Gardar Sveinbjornsson
33PUBLICATIONS
457CO-AUTHORS
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Publications (33)
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|Feb 16, 2026
A frameshift variant in PKP2 can be associated with a complex phenotype in sudden cardiac death: a case report.Gustav A Davidsson, Gudny A Arnadottir, Gardar Sveinbjornsson
|Mar 26, 2025
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder.Thorgeir E Thorgeirsson, Vinicius Tragante, Gardar Sveinbjornsson
|Mar 26, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestries.Andrea B Jonsdottir, Gardar Sveinbjornsson, Rosa B Thorolfsdottir
|Mar 06, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.Seung Hoan Choi, Sean J Jurgens, Ling Xiao
|Mar 06, 2025
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases.Carolina Roselli, Ida Surakka, Morten S Olesen
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Frequent Collaborators
27 joint publications
Daniel Gudbjartsson
25 joint publications
Kari Stefansson
23 joint publications
Patrick Sulem
22 joint publications
Hilma Holm
19 joint publications
Vinicius Tragante
18 joint publications
Ole Birger Pedersen
17 joint publications
Christian Erikstrup
16 joint publications
Gisli Hreinn Halldorsson
16 joint publications
Gudmar Thorleifsson
16 joint publications
Asmundur Oddsson