abend, N., Balvers, M., Jahner, D., Northemann, W. and Ivell, R. (1995) Novel splicing variants of the human thyrotropin receptor encode truncated polypeptides without a membrane-spanning domain. Endocrine, 3, 233-240.
-
(1995)
Endocrine
, vol.3
, pp. 233-240
-
-
Hunt, N.1
Wiley, K.P.2
Abend, N.3
Balvers, M.4
Jahner, D.5
Northemann, W.6
Ivell, R.7
-
30
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
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. et al. (2007) A second generation human haplotype map of over 3.1 million SNPs. Nature, 449, 851-861.
-
(2007)
Nature
, vol.449
, 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
-
31
-
-
55549089660
-
Accurate whole human genome sequencing using reversible terminator chemistry
-
Bentley, D.R., Balasubramanian, S., Swerdlow, H.P., Smith, G.P., Milton, J., Brown, C.G., Hall, K.P., Evers, D.J., Barnes, C.L., Bignell, H.R. et al. (2008) Accurate whole human genome sequencing using reversible terminator chemistry. Nature, 456, 53-59.
-
(2008)
Nature
, vol.456
, pp. 53-59
-
-
Bentley, D.R.1
Balasubramanian, S.2
Swerdlow, H.P.3
Smith, G.P.4
Milton, J.5
Brown, C.G.6
Hall, K.P.7
Evers, D.J.8
Barnes, C.L.9
Bignell, H.R.10
-
32
-
-
33750953227
-
Whole-genome re-sequencing
-
Bentley, D.R. (2006) Whole-genome re-sequencing. Curr. Opin. Genet. Dev., 16, 545-552.
-
(2006)
Curr. Opin. Genet. Dev
, vol.16
, pp. 545-552
-
-
Bentley, D.R.1
-
33
-
-
0031756989
-
Production of bioactive amino-terminal domain of the thyrotropin receptor via insertion in the plasma membrane by a glycosylphosphatidylinositol anchor
-
Costagliola, S., Khoo, D. and Vassart, G. (1998) Production of bioactive amino-terminal domain of the thyrotropin receptor via insertion in the plasma membrane by a glycosylphosphatidylinositol anchor. FEBS Lett. 436, 427-433.
-
(1998)
FEBS Lett
, vol.436
, pp. 427-433
-
-
Costagliola, S.1
Khoo, D.2
Vassart, G.3
-
34
-
-
0042744788
-
The thyrotropin receptor autoantigen in Graves disease is the culprit as well as the victim
-
Chen, C.R., Pichurin, P., Nagayama, Y., Latrofa, F., Rapoport, B. and McLachlan, S.M. (2003) The thyrotropin receptor autoantigen in Graves disease is the culprit as well as the victim. J. Clin. Invest., 111, 1897-1904.
-
(2003)
J. Clin. Invest
, vol.111
, pp. 1897-1904
-
-
Chen, C.R.1
Pichurin, P.2
Nagayama, Y.3
Latrofa, F.4
Rapoport, B.5
McLachlan, S.M.6
-
35
-
-
38749132020
-
Admixture mapping of white cell count: Genetic locus responsible for lower white blood cell count in the Health ABC and Jackson Heart studies
-
Nalls, M.A., Wilson, J.G., Patterson, N.J., Tandon, A., Zmuda, J.M., Huntsman, S., Garcia, M., Hu, D., Li, R., Beamer, B.A. et al. (2008) Admixture mapping of white cell count: Genetic locus responsible for lower white blood cell count in the Health ABC and Jackson Heart studies. Am. J. Hum. Genet., 82, 81-87.
-
(2008)
Am. J. Hum. Genet
, vol.82
, pp. 81-87
-
-
Nalls, M.A.1
Wilson, J.G.2
Patterson, N.J.3
Tandon, A.4
Zmuda, J.M.5
Huntsman, S.6
Garcia, M.7
Hu, D.8
Li, R.9
Beamer, B.A.10
-
36
-
-
39749197456
-
Genotype, haplotype and copy-number variation in worldwide human populations
-
Jakobsson, M., Scholz, S.W., Scheet, P., Gibbs, J.R., VanLiere, J.M., Fung, H.C., Szpiech, Z.A., Degnan, J.H., Wang, K., Guerreiro, R. et al. (2008) Genotype, haplotype and copy-number variation in worldwide human populations. Nature, 451, 998-1003.
-
(2008)
Nature
, vol.451
, pp. 998-1003
-
-
Jakobsson, M.1
Scholz, S.W.2
Scheet, P.3
Gibbs, J.R.4
VanLiere, J.M.5
Fung, H.C.6
Szpiech, Z.A.7
Degnan, J.H.8
Wang, K.9
Guerreiro, R.10
-
37
-
-
50449085212
-
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
-
Unoki, H., Takahashi, A., Kawaguchi, T., Hara, K., Horikoshi, M., Andersen, G., Ng, D.P., Holmkvist, J., Borch-Johnsen, K., Jorgensen, T. et al. (2008) SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. Nat. Genet. 40, 1039-1040.
-
(2008)
Nat. Genet
, vol.40
, pp. 1039-1040
-
-
Unoki, H.1
Takahashi, A.2
Kawaguchi, T.3
Hara, K.4
Horikoshi, M.5
Andersen, G.6
Ng, D.P.7
Holmkvist, J.8
Borch-Johnsen, K.9
Jorgensen, T.10
-
38
-
-
58149347486
-
Genome-wide association studies: Potential next steps on a genetic journey
-
McCarthy, M.I. and Hirschhorn, J.N. (2008) Genome-wide association studies: Potential next steps on a genetic journey. Hum. Mol. Genet. 17, R156-R165.
-
(2008)
Hum. Mol. Genet
, vol.17
-
-
McCarthy, M.I.1
Hirschhorn, J.N.2
-
39
-
-
15144361587
-
Linkage disequilibrium between the human leukocyte antigen class II region of the major histocompatibility complex and Graves' disease: Replication using a population case control and family-based study
-
Heward, J.M., Allahabadia, A., Daykin, J., Carr-Smith, J., Daly, A., Armitage, M., Dodson, P.M., Sheppard, M.C., Barnett, A.H., Franklyn, J.A. et al. (1998) Linkage disequilibrium between the human leukocyte antigen class II region of the major histocompatibility complex and Graves' disease: Replication using a population case control and family-based study. J. Clin. Endocrinol. Metab., 83, 3394-3397.
-
(1998)
J. Clin. Endocrinol. Metab
, vol.83
, pp. 3394-3397
-
-
Heward, J.M.1
Allahabadia, A.2
Daykin, J.3
Carr-Smith, J.4
Daly, A.5
Armitage, M.6
Dodson, P.M.7
Sheppard, M.C.8
Barnett, A.H.9
Franklyn, J.A.10
-
40
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett, J.C., Fry, B., Maller, J. and Daly, M.J. (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
-
41
-
-
27644439141
-
Efficiency and power in genetic association studies
-
de Bakker, P.I., Yelensky, R., Pe'er, I., Gabriel, S.B., Daly, M.J. and Altshuler, D. (2005) Efficiency and power in genetic association studies. Nat. Genet., 37, 1217-1223.
-
(2005)
Nat. Genet
, vol.37
, pp. 1217-1223
-
-
de Bakker, P.I.1
Yelensky, R.2
Pe'er, I.3
Gabriel, S.B.4
Daly, M.J.5
Altshuler, D.6
-
42
-
-
0028847909
-
Novel splicing variants of the human thyrotropin receptor encode truncated polypeptides without a membrane-spanning domain
-
Nicholas Hunt, K.P.W., Abend, N., Balvers, M., Jahner, D., Northemann, W. and Ivell, R. (1995) Novel splicing variants of the human thyrotropin receptor encode truncated polypeptides without a membrane-spanning domain. Endocrine, 3, 233-240.
-
(1995)
Endocrine
, vol.3
, pp. 233-240
-
-
Nicholas Hunt, K.P.W.1
Abend, N.2
Balvers, M.3
Jahner, D.4
Northemann, W.5
Ivell, R.6
|