Brynjar O. Jensson
Brynjar O. Jensson
Research Associate, deCODE genetics
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Cited by
Cited by
Spread of SARS-CoV-2 in the Icelandic population
DF Gudbjartsson, A Helgason, H Jonsson, OT Magnusson, P Melsted, ...
New England Journal of Medicine 382 (24), 2302-2315, 2020
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
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
Epigenetic and genetic components of height regulation
S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ...
Nature communications 7 (1), 1-10, 2016
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
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
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
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
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
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
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
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
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease
A Helgadottir, G Thorleifsson, KF Alexandersson, V Tragante, ...
European heart journal 41 (28), 2618-2628, 2020
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
Sequence variants associating with urinary biomarkers
S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ...
Human molecular genetics 28 (7), 1199-1211, 2019
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
Sequence variant at 4q25 near PITX2 associates with appendicitis
RP Kristjansson, S Benonisdottir, A Oddsson, TE Galesloot, ...
Scientific reports 7 (1), 1-7, 2017
A rare missense variant in NR1H4 associates with lower cholesterol levels
AM Deaton, P Sulem, P Nioi, S Benonisdottir, LD Ward, OB Davidsson, ...
Communications biology 1 (1), 1-9, 2018
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), 1-10, 2020
Recurrence of de novo mutations in families
H Jónsson, P Sulem, GA Arnadottir, G Pálsson, HP Eggertsson, ...
BioRxiv, 221259, 2017
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