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Birte Kehr
Birte Kehr
Leibniz Institute for Immunotherapy (formerly RCI)
Verified email at ukr.de
Title
Cited by
Cited by
Year
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
8592017
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
2102017
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
1332017
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
1322017
New basal cell carcinoma susceptibility loci
SN Stacey, H Helgason, SA Gudjonsson, G Thorleifsson, F Zink, ...
Nature communications 6 (1), 6825, 2015
1262015
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
1052018
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
912014
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
882016
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
752017
Genome alignment with graph data structures: a comparison
B Kehr, K Trappe, M Holtgrewe, K Reinert
BMC bioinformatics 15, 1-20, 2014
562014
PopIns: population-scale detection of novel sequence insertions
B Kehr, P Melsted, BV Halldórsson
Bioinformatics 32 (7), 961-967, 2016
492016
STELLAR: fast and exact local alignments
B Kehr, D Weese, K Reinert
BMC bioinformatics 12, 1-12, 2011
412011
Sequence variants associating with urinary biomarkers
S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ...
Human Molecular Genetics 28 (7), 1199-1211, 2019
292019
popSTR: population-scale detection of STR variants
S Kristmundsdóttir, BD Sigurpálsdóttir, B Kehr, BV Halldórsson
Bioinformatics 33 (24), 4041-4048, 2017
292017
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
292016
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
252010
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
212017
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
202021
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
152022
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
132021
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