Laivuori H - Search Results

1

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.

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

Heterogeneity-based genome search meta-analysis for preeclampsia.

Zintzaras E, Kitsios G, Harrison GA, Laivuori H, Kivinen K, Kere J, Messinis I, Stefanidis I, Ioannidis JP. Zintzaras E, et al. Among authors: laivuori h. Hum Genet. 2006 Oct;120(3):360-70. doi: 10.1007/s00439-006-0214-1. Epub 2006 Jul 26. Hum Genet. 2006. PMID: 16868762

4

Genetic aspects of preeclampsia.

Laivuori H. Laivuori H. Front Biosci. 2007 Jan 1;12:2372-82. doi: 10.2741/2239. Front Biosci. 2007. PMID: 17127247 Review.

5

Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample.

Kivinen K, Peterson H, Hiltunen L, Laivuori H, Heino S, Tiala I, Knuutila S, Rasi V, Kere J. Kivinen K, et al. Among authors: laivuori h. Eur J Hum Genet. 2007 Apr;15(4):494-7. doi: 10.1038/sj.ejhg.5201788. Epub 2007 Feb 7. Eur J Hum Genet. 2007. PMID: 17290274

6

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.

7

Blood group AB and factor V Leiden as risk factors for pre-eclampsia: a population-based nested case-control study.

Hiltunen LM, Laivuori H, Rautanen A, Kaaja R, Kere J, Krusius T, Paunio M, Rasi V. Hiltunen LM, et al. Among authors: laivuori h. Thromb Res. 2009 Jun;124(2):167-73. doi: 10.1016/j.thromres.2008.11.012. Epub 2008 Dec 24. Thromb Res. 2009. PMID: 19110300

8

Does the Y chromosome have a role in Müllerian aplasia?

Sandbacka M, Painter J, Puhakka M, Halttunen M, Laivuori H, Aittomäki K. Sandbacka M, et al. Among authors: laivuori h. Fertil Steril. 2010 Jun;94(1):120-5. doi: 10.1016/j.fertnstert.2009.02.004. Epub 2009 Mar 26. Fertil Steril. 2010. PMID: 19324347 Free article.

9

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

10

ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population.

Peterson H, Laivuori H, Kerkelä E, Jiao H, Hiltunen L, Heino S, Tiala I, Knuutila S, Rasi V, Kere J, Kivinen K. Peterson H, et al. Among authors: laivuori h. Mol Hum Reprod. 2009 Jul;15(7):443-9. doi: 10.1093/molehr/gap032. Epub 2009 May 12. Mol Hum Reprod. 2009. PMID: 19435756

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