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A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use-The P5 Study.
Marjonen H, Marttila M, Paajanen T, Vornanen M, Brunfeldt M, Joensuu A, Halmesvaara O, Aro K, Alanne-Kinnunen M, Jousilahti P, Borodulin K, Koskinen S, Tuomi T, Ilanne-Parikka P, Lindström J, Laine MK, Auro K, Kääriäinen H, Perola M, Kristiansson K. Marjonen H, et al. Front Genet. 2021 Oct 29;12:763159. doi: 10.3389/fgene.2021.763159. eCollection 2021. Front Genet. 2021. PMID: 34777479 Free PMC article. Review.
Economic evaluation of using polygenic risk score to guide risk screening and interventions for the prevention of type 2 diabetes in individuals with high overall baseline risk.
Martikainen J, Lehtimäki AV, Jalkanen K, Lavikainen P, Paajanen T, Marjonen H, Kristiansson K, Lindström J, Perola M. Martikainen J, et al. Among authors: marjonen h. Front Genet. 2022 Sep 15;13:880799. doi: 10.3389/fgene.2022.880799. eCollection 2022. Front Genet. 2022. PMID: 36186460 Free PMC article.
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration.
Rämö JT, Abner E, van Dijk EHC, Wang X, Brinks J, Nikopensius T, Nõukas M, Marjonen H, Silander K, Jukarainen S, Kiiskinen T, Choi SH, Kajanne R, Mehtonen J, Palta P, Lubitz SA, Kaarniranta K, Sobrin L, Kurki M, Yzer S, Ellinor PT, Esko T, Daly MJ, den Hollander AI, Palotie A, Turunen JA, Boon CJF, Rossin EJ; FinnGen Study; Estonian Biobank Research Team. Rämö JT, et al. Among authors: marjonen h. JAMA Ophthalmol. 2023 May 1;141(5):449-457. doi: 10.1001/jamaophthalmol.2023.0706. JAMA Ophthalmol. 2023. PMID: 37079300 Free PMC article.
rs10732516 polymorphism at the IGF2/H19 locus associates with genotype-specific effects on placental DNA methylation and birth weight of newborns conceived by assisted reproductive technology.
Marjonen H, Auvinen P, Kahila H, Tšuiko O, Kõks S, Tiirats A, Viltrop T, Tuuri T, Söderström-Anttila V, Suikkari AM, Salumets A, Tiitinen A, Kaminen-Ahola N. Marjonen H, et al. Clin Epigenetics. 2018 Jun 18;10:80. doi: 10.1186/s13148-018-0511-2. eCollection 2018. Clin Epigenetics. 2018. PMID: 29946374 Free PMC article.
In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages.
Zamani Esteki M, Viltrop T, Tšuiko O, Tiirats A, Koel M, Nõukas M, Žilina O, Teearu K, Marjonen H, Kahila H, Meekels J, Söderström-Anttila V, Suikkari AM, Tiitinen A, Mägi R, Kõks S, Kaminen-Ahola N, Kurg A, Voet T, Vermeesch JR, Salumets A. Zamani Esteki M, et al. Among authors: marjonen h. Nat Med. 2019 Nov;25(11):1699-1705. doi: 10.1038/s41591-019-0620-2. Epub 2019 Nov 4. Nat Med. 2019. PMID: 31686035
Chromatin modifier developmental pluripotency associated factor 4 (DPPA4) is a candidate gene for alcohol-induced developmental disorders.
Auvinen P, Vehviläinen J, Marjonen H, Modhukur V, Sokka J, Wallén E, Rämö K, Ahola L, Salumets A, Otonkoski T, Skottman H, Ollikainen M, Trokovic R, Kahila H, Kaminen-Ahola N. Auvinen P, et al. Among authors: marjonen h. BMC Med. 2022 Dec 30;20(1):495. doi: 10.1186/s12916-022-02699-1. BMC Med. 2022. PMID: 36581877 Free PMC article.