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Items: 40

1.

Identification and analysis of mtDNA genomes attributed to Finns reveal long-stagnant demographic trends obscured in the total diversity.

Översti S, Onkamo P, Stoljarova M, Budowle B, Sajantila A, Palo JU.

Sci Rep. 2017 Jul 21;7(1):6193. doi: 10.1038/s41598-017-05673-7.

2.

Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia.

Lokki AI, Kaartokallio T, Holmberg V, Onkamo P, Koskinen LLE, Saavalainen P, Heinonen S, Kajantie E, Kere J, Kivinen K, Pouta A, Villa PM, Hiltunen L, Laivuori H, Meri S.

Front Immunol. 2017 May 29;8:589. doi: 10.3389/fimmu.2017.00589. eCollection 2017.

3.

Convergent evidence for the molecular basis of musical traits.

Oikkonen J, Onkamo P, Järvelä I, Kanduri C.

Sci Rep. 2016 Dec 22;6:39707. doi: 10.1038/srep39707.

4.

Creative Activities in Music--A Genome-Wide Linkage Analysis.

Oikkonen J, Kuusi T, Peltonen P, Raijas P, Ukkola-Vuoti L, Karma K, Onkamo P, Järvelä I.

PLoS One. 2016 Feb 24;11(2):e0148679. doi: 10.1371/journal.pone.0148679. eCollection 2016.

5.

The genetic variant rs4073 A→T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degeneration.

Hautamäki A, Seitsonen S, Holopainen JM, Moilanen JA, Kivioja J, Onkamo P, Järvelä I, Immonen I.

Acta Ophthalmol. 2015 Dec;93(8):726-33. doi: 10.1111/aos.12799. Epub 2015 Jul 8.

6.

Vestiges of an Ancient Border in the Contemporary Genetic Diversity of North-Eastern Europe.

Neuvonen AM, Putkonen M, Översti S, Sundell T, Onkamo P, Sajantila A, Palo JU.

PLoS One. 2015 Jul 1;10(7):e0130331. doi: 10.1371/journal.pone.0130331. eCollection 2015.

7.

Association and Promoter Analysis of AVPR1A in Finnish Autism Families.

Kantojärvi K, Oikkonen J, Kotala I, Kallela J, Vanhala R, Onkamo P, Järvelä I.

Autism Res. 2015 Oct;8(5):634-9. doi: 10.1002/aur.1473. Epub 2015 Feb 23.

PMID:
25707602
8.

Neolithic dairy farming at the extreme of agriculture in northern Europe.

Cramp LJ, Evershed RP, Lavento M, Halinen P, Mannermaa K, Oinonen M, Kettunen J, Perola M, Onkamo P, Heyd V.

Proc Biol Sci. 2014 Sep 22;281(1791):20140819. doi: 10.1098/rspb.2014.0819.

9.

A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions.

Oikkonen J, Huang Y, Onkamo P, Ukkola-Vuoti L, Raijas P, Karma K, Vieland VJ, Järvelä I.

Mol Psychiatry. 2015 Feb;20(2):275-82. doi: 10.1038/mp.2014.8. Epub 2014 Mar 11.

10.

Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration.

Hautamäki A, Kivioja J, Vavuli S, Kakko S, Savolainen ER, Savolainen MJ, Liinamaa MJ, Seitsonen S, Onkamo P, Järvelä I, Immonen I.

Retina. 2013 Oct;33(9):1815-27. doi: 10.1097/IAE.0b013e318285cf92.

PMID:
23584701
11.

Correlation between components of newly diagnosed exudative age-related macular degeneration lesion and focal retinal sensitivity.

Hautamäki A, Oikkonen J, Onkamo P, Immonen I.

Acta Ophthalmol. 2014 Feb;92(1):51-8. doi: 10.1111/j.1755-3768.2012.02556.x. Epub 2012 Sep 23.

12.

Mutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malaria.

Holmberg V, Onkamo P, Lahtela E, Lahermo P, Bedu-Addo G, Mockenhaupt FP, Meri S.

Malar J. 2012 Mar 2;11:61. doi: 10.1186/1475-2875-11-61.

13.

Genetic background and the risk of otitis media.

Hafrén L, Kentala E, Järvinen TM, Leinonen E, Onkamo P, Kere J, Mattila PS.

Int J Pediatr Otorhinolaryngol. 2012 Jan;76(1):41-4. doi: 10.1016/j.ijporl.2011.09.026. Epub 2011 Oct 21.

PMID:
22018929
14.

Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to music.

Ukkola-Vuoti L, Oikkonen J, Onkamo P, Karma K, Raijas P, Järvelä I.

J Hum Genet. 2011 Apr;56(4):324-9. doi: 10.1038/jhg.2011.13. Epub 2011 Feb 10.

PMID:
21307861
15.

SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.

Matsson H, Tammimies K, Zucchelli M, Anthoni H, Onkamo P, Nopola-Hemmi J, Lyytinen H, Leppanen PH, Neuhoff N, Warnke A, Schulte-Körne G, Schumacher J, Nöthen MM, Kere J, Peyrard-Janvid M.

Behav Genet. 2011 Jan;41(1):134-40. doi: 10.1007/s10519-010-9431-4. Epub 2011 Jan 4.

PMID:
21203819
16.

Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample.

Kantojärvi K, Onkamo P, Vanhala R, Alen R, Hedman M, Sajantila A, Nieminen-von Wendt T, Järvelä I.

Psychiatr Genet. 2010 Jun;20(3):102-8. doi: 10.1097/YPG.0b013e32833a2080.

PMID:
20410850
17.

Screening of DNA-variants in the properdin gene (CFP) in age-related macular degeneration (AMD).

Seitsonen S, Onkamo P, Torniainen S, Ihalainen M, Immonen I, Meri S, Järvelä I.

Mol Immunol. 2010 Mar;47(6):1334-6. doi: 10.1016/j.molimm.2010.01.001. Epub 2010 Jan 31.

PMID:
20122735
18.

[Identification of susceptibility genes for age-related macular degeneration--a success story of molecular genetics].

Seitsonen S, Onkamo P, Immonen I, Järvelä I.

Duodecim. 2009;125(21):2360-4. Finnish.

PMID:
19999660
19.

Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE).

Hellquist A, Zucchelli M, Lindgren CM, Saarialho-Kere U, Järvinen TM, Koskenmies S, Julkunen H, Onkamo P, Skoog T, Panelius J, Räisänen-Sokolowski A, Hasan T, Widen E, Gunnarson I, Svenungsson E, Padyukov L, Assadi G, Berglind L, Mäkelä VV, Kivinen K, Wong A, Cunningham Graham DS, Vyse TJ, D'Amato M, Kere J.

PLoS One. 2009 Dec 7;4(12):e8037. doi: 10.1371/journal.pone.0008037.

20.

Musical aptitude is associated with AVPR1A-haplotypes.

Ukkola LT, Onkamo P, Raijas P, Karma K, Järvelä I.

PLoS One. 2009 May 20;4(5):e5534. doi: 10.1371/journal.pone.0005534.

21.

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.

J Hum Genet. 2009 May;54(5):289-97. doi: 10.1038/jhg.2009.28. Epub 2009 Apr 3.

PMID:
19343041
22.

Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration.

Seitsonen SP, Onkamo P, Peng G, Xiong M, Tommila PV, Ranta PH, Holopainen JM, Moilanen JA, Palosaari T, Kaarniranta K, Meri S, Immonen IR, Järvelä IE.

PLoS One. 2008;3(12):e3833. doi: 10.1371/journal.pone.0003833. Epub 2008 Dec 2.

23.

Clinical and laboratory characteristics of Finnish lupus erythematosus patients with cutaneous manifestations.

Koskenmies S, Järvinen TM, Onkamo P, Panelius J, Tuovinen U, Hasan T, Ranki A, Saarialho-Kere U.

Lupus. 2008 Apr;17(4):337-47. doi: 10.1177/0961203307087403.

PMID:
18413417
24.

Clinical associations of the risk alleles of HLA-Cw6 and CCHCR1*WWCC in psoriasis.

Suomela S, Kainu K, Onkamo P, Tiala I, Himberg J, Koskinen L, Snellman E, Karvonen SL, Karvonen J, Uurasmaa T, Reunala T, Kivikäs K, Jansén CT, Holopainen P, Elomaa O, Kere J, Saarialho-Kere U.

Acta Derm Venereol. 2007;87(2):127-34.

25.

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.

Anthoni H, Zucchelli M, Matsson H, Müller-Myhsok B, Fransson I, Schumacher J, Massinen S, Onkamo P, Warnke A, Griesemann H, Hoffmann P, Nopola-Hemmi J, Lyytinen H, Schulte-Körne G, Kere J, Nöthen MM, Peyrard-Janvid M.

Hum Mol Genet. 2007 Mar 15;16(6):667-77. Epub 2007 Feb 19.

PMID:
17309879
26.

A survey of data mining methods for linkage disequilibrium mapping.

Onkamo P, Toivonen H.

Hum Genomics. 2006 Mar;2(5):336-40. Review.

27.

Genome scan on Swedish Alzheimer's disease families.

Sillén A, Forsell C, Lilius L, Axelman K, Björk BF, Onkamo P, Kere J, Winblad B, Graff C.

Mol Psychiatry. 2006 Feb;11(2):182-6.

PMID:
16288313
28.

An empirical comparison of case-control and trio based study designs in high throughput association mapping.

Hintsanen P, Sevon P, Onkamo P, Eronen L, Toivonen H.

J Med Genet. 2006 Jul;43(7):617-24. Epub 2005 Oct 28.

29.

Increasing incidence of Type 1 diabetes--role for genes?

Pitkäniemi J, Onkamo P, Tuomilehto J, Arjas E.

BMC Genet. 2004 Apr 2;5:5.

30.

Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus.

Koskenmies S, Widén E, Onkamo P, Sevón P, Julkunen H, Kere J.

Eur J Hum Genet. 2004 Jun;12(6):489-94.

31.

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.

Peyrard-Janvid M, Anthoni H, Onkamo P, Lahermo P, Zucchelli M, Kaminen N, Hannula-Jouppi K, Nopola-Hemmi J, Voutilainen A, Lyytinen H, Kere J.

Hum Genet. 2004 Apr;114(5):510-6. Epub 2004 Mar 6.

PMID:
15007729
32.

Association analysis for quantitative traits by data mining: QHPM.

Onkamo P, Ollikainen V, Sevon P, Toivonen HT, Mannila H, Kere J.

Ann Hum Genet. 2002 Nov;66(Pt 5-6):419-29.

33.

A novel low-penetrance locus for familial glioma at 15q23-q26.3.

Paunu N, Lahermo P, Onkamo P, Ollikainen V, Rantala I, Helén P, Simola KO, Kere J, Haapasalo H.

Cancer Res. 2002 Jul 1;62(13):3798-802.

34.

Bayesian association mapping for quantitative traits in a mixture of two populations.

Sillanpää MJ, Kilpikari R, Ripatti S, Onkamo P, Uimari P.

Genet Epidemiol. 2001;21 Suppl 1:S692-9.

PMID:
11793763
35.

Mining associations between genetic markers, phenotypes, and covariates.

Sevon P, Ollikainen V, Onkamo P, Toivonen HT, Mannila H, Kere J.

Genet Epidemiol. 2001;21 Suppl 1:S588-93.

PMID:
11793743
37.

Data mining applied to linkage disequilibrium mapping.

Toivonen HT, Onkamo P, Vasko K, Ollikainen V, Sevon P, Mannila H, Herr M, Kere J.

Am J Hum Genet. 2000 Jul;67(1):133-45. Epub 2000 Jun 9.

38.

Worldwide increase in incidence of Type I diabetes--the analysis of the data on published incidence trends.

Onkamo P, Väänänen S, Karvonen M, Tuomilehto J.

Diabetologia. 1999 Dec;42(12):1395-403. Erratum in: Diabetologia 2000 May;43(5):685.

PMID:
10651256
39.

A Bayesian Markov chain Monte Carlo approach to map disease genes in simulated GAW11 data.

Uimari P, Pitkäniemi J, Onkamo P.

Genet Epidemiol. 1999;17 Suppl 1:S743-8.

PMID:
10597524
40.

Neonatal anthropometric measurements and risk of childhood-onset type 1 diabetes. DiMe Study Group.

Podar T, Onkamo P, Forsen T, Karvonen M, Tuomilehto-Wolf E, Tuomilehto J.

Diabetes Care. 1999 Dec;22(12):2092-4. No abstract available.

PMID:
10587856

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