Laivuori H - Search Results

1

Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia.

Sandbacka M, Bruce S, Halttunen M, Puhakka M, Lahermo P, Hannula-Jouppi K, Lipsanen-Nyman M, Kere J, Aittomäki K, Laivuori H. Sandbacka M, et al. Among authors: laivuori h. Fertil Steril. 2011 Jun 30;95(8):2703-6. doi: 10.1016/j.fertnstert.2011.03.019. Epub 2011 Apr 2. Fertil Steril. 2011. PMID: 21458801 Free 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

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

4

Large genomic rearrangements and germline epimutations in Lynch syndrome.

Gylling A, Ridanpää M, Vierimaa O, Aittomäki K, Avela K, Kääriäinen H, Laivuori H, Pöyhönen M, Sallinen SL, Wallgren-Pettersson C, Järvinen HJ, Mecklin JP, Peltomäki P. Gylling A, et al. Among authors: laivuori h. Int J Cancer. 2009 May 15;124(10):2333-40. doi: 10.1002/ijc.24230. Int J Cancer. 2009. PMID: 19173287

5

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.

6

Factor V Leiden as risk factor for unexplained stillbirth--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. 2010 Jun;125(6):505-10. doi: 10.1016/j.thromres.2009.09.016. Epub 2009 Oct 13. Thromb Res. 2010. PMID: 19828176

7

Factor V Leiden as a risk factor for preterm birth--a population-based nested case-control study.

Hiltunen LM, Laivuori H, Rautanen A, Kaaja R, Kere J, Krusius T, Rasi V, Paunio M. Hiltunen LM, et al. Among authors: laivuori h. J Thromb Haemost. 2011 Jan;9(1):71-8. doi: 10.1111/j.1538-7836.2010.04104.x. J Thromb Haemost. 2011. PMID: 20946152 Free article.

8

Evaluation of SHOX copy number variations in patients with Müllerian aplasia.

Sandbacka M, Halttunen M, Jokimaa V, Aittomäki K, Laivuori H. Sandbacka M, et al. Among authors: laivuori h. Orphanet J Rare Dis. 2011 Aug 2;6:53. doi: 10.1186/1750-1172-6-53. Orphanet J Rare Dis. 2011. PMID: 21806840 Free PMC article.

9

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.

10

TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia.

Sandbacka M, Laivuori H, Freitas É, Halttunen M, Jokimaa V, Morin-Papunen L, Rosenberg C, Aittomäki K. Sandbacka M, et al. Among authors: laivuori h. Orphanet J Rare Dis. 2013 Aug 16;8:125. doi: 10.1186/1750-1172-8-125. Orphanet J Rare Dis. 2013. PMID: 23954021 Free PMC article.

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