Comparison of methods for transcriptome imputation through application to two common complex diseases by Fryett, J, Inshaw, J, Morris, A, Cordell, H

A genome-wide search for human type 1 diabetes susceptibility genes. by Davies, J, Kawaguchi, Y, Bennett, S, Copeman, J, Cordell, H, Pritchard, L, Reed, P, Gough, S, Jenkins, S, Palmer, S

Dissection of the pathophysiology of type 1 diabetes by genetic analysis. by Todd, J, Reed, P, Prins, J, Bain, S, Palmer, S, Cordell, H, Pritchard, L, Ghosh, S, Cornall, R, Aitman, T

Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping. by Reed, P, Davies, J, Copeman, J, Bennett, S, Palmer, S, Pritchard, L, Gough, S, Kawaguchi, Y, Cordell, H, Balfour, K

MHC class II and III genes are associated with ankylosing spondylitis independent of HLA-B27. by Sims, A, Cordell, H, Barnardo, M, Broxholme, S, Herzberg, I, Bradbury, L, Calin, A, Wordsworth, B, Darke, C, Brown, M

Polygenic control of autoimmune diabetes in nonobese diabetic mice. by Ghosh, S, Palmer, S, Rodrigues, N, Cordell, H, Hearne, C, Cornall, R, Prins, J, McShane, P, Lathrop, G, Peterson, L

Mapping of MHC class II and III genes associated with Ankylosing spondylitis independent of HLA-B27 by Sims, A, Cordell, H, Barnardo, M, Broxholme, S, Herzberg, I, Bradbury, L, Calin, A, Wordsworth, B, Darke, C, Brown, M

THE IL1 GENE CLUSTER IS A MAJOR LOCUS DETERMINING SUSCEPTIBILITY TO ANKYLOSING SPONDYLITIS by Timms, A, Crane, A, Sims, A, Cordell, H, Bradbury, L, Beynon, O, Duff, G, Cardon, L, Calin, A, Wordsworth, P, Brown, M

Marked variation in heritability estimates of left ventricular mass depending on modality of measurement by Nethononda, R, McGurk, K, Whitworth, P, Francis, J, Mamasoula, C, Cordell, H, Neubauer, S, Keavney, B, Mayosi, B, Farrall, M, Watkins, H

Regression mapping of association between the human leukocyte antigen region and Graves disease. by Simmonds, M, Howson, J, Heward, J, Cordell, H, Foxall, H, Carr-Smith, J, Gibson, S, Walker, N, Tomer, Y, Franklyn, J, Todd, J, Gough, S

Association between aldosterone production and variation in the gene encoding 11-beta hydroxylase (CYP11B1) by Imrie, H, Freel, M, Mayosi, B, Davies, E, Fraser, R, Ingram, M, Cordell, H, Avery, P, Farrall, M, Watkins, H, Connell, J, Keavney, B

FINE MAPPING OF THE IL-2/IL-21 AND IL2RA LOCI IN PRIMARY SCLEROSING CHOLANGITIS by Srivastava, B, Mells, G, Cordell, H, Muriithi, A, Brown, M, Ellinghaus, E, Franke, A, Karlsen, T, Sandford, R, Alexander, G, Chapman, R, Rushbrook, S, Melum, E

Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene. by Imrie, H, Freel, M, Mayosi, B, Davies, E, Fraser, R, Ingram, M, Cordell, H, Farrall, M, Avery, P, Watkins, H, Keavney, B, Connell, J

Fine mapping and replication of genetic risk loci in primary sclerosing cholangitis. by Srivastava, B, Mells, G, Cordell, H, Muriithi, A, Brown, M, Ellinghaus, E, Franke, A, Consortium, UP, Karlsen, T, Sandford, R, Alexander, G, Chapman, R, Rushbrook, S, Melum, E

FINE MAPPING OF THE IL-2/IL-21 AND IL2RA LOCI IN PRIMARY SCLEROSING CHOLANGITIS by Srivastava, B, Mells, G, Cordell, H, Murithii, A, Brown, M, Ellinghaus, E, Franke, A, Karlsen, T, Sandford, R, Alexander, G, Chapman, R, Rushbrook, S, Melum, E, Consortium, UK-PSC

The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis. by Timms, A, Crane, A, Sims, A, Cordell, H, Bradbury, L, Abbott, A, Coyne, MR, Beynon, O, Herzberg, I, Duff, G, Calin, A, Cardon, L, Wordsworth, B, Brown, M

Aetiological Role Of Folate Deficiency In Congenital Cardiovascular Malformation: Evidence From "Mendelian Randomisation" And Meta-Analysis by Mamasoula, C, Pierscionek, T, Hall, D, Topf, A, Doza, J, Rahman, T, Tan, A, Bentham, J, Bhattacharya, S, Cosgrove, C, Brook, D, Riveron, J, Bu'Lock, F, O'Sullivan, J, Wren, C, Goodship, J, Cordell, H, Keavney, B

Haplotype tagging for the identification of common disease genes. by Johnson, G, Esposito, L, Barratt, B, Smith, A, Heward, J, Di Genova, G, Ueda, H, Cordell, H, Eaves, I, Dudbridge, F, Twells, R, Payne, F, Hughes, W, Nutland, S, Stevens, H, Carr, P, Tuomilehto-Wolf, E, Tuomilehto, J, Gough, S, Clayton, D, Todd, J

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot. by Goodship, J, Hall, D, Topf, A, Mamasoula, C, Griffin, H, Rahman, T, Glen, E, Tan, H, Palomino Doza, J, Relton, C, Bentham, J, Bhattacharya, S, Cosgrove, C, Brook, D, Granados-Riveron, J, Bu'Lock, F, O'Sullivan, J, Stuart, A, Parsons, J, Cordell, H, Keavney, B

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation. by Griffin, H, Hall, D, Topf, A, Eden, J, Stuart, A, Parsons, J, Peart, I, Deanfield, J, O'Sullivan, J, Babu-Narayan, S, Gatzoulis, M, Bu'lock, F, Bhattacharya, S, Bentham, J, Farrall, M, Granados Riveron, J, Brook, J, Burn, J, Cordell, H, Goodship, J, Keavney, B