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Communications Biology|September 6, 2022
HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2Thorunn A Olafsdottir, Kristbjorg Bjarnadottir, Gudmundur L Norddahl, et al.Communications Biology|September 28, 2021
Genetic variants associated with platelet count are predictive of human disease and physiological markersEvgenia Mikaelsdottir, Gudmar Thorleifsson, Lilja Stefansdottir, et al.Nature|October 4, 2023
Large-scale plasma proteomics comparisons through genetics and disease associationsGrimur Hjorleifsson Eldjarn, Egil Ferkingstad, Sigrun H Lund, et al.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 Communications|September 14, 2024
Sequence variants influencing the regulation of serum IgG subclass levelsThorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, et al.Communications Biology|July 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticariaRagnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir, et al.Cancer Research|February 19, 2021
Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer RiskThorhildur Olafsdottir, Simon N Stacey, Gardar Sveinbjornsson, 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.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.Pageof 4