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BMC Bioinformatics|June 1, 2010
GWAMA: software for genome-wide association meta-analysisReedik Mägi, Andrew P Morris
BMC Proceedings|March 1, 2012
Assessing the impact of missing genotype data in rare variant association analysisReedik Mägi, Ashish Kumar, Andrew P Morris
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.
European Journal of Human Genetics : EJHG|May 25, 2017
A rare-variant test for high-dimensional dataMarika Kaakinen, Reedik Mägi, Krista Fischer, et al.
BMC Bioinformatics|February 18, 2017
MARV: a tool for genome-wide multi-phenotype analysis of rare variantsMarika Kaakinen, Reedik Mägi, Krista Fischer, et al.
BMC Bioinformatics|January 13, 2017
SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypesReedik Mägi, Yury V Suleimanov, Geraldine M Clarke, et al.
Epigenomics|March 24, 2016
Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissuesNatalia Pervjakova, Silva Kasela, Andrew P Morris, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|November 11, 2006
The whole genome tagSNP selection and transferability among HapMap populationsReedik Mägi, Lauris Kaplinski, Maido Remm
Human Reproduction (Oxford, England)|October 25, 2023
Genome-wide association study meta-analysis supports association between MUC1 and ectopic pregnancyNatàlia Pujol Gualdo, , Reedik Mägi, et al.
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