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Gudny A. Arnadottir
Gudny A. Arnadottir
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Year
Humoral immune response to SARS-CoV-2 in Iceland
DF Gudbjartsson, GL Norddahl, P Melsted, K Gunnarsdottir, H Holm, ...
New England Journal of Medicine 383 (18), 1724-1734, 2020
9642020
Parental influence on human germline de novo mutations in 1,548 trios from Iceland
H Jónsson, P Sulem, B Kehr, S Kristmundsdottir, F Zink, E Hjartarson, ...
Nature 549 (7673), 519-522, 2017
6352017
Whole genome characterization of sequence diversity of 15,220 Icelanders
H Jónsson, P Sulem, B Kehr, S Kristmundsdottir, F Zink, E Hjartarson, ...
Scientific data 4 (1), 1-9, 2017
1032017
Large-scale integration of the plasma proteome with genetics and disease
E Ferkingstad, P Sulem, BA Atlason, G Sveinbjornsson, MI Magnusson, ...
Nature genetics 53 (12), 1712-1721, 2021
882021
Multiple transmissions of de novo mutations in families
H Jónsson, P Sulem, GA Arnadottir, G Pálsson, HP Eggertsson, ...
Nature genetics 50 (12), 1674-1680, 2018
812018
A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease
GA Arnadottir, GL Norddahl, S Gudmundsdottir, AB Agustsdottir, ...
Nature Communications 9 (1), 4447, 2018
812018
Differences between germline genomes of monozygotic twins
H Jonsson, E Magnusdottir, HP Eggertsson, OA Stefansson, GA Arnadottir, ...
Nature Genetics 53 (1), 27-34, 2021
792021
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
T Rafnar, B Gunnarsson, OA Stefansson, P Sulem, A Ingason, ML Frigge, ...
Nature communications 9 (1), 3636, 2018
712018
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
RP Kristjansson, A Oddsson, H Helgason, G Sveinbjornsson, ...
Nature communications 7 (1), 10572, 2016
712016
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
RP Kristjansson, S Benonisdottir, OB Davidsson, A Oddsson, V Tragante, ...
Nature genetics 51 (2), 267-276, 2019
682019
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease
A Helgadottir, P Sulem, G Thorgeirsson, S Gretarsdottir, G Thorleifsson, ...
European Heart Journal 39 (23), 2172-2178, 2018
612018
Genome-wide association meta-analysis yields 20 loci associated with gallstone disease
E Ferkingstad, A Oddsson, S Gretarsdottir, S Benonisdottir, G Thorleifsson, ...
Nature communications 9 (1), 5101, 2018
592018
Epigenetic and genetic components of height regulation
S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ...
Nature communications 7 (1), 13490, 2016
552016
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA
BO Jensson, S Hansdottir, GA Arnadottir, G Sulem, RP Kristjansson, ...
BMC medical genetics 18 (1), 1-5, 2017
402017
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death
G Sveinbjornsson, EF Olafsdottir, RB Thorolfsdottir, OB Davidsson, ...
Circulation: Genomic and Precision Medicine 11 (8), e002151, 2018
262018
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters
GA Arnadottir, BO Jensson, SE Marelsson, G Sulem, A Oddsson, ...
BMC medical genetics 18, 1-5, 2017
232017
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
GR Oskarsson, A Oddsson, MK Magnusson, RP Kristjansson, ...
Communications Biology 3 (1), 189, 2020
222020
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density
EV Ivarsdottir, S Benonisdottir, G Thorleifsson, P Sulem, A Oddsson, ...
Nature Communications 10 (1), 1284, 2019
222019
Sequence variants in TAAR5 and other loci affect human odor perception and naming
RS Gisladottir, EV Ivarsdottir, A Helgason, L Jonsson, NK Hannesdottir, ...
Current Biology 30 (23), 4643-4653. e3, 2020
192020
Sequence variants associating with urinary biomarkers
S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ...
Human Molecular Genetics 28 (7), 1199-1211, 2019
192019
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