Birte Kehr
Birte Kehr
Leibniz Institute for Immunotherapy (formerly RCI)
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Cited by
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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
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
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
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
New basal cell carcinoma susceptibility loci
SN Stacey, H Helgason, SA Gudjonsson, G Thorleifsson, F Zink, ...
Nature communications 6 (1), 6825, 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
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
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
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
Genome alignment with graph data structures: a comparison
B Kehr, K Trappe, M Holtgrewe, K Reinert
BMC bioinformatics 15, 1-20, 2014
PopIns: population-scale detection of novel sequence insertions
B Kehr, P Melsted, BV Halldórsson
Bioinformatics 32 (7), 961-967, 2016
STELLAR: fast and exact local alignments
B Kehr, D Weese, K Reinert
BMC bioinformatics 12, 1-12, 2011
Sequence variants associating with urinary biomarkers
S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ...
Human Molecular Genetics 28 (7), 1199-1211, 2019
popSTR: population-scale detection of STR variants
S Kristmundsdóttir, BD Sigurpálsdóttir, B Kehr, BV Halldórsson
Bioinformatics 33 (24), 4041-4048, 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
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
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
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
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
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
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