Mannila H - Search Results

1

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci.

Hovatta I, Varilo T, Suvisaari J, Terwilliger JD, Ollikainen V, Arajärvi R, Juvonen H, Kokko-Sahin ML, Väisänen L, Mannila H, Lönnqvist J, Peltonen L. Hovatta I, et al. Among authors: mannila h. Am J Hum Genet. 1999 Oct;65(4):1114-24. doi: 10.1086/302567. Am J Hum Genet. 1999. PMID: 10486331 Free PMC article.

2

Minimum description length block finder, a method to identify haplotype blocks and to compare the strength of block boundaries.

Mannila H, Koivisto M, Perola M, Varilo T, Hennah W, Ekelund J, Lukk M, Peltonen L, Ukkonen E. Mannila H, et al. Am J Hum Genet. 2003 Jul;73(1):86-94. doi: 10.1086/376438. Epub 2003 May 20. Am J Hum Genet. 2003. Retraction in: Am J Hum Genet. 2003 Aug;73(2):444. doi: 10.1086/378685 PMID: 12761696 Free PMC article. Retracted.

3

Data mining applied to linkage disequilibrium mapping.

Toivonen HT, Onkamo P, Vasko K, Ollikainen V, Sevon P, Mannila H, Herr M, Kere J. Toivonen HT, et al. Among authors: mannila h. Am J Hum Genet. 2000 Jul;67(1):133-45. doi: 10.1086/302954. Epub 2000 Jun 9. Am J Hum Genet. 2000. PMID: 10848493 Free PMC article.

4

The IL9R region contribution in asthma is supported by genetic association in an isolated population.

Kauppi P, Laitinen T, Ollikainen V, Mannila H, Laitinen LA, Kere J. Kauppi P, et al. Among authors: mannila h. Eur J Hum Genet. 2000 Oct;8(10):788-92. doi: 10.1038/sj.ejhg.5200541. Eur J Hum Genet. 2000. PMID: 11039580

5

Association study of the chromosomal region containing the FCER2 gene suggests it has a regulatory role in atopic disorders.

Laitinen T, Ollikainen V, Lázaro C, Kauppi P, de Cid R, Antó JM, Estivill X, Lokki H, Mannila H, Laitinen LA, Kere J. Laitinen T, et al. Among authors: mannila h. Am J Respir Crit Care Med. 2000 Mar;161(3 Pt 1):700-6. doi: 10.1164/ajrccm.161.3.9810056. Am J Respir Crit Care Med. 2000. PMID: 10712310

6

Mining associations between genetic markers, phenotypes, and covariates.

Sevon P, Ollikainen V, Onkamo P, Toivonen HT, Mannila H, Kere J. Sevon P, et al. Among authors: mannila h. Genet Epidemiol. 2001;21 Suppl 1:S588-93. doi: 10.1002/gepi.2001.21.s1.s588. Genet Epidemiol. 2001. PMID: 11793743

7

An MDL method for finding haplotype blocks and for estimating the strength of haplotype block boundaries.

Koivisto M, Perola M, Varilo T, Hennah W, Ekelund J, Lukk M, Peltonen L, Ukkonen E, Mannila H. Koivisto M, et al. Among authors: mannila h. Pac Symp Biocomput. 2003:502-13. doi: 10.1142/9789812776303_0047. Pac Symp Biocomput. 2003. PMID: 12603053 Free article.

8

Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia.

Wessman J, Paunio T, Tuulio-Henriksson A, Koivisto M, Partonen T, Suvisaari J, Turunen JA, Wedenoja J, Hennah W, Pietiläinen OP, Lönnqvist J, Mannila H, Peltonen L. Wessman J, et al. Among authors: mannila h. Biol Psychiatry. 2009 Dec 1;66(11):990-6. doi: 10.1016/j.biopsych.2009.05.034. Epub 2009 Sep 27. Biol Psychiatry. 2009. PMID: 19782967

9

Association analysis for quantitative traits by data mining: QHPM.

Onkamo P, Ollikainen V, Sevon P, Toivonen HT, Mannila H, Kere J. Onkamo P, et al. Among authors: mannila h. Ann Hum Genet. 2002 Nov;66(Pt 5-6):419-29. doi: 10.1017/S0003480002001318. Ann Hum Genet. 2002. PMID: 12485474

10

Evaluation of HapMap data in six populations of European descent.

Lundmark PE, Liljedahl U, Boomsma DI, Mannila H, Martin NG, Palotie A, Peltonen L, Perola M, Spector TD, Syvänen AC. Lundmark PE, et al. Among authors: mannila h. Eur J Hum Genet. 2008 Sep;16(9):1142-50. doi: 10.1038/ejhg.2008.77. Epub 2008 Apr 9. Eur J Hum Genet. 2008. PMID: 18398430 Free article.

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