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Leisure-time physical activity is associated with the metabolic syndrome in type 1 diabetes: effect of the PPARgamma Pro12Ala polymorphism: the FinnDiane Study.
Wadén J, Thorn LM, Forsblom C, Lakka T, Saraheimo M, Rosengård-Bärlund M, Heikkilä O, Wessman M, Turunen JA, Parkkonen M, Tikkanen H, Groop PH; FinnDiane Study Group. Wadén J, et al. Among authors: turunen ja. Diabetes Care. 2007 Jun;30(6):1618-20. doi: 10.2337/dc06-2467. Epub 2007 Mar 10. Diabetes Care. 2007. PMID: 17351273 No abstract available.
Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample.
Soronen P, Silander K, Antila M, Palo OM, Tuulio-Henriksson A, Kieseppä T, Ellonen P, Wedenoja J, Turunen JA, Pietiläinen OP, Hennah W, Lönnqvist J, Peltonen L, Partonen T, Paunio T. Soronen P, et al. Among authors: turunen ja. Biol Psychiatry. 2008 Sep 1;64(5):438-42. doi: 10.1016/j.biopsych.2008.03.028. Epub 2008 May 7. Biol Psychiatry. 2008. PMID: 18466879 Free PMC article.
The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland.
Turunen JA, Peltonen JO, Pietiläinen OP, Hennah W, Loukola A, Paunio T, Silander K, Ekelund J, Varilo T, Partonen T, Lönnqvist J, Peltonen L. Turunen JA, et al. Schizophr Res. 2007 Mar;91(1-3):27-36. doi: 10.1016/j.schres.2006.11.028. Epub 2007 Feb 14. Schizophr Res. 2007. PMID: 17300918
Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins.
Pietiläinen OP, Paunio T, Loukola A, Tuulio-Henriksson A, Kieseppä T, Thompson P, Toga AW, van Erp TG, Silventoinen K, Soronen P, Hennah W, Turunen JA, Wedenoja J, Palo OM, Silander K, Lönnqvist J, Kaprio J, Cannon TD, Peltonen L. Pietiläinen OP, et al. Among authors: turunen ja. Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 5;150B(5):683-92. doi: 10.1002/ajmg.b.30890. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19051289 Free PMC article.
Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q.
Paunio T, Ekelund J, Varilo T, Parker A, Hovatta I, Turunen JA, Rinard K, Foti A, Terwilliger JD, Juvonen H, Suvisaari J, Arajärvi R, Suokas J, Partonen T, Lönnqvist J, Meyer J, Peltonen L. Paunio T, et al. Among authors: turunen ja. Hum Mol Genet. 2001 Dec 15;10(26):3037-48. doi: 10.1093/hmg/10.26.3037. Hum Mol Genet. 2001. PMID: 11751686
Analysis of four neuroligin genes as candidates for autism.
Ylisaukko-oja T, Rehnström K, Auranen M, Vanhala R, Alen R, Kempas E, Ellonen P, Turunen JA, Makkonen I, Riikonen R, Nieminen-von Wendt T, von Wendt L, Peltonen L, Järvelä I. Ylisaukko-oja T, et al. Among authors: turunen ja. Eur J Hum Genet. 2005 Dec;13(12):1285-92. doi: 10.1038/sj.ejhg.5201474. Eur J Hum Genet. 2005. PMID: 16077734
71 results