Remm M - Search Results

1

Haplotypes in the human Foxo1a and Foxo3a genes; impact on disease and mortality at old age.

Kuningas M, Mägi R, Westendorp RG, Slagboom PE, Remm M, van Heemst D. Kuningas M, et al. Among authors: remm m. Eur J Hum Genet. 2007 Mar;15(3):294-301. doi: 10.1038/sj.ejhg.5201766. Epub 2007 Jan 24. Eur J Hum Genet. 2007. PMID: 17245409

2

Shared and unique components of human population structure and genome-wide signals of positive selection in South Asia.

Metspalu M, Romero IG, Yunusbayev B, Chaubey G, Mallick CB, Hudjashov G, Nelis M, Mägi R, Metspalu E, Remm M, Pitchappan R, Singh L, Thangaraj K, Villems R, Kivisild T. Metspalu M, et al. Among authors: remm m. Am J Hum Genet. 2011 Dec 9;89(6):731-44. doi: 10.1016/j.ajhg.2011.11.010. Am J Hum Genet. 2011. PMID: 22152676 Free PMC article.

3

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: remm m. 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.

4

The whole genome tagSNP selection and transferability among HapMap populations.

Mägi R, Kaplinski L, Remm M. Mägi R, et al. Among authors: remm m. Pac Symp Biocomput. 2006:535-43. Pac Symp Biocomput. 2006. PMID: 17094267 Free article.

5

Linkage disequilibrium patterns and tagSNP transferability among European populations.

Mueller JC, Lõhmussaar E, Mägi R, Remm M, Bettecken T, Lichtner P, Biskup S, Illig T, Pfeufer A, Luedemann J, Schreiber S, Pramstaller P, Pichler I, Romeo G, Gaddi A, Testa A, Wichmann HE, Metspalu A, Meitinger T. Mueller JC, et al. Among authors: remm m. Am J Hum Genet. 2005 Mar;76(3):387-98. doi: 10.1086/427925. Epub 2005 Jan 6. Am J Hum Genet. 2005. PMID: 15637659 Free PMC article.

6

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: remm m. 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

7

An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population.

Montpetit A, Nelis M, Laflamme P, Magi R, Ke X, Remm M, Cardon L, Hudson TJ, Metspalu A. Montpetit A, et al. Among authors: remm m. PLoS Genet. 2006 Mar;2(3):e27. doi: 10.1371/journal.pgen.0020027. Epub 2006 Mar 10. PLoS Genet. 2006. PMID: 16532062 Free PMC article.

8

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: remm m. Clin Chem Lab Med. 2008;46(7):974-9. doi: 10.1515/CCLM.2008.187. Clin Chem Lab Med. 2008. PMID: 18605963

9

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. Among authors: remm m. BMC Genomics. 2007 Jun 11;8:159. doi: 10.1186/1471-2164-8-159. BMC Genomics. 2007. PMID: 17562002 Free PMC article.

10

A first-generation linkage disequilibrium map of human chromosome 22.

Dawson E, Abecasis GR, Bumpstead S, Chen Y, Hunt S, Beare DM, Pabial J, Dibling T, Tinsley E, Kirby S, Carter D, Papaspyridonos M, Livingstone S, Ganske R, Lõhmussaar E, Zernant J, Tõnisson N, Remm M, Mägi R, Puurand T, Vilo J, Kurg A, Rice K, Deloukas P, Mott R, Metspalu A, Bentley DR, Cardon LR, Dunham I. Dawson E, et al. Among authors: remm m. Nature. 2002 Aug 1;418(6897):544-8. doi: 10.1038/nature00864. Epub 2002 Jul 10. Nature. 2002. PMID: 12110843 Free article.

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