Cardiovascular twist to the rapidly evolving apolipoprotein L1 story. by Farrall, M

Interpreting gene-association studies. by Farrall, M

Reports of the death of the epistasis model are greatly exaggerated. by Farrall, M

Quantitative genetic variation: a post-modern view. by Farrall, M

Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour. by Peden, J, Farrall, M

Integrating case-control and TDT studies. by Kazeem, G, Farrall, M

Gearing up for genome-wide gene-association studies. by Farrall, M, Morris, A

A power comparison of multilocus mapping approaches in the presence of epistasis and heterogeneity by Tzenova, J, Farrall, M

Genetic susceptibility to coronary artery disease: from promise to progress. by Watkins, H, Farrall, M

Detecting Gene-gene Interactions in Complex Diseases using Lasso Penalized Regression by Keildson, S, Morris, A, Farrall, M

Model selection methods applied to genetic association studies by Keildson, S, Farrall, M, Morris, A

Model Selection Strategies in Genome-Wide Association Studies by Keildson, S, Farrall, M, Morris, A

The authors reply by Farrall, M, Clarke, R, Watkins, H

Reports of the Death of the Epistasis Model Are Greatly Exaggerated [2] (multiple letters) by Farrall, M, Vieland, V, Huang, J

Genetic Variants in Lp(a) Lipoprotein and Coronary Disease REPLY by Farrall, M, Clarke, R, Watkins, H

Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease by Magosi, LE, Goel, A, Hopewell, JC, Farrall, M

Measured haplotype analysis of the aldosterone synthase gene and cardiac hypertrophy by Mayosi, B, Keavney, B, Watkins, H, Farrall, M

Measured haplotype analysis of the aldosterone synthase gene and heart size (vol 11, pg 395, 2005) by Mayosi, B, Keavney, B, Watkins, H, Farrall, M

Finding associations in dense genetic maps: a genetic algorithm approach. by Clark, T, De Iorio, M, Griffiths, R, Farrall, M

Association of prion protein gene single nucleotide polymorphism haplotypes with Creutzfeldt-Jakob disease. by Mead, S, Mahal, S, Farrall, M, Fisher, E, Collinge, J