Gudjon R Oskarsson

6PUBLICATIONS
63CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Gene mappingNutritional epidemiologyCell and nuclear division
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Publications (6)

|Aug 27, 2024
Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency.

Asmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson

|Jul 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.

Ragnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir

|Jul 03, 2023
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson

|Jun 10, 2023
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson

|Oct 25, 2022
Multiomics study of nonalcoholic fatty liver disease.

Gardar Sveinbjornsson, Magnus O Ulfarsson, Rosa B Thorolfsdottir

|Jun 01, 2022
Genetic architecture of band neutrophil fraction in Iceland.

Gudjon R Oskarsson, Magnus K Magnusson, Asmundur Oddsson

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