Gudny Anna Arnadottir

28PUBLICATIONS
121CO-AUTHORS
Gene mappingEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Cancer geneticsMedical infection agents (incl. prions)
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Publications (28)

|Aug 26, 2026
Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.

|May 21, 2025
Sequence diversity lost in early pregnancy.

Gudny A Arnadottir, Hakon Jonsson, Tanja Schlaikjær Hartwig

|Mar 26, 2025
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder.

Thorgeir E Thorgeirsson, Vinicius Tragante, Gardar Sveinbjornsson

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

Asmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson

|Jan 29, 2024
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination.

Valgerdur Steinthorsdottir, Bjarni V Halldorsson, Hakon Jonsson

|Sep 08, 2023
A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome.

Elin Ola Klemenzdottir, Gudny Anna Arnadottir, Brynjar Orn Jensson

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Frequent Collaborators

26 joint publications

Patrick Sulem

21 joint publications

Daniel F Gudbjartsson

19 joint publications

Kari Stefansson

19 joint publications

Asmundur Oddsson