Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome.
Jaakko S TyrmiRiikka K ArffmanNatàlia Pujol-GualdoVenla KurraLaure Morin-PapunenEeva Sliznull nullAnnemieke HoekTriin LaiskJohannes KettunenFinnpec Hannele LaivuoriPublished in: Human reproduction (Oxford, England) (2021)
This work has received funding from the European Union's Horizon 2020 research and innovation programme under the MATER Marie Skłodowska-Curie grant agreement No. 813707 (N.P.-G., T.L., T.P.), the Estonian Research Council grant (PRG687, T.L.), the Academy of Finland grants 315921 (T.P.), 321763 (T.P.), 297338 (J.K.), 307247 (J.K.), 344695 (H.L.), Novo Nordisk Foundation grant NNF17OC0026062 (J.K.), the Sigrid Juselius Foundation project grants (T.L., J.K., T.P.), Finska Läkaresällskapet (H.L.) and Jane and Aatos Erkko Foundation (H.L.). The funders had no role in study design, data collection and analysis, publishing or preparation of the manuscript. The authors declare no conflicts of interest.