Copy number variation in common disease. by Brand, O, Gough, S

Genetics of thyroid autoimmunity and the role of the TSHR. by Brand, O, Gough, S

Immunogenetic mechanisms leading to thyroid autoimmunity: recent advances in identifying susceptibility genes and regions. by Brand, O, Gough, S

CMOS-MEMS / by Brand, O., Fedder, G. K.

HLA , CTLA-4 and PTPN22 : the shared genetic master-key to autoimmunity? by Brand, O, Gough, S, Heward, J

Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3. by Simmonds, M, Brand, O, Barrett, J, Newby, P, Franklyn, J, Gough, S

Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy. by Syed, A, Simmonds, M, Brand, O, Franklyn, J, Gough, S, Heward, J

Confirmation of association of chromosome 5q31-33 with United Kingdom Caucasian Graves' disease. by Simmonds, M, Yesmin, K, Newby, P, Brand, O, Franklyn, J, Gough, S

Association of PTPN22 haplotypes with Graves' disease. by Heward, J, Brand, O, Barrett, J, Carr-Smith, J, Franklyn, J, Gough, S

Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves' disease. by Zeitlin, A, Heward, J, Brand, O, Newby, P, Franklyn, J, Gough, S, Simmonds, M

Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs. by Brand, O, Lowe, C, Heward, J, Franklyn, J, Cooper, J, Todd, J, Gough, S

Tag SNP screening of the PDCD1 gene for association with Graves' disease. by Newby, P, Roberts-Davies, E, Brand, O, Heward, J, Franklyn, J, Gough, S, Simmonds, M

Skewed X chromosome inactivation and female preponderance in autoimmune thyroid disease: an association study and meta-analysis. by Simmonds, M, Kavvoura, F, Brand, O, Newby, P, Jackson, L, Hargreaves, C, Franklyn, J, Gough, S

Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression. by Yesmin, K, Hargreaves, C, Newby, P, Brand, O, Heward, J, Franklyn, J, Gough, S, Simmonds, M

Skewing of female X-chromosome inactivation: an epigenetic risk factor for kidney transplantation outcome. by Simmonds, M, Benavente, D, Brand, O, Moore, J, Ball, S, Ferro, C, Briggs, D, Gough, S, Borrows, R

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. by Newby, P, Pickles, O, Mazumdar, S, Brand, O, Carr-Smith, J, Pearce, S, Franklyn, J, Evans, D, Simmonds, M, Gough, S

Seven newly identified loci for autoimmune thyroid disease. by Cooper, J, Simmonds, M, Walker, N, Burren, O, Brand, O, Guo, H, Wallace, C, Stevens, H, Coleman, G, Franklyn, J, Todd, J, Gough, S

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts. by Płoski, R, Brand, O, Jurecka-Lubieniecka, B, Franaszczyk, M, Kula, D, Krajewski, P, Karamat, M, Simmonds, M, Franklyn, J, Gough, S, Jarząb, B, Bednarczuk, T

Association of caveolin-1 gene polymorphism with kidney transplant fibrosis and allograft failure. by Moore, J, McKnight, A, Simmonds, M, Courtney, A, Hanvesakul, R, Brand, O, Briggs, D, Ball, S, Cockwell, P, Patterson, C, Maxwell, A, Gough, S, Borrows, R

Donor ABCB1 variant associates with increased risk for kidney allograft failure. by Moore, J, McKnight, A, Döhler, B, Simmonds, M, Courtney, A, Brand, O, Briggs, D, Ball, S, Cockwell, P, Patterson, C, Maxwell, A, Gough, S, Opelz, G, Borrows, R