Perola M - Search Results

1

An interaction map of circulating metabolites, immune gene networks, and their genetic regulation.

Nath AP, Ritchie SC, Byars SG, Fearnley LG, Havulinna AS, Joensuu A, Kangas AJ, Soininen P, Wennerström A, Milani L, Metspalu A, Männistö S, Würtz P, Kettunen J, Raitoharju E, Kähönen M, Juonala M, Palotie A, Ala-Korpela M, Ripatti S, Lehtimäki T, Abraham G, Raitakari O, Salomaa V, Perola M, Inouye M. Nath AP, et al. Among authors: perola m. Genome Biol. 2017 Aug 1;18(1):146. doi: 10.1186/s13059-017-1279-y. Genome Biol. 2017. PMID: 28764798 Free PMC article.

2

Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups.

Perola M, Ohman M, Hiekkalinna T, Leppävuori J, Pajukanta P, Wessman M, Koskenvuo M, Palotie A, Lange K, Kaprio J, Peltonen L. Perola M, et al. Am J Hum Genet. 2001 Jul;69(1):117-23. doi: 10.1086/321286. Epub 2001 Jun 15. Am J Hum Genet. 2001. PMID: 11410840 Free PMC article.

3

Coronary artery complicated lesion area is related to functional polymorphism of matrix metalloproteinase 9 gene: an autopsy study.

Pöllänen PJ, Karhunen PJ, Mikkelsson J, Laippala P, Perola M, Penttilä A, Mattila KM, Koivula T, Lehtimäki T. Pöllänen PJ, et al. Among authors: perola m. Arterioscler Thromb Vasc Biol. 2001 Sep;21(9):1446-50. doi: 10.1161/hq0901.095545. Arterioscler Thromb Vasc Biol. 2001. PMID: 11557670

4

Coronary artery wall atherosclerosis in relation to the estrogen receptor 1 gene polymorphism: an autopsy study.

Lehtimäki T, Kunnas TA, Mattila KM, Perola M, Penttilä A, Koivula T, Karhunen PJ. Lehtimäki T, et al. Among authors: perola m. J Mol Med (Berl). 2002 Mar;80(3):176-80. doi: 10.1007/s00109-001-0311-5. Epub 2002 Jan 17. J Mol Med (Berl). 2002. PMID: 11894143

5

Myeloperoxidase gene variation as a determinant of atherosclerosis progression in the abdominal and thoracic aorta: an autopsy study.

Mäkelä R, Karhunen PJ, Kunnas TA, Ilveskoski E, Kajander OA, Mikkelsson J, Perola M, Penttilä A, Lehtimäki T. Mäkelä R, et al. Among authors: perola m. Lab Invest. 2003 Jul;83(7):919-25. doi: 10.1097/01.lab.0000077981.49367.46. Lab Invest. 2003. PMID: 12861032 Free article.

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: perola m. Twin Res Hum Genet. 2005 Aug;8(4):368-75. doi: 10.1375/1832427054936664. Twin Res Hum Genet. 2005. PMID: 16176722

7

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: perola m. 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

8

Lessons from studying monogenic disease for common disease.

Peltonen L, Perola M, Naukkarinen J, Palotie A. Peltonen L, et al. Among authors: perola m. Hum Mol Genet. 2006 Apr 15;15 Spec No 1:R67-74. doi: 10.1093/hmg/ddl060. Hum Mol Genet. 2006. PMID: 16651371 Review. No abstract available.

9

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: perola m. 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.

10

Genetic component of identification, intensity and pleasantness of odours: a Finnish family study.

Knaapila A, Keskitalo K, Kallela M, Wessman M, Sammalisto S, Hiekkalinna T, Palotie A, Peltonen L, Tuorila H, Perola M. Knaapila A, et al. Among authors: perola m. Eur J Hum Genet. 2007 May;15(5):596-602. doi: 10.1038/sj.ejhg.5201804. Epub 2007 Mar 7. Eur J Hum Genet. 2007. PMID: 17342154

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