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Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder.
Häkkinen K, Kiiski JI, Lähteenvuo M, Jukuri T, Suokas K, Niemi-Pynttäri J, Kieseppä T, Männynsalo T, Wegelius A, Haaki W, Lahdensuo K, Kajanne R, Kaunisto MA, Tuulio-Henriksson A, Kampman O, Hietala J, Veijola J, Lönnqvist J, Isometsä E, Paunio T, Suvisaari J, Kalso E, Niemi M, Tiihonen J, Daly M, Palotie A, Ahola-Olli AV. Häkkinen K, et al. Among authors: veijola j. Pharmacogenomics J. 2022 May;22(3):166-172. doi: 10.1038/s41397-022-00270-y. Epub 2022 Feb 23. Pharmacogenomics J. 2022. PMID: 35197553 Free PMC article.
Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort.
Nyman ES, Sulkava S, Soronen P, Miettunen J, Loukola A, Leppä V, Joukamaa M, Mäki P, Järvelin MR, Freimer N, Peltonen L, Veijola J, Paunio T. Nyman ES, et al. Among authors: veijola j. BMJ Open. 2011 Aug 27;1(1):e000087. doi: 10.1136/bmjopen-2011-000087. BMJ Open. 2011. PMID: 22021758 Free PMC article.
Default mode network in young people with familial risk for psychosis--the Oulu Brain and Mind study.
Jukuri T, Kiviniemi V, Nikkinen J, Miettunen J, Mäki P, Jääskeläinen E, Mukkala S, Koivukangas J, Nordström T, Taanila A, Moilanen I, Heinimaa M, Barnett JH, Jones PB, Murray GK, Veijola J. Jukuri T, et al. Among authors: veijola j. Schizophr Res. 2013 Feb;143(2-3):239-45. doi: 10.1016/j.schres.2012.11.020. Epub 2012 Dec 12. Schizophr Res. 2013. PMID: 23245776
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.
Gusev A, Lee SH, Trynka G, Finucane H, Vilhjálmsson BJ, Xu H, Zang C, Ripke S, Bulik-Sullivan B, Stahl E; Schizophrenia Working Group of the Psychiatric Genomics Consortium; SWE-SCZ Consortium; Kähler AK, Hultman CM, Purcell SM, McCarroll SA, Daly M, Pasaniuc B, Sullivan PF, Neale BM, Wray NR, Raychaudhuri S, Price AL; Schizophrenia Working Group of the Psychiatric Genomics Consortium; SWE-SCZ Consortium. Gusev A, et al. Am J Hum Genet. 2014 Nov 6;95(5):535-52. doi: 10.1016/j.ajhg.2014.10.004. Epub 2014 Nov 6. Am J Hum Genet. 2014. PMID: 25439723 Free PMC article.
Association between Dopamine Receptor D2 (DRD2) Variations rs6277 and rs1800497 and Cognitive Performance According to Risk Type for Psychosis: A Nested Case Control Study in a Finnish Population Sample.
Ramsay H, Barnett JH, Miettunen J, Mukkala S, Mäki P, Liuhanen J, Murray GK, Jarvelin MR, Ollila H, Paunio T, Veijola J. Ramsay H, et al. Among authors: veijola j. PLoS One. 2015 Jun 26;10(6):e0127602. doi: 10.1371/journal.pone.0127602. eCollection 2015. PLoS One. 2015. PMID: 26114663 Free PMC article.
272 results