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Journal of the American Academy of Dermatology|December 7, 2024
A genome-wide association meta-analysis links hidradenitis suppurativa to common and rare sequence variants causing disruption of the Notch and Wnt/β-catenin signaling pathwaysRune Kjærsgaard Andersen, Lilja Stefansdottir, Peter Theut Riis, et al.Nature Genetics|June 20, 2017
Variants in the fetal genome near FLT1 are associated with risk of preeclampsiaRalph McGinnis, Valgerdur Steinthorsdottir, Nicholas O Williams, et al.European Heart Journal|October 25, 2022
Genetic insight into sick sinus syndromeRosa B Thorolfsdottir, Gardar Sveinbjornsson, Hildur M Aegisdottir, et al.Nature Communications|February 3, 2022
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathologyGyda Bjornsdottir, Lilja Stefansdottir, Gudmar Thorleifsson, et al.Nature Communications|August 5, 2024
Deciphering the genetics and mechanisms of predisposition to multiple myelomaMolly Went, Laura Duran-Lozano, Gisli H Halldorsson, et al.Medrxiv : the Preprint Server for Health Sciences|September 26, 2025
The genetic architecture of fibromyalgia across 2.5 million individualsIsabel Kerrebijn, Gyda Bjornsdottir, Keon Arbabi, et al.Hypertension (Dallas, Tex. : 1979)|July 9, 2026
Resistant Hypertension Variants Link to Hyperaldosteronism and Potassium LevelsVinicius Tragante, Patrick Sulem, Gudmar Thorleifsson, et al.Nature Communications|May 5, 2019
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fracturesUnnur Styrkarsdottir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, et al.Nature Communications|May 26, 2019
Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fracturesUnnur Styrkarsdottir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, et al.Nature Medicine|July 28, 2026
The genetic architecture of fibromyalgia across 2.5 million individualsIsabel Kerrebijn, Gyda Bjornsdottir, Keon Arbabi, et al.Pageof 6