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The Finnish genetic heritage in 2022 - from diagnosis to translational research.
Uusimaa J, Kettunen J, Varilo T, Järvelä I, Kallijärvi J, Kääriäinen H, Laine M, Lapatto R, Myllynen P, Niinikoski H, Rahikkala E, Suomalainen A, Tikkanen R, Tyynismaa H, Vieira P, Zarybnicky T, Sipilä P, Kuure S, Hinttala R. Uusimaa J, et al. Among authors: kaariainen h. Dis Model Mech. 2022 Oct 1;15(10):dmm049490. doi: 10.1242/dmm.049490. Epub 2022 Oct 26. Dis Model Mech. 2022. PMID: 36285626 Free PMC article. Review.
Infertility following trisomic pregnancies: A nationwide cohort study.
Wedenoja S, Pihlajamäki M, Gissler M, Wedenoja J, Öhman H, Heinonen S, Kere J, Kääriäinen H, Tanner L. Wedenoja S, et al. Among authors: kaariainen h. Int J Gynaecol Obstet. 2025 Jan;168(1):326-332. doi: 10.1002/ijgo.15828. Epub 2024 Jul 26. Int J Gynaecol Obstet. 2025. PMID: 39056516 Free PMC article.
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. Among authors: kaariainen h. Front Genet. 2021 Oct 29;12:763159. doi: 10.3389/fgene.2021.763159. eCollection 2021. Front Genet. 2021. PMID: 34777479 Free PMC article. Review.
Rare diseases: past achievements and future prospects.
Tumiene B, Kristoffersson U, Hedley V, Kääriäinen H. Tumiene B, et al. Among authors: kaariainen h. J Community Genet. 2021 Apr;12(2):205-206. doi: 10.1007/s12687-021-00529-0. J Community Genet. 2021. PMID: 33945116 Free PMC article. No abstract available.
The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.
Black GC, Sergouniotis P, Sodi A, Leroy BP, Van Cauwenbergh C, Liskova P, Grønskov K, Klett A, Kohl S, Taurina G, Sukys M, Haer-Wigman L, Nowomiejska K, Marques JP, Leroux D, Cremers FPM, De Baere E, Dollfus H; ERN-EYE study group. Black GC, et al. Orphanet J Rare Dis. 2021 Mar 20;16(1):142. doi: 10.1186/s13023-021-01756-x. Orphanet J Rare Dis. 2021. PMID: 33743793 Free PMC article.
168 results