Peltonen L - Search Results

1

Combined effects of thrombosis pathway gene variants predict cardiovascular events.

Auro K, Alanne M, Kristiansson K, Silander K, Kuulasmaa K, Salomaa V, Peltonen L, Perola M. Auro K, et al. Among authors: peltonen l. PLoS Genet. 2007 Jul;3(7):e120. doi: 10.1371/journal.pgen.0030120. Epub 2007 Jun 7. PLoS Genet. 2007. PMID: 17677000 Free PMC article.

2

Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.

Komulainen K, Alanne M, Auro K, Kilpikari R, Pajukanta P, Saarela J, Ellonen P, Salminen K, Kulathinal S, Kuulasmaa K, Silander K, Salomaa V, Perola M, Peltonen L. Komulainen K, et al. Among authors: peltonen l. PLoS Genet. 2006 May;2(5):e69. doi: 10.1371/journal.pgen.0020069. Epub 2006 May 12. PLoS Genet. 2006. PMID: 16699592 Free PMC article.

3

Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts.

Alanne M, Kristiansson K, Auro K, Silander K, Kuulasmaa K, Peltonen L, Salomaa V, Perola M. Alanne M, et al. Among authors: peltonen l. Hum Genet. 2007 Nov;122(3-4):355-65. doi: 10.1007/s00439-007-0402-7. Epub 2007 Jul 20. Hum Genet. 2007. PMID: 17641917

4

Gender differences in genetic risk profiles for cardiovascular disease.

Silander K, Alanne M, Kristiansson K, Saarela O, Ripatti S, Auro K, Karvanen J, Kulathinal S, Niemelä M, Ellonen P, Vartiainen E, Jousilahti P, Saarela J, Kuulasmaa K, Evans A, Perola M, Salomaa V, Peltonen L. Silander K, et al. Among authors: peltonen l. PLoS One. 2008;3(10):e3615. doi: 10.1371/journal.pone.0003615. Epub 2008 Oct 31. PLoS One. 2008. PMID: 18974842 Free PMC article.

5

The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories.

Varilo T, Paunio T, Parker A, Perola M, Meyer J, Terwilliger JD, Peltonen L. Varilo T, et al. Among authors: peltonen l. Hum Mol Genet. 2003 Jan 1;12(1):51-9. doi: 10.1093/hmg/ddg005. Hum Mol Genet. 2003. PMID: 12490532

6

Evaluating whole genome amplification via multiply-primed rolling circle amplification for SNP genotyping of samples with low DNA yield.

Silander K, Komulainen K, Ellonen P, Jussila M, Alanne M, Levander M, Tainola P, Kuulasmaa K, Salomaa V, Perola M, Peltonen L, Saarela J. Silander K, et al. Among authors: peltonen l. Twin Res Hum Genet. 2005 Aug;8(4):368-75. doi: 10.1375/1832427054936664. Twin Res Hum Genet. 2005. PMID: 16176722

7

Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.

Palo OM, Antila M, Silander K, Hennah W, Kilpinen H, Soronen P, Tuulio-Henriksson A, Kieseppä T, Partonen T, Lönnqvist J, Peltonen L, Paunio T. Palo OM, et al. Among authors: peltonen l. Hum Mol Genet. 2007 Oct 15;16(20):2517-28. doi: 10.1093/hmg/ddm207. Epub 2007 Aug 2. Hum Mol Genet. 2007. PMID: 17673452

8

Association analysis of allelic variants of USF1 in coronary atherosclerosis.

Kristiansson K, Ilveskoski E, Lehtimäki T, Peltonen L, Perola M, Karhunen PJ. Kristiansson K, et al. Among authors: peltonen l. Arterioscler Thromb Vasc Biol. 2008 May;28(5):983-9. doi: 10.1161/ATVBAHA.107.156463. Epub 2008 Feb 14. Arterioscler Thromb Vasc Biol. 2008. PMID: 18276913 Free PMC article.

9

Further evidence for the role of ENPP1 in obesity: association with morbid obesity in Finns.

Valli-Jaakola K, Suviolahti E, Schalin-Jäntti C, Ripatti S, Silander K, Oksanen L, Salomaa V, Peltonen L, Kontula K. Valli-Jaakola K, et al. Among authors: peltonen l. Obesity (Silver Spring). 2008 Sep;16(9):2113-9. doi: 10.1038/oby.2008.313. Obesity (Silver Spring). 2008. PMID: 18551113 Free article.

10

Isolated populations and complex disease gene identification.

Kristiansson K, Naukkarinen J, Peltonen L. Kristiansson K, et al. Among authors: peltonen l. Genome Biol. 2008;9(8):109. doi: 10.1186/gb-2008-9-8-109. Epub 2008 Aug 26. Genome Biol. 2008. PMID: 18771588 Free PMC article.

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