Remm M - Search Results

1

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.

2

High-density genotyping and linkage disequilibrium in the human genome using chromosome 22 as a model.

Remm M, Metspalu A. Remm M, et al. Curr Opin Chem Biol. 2002 Feb;6(1):24-30. doi: 10.1016/s1367-5931(01)00285-x. Curr Opin Chem Biol. 2002. PMID: 11827819 Review.

3

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.

4

MultiPLX: automatic grouping and evaluation of PCR primers.

Kaplinski L, Andreson R, Puurand T, Remm M. Kaplinski L, et al. Among authors: remm m. Bioinformatics. 2005 Apr 15;21(8):1701-2. doi: 10.1093/bioinformatics/bti219. Epub 2004 Dec 14. Bioinformatics. 2005. PMID: 15598831

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

X-chromosome as a marker for population history: linkage disequilibrium and haplotype study in Eurasian populations.

Laan M, Wiebe V, Khusnutdinova E, Remm M, Pääbo S. Laan M, et al. Among authors: remm m. Eur J Hum Genet. 2005 Apr;13(4):452-62. doi: 10.1038/sj.ejhg.5201340. Eur J Hum Genet. 2005. PMID: 15657606 Free PMC article.

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

SNPmasker: automatic masking of SNPs and repeats across eukaryotic genomes.

Andreson R, Puurand T, Remm M. Andreson R, et al. Among authors: remm m. Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W651-5. doi: 10.1093/nar/gkl125. Nucleic Acids Res. 2006. PMID: 16845091 Free PMC article.

9

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.

10

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

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