Author
deCODE Genetics (Iceland)ORCID 0000-0001-7067-9862Unclaimed ORCID profile · follow to get notified of new preprints
6 papers
Recent·Most cited
Zain Ali, Aitzkoa Lopez de Lapuente Portilla, Guðmar Þorleifsson…·Björn Nilsson
The paper uses population-scale Ig genetics to identify genetic associations and map their effects on the human B-cell system, revealing new genes and regulatory mechanisms in humoral immunity.
Aitzkoa Lopez de Lapuente Portilla, Ludvig Ekdahl, Guðmar Þorleifsson…·Björn Nilsson
BloodVariome identifies 259 genetic associations across 127 immune cell populations in 11,983 individuals, revealing fine-grained genetic compartmentalization of the immune system.
Søren Albertsen Rand, Johan Skov Bundgaard, Vinicius Tragante…·Jonas Ghouse
This paper identifies genetic variants associated with amiodarone-induced thyroid dysfunction and shows they improve risk prediction beyond general thyroid disease PRS.
Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore…·Kāri Stefánsson
The paper analyzes whole genome sequences of 150,119 UK Biobank individuals, identifying variants and associations with traits, and provides a haplotype reference panel for imputation.
Grímur Hjörleifsson Eldjárn, Egil Ferkingstad, Sigrún H. Lund…·Kāri Stefánsson
The paper was withdrawn due to premature posting and is not intended to be cited for the UK Biobank Pharma Proteomics Project.
Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson, Patrick Sulem…·Kāri Stefánsson
This study identifies mutations in RPL3L and MYZAP as risk factors for atrial fibrillation through genome-wide association analysis and functional validation.