Author

Jona Saemundsdottir

deCODE Genetics (Iceland)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Research Focus:benchmarking· 1 Research Focus:clustering· 1 Research Focus:GWAS / association mapping· 1 Research Focus:imputation· 1 Assay:proteomics· 1

Frequent Co-Authors

Ingileif JónsdóttiriD· 3 shared Kāri StefánssoniD· 3 shared Ólafur Þ. MagnússoniD· 3 shared Agnar HelgasoniD· 2 shared Ásmundur OddssoniD· 2 shared Bjarni V. HalldórssoniD· 2 shared Daniel Fannar GudbjartssoniD· 2 shared Droplaug N. Magnúsdóttir· 2 shared

Activity by Year

2022-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Ingileif JónsdóttirORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Endometriosis lesions are oligoclonal structures derived from the normal endometrium

Sigurgeir Ólafsson, Asgeir Orn Arnthorsson, Kirsten Kübler, Ásgeir Sigurðsson, Helga Sigrun Gunnarsdottir, Hákon Jónsson, Bergrún Ásbjörnsdóttir, Louise le Roux, Jona Saemundsdottir, Valgerður Steinthórsdóttir, Gudmundur Logi Norddahl, Ingileif Jónsdóttir, Jon Gunnlaugur Jonasson, Droplaug N. Magnúsdóttir, Ólafur Þ. Magnússon, , Kāri Stefánsson

This study shows endometriosis lesions originate from the normal endometrium through clonal expansion, with distinct clones at different body sites.

bioRxiv · Feb 26, 2026 · PreprintGenetics

The sequences of 150,119 genomes in the UK biobank

Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore, Hannes Hauswedell, Ögmundur Eiríksson, Magnus Orn Ulfarsson, Gunnar Pálsson, Marteinn Thor Hardarson, Ásmundur Oddsson, Brynjar Ö. Jensson, Snædís Kristmundsdóttir, Brynja D. Sigurpalsdottir, Ólafur Andri Stefánsson, Doruk Beyter, Guillaume Holley, , 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.

Nature · Jul 20, 2022Peer-reviewedGenetics

Large-scale comparison of immunoassay- and aptamer-based plasma proteomics through genetics and disease

Grímur Hjörleifsson Eldjárn, Egil Ferkingstad, Sigrún H. Lund, Hannes Helgason, Ólafur Þ. Magnússon, Thorunn Asta Olafsdottir, Bjarni V. Halldórsson, Pall I. Olason, Florian Zink, Sigurjon Axel Gudjonsson, Garðar Sveinbjörnsson, Magnus I. Magnusson, Agnar Helgason, Ásmundur Oddsson, Gisli Hreinn Halldorsson, , Kāri Stefánsson

The paper was withdrawn due to premature posting and is not intended to be cited for the UK Biobank Pharma Proteomics Project.

bioRxiv · Feb 18, 2022 · PreprintGenomics