| 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 | 831 | 2017 |
| Graphtyper enables population-scale genotyping using pangenome graphs HP Eggertsson, H Jonsson, S Kristmundsdottir, E Hjartarson, B Kehr, ... Nature genetics 49 (11), 1654-1660, 2017 | 200 | 2017 |
| 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 | 128 | 2017 |
| Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2 S Haraldsdottir, T Rafnar, WL Frankel, S Einarsdottir, A Sigurdsson, ... Nature communications 8 (1), 14755, 2017 | 127 | 2017 |
| New basal cell carcinoma susceptibility loci SN Stacey, H Helgason, SA Gudjonsson, G Thorleifsson, F Zink, ... Nature communications 6 (1), 6825, 2015 | 125 | 2015 |
| 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 | 101 | 2018 |
| NetCoffee: a fast and accurate global alignment approach to identify functionally conserved proteins in multiple networks J Hu, B Kehr, K Reinert Bioinformatics 30 (4), 540-548, 2014 | 89 | 2014 |
| The rate of meiotic gene conversion varies by sex and age BV Halldorsson, MT Hardarson, B Kehr, U Styrkarsdottir, A Gylfason, ... Nature genetics 48 (11), 1377-1384, 2016 | 85 | 2016 |
| Diversity in non-repetitive human sequences not found in the reference genome B Kehr, A Helgadottir, P Melsted, H Jonsson, H Helgason, A Jonasdottir, ... Nature Genetics 49 (4), 588-593, 2017 | 76 | 2017 |
| Genome alignment with graph data structures: a comparison B Kehr, K Trappe, M Holtgrewe, K Reinert BMC bioinformatics 15, 1-20, 2014 | 55 | 2014 |
| PopIns: population-scale detection of novel sequence insertions B Kehr, P Melsted, BV Halldórsson Bioinformatics 32 (7), 961-967, 2016 | 49 | 2016 |
| STELLAR: fast and exact local alignments B Kehr, D Weese, K Reinert BMC bioinformatics 12, 1-12, 2011 | 41 | 2011 |
| popSTR: population-scale detection of STR variants S Kristmundsdóttir, BD Sigurpálsdóttir, B Kehr, BV Halldórsson Bioinformatics 33 (24), 4041-4048, 2017 | 29 | 2017 |
| Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer SN Stacey, B Kehr, J Gudmundsson, F Zink, A Jonasdottir, ... Human molecular genetics 25 (5), 1008-1018, 2016 | 29 | 2016 |
| Sequence variants associating with urinary biomarkers S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ... Human Molecular Genetics 28 (7), 1199-1211, 2019 | 26 | 2019 |
| Determination of glycan structure from tandem mass spectra S Bocker, B Kehr, F Rasche IEEE/ACM Transactions on Computational Biology and Bioinformatics 8 (4), 976-986, 2010 | 25 | 2010 |
| A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease E Bjornsson, H Helgason, G Halldorsson, A Helgadottir, A Gylfason, ... Human molecular genetics 26 (12), 2364-2376, 2017 | 21 | 2017 |
| Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in LDLR E Bjornsson, K Gunnarsdottir, GH Halldorsson, A Sigurdsson, ... Circulation: Genomic and Precision Medicine 14 (1), e003029, 2021 | 16 | 2021 |
| The collaborative research center fonda U Leser, M Hilbrich, C Draxl, P Eisert, L Grunske, P Hostert, D Kainmüller, ... Datenbank-Spektrum 21, 255-260, 2021 | 13 | 2021 |
| Population-scale detection of non-reference sequence variants using colored de Bruijn graphs T Krannich, WTJ White, S Niehus, G Holley, BV Halldórsson, B Kehr Bioinformatics 38 (3), 604-611, 2022 | 10 | 2022 |
Bjarni V. HalldorssondeCODE genetics/Reykjavik UniversityПодтвержден адрес электронной почты в домене ru.is
