GWAS in autoimmune thyroid disease: redefining our understanding of pathogenesis. by Simmonds, M

GWAS in autoimmune thyroid disease: Redefining our understanding of pathogenesis by Simmonds, M

The search for the genetic contribution to autoimmune thyroid disease: the never ending story? by Simmonds, M, Gough, S

Genetic insights into disease mechanisms of autoimmunity. by Simmonds, M, Gough, S

Unravelling the genetic complexity of autoimmune thyroid disease: HLA, CTLA-4 and beyond. by Simmonds, M, Gough, S

The HLA Region and Autoimmune Disease: Associations and Mechanisms of Action. by Gough, S, Simmonds, M

Identification of the regions of the HPV 5 E6 protein involved in Bak degradation and inhibition of apoptosis. by Simmonds, M, Storey, A

Interaction between ultraviolet radiation and human papillomavirus. by Storey, A, Simmonds, M

Genetic developments in autoimmune thyroid disease: an evolutionary process. by Zeitlin, A, Simmonds, M, Gough, S

The CD40 Kozak SNP: a new susceptibility loci for Graves' disease? by Simmonds, M, Heward, J, Franklyn, J, Gough, S

IL-13 and chromosome 5q31-q33: problems of identifying association within regions of linkage to Graves' disease. by Simmonds, M, Heward, J, Franklyn, J, Gough, S

Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74. by Simmonds, M, Heward, J, Barrett, J, Franklyn, J, Gough, S

Variation in the surfactant protein B gene is associated with development of emphysema in alpha 1 anti-trypsin deficiency by Wood, A, Simmonds, M, Newby, P, Gough, S, Stockley, R

Cost-effectiveness of diagnosis of high blood pressure in primary care by Wald, D, Simmonds, M, Morris, J, Rothwell, P, Wald, N

Cost-effectiveness of diagnosis of high blood pressure in primary care. by Wald, D, Simmonds, M, Morris, J, Rothwell, P, Wald, N

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

The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency. by Wood, A, Simmonds, M, Bayley, D, Newby, P, Gough, S, Stockley, R

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

Phenotypic differences in alpha 1 antitrypsin-deficient sibling pairs may relate to genetic variation. by Wood, A, Needham, M, Simmonds, M, Newby, P, Gough, S, Stockley, R