| Large-scale whole-genome sequencing of the Icelandic population DF Gudbjartsson, H Helgason, SA Gudjonsson, F Zink, A Oddson, ... Nature genetics 47 (5), 435-444, 2015 | 723 | 2015 |
| The nature of nurture: Effects of parental genotypes A Kong, G Thorleifsson, ML Frigge, BJ Vilhjalmsson, AI Young, ... Science 359 (6374), 424-428, 2018 | 627 | 2018 |
| Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits U Styrkarsdottir, G Thorleifsson, P Sulem, DF Gudbjartsson, A Sigurdsson, ... Nature 497 (7450), 517-520, 2013 | 268 | 2013 |
| Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease A Helgadottir, S Gretarsdottir, G Thorleifsson, E Hjartarson, A Sigurdsson, ... Nature genetics 48 (6), 634-639, 2016 | 227 | 2016 |
| Identification of a large set of rare complete human knockouts P Sulem, H Helgason, A Oddson, H Stefansson, SA Gudjonsson, F Zink, ... Nature genetics 47 (5), 448-452, 2015 | 221 | 2015 |
| Weighting sequence variants based on their annotation increases power of whole-genome association studies G Sveinbjornsson, A Albrechtsen, F Zink, SA Gudjonsson, A Oddson, ... Nature genetics 48 (3), 314-317, 2016 | 184 | 2016 |
| Characterizing mutagenic effects of recombination through a sequence-level genetic map BV Halldorsson, G Palsson, OA Stefansson, H Jonsson, MT Hardarson, ... Science 363 (6425), eaau1043, 2019 | 181 | 2019 |
| Loss-of-function variants in ATM confer risk of gastric cancer H Helgason, T Rafnar, HS Olafsdottir, JG Jonasson, A Sigurdsson, ... Nature genetics 47 (8), 906-910, 2015 | 144 | 2015 |
| Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis U Styrkarsdottir, SH Lund, G Thorleifsson, F Zink, OA Stefansson, ... Nature genetics 50 (12), 1681-1687, 2018 | 127 | 2018 |
| Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits D Beyter, H Ingimundardottir, A Oddsson, HP Eggertsson, E Bjornsson, ... Nature Genetics 53 (6), 779-786, 2021 | 123 | 2021 |
| Common and rare variants associated with kidney stones and biochemical traits A Oddsson, P Sulem, H Helgason, VO Edvardsson, G Thorleifsson, ... Nature communications 6 (1), 7975, 2015 | 121 | 2015 |
| The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms A Oddsson, SY Kristinsson, H Helgason, DF Gudbjartsson, G Masson, ... Leukemia 28 (6), 1371-1374, 2014 | 99 | 2014 |
| 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 | 88 | 2021 |
| Expression and subcellular distribution of novel glomerulus-associated proteins dendrin, ehd3, sh2d4a, plekhh2, and 2310066E14Rik J Patrakka, Z Xiao, M Nukui, M Takemoto, L He, A Oddsson, L Perisic, ... Journal of the American Society of Nephrology 18 (3), 689-697, 2007 | 87 | 2007 |
| 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 | 81 | 2018 |
| Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis U Styrkarsdottir, H Helgason, A Sigurdsson, GL Norddahl, AB Agustsdottir, ... Nature genetics 49 (5), 801-805, 2017 | 80 | 2017 |
| Identification of sequence variants influencing immunoglobulin levels S Jonsson, G Sveinbjornsson, AL de Lapuente Portilla, B Swaminathan, ... Nature genetics 49 (8), 1182-1191, 2017 | 75 | 2017 |
| A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation DF Gudbjartsson, H Holm, P Sulem, G Masson, A Oddsson, ... European heart journal, ehw379, 2016 | 74 | 2016 |
| 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 | 71 | 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 | 71 | 2016 |
Daniel GudbjartssonStatistician, Decode GeneticsVerified email at decode.is
