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European Journal of Clinical Investigation|December 16, 2010
The effect of next-generation sequencing technology on complex trait researchAaron G Day-Williams, Eleftheria ZegginiHuman Heredity|March 24, 2012
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing dataJennifer L Asimit, Aaron G Day-Williams, Andrew P Morris, et al.BMC Bioinformatics|October 23, 2010
CCRaVAT and QuTie-enabling analysis of rare variants in large-scale case control and quantitative trait association studiesRobert Lawrence, Aaron G Day-Williams, Katherine S Elliott, et al.Genetic Epidemiology|September 7, 2012
Genome-wide association analysis of imputed rare variants: application to seven common complex diseasesReedik Mägi, Jennifer L Asimit, Aaron G Day-Williams, et al.BMC Bioinformatics|November 3, 2009
GLIDERS--a web-based search engine for genome-wide linkage disequilibrium between HapMap SNPsRobert Lawrence, Aaron G Day-Williams, Richard Mott, et al.Plos One|November 10, 2011
An evaluation of different target enrichment methods in pooled sequencing designs for complex disease association studiesAaron G Day-Williams, Kirsten McLay, Eleanor Drury, et al.Nature Genetics|March 30, 2011
Next-generation association studies for complex traitsEleftheria ZegginiGenome Medicine|December 5, 2014
Using genetically isolated populations to understand the genomic basis of diseaseEleftheria ZegginiGenome Medicine|May 6, 2011
Testing for rare variant associations in complex diseasesJennifer Asimit, Eleftheria ZegginiJournal of Medical Genetics|July 23, 2013
Advances in osteoarthritis geneticsKalliope Panoutsopoulou, Eleftheria ZegginiPageof 33