Unexplained sudden death: next-generation sequencing to the rescue?
David O Arnar , David O Arnar , Gudny A Arnadottir
Europace 23 ( 3) 327 -328
2021
Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency.
Hrafnhildur L Runolfsdottir , John A Sayer , Olafur S Indridason , Vidar O Edvardsson
European Journal of Human Genetics 1 -10
2021
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease.
Anna Helgadottir , Patrick Sulem , Gudmundur Thorgeirsson , Solveig Gretarsdottir
European Heart Journal 39 ( 23) 2172 -2178
28
2018
Sequence variants associating with urinary biomarkers.
Stefania Benonisdottir , Ragnar P Kristjansson , Asmundur Oddsson , Valgerdur Steinthorsdottir
Human Molecular Genetics 28 ( 7) 1199 -1211
13
2019
popSTR2 enables clinical and population-scale genotyping of microsatellites.
Snædis Kristmundsdottir , Hannes P Eggertsson , Gudny A Arnadottir , Bjarni V Halldorsson
Bioinformatics 36 ( 7) 2269 -2271
6
2020
Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene
Gudny A Arnadottir , Asmundur Oddsson , Brynjar O Jensson , Svanborg Gisladottir
Nature communications 13 ( 1) 705
2
2022
Large-scale integration of the plasma proteome with genetics and disease
Egil Ferkingstad , Patrick Sulem , Bjarni A Atlason , Gardar Sveinbjornsson
Nature genetics 53 ( 12) 1712 -1721
100
2021
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
Asmundur Oddsson , Patrick Sulem , Gardar Sveinbjornsson , Gudny A Arnadottir
nature communications 14 ( 1) 3453 -3453
7
2023
Complex effects of sequence variants on lipid levels and coronary artery disease
Audunn S Snaebjarnarson , Anna Helgadottir , Gudny A Arnadottir , Erna V Ivarsdottir
Cell 186 ( 19) 4085 -4099. e15
2
2023
Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination
Valgerdur Steinthorsdottir , Bjarni V Halldorsson , Hakon Jonsson , Gunnar Palsson
Nature structural & molecular biology 1 -7
1
2024
Actionable genotypes and their association with life span in Iceland
Brynjar O Jensson , Gudny A Arnadottir , Hildigunnur Katrinardottir , Run Fridriksdottir
New England Journal of Medicine 389 ( 19) 1741 -1752
6
2023
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis
Erna V Ivarsdottir , Hilma Holm , Stefania Benonisdottir , Thorhildur Olafsdottir
Communications Biology 4 ( 1) 706 -706
34
2021
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria
Ragnar P Kristjansson , Gudjon R Oskarsson , Astros Skuladottir , Asmundur Oddsson
Communications Biology 6 ( 1) 703 -703
3
2023
Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database
Run Fridriksdottir , Arnar J Jonsson , Brynjar O Jensson , Kristinn O Sverrisson
European Journal of Human Genetics 29 ( 12) 1819 -1824
6
2021
Sequence variants affecting the genome-wide rate of germline microsatellite mutations
Snaedis Kristmundsdottir , Hakon Jonsson , Marteinn T Hardarson , Gunnar Palsson
Nature Communications 14 ( 1) 3855 -3855
7
2023
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
Thorunn Rafnar , Bjarni Gunnarsson , Olafur A Stefansson , Patrick Sulem
Nature Communications 9 ( 1) 3636 -3636
25
2018
Genetic architecture of band neutrophil fraction in Iceland
Gudjon R Oskarsson , Magnus K Magnusson , Asmundur Oddsson , Brynjar O Jensson
Communications Biology 5 ( 1) 525 -525
2
2022
Screening for rare coding variants that associate with the QTc interval in Iceland
Gardar Sveinbjornsson , Bara D Benediktsdottir , Gunnlaugur Sigfusson , Kristjan Norland
Journal of the American Heart Association 12 ( 14) e029845 -e029845
1
2023
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Ragnar P Kristjansson , Stefania Benonisdottir , Olafur B Davidsson , Asmundur Oddsson
Nature Genetics 51 ( 2) 267 -276
72
2019
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
Ragnar P Kristjansson , Asmundur Oddsson , Hannes Helgason , Gardar Sveinbjornsson
Nature Communications 7 ( 1) 10572 -10572
38
2016