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Scientific Reports|October 18, 2023
GeneToCN: an alignment-free method for gene copy number estimation directly from next-generation sequencing readsFanny-Dhelia Pajuste, Maido RemmMobile DNA|July 31, 2019
AluMine: alignment-free method for the discovery of polymorphic Alu element insertionsTarmo Puurand, Viktoria Kukuškina, Fanny-Dhelia Pajuste, et al.Human Mutation|March 14, 2021
KATK: Fast genotyping of rare variants directly from unmapped sequencing readsLauris Kaplinski, Märt Möls, Tarmo Puurand, et al.Scientific Reports|June 2, 2017
FastGT: an alignment-free method for calling common SNVs directly from raw sequencing readsFanny-Dhelia Pajuste, Lauris Kaplinski, Märt Möls, et al.Nature Communications|July 25, 2024
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure eventsHenrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner, et al.Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure eventsHenrike O Heyne, Fanny-Dhelia Pajuste, Julian Wanner, et al.Nature|August 6, 2025
Parent-of-origin effects on complex traits in up to 236,781 individualsRobin J Hofmeister, Théo Cavinato, Roya Karimi, et al.Nature Medicine|March 12, 2025
Atlas of genetic and phenotypic associations across 42 female reproductive health diagnosesNatàlia Pujol Gualdo, Jelisaveta Džigurski, Valentina Rukins, et al.Nature Genetics|October 1, 2025
Limited overlap between genetic effects on disease susceptibility and disease survivalZhiyu Yang, Fanny-Dhelia Pajuste, Kristina Zguro, et al.Nature|June 12, 2024
Genetic drivers and cellular selection of female mosaic X chromosome lossAoxing Liu, Giulio Genovese, Yajie Zhao, et al.Pageof 2