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Page 1
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. Lokki AI, et al. Among authors: onkamo p. Front Immunol. 2017 May 29;8:589. doi: 10.3389/fimmu.2017.00589. eCollection 2017. Front Immunol. 2017. PMID: 28611769 Free PMC article.
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. Hellquist A, et al. Among authors: onkamo p. PLoS One. 2009 Dec 7;4(12):e8037. doi: 10.1371/journal.pone.0008037. PLoS One. 2009. PMID: 19997561 Free PMC article.
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. Lemmelä S, et al. Among authors: onkamo p. J Hum Genet. 2009 May;54(5):289-97. doi: 10.1038/jhg.2009.28. Epub 2009 Apr 3. J Hum Genet. 2009. PMID: 19343041
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. Anthoni H, et al. Among authors: onkamo p. Hum Mol Genet. 2007 Mar 15;16(6):667-77. doi: 10.1093/hmg/ddm009. Epub 2007 Feb 19. Hum Mol Genet. 2007. PMID: 17309879
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. Suomela S, et al. Among authors: onkamo p. Acta Derm Venereol. 2007;87(2):127-34. doi: 10.2340/00015555-0184. Acta Derm Venereol. 2007. PMID: 17340018 Free article.
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. Matsson H, et al. Among authors: onkamo p. Behav Genet. 2011 Jan;41(1):134-40. doi: 10.1007/s10519-010-9431-4. Epub 2011 Jan 4. Behav Genet. 2011. PMID: 21203819
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. Seitsonen SP, et al. Among authors: onkamo p. PLoS One. 2008;3(12):e3833. doi: 10.1371/journal.pone.0003833. Epub 2008 Dec 2. PLoS One. 2008. PMID: 19048105 Free PMC article.
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