| Strelka2: fast and accurate calling of germline and somatic variants S Kim, K Scheffler, AL Halpern, MA Bekritsky, E Noh, M Källberg, X Chen, ... Nature methods 15 (8), 591-594, 2018 | 1041 | 2018 |
| Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity KM Turner, V Deshpande, D Beyter, T Koga, J Rusert, C Lee, B Li, ... Nature 543 (7643), 122-125, 2017 | 609 | 2017 |
| The sequences of 150,119 genomes in the UK Biobank BV Halldorsson, HP Eggertsson, KHS Moore, H Hauswedell, O Eiriksson, ... Nature 607 (7920), 732-740, 2022 | 210 | 2022 |
| 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 | 206 | 2021 |
| GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs HP Eggertsson, S Kristmundsdottir, D Beyter, H Jonsson, A Skuladottir, ... Nature communications 10 (1), 5402, 2019 | 135 | 2019 |
| Differences between germline genomes of monozygotic twins H Jonsson, E Magnusdottir, HP Eggertsson, OA Stefansson, GA Arnadottir, ... Nature Genetics 53 (1), 27-34, 2021 | 121 | 2021 |
| Diversity, productivity, and stability of an industrial microbial ecosystem D Beyter, PZ Tang, S Becker, T Hoang, D Bilgin, YW Lim, TC Peterson, ... Applied and environmental microbiology 82 (8), 2494-2505, 2016 | 59 | 2016 |
| Ratatosk: hybrid error correction of long reads enables accurate variant calling and assembly G Holley, D Beyter, H Ingimundardottir, PL Møller, S Kristmundsdottir, ... Genome Biology 22 (1), 28, 2021 | 43 | 2021 |
| Proteostorm: An ultrafast metaproteomics database search framework D Beyter, MS Lin, Y Yu, R Pieper, V Bafna Cell systems 7 (4), 463-467. e6, 2018 | 29 | 2018 |
| PopDel identifies medium-size deletions simultaneously in tens of thousands of genomes S Niehus, H Jónsson, J Schönberger, E Björnsson, D Beyter, ... Nature communications 12 (1), 730, 2021 | 18* | 2021 |
| Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program MM Wheeler, AM Stilp, S Rao, BV Halldórsson, D Beyter, J Wen, ... Medrxiv, 2021.12. 16.21267871, 2021 | 7* | 2021 |
| Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality A Oddsson, P Sulem, G Sveinbjornsson, GA Arnadottir, V Steinthorsdottir, ... nature communications 14 (1), 3453, 2023 | 6 | 2023 |
| Benchmarking small variant detection with ONT reveals high performance in challenging regions PL Møller, G Holley, D Beyter, M Nyegaard, BV Halldórsson bioRxiv, 2020.10. 22.350009, 2020 | 6 | 2020 |
| Methods of diagnosing and treating cancer targeting extrachromosomal DNA P Mischel, P Mali, V Bafna, K Turner, V Deshpande, D Beyter US Patent 11,193,164, 2021 | 5 | 2021 |
| Variants at the Interleukin 1 gene locus and pericarditis RB Thorolfsdottir, AB Jonsdottir, G Sveinbjornsson, HM Aegisdottir, ... JAMA cardiology 9 (2), 165-172, 2024 | 4 | 2024 |
| Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura G Bjornsdottir, MA Chalmer, L Stefansdottir, AT Skuladottir, G Einarsson, ... Nature Genetics 55 (11), 1843-1853, 2023 | 3 | 2023 |
| Sequence variants affecting the genome-wide rate of germline microsatellite mutations S Kristmundsdottir, H Jonsson, MT Hardarson, G Palsson, D Beyter, ... Nature Communications 14 (1), 3855, 2023 | 3 | 2023 |
| Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria RP Kristjansson, GR Oskarsson, A Skuladottir, A Oddsson, ... Communications Biology 6 (1), 703, 2023 | 2 | 2023 |
| A comparison of methods for detecting DNA methylation from long-read sequencing of human genomes BD Sigurpalsdottir, OA Stefansson, G Holley, D Beyter, F Zink, ... Genome Biology 25 (1), 69, 2024 | 1 | 2024 |
| Methods of diagnosing and treating cancer targeting extrachromosomal dna P Mischel, P Mali, V Bafna, K Turner, V Deshpande, D Beyter US Patent App. 17/518,396, 2022 | | 2022 |
Bjarni V. HalldorssondeCODE genetics/Reykjavik UniversityVerified email at ru.is
