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Communications Biology|October 2, 2018
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.Nature Genetics|December 3, 2021
Large-scale integration of the plasma proteome with genetics and diseaseEgil Ferkingstad, Patrick Sulem, Bjarni A Atlason, et al.Nature Genetics|August 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiencyAsmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson, et al.The New England Journal of Medicine|November 8, 2023
Actionable Genotypes and Their Association with Life Span in IcelandBrynjar O Jensson, Gudny A Arnadottir, Hildigunnur Katrinardottir, et al.Nature Communications|February 15, 2017
A genome-wide association study yields five novel thyroid cancer risk lociJulius Gudmundsson, Gudmar Thorleifsson, Jon K Sigurdsson, et al.Nature Genetics|January 16, 2019
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitisRagnar P Kristjansson, Stefania Benonisdottir, Olafur B Davidsson, et al.Nature Communications|July 9, 2024
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, et al.JAMA Cardiology|September 4, 2024
Genome-Wide Association Study of Accessory Atrioventricular PathwaysHildur M Aegisdottir, Laura Andreasen, Rosa B Thorolfsdottir, et al.Nature|June 26, 2020
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid diseaseSaedis Saevarsdottir, Thorunn A Olafsdottir, Erna V Ivarsdottir, et al.European Heart Journal|October 25, 2022
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.Pageof 25