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Page 1
Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.
Komulainen K, Alanne M, Auro K, Kilpikari R, Pajukanta P, Saarela J, Ellonen P, Salminen K, Kulathinal S, Kuulasmaa K, Silander K, Salomaa V, Perola M, Peltonen L. Komulainen K, et al. Among authors: ellonen p. PLoS Genet. 2006 May;2(5):e69. doi: 10.1371/journal.pgen.0020069. Epub 2006 May 12. PLoS Genet. 2006. PMID: 16699592 Free PMC article.
A quality assessment survey of SNP genotyping laboratories.
Lahermo P, Liljedahl U, Alnaes G, Axelsson T, Brookes AJ, Ellonen P, Groop PH, Halldén C, Holmberg D, Holmberg K, Keinänen M, Kepp K, Kere J, Kiviluoma P, Kristensen V, Lindgren C, Odeberg J, Osterman P, Parkkonen M, Saarela J, Sterner M, Strömqvist L, Talas U, Wessman M, Palotie A, Syvänen AC. Lahermo P, et al. Among authors: ellonen p. Hum Mutat. 2006 Jul;27(7):711-4. doi: 10.1002/humu.20346. Hum Mutat. 2006. PMID: 16786507
Gender differences in genetic risk profiles for cardiovascular disease.
Silander K, Alanne M, Kristiansson K, Saarela O, Ripatti S, Auro K, Karvanen J, Kulathinal S, Niemelä M, Ellonen P, Vartiainen E, Jousilahti P, Saarela J, Kuulasmaa K, Evans A, Perola M, Salomaa V, Peltonen L. Silander K, et al. Among authors: ellonen p. PLoS One. 2008;3(10):e3615. doi: 10.1371/journal.pone.0003615. Epub 2008 Oct 31. PLoS One. 2008. PMID: 18974842 Free PMC article.
Allelic variants in HTR3C show association with autism.
Rehnström K, Ylisaukko-oja T, Nummela I, Ellonen P, Kempas E, Vanhala R, von Wendt L, Järvelä I, Peltonen L. Rehnström K, et al. Among authors: ellonen p. Am J Med Genet B Neuropsychiatr Genet. 2009 Jul 5;150B(5):741-6. doi: 10.1002/ajmg.b.30882. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19035560 Free PMC article.
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: ellonen p. 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.
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: ellonen p. Eur J Hum Genet. 2005 Dec;13(12):1285-92. doi: 10.1038/sj.ejhg.5201474. Eur J Hum Genet. 2005. PMID: 16077734
No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.
Sulonen AM, Kallio SP, Ellonen P, Suvela M, Elovaara I, Koivisto K, Pirttilä T, Reunanen M, Tienari PJ, Palotie A, Peltonen L, Saarela J. Sulonen AM, et al. Among authors: ellonen p. J Neuroimmunol. 2009 Jan 3;206(1-2):86-90. doi: 10.1016/j.jneuroim.2008.10.005. Epub 2008 Nov 18. J Neuroimmunol. 2009. PMID: 19019460 Free PMC article.
Comparison of solution-based exome capture methods for next generation sequencing.
Sulonen AM, Ellonen P, Almusa H, Lepistö M, Eldfors S, Hannula S, Miettinen T, Tyynismaa H, Salo P, Heckman C, Joensuu H, Raivio T, Suomalainen A, Saarela J. Sulonen AM, et al. Among authors: ellonen p. Genome Biol. 2011 Sep 28;12(9):R94. doi: 10.1186/gb-2011-12-9-r94. Genome Biol. 2011. PMID: 21955854 Free PMC article.
77 results