Jeffrey Barrett

L Jostins, J Barrett (2011) Genetic risk prediction in complex disease, 1-7. In Human Molecular Genetics.

L Jostins, K I Morley, J C Barrett (2011) Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets, 1-5. In European Journal of Human Genetics.

C A Anderson, G Boucher, C W Lees et al. (2011) Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47, 1-9. In Nature genetics.

C Lees, J Barrett, M Parkes et al. (2011) New IBD genetics: common pathways with other diseases, 1-16. In Gut.

C Cotsapas, B Voight, E Rossin et al. (2011) Pervasive Sharing of Genetic Effects in Autoimmune Disease, e1002254. In PLoS Genetics 7 (8).

C A Anderson, N Soranzo, E Zeggini et al. (2011) Synthetic Associations Are Unlikely to Account for Many Common Disease Genome-Wide Association Signals, e1000580. In PLoS Biology 9 (1).

the International Headache Genetics Consortium, V Anttila, H Stefansson et al. (2010) Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. In Nature genetics.

A Franke, D P B Mcgovern, J C Barrett et al. (2010) Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci, 1-9. In Nature genetics.

P C A Dubois, G Trynka, L Franke et al. (2010) Multiple common variants for celiac disease influencing immune gene expression, 1-10. In Nature genetics.

G Orozco, J Barrett, E Zeggini (2010) Synthetic associations in the context of genome-wide association scan signals, R137-R144. In Human Molecular Genetics 19 (R2).