Hakon Jonsson

22PUBLICATIONS
113CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Cancer geneticsHaematologyGene mapping
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Publications (22)

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

Gudny A Arnadottir, Hakon Jonsson, Tanja Schlaikjær Hartwig

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

Asmundur Oddsson, Valgerdur Steinthorsdottir, Gudjon R Oskarsson

|Jul 24, 2024
The correlation between CpG methylation and gene expression is driven by sequence variants.

Olafur Andri Stefansson, Brynja Dogg Sigurpalsdottir, Solvi Rognvaldsson

|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

|Nov 06, 2023
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.

Simon N Stacey, Florian Zink, Gisli H Halldorsson

|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

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