Peltonen L - Search Results

1

Angiotensin-converting enzyme genotypes in the high- and low-risk area for coronary heart disease in Finland.

Perola M, Sajantila A, Sarti C, Stengård J, Tamminen M, Puska P, Huttunen J, Tuomilehto J, Peltonen L. Perola M, et al. Among authors: peltonen l. Genet Epidemiol. 1995;12(4):391-9. doi: 10.1002/gepi.1370120407. Genet Epidemiol. 1995. PMID: 8536956

2

Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population.

Pastinen T, Perola M, Niini P, Terwilliger J, Salomaa V, Vartiainen E, Peltonen L, Syvänen A. Pastinen T, et al. Among authors: peltonen l. Hum Mol Genet. 1998 Sep;7(9):1453-62. doi: 10.1093/hmg/7.9.1453. Hum Mol Genet. 1998. PMID: 9700201

3

Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension.

Kainulainen K, Perola M, Terwilliger J, Kaprio J, Koskenvuo M, Syvänen AC, Vartiainen E, Peltonen L, Kontula K. Kainulainen K, et al. Among authors: peltonen l. Hypertension. 1999 Mar;33(3):844-9. doi: 10.1161/01.hyp.33.3.844. Hypertension. 1999. PMID: 10082497

4

Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.

Pajukanta P, Cargill M, Viitanen L, Nuotio I, Kareinen A, Perola M, Terwilliger JD, Kempas E, Daly M, Lilja H, Rioux JD, Brettin T, Viikari JS, Rönnemaa T, Laakso M, Lander ES, Peltonen L. Pajukanta P, et al. Among authors: peltonen l. Am J Hum Genet. 2000 Dec;67(6):1481-93. doi: 10.1086/316902. Epub 2000 Nov 13. Am J Hum Genet. 2000. PMID: 11078477 Free PMC article.

5

Thrombomodulin gene polymorphisms and haplotypes and the risk of cardiovascular events: a prospective follow-up study.

Auro K, Komulainen K, Alanne M, Silander K, Peltonen L, Perola M, Salomaa V. Auro K, et al. Among authors: peltonen l. Arterioscler Thromb Vasc Biol. 2006 Apr;26(4):942-7. doi: 10.1161/01.ATV.0000208365.45200.41. Epub 2006 Feb 2. Arterioscler Thromb Vasc Biol. 2006. PMID: 16456088

6

Association of FXIII Val34Leu with decreased risk of myocardial infarction in Finnish males.

Wartiovaara U, Perola M, Mikkola H, Tötterman K, Savolainen V, Penttilä A, Grant PJ, Tikkanen MJ, Vartiainen E, Karhunen PJ, Peltonen L, Palotie A. Wartiovaara U, et al. Among authors: peltonen l. Atherosclerosis. 1999 Feb;142(2):295-300. doi: 10.1016/s0021-9150(98)00241-x. Atherosclerosis. 1999. PMID: 10030380

7

PCR amplification of alleles at the DIS80 locus: comparison of a Finnish and a North American Caucasian population sample, and forensic casework evaluation.

Sajantila A, Budowle B, Ström M, Johnsson V, Lukka M, Peltonen L, Ehnholm C. Sajantila A, et al. Among authors: peltonen l. Am J Hum Genet. 1992 Apr;50(4):816-25. Am J Hum Genet. 1992. PMID: 1347970 Free PMC article.

8

DNA profiling in a genetically isolated population using three hypervariable DNA markers.

Sajantila A, Makkonen K, Ehnholm C, Peltonen L. Sajantila A, et al. Among authors: peltonen l. Hum Hered. 1992;42(6):372-9. doi: 10.1159/000154100. Hum Hered. 1992. PMID: 1362961

9

Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene.

Tienari PJ, Wikström J, Sajantila A, Palo J, Peltonen L. Tienari PJ, et al. Among authors: peltonen l. Lancet. 1992 Oct 24;340(8826):987-91. doi: 10.1016/0140-6736(92)93007-a. Lancet. 1992. PMID: 1383661

10

The distribution of the HLA-DQ alpha alleles and genotypes in the Finnish population as determined by the use of DNA amplification and allele specific oligonucleotides.

Sajantila A, Ström M, Budowle B, Tienari PJ, Ehnholm C, Peltonen L. Sajantila A, et al. Among authors: peltonen l. Int J Legal Med. 1991;104(4):181-4. doi: 10.1007/BF01369802. Int J Legal Med. 1991. PMID: 1931734

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