Birte Kehr

5.2k total citations
20 papers, 405 citations indexed

About

Birte Kehr is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Birte Kehr has authored 20 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Plant Science. Recurrent topics in Birte Kehr's work include Genomics and Phylogenetic Studies (12 papers), Genomics and Chromatin Dynamics (5 papers) and Genomics and Rare Diseases (4 papers). Birte Kehr is often cited by papers focused on Genomics and Phylogenetic Studies (12 papers), Genomics and Chromatin Dynamics (5 papers) and Genomics and Rare Diseases (4 papers). Birte Kehr collaborates with scholars based in Germany, Iceland and Denmark. Birte Kehr's co-authors include Bjarni V. Halldórsson, Knut Reinert, Jialu Hu, Páll Melsted, Kāri Stefánsson, Snædís Kristmundsdóttir, Daníel F. Guðbjartsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir and Gísli Másson and has published in prestigious journals such as New England Journal of Medicine, Nature Communications and Nature Genetics.

In The Last Decade

Birte Kehr

19 papers receiving 400 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Birte Kehr Germany	10	312	172	98	36	25	20	405
Wyatt T. Clark United States	11	580 1.9×	135 0.8×	57 0.6×	37 1.0×	27 1.1×	16	685
Keun-Joon Park Japan	6	563 1.8×	57 0.3×	118 1.2×	17 0.5×	10 0.4×	10	682
Daniela Butano United Kingdom	3	253 0.8×	50 0.3×	46 0.5×	9 0.3×	21 0.8×	5	331
Christopher A. Penfold United Kingdom	17	733 2.3×	91 0.5×	331 3.4×	33 0.9×	27 1.1×	32	902
Domenica D’Elia Italy	15	334 1.1×	51 0.3×	35 0.4×	53 1.5×	106 4.2×	38	470
Aïda Ouangraoua Canada	12	353 1.1×	70 0.4×	70 0.7×	30 0.8×	28 1.1×	38	405
Morteza Mohammad-Noori Iran	9	682 2.2×	67 0.4×	41 0.4×	57 1.6×	45 1.8×	14	770
Antonio Turi Italy	8	367 1.2×	50 0.3×	28 0.3×	16 0.4×	60 2.4×	10	472
Daniel Visentin United Kingdom	2	408 1.3×	91 0.5×	30 0.3×	42 1.2×	37 1.5×	2	489

Countries citing papers authored by Birte Kehr

Since Specialization

Citations

This map shows the geographic impact of Birte Kehr's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Birte Kehr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birte Kehr more than expected).

Fields of papers citing papers by Birte Kehr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Birte Kehr. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Birte Kehr. The network helps show where Birte Kehr may publish in the future.

Co-authorship network of co-authors of Birte Kehr

This figure shows the co-authorship network connecting the top 25 collaborators of Birte Kehr. A scholar is included among the top collaborators of Birte Kehr based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Birte Kehr. Birte Kehr is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kehr, Birte, et al.. (2024). How Do Users Design Scientific Workflows? The Case of Snakemake and Nextflow. 1–12.

Lohmayer, Robert, et al.. (2024). GGTyper: genotyping complex structural variants using short-read sequencing data. Bioinformatics. 40(Supplement_2). ii11–ii19. 2 indexed citations

Markowski, Julia, Rieke Kempfer, Alexander Kukalev, et al.. (2021). GAMIBHEAR: whole-genome haplotype reconstruction from Genome Architecture Mapping data. Bioinformatics. 37(19). 3128–3135. 4 indexed citations

Niehus, Sebastian, et al.. (2021). Population-scale detection of non-reference sequence variants using colored de Bruijn graphs. Bioinformatics. 38(3). 604–611. 7 indexed citations

Niehus, Sebastian, Hákon Jónsson, Eyþór Björnsson, et al.. (2021). PopDel identifies medium-size deletions simultaneously in tens of thousands of genomes. Nature Communications. 12(1). 730–730. 9 indexed citations

Schwarz, Jana Marie, et al.. (2021). Novel sequencing technologies and bioinformatic tools for deciphering the non-coding genome. Medizinische Genetik. 33(2). 133–145. 2 indexed citations

Niehus, Sebastian, et al.. (2020). PopDel - Population wide deletion calling (v1.2.2). Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations

Eggertsson, Hannes P., Hákon Jónsson, Snædís Kristmundsdóttir, et al.. (2017). Graphtyper enables population-scale genotyping using pangenome graphs. Nature Genetics. 49(11). 1654–1660. 113 indexed citations

Kehr, Birte, Anna Helgadóttir, Páll Melsted, et al.. (2017). Diversity in non-repetitive human sequences not found in the reference genome. Nature Genetics. 49(4). 588–593. 38 indexed citations

10.

Halldórsson, Bjarni V., Marteinn T. Hardarson, Birte Kehr, et al.. (2016). The rate of meiotic gene conversion varies by sex and age. Nature Genetics. 48(11). 1377–1384. 61 indexed citations

11.

Haraldsdóttir, Sigurdís, Þórunn Rafnar, Wendy L. Frankel, et al.. (2016). Comprehensive population-wide detection of Lynch syndrome in Iceland.. Journal of Clinical Oncology. 34(15_suppl). 1542–1542. 2 indexed citations

12.

Kristmundsdóttir, Snædís, Brynja D. Sigurpalsdottir, Birte Kehr, & Bjarni V. Halldórsson. (2016). popSTR: population-scale detection of STR variants. Bioinformatics. 33(24). 4041–4048. 20 indexed citations

13.

Qian, Yu, Birte Kehr, & Bjarni V. Halldórsson. (2015). PopAlu: population-scale detection of Alu polymorphisms. PeerJ. 3. e1269–e1269. 7 indexed citations

14.

Kehr, Birte, Páll Melsted, & Bjarni V. Halldórsson. (2015). PopIns: population-scale detection of novel sequence insertions. Bioinformatics. 32(7). 961–967. 19 indexed citations

15.

Kehr, Birte, Kathrin Trappe, Manuel Holtgrewe, & Knut Reinert. (2014). Genome alignment with graph data structures: a comparison. BMC Bioinformatics. 15(1). 99–99. 20 indexed citations

16.

Hu, Jialu, Birte Kehr, & Knut Reinert. (2013). NetCoffee: a fast and accurate global alignment approach to identify functionally conserved proteins in multiple networks. Bioinformatics. 30(4). 540–548. 50 indexed citations

17.

Kehr, Birte, David Weese, & Knut Reinert. (2011). STELLAR: fast and exact local alignments. BMC Bioinformatics. 12(S9). S15–S15. 22 indexed citations

18.

Böcker, Sebastian, Birte Kehr, & Frank Rasche. (2010). Determination of Glycan Structure from Tandem Mass Spectra. IEEE/ACM Transactions on Computational Biology and Bioinformatics. 8(4). 976–986. 18 indexed citations

19.

Gebel, Jürgen, Andreas Vogt, Birte Kehr, et al.. (2008). Hygiene-Tipps für Kids. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 51(11). 1304–1313. 4 indexed citations

20.

Kehr, Birte, et al.. (1979). Code or No Code Decisions. New England Journal of Medicine. 300(18). 1057–1059. 6 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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