Perola M - Search Results

1

Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.

Leskelä J, Toppila I, Härma MA, Palviainen T, Salminen A, Sandholm N, Pietiäinen M, Kopra E, Pais de Barros JP; FinnGen; Lassenius MI, Kumar A, Harjutsalo V, Roslund K, Forsblom C, Loukola A, Havulinna AS, Lagrost L, Salomaa V, Groop PH, Perola M, Kaprio J, Lehto M, Pussinen PJ. Leskelä J, et al. Among authors: perola m. J Am Heart Assoc. 2021 Nov 2;10(21):e022482. doi: 10.1161/JAHA.121.022482. Epub 2021 Oct 20. J Am Heart Assoc. 2021. PMID: 34668383 Free PMC article.

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: perola m. Hum Mol Genet. 1998 Sep;7(9):1453-62. doi: 10.1093/hmg/7.9.1453. Hum Mol Genet. 1998. PMID: 9700201

3

Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings.

Perola M, Kainulainen K, Pajukanta P, Terwilliger JD, Hiekkalinna T, Ellonen P, Kaprio J, Koskenvuo M, Kontula K, Peltonen L. Perola M, et al. J Hypertens. 2000 Nov;18(11):1579-85. doi: 10.1097/00004872-200018110-00008. J Hypertens. 2000. PMID: 11081770

4

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.

5

The functional -374 T/A RAGE gene polymorphism is associated with proteinuria and cardiovascular disease in type 1 diabetic patients.

Pettersson-Fernholm K, Forsblom C, Hudson BI, Perola M, Grant PJ, Groop PH; Finn-Diane Study Group. Pettersson-Fernholm K, et al. Among authors: perola m. Diabetes. 2003 Mar;52(3):891-4. doi: 10.2337/diabetes.52.3.891. Diabetes. 2003. PMID: 12606536

6

Polymorphisms in the nephrin gene and diabetic nephropathy in type 1 diabetic patients.

Pettersson-Fernholm K, Forsblom C, Perola M, Groop PH; FinnDiane Study Group. Pettersson-Fernholm K, et al. Among authors: perola m. Kidney Int. 2003 Apr;63(4):1205-10. doi: 10.1046/j.1523-1755.2003.00855.x. Kidney Int. 2003. PMID: 12631336 Free article.

7

Dopamine D3 receptor gene polymorphisms, blood pressure and nephropathy in type 1 diabetic patients.

Pettersson-Fernholm KJ, Forsblom CM, Perola M, Fagerudd JA, Groop PH; FinnDiane Study Group. Pettersson-Fernholm KJ, et al. Among authors: perola m. Nephrol Dial Transplant. 2004 Jun;19(6):1432-6. doi: 10.1093/ndt/gfh174. Epub 2004 Mar 5. Nephrol Dial Transplant. 2004. PMID: 15004255

8

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

9

Linkage of nicotine dependence and smoking behavior on 10q, 7q and 11p in twins with homogeneous genetic background.

Loukola A, Broms U, Maunu H, Widén E, Heikkilä K, Siivola M, Salo A, Pergadia ML, Nyman E, Sammalisto S, Perola M, Agrawal A, Heath AC, Martin NG, Madden PA, Peltonen L, Kaprio J. Loukola A, et al. Among authors: perola m. Pharmacogenomics J. 2008 Jun;8(3):209-19. doi: 10.1038/sj.tpj.6500464. Epub 2007 Jun 5. Pharmacogenomics J. 2008. PMID: 17549066

10

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: perola m. 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

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