Gudny A. Arnadottir
Gudny A. Arnadottir
Verified email at decode.is
Title
Cited by
Cited by
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
2972020
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
2952017
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
522017
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), 1-8, 2016
482016
Epigenetic and genetic components of height regulation
S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ...
Nature communications 7 (1), 1-10, 2016
422016
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), 1-9, 2018
412018
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
402018
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
292019
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), 1-9, 2018
292018
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
292018
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
292017
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), 1-11, 2018
192018
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), 1-5, 2017
142017
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
112018
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), 1-10, 2019
102019
Identification of Lynch syndrome risk variants in the Romanian population
PD Iordache, D Mates, B Gunnarsson, HP Eggertsson, P Sulem, ...
Journal of cellular and molecular medicine 22 (12), 6068-6076, 2018
102018
Sequence variants associating with urinary biomarkers
S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ...
Human molecular genetics 28 (7), 1199-1211, 2019
82019
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
52020
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin
GR Oskarsson, RP Kristjansson, AL Lee, G Sveinbjornsson, ...
Communications biology 1 (1), 1-7, 2018
52018
Sequence variant at 4q25 near PITX2 associates with appendicitis
RP Kristjansson, S Benonisdottir, A Oddsson, TE Galesloot, ...
Scientific reports 7 (1), 1-7, 2017
42017
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