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Chromosome 1 loci in Finnish schizophrenia families.
Ekelund J, Hovatta I, Parker A, Paunio T, Varilo T, Martin R, Suhonen J, Ellonen P, Chan G, Sinsheimer JS, Sobel E, Juvonen H, Arajärvi R, Partonen T, Suvisaari J, Lönnqvist J, Meyer J, Peltonen L. Ekelund J, et al. Among authors: ellonen p. Hum Mol Genet. 2001 Jul 15;10(15):1611-7. doi: 10.1093/hmg/10.15.1611. Hum Mol Genet. 2001. PMID: 11468279
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
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.
Genetic Control of Myelin Plasticity after Chronic Psychosocial Stress.
Laine MA, Trontti K, Misiewicz Z, Sokolowska E, Kulesskaya N, Heikkinen A, Saarnio S, Balcells I, Ameslon P, Greco D, Mattila P, Ellonen P, Paulin L, Auvinen P, Jokitalo E, Hovatta I. Laine MA, et al. Among authors: ellonen p. eNeuro. 2018 Jul 11;5(4):ENEURO.0166-18.2018. doi: 10.1523/ENEURO.0166-18.2018. eCollection 2018 Jul-Aug. eNeuro. 2018. PMID: 30073192 Free PMC article.
NCOR2 is a novel candidate gene for migraine-epilepsy phenotype.
Nuottamo ME, Häppölä P, Artto V, Hautakangas H, Pirinen M, Hiekkalinna T, Ellonen P, Lepistö M, Hämäläinen E; International Headache Genetics Consortium (IHGC), FinnGenConsortium; Siren A, Lehesjoki AE, Kallela M, Palotie A, Kaunisto MA, Wessman M. Nuottamo ME, et al. Among authors: ellonen p. Cephalalgia. 2022 Jun;42(7):631-644. doi: 10.1177/03331024211068065. Epub 2022 Feb 15. Cephalalgia. 2022. PMID: 35166138
Discovery of mitochondrial DNA variants associated with genome-wide blood cell gene expression: a population-based mtDNA sequencing study.
Laaksonen J, Seppälä I, Raitoharju E, Mononen N, Lyytikäinen LP, Waldenberger M, Illig T, Lepistö M, Almusa H, Ellonen P, Hutri-Kähönen N, Juonala M, Kähönen M, Raitakari O, Salonen JT, Lehtimäki T. Laaksonen J, et al. Among authors: ellonen p. Hum Mol Genet. 2019 Apr 15;28(8):1381-1391. doi: 10.1093/hmg/ddz011. Hum Mol Genet. 2019. PMID: 30629177 Free article.
77 results