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 | 1112 | 2020 |
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 | 868 | 2017 |
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 | 515 | 2021 |
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 | 132 | 2017 |
Differences between germline genomes of monozygotic twins H Jonsson, E Magnusdottir, HP Eggertsson, OA Stefansson, GA Arnadottir, ... Nature Genetics 53 (1), 27-34, 2021 | 131 | 2021 |
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 | 110 | 2019 |
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 | 107 | 2018 |
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 | 106 | 2018 |
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 | 99 | 2018 |
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 | 93 | 2018 |
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 | 88 | 2016 |
Epigenetic and genetic components of height regulation S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ... Nature communications 7 (1), 13490, 2016 | 67 | 2016 |
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 | 66 | 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, 1-5, 2017 | 52 | 2017 |
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 | 34 | 2020 |
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis EV Ivarsdottir, H Holm, S Benonisdottir, T Olafsdottir, G Sveinbjornsson, ... Communications Biology 4 (1), 706, 2021 | 33 | 2021 |
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 | 33 | 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, 1-5, 2017 | 32 | 2017 |
Sequence variants associating with urinary biomarkers S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ... Human Molecular Genetics 28 (7), 1199-1211, 2019 | 30 | 2019 |
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 | 30 | 2019 |