Gyda Bjornsdottir

16PUBLICATIONS
111CO-AUTHORS
Gene mappingGene expression (incl. microarray and other genome-wide approaches)Genetic immunologyMajor global burdens of diseaseEpigenetics (incl. genome methylation and epigenomics)
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Publications (16)

|Sep 26, 2025
The genetic architecture of fibromyalgia across 2.5 million individuals.

Isabel Kerrebijn, Gyda Bjornsdottir, Keon Arbabi

|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

|Nov 12, 2024
Sequence variants associated with BMI affect disease risk through BMI itself.

Gudmundur Einarsson, Gudmar Thorleifsson, Valgerdur Steinthorsdottir

|Aug 15, 2024
Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

Astros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjornsson

|Apr 26, 2024
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis.

Astros Th Skuladottir, Lilja Stefansdottir, Gisli H Halldorsson

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Frequent Collaborators

14 joint publications

Kari Stefansson

13 joint publications

Daniel F Gudbjartsson

12 joint publications

Patrick Sulem

9 joint publications

Astros Th Skuladottir