GWAMA: software for genome-wide association meta-analysis

por Mägi, Reedik, Morris, Andrew P
Publicado 2010

Genome-wide association study meta-analysis supports association between MUC1 and ectopic pregnancy

por Pujol Gualdo, Natàlia, Mägi, Reedik, Laisk, Triin
Publicado 2023

Assessing the impact of missing genotype data in rare variant association analysis

por Mägi, Reedik, Kumar, Ashish, Morris, Andrew P
Publicado 2011

Meta-analysis of sex-specific genome-wide association studies

por Magi, Reedik, Lindgren, Cecilia M, Morris, Andrew P
Publicado 2010

Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk

por Zhou, Yitian, Mägi, Reedik, Milani, Lili, Lauschke, Volker M.
Publicado 2018

RegScan: a GWAS tool for quick estimation of allele effects on continuous traits and their combinations

por Haller, Toomas, Kals, Mart, Esko, Tõnu, Mägi, Reedik, Fischer, Krista
Publicado 2015

Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores

por Läll, Kristi, Mägi, Reedik, Morris, Andrew, Metspalu, Andres, Fischer, Krista
Publicado 2017

Parents of early‐maturing girls die younger

por Hõrak, Peeter, Valge, Markus, Fischer, Krista, Mägi, Reedik, Kaart, Tanel
Publicado 2019

Genome-wide association study identifies five risk loci for pernicious anemia

por Laisk, Triin, Lepamets, Maarja, Koel, Mariann, Abner, Erik, Mägi, Reedik
Publicado 2021

Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation

por Mägi, Reedik, Pfeufer, Arne, Nelis, Mari, Montpetit, Alexandre, Metspalu, Andres, Remm, Maido
Publicado 2007

Genetic variants in humanin nuclear isoform gene regions show no association with coronary artery disease

por Eltermaa, Mall, Jakobson, Maili, Utt, Meeme, Kõks, Sulev, Mägi, Reedik, Starkopf, Joel
Publicado 2019

Polygenic Risk Score Predicts Modified Risk in BRCA1 Pathogenic Variant c.4035del and c.5266dup Carriers in Breast Cancer Patients

por Berga-Švītiņa, Egija, Maksimenko, Jeļena, Miklaševičs, Edvīns, Fischer, Krista, Vilne, Baiba, Mägi, Reedik
Publicado 2023

Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases

por Mägi, Reedik, Asimit, Jennifer L, Day-Williams, Aaron G, Zeggini, Eleftheria, Morris, Andrew P
Publicado 2012

Reconstructing recent population history while mapping rare variants using haplotypes

por Yunusbaev, Ural, Valeev, Albert, Yunusbaeva, Milyausha, Kwon, Hyung Wook, Mägi, Reedik, Metspalu, Mait, Yunusbayev, Bayazit
Publicado 2019

MARV: a tool for genome-wide multi-phenotype analysis of rare variants

por Kaakinen, Marika, Mägi, Reedik, Fischer, Krista, Heikkinen, Jani, Järvelin, Marjo-Riitta, Morris, Andrew P., Prokopenko, Inga
Publicado 2017

A rare-variant test for high-dimensional data

por Kaakinen, Marika, Mägi, Reedik, Fischer, Krista, Heikkinen, Jani, Järvelin, Marjo-Riitta, Morris, Andrew P, Prokopenko, Inga
Publicado 2017

SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes

por Mägi, Reedik, Suleimanov, Yury V., Clarke, Geraldine M., Kaakinen, Marika, Fischer, Krista, Prokopenko, Inga, Morris, Andrew P.
Publicado 2017

Genetic insights into the age-specific biological mechanisms governing human ovarian aging

por Ojavee, Sven E., Darrous, Liza, Patxot, Marion, Läll, Kristi, Fischer, Krista, Mägi, Reedik, Kutalik, Zoltan, Robinson, Matthew R.
Publicado 2023

Imprinted genes and imprinting control regions show predominant intermediate methylation in adult somatic tissues

por Pervjakova, Natalia, Kasela, Silva, Morris, Andrew P, Kals, Mart, Metspalu, Andres, Lindgren, Cecilia M, Salumets, Andres, Mägi, Reedik
Publicado 2016

Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification

por Läll, Kristi, Lepamets, Maarja, Palover, Marili, Esko, Tõnu, Metspalu, Andres, Tõnisson, Neeme, Padrik, Peeter, Mägi, Reedik, Fischer, Krista
Publicado 2019