Mägi R - Search Results

1

Orthofer M, Valsesia A, Mägi R, Wang QP, Kaczanowska J, Kozieradzki I, Leopoldi A, Cikes D, Zopf LM, Tretiakov EO, Demetz E, Hilbe R, Boehm A, Ticevic M, Nõukas M, Jais A, Spirk K, Clark T, Amann S, Lepamets M, Neumayr C, Arnold C, Dou Z, Kuhn V, Novatchkova M, Cronin SJF, Tietge UJF, Müller S, Pospisilik JA, Nagy V, Hui CC, Lazovic J, Esterbauer H, Hagelkruys A, Tancevski I, Kiefer FW, Harkany T, Haubensak W, Neely GG, Metspalu A, Hager J, Gheldof N, Penninger JM. Orthofer M, et al. Among authors: magi r. Cell. 2020 Jun 11;181(6):1246-1262.e22. doi: 10.1016/j.cell.2020.04.034. Epub 2020 May 21. Cell. 2020. PMID: 32442405 Free article.

2

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

Mägi R, Pfeufer A, Nelis M, Montpetit A, Metspalu A, Remm M. Mägi R, et al. BMC Genomics. 2007 Jun 11;8:159. doi: 10.1186/1471-2164-8-159. BMC Genomics. 2007. PMID: 17562002 Free PMC article.

3

Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population.

Tamm R, Oselin K, Kallassalu K, Magi R, Anier K, Remm M, Metspalu A. Tamm R, et al. Among authors: magi r. Clin Chem Lab Med. 2008;46(7):974-9. doi: 10.1515/CCLM.2008.187. Clin Chem Lab Med. 2008. PMID: 18605963

4

A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.

Männik K, Parkel S, Palta P, Zilina O, Puusepp H, Esko T, Mägi R, Nõukas M, Veidenberg A, Nelis M, Metspalu A, Remm M, Ounap K, Kurg A. Männik K, et al. Among authors: magi r. Eur J Med Genet. 2011 Mar-Apr;54(2):136-43. doi: 10.1016/j.ejmg.2010.11.005. Epub 2010 Nov 26. Eur J Med Genet. 2011. PMID: 21112420

5

Copy number variations and cognitive phenotypes in unselected populations.

Männik K, Mägi R, Macé A, Cole B, Guyatt AL, Shihab HA, Maillard AM, Alavere H, Kolk A, Reigo A, Mihailov E, Leitsalu L, Ferreira AM, Nõukas M, Teumer A, Salvi E, Cusi D, McGue M, Iacono WG, Gaunt TR, Beckmann JS, Jacquemont S, Kutalik Z, Pankratz N, Timpson N, Metspalu A, Reymond A. Männik K, et al. Among authors: magi r. JAMA. 2015 May 26;313(20):2044-54. doi: 10.1001/jama.2015.4845. JAMA. 2015. PMID: 26010633 Free PMC article.

6

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

Läll K, Mägi R, Morris A, Metspalu A, Fischer K. Läll K, et al. Among authors: magi r. Genet Med. 2017 Mar;19(3):322-329. doi: 10.1038/gim.2016.103. Epub 2016 Aug 11. Genet Med. 2017. PMID: 27513194 Free PMC article.

7

Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions.

Reisberg S, Krebs K, Lepamets M, Kals M, Mägi R, Metsalu K, Lauschke VM, Vilo J, Milani L. Reisberg S, et al. Among authors: magi r. Genet Med. 2019 Jun;21(6):1345-1354. doi: 10.1038/s41436-018-0337-5. Epub 2018 Oct 16. Genet Med. 2019. PMID: 30327539 Free PMC article.

8

Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records.

Tasa T, Krebs K, Kals M, Mägi R, Lauschke VM, Haller T, Puurand T, Remm M, Esko T, Metspalu A, Vilo J, Milani L. Tasa T, et al. Among authors: magi r. Eur J Hum Genet. 2019 Mar;27(3):442-454. doi: 10.1038/s41431-018-0300-6. Epub 2018 Nov 12. Eur J Hum Genet. 2019. PMID: 30420678 Free PMC article.

9

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

Läll K, Lepamets M, Palover M, Esko T, Metspalu A, Tõnisson N, Padrik P, Mägi R, Fischer K. Läll K, et al. Among authors: magi r. BMC Cancer. 2019 Jun 10;19(1):557. doi: 10.1186/s12885-019-5783-1. BMC Cancer. 2019. PMID: 31182048 Free PMC article.

10

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

Laisk T, Lepamets M, Koel M, Abner E; Estonian Biobank Research Team; Mägi R. Laisk T, et al. Among authors: magi r. Nat Commun. 2021 Jun 18;12(1):3761. doi: 10.1038/s41467-021-24051-6. Nat Commun. 2021. PMID: 34145262 Free PMC article.

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