Perola M - Search Results

1

Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.

Saarentaus EC, Havulinna AS, Mars N, Ahola-Olli A, Kiiskinen TTJ, Partanen J, Ruotsalainen S, Kurki M, Urpa LM, Chen L, Perola M, Salomaa V, Veijola J, Männikkö M, Hall IM, Pietiläinen O, Kaprio J, Ripatti S, Daly M, Palotie A. Saarentaus EC, et al. Among authors: perola m. Mol Psychiatry. 2021 Sep;26(9):4884-4895. doi: 10.1038/s41380-021-01026-z. Epub 2021 Feb 1. Mol Psychiatry. 2021. PMID: 33526825 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

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: perola m. Hypertension. 1999 Mar;33(3):844-9. doi: 10.1161/01.hyp.33.3.844. Hypertension. 1999. PMID: 10082497

4

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

5

Heritability and risk factors of uterine fibroids--the Finnish Twin Cohort study.

Luoto R, Kaprio J, Rutanen EM, Taipale P, Perola M, Koskenvuo M. Luoto R, et al. Among authors: perola m. Maturitas. 2000 Nov 30;37(1):15-26. doi: 10.1016/s0378-5122(00)00160-2. Maturitas. 2000. PMID: 11099869

6

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.

7

Bipolar disorder susceptibility region on Xq24-q27.1 in Finnish families.

Ekholm JM, Pekkarinen P, Pajukanta P, Kieseppä T, Partonen T, Paunio T, Varilo T, Perola M, Lönnqvist J, Peltonen L. Ekholm JM, et al. Among authors: perola m. Mol Psychiatry. 2002;7(5):453-9. doi: 10.1038/sj.mp.4001104. Mol Psychiatry. 2002. PMID: 12082562

8

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

9

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

10

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.

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