Brynjar Orn Jensson
10PUBLICATIONS
71CO-AUTHORS
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Publications (10)
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|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
|Aug 15, 2024
Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.Astros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjornsson
|Nov 08, 2023
Actionable Genotypes and Their Association with Life Span in Iceland.Brynjar O Jensson, Gudny A Arnadottir, Hildigunnur Katrinardottir
|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
|Jul 10, 2023
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.Ragnar P Kristjansson, Gudjon R Oskarsson, Astros Skuladottir
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Frequent Collaborators
9 joint publications
Patrick Sulem
8 joint publications
Kari Stefansson
7 joint publications
Gudny Anna Arnadottir
7 joint publications
Hilma Holm
7 joint publications
Daniel F Gudbjartsson
6 joint publications
Asmundur Oddsson
6 joint publications
Gisli H Halldorsson
6 joint publications
Gardar Sveinbjornsson
6 joint publications
Ingileif Jonsdottir
5 joint publications
Gudjon R Oskarsson
