Laivuori H - Search Results

1

Association of LOXL1 gene with Finnish exfoliation syndrome patients.

Lemmelä S, Forsman E, Onkamo P, Nurmi H, Laivuori H, Kivelä T, Puska P, Heger M, Eriksson A, Forsius H, Järvelä I. Lemmelä S, et al. Among authors: laivuori h. J Hum Genet. 2009 May;54(5):289-97. doi: 10.1038/jhg.2009.28. Epub 2009 Apr 3. J Hum Genet. 2009. PMID: 19343041

2

Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families.

Laivuori H, Lahermo P, Ollikainen V, Widen E, Häivä-Mällinen L, Sundström H, Laitinen T, Kaaja R, Ylikorkala O, Kere J. Laivuori H, et al. Am J Hum Genet. 2003 Jan;72(1):168-77. doi: 10.1086/345311. Epub 2002 Dec 9. Am J Hum Genet. 2003. PMID: 12474145 Free PMC article.

3

Non-synonymous sequence variants within the oxygen-dependent degradation domain of the HIF1A gene are not associated with pre-eclampsia in the Finnish population.

Heino S, Kaare M, Andersson S, Laivuori H. Heino S, et al. Among authors: laivuori h. BMC Med Genet. 2008 Nov 3;9:96. doi: 10.1186/1471-2350-9-96. BMC Med Genet. 2008. PMID: 18980686 Free PMC article.

4

Complement factor H variant Y402H is not a risk factor for preeclampsia in the Finnish population.

Kaare M, Seitsonen S, Jarvela I, Meri S, Laivuori H. Kaare M, et al. Among authors: laivuori h. Hypertens Pregnancy. 2008;27(4):328-36. doi: 10.1080/10641950801955691. Hypertens Pregnancy. 2008. PMID: 19003634

5

A follow-up linkage study of Finnish pre-eclampsia families identifies a new fetal susceptibility locus on chromosome 18.

Majander KK, Villa PM, Kivinen K, Kere J, Laivuori H. Majander KK, et al. Among authors: laivuori h. Eur J Hum Genet. 2013 Sep;21(9):1024-6. doi: 10.1038/ejhg.2013.6. Epub 2013 Feb 6. Eur J Hum Genet. 2013. PMID: 23386034 Free PMC article.

6

An RGS2 3'UTR polymorphism is associated with preeclampsia in overweight women.

Karppanen T, Kaartokallio T, Klemetti MM, Heinonen S, Kajantie E, Kere J, Kivinen K, Pouta A, Staff AC, Laivuori H. Karppanen T, et al. Among authors: laivuori h. BMC Genet. 2016 Aug 24;17(1):121. doi: 10.1186/s12863-016-0428-8. BMC Genet. 2016. PMID: 27558088 Free PMC article.

7

SIRT6 polymorphism rs117385980 is associated with longevity and healthy aging in Finnish men.

Hirvonen K, Laivuori H, Lahti J, Strandberg T, Eriksson JG, Hackman P. Hirvonen K, et al. Among authors: laivuori h. BMC Med Genet. 2017 Apr 11;18(1):41. doi: 10.1186/s12881-017-0401-z. BMC Med Genet. 2017. PMID: 28399814 Free PMC article.

8

Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.

Lokki AI, Kaartokallio T, Holmberg V, Onkamo P, Koskinen LLE, Saavalainen P, Heinonen S, Kajantie E, Kere J, Kivinen K, Pouta A, Villa PM, Hiltunen L, Laivuori H, Meri S. Lokki AI, et al. Among authors: laivuori h. Front Immunol. 2017 May 29;8:589. doi: 10.3389/fimmu.2017.00589. eCollection 2017. Front Immunol. 2017. PMID: 28611769 Free PMC article.

9

Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers.

Mars N, Koskela JT, Ripatti P, Kiiskinen TTJ, Havulinna AS, Lindbohm JV, Ahola-Olli A, Kurki M, Karjalainen J, Palta P; FinnGen; Neale BM, Daly M, Salomaa V, Palotie A, Widén E, Ripatti S. Mars N, et al. Nat Med. 2020 Apr;26(4):549-557. doi: 10.1038/s41591-020-0800-0. Epub 2020 Apr 7. Nat Med. 2020. PMID: 32273609

10

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease.

Ruotsalainen SE, Partanen JJ, Cichonska A, Lin J, Benner C, Surakka I; FinnGen; Reeve MP, Palta P, Salmi M, Jalkanen S, Ahola-Olli A, Palotie A, Salomaa V, Daly MJ, Pirinen M, Ripatti S, Koskela J. Ruotsalainen SE, et al. Eur J Hum Genet. 2021 Feb;29(2):309-324. doi: 10.1038/s41431-020-00730-8. Epub 2020 Oct 27. Eur J Hum Genet. 2021. PMID: 33110245 Free PMC article.

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