| 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 | 940 | 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 | 297 | 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 | 48 | 2016 |
| Epigenetic and genetic components of height regulation S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ... Nature communications 7 (1), 1-10, 2016 | 42 | 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 | 41 | 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 | 40 | 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 | 29 | 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 | 29 | 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 | 29 | 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 | 19 | 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 | 14 | 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 | 11 | 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 | 10 | 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 | 10 | 2018 |
| Sequence variants associating with urinary biomarkers S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ... Human molecular genetics 28 (7), 1199-1211, 2019 | 8 | 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 | 5 | 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 | 4 | 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 | 3 | 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 | 2 | 2020 |
| Recurrence of de novo mutations in families H Jónsson, P Sulem, GA Arnadottir, G Pálsson, HP Eggertsson, ... BioRxiv, 221259, 2017 | 2 | 2017 |
