Daniela Endt

789 total citations
5 papers, 564 citations indexed

About

Daniela Endt is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Daniela Endt has authored 5 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Public Health, Environmental and Occupational Health. Recurrent topics in Daniela Endt's work include DNA Repair Mechanisms (4 papers), BRCA gene mutations in cancer (3 papers) and Genomics and Chromatin Dynamics (2 papers). Daniela Endt is often cited by papers focused on DNA Repair Mechanisms (4 papers), BRCA gene mutations in cancer (3 papers) and Genomics and Chromatin Dynamics (2 papers). Daniela Endt collaborates with scholars based in Germany, United States and United Kingdom. Daniela Endt's co-authors include Detlev Schindler, Kornelia Neveling, Holger Hoehn, Constanze Wiek, Helmut Hanenberg, Marcel Freund, David Grimwade, Christopher G. Mathew, Flavia Autore and Ian Kesterton and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

In The Last Decade

Daniela Endt

5 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Daniela Endt Germany	5	473	237	139	111	51	5	564
Beatrice Schuster Germany	6	559 1.2×	212 0.9×	144 1.0×	117 1.1×	38 0.7×	6	639
Ian Kesterton United Kingdom	6	352 0.7×	137 0.6×	128 0.9×	100 0.9×	38 0.7×	8	444
Britta Wieland Germany	8	328 0.7×	136 0.6×	139 1.0×	133 1.2×	55 1.1×	9	453
Scott Houghtaling United States	8	475 1.0×	96 0.4×	174 1.3×	110 1.0×	25 0.5×	11	544
Adam J.W. Paige United Kingdom	11	399 0.8×	346 1.5×	53 0.4×	78 0.7×	35 0.7×	14	544
Michael R. Dufault United States	8	287 0.6×	124 0.5×	126 0.9×	87 0.8×	44 0.9×	14	441
Betty K. Martin United States	13	661 1.4×	245 1.0×	231 1.7×	145 1.3×	50 1.0×	17	799
N C Cheng Netherlands	8	299 0.6×	99 0.4×	122 0.9×	100 0.9×	26 0.5×	11	454
Dominique Stoppa-Lyonnet France	6	185 0.4×	217 0.9×	58 0.4×	65 0.6×	40 0.8×	6	350
Åsa Ehlén France	9	445 0.9×	123 0.5×	75 0.5×	83 0.7×	25 0.5×	13	510

Countries citing papers authored by Daniela Endt

Since Specialization

Citations

This map shows the geographic impact of Daniela Endt'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 Daniela Endt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Endt more than expected).

Fields of papers citing papers by Daniela Endt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniela Endt. 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 Daniela Endt. The network helps show where Daniela Endt may publish in the future.

Co-authorship network of co-authors of Daniela Endt

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Endt. A scholar is included among the top collaborators of Daniela Endt 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 Daniela Endt. Daniela Endt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

1.

Osório, Ana, Daniela Endt, Fernando Fernández, et al.. (2012). Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. Human Molecular Genetics. 21(13). 2889–2898. 76 indexed citations

2.

Hansmann, T., Galyna Pliushch, Daniela Endt, et al.. (2012). Constitutive promoter methylation of BRCA1 and RAD51C in patients with familial ovarian cancer and early-onset sporadic breast cancer. Human Molecular Genetics. 21(21). 4669–4679. 74 indexed citations

3.

Meindl, Alfons, Katharina Eirich, Stefanie Engert, et al.. (2012). Germline RAD51C mutations confer susceptibility to ovarian cancer. Nature Genetics. 44(5). 476–476. 5 indexed citations

4.

Hanenberg, Helmut, Beatrice Schuster, Karen Barker, et al.. (2010). Mutation of the RAD51C gene in a Fanconi anemia–like disorder. Nature Genetics. 42(5). 406–409. 310 indexed citations

5.

Neveling, Kornelia, Daniela Endt, Holger Hoehn, & Detlev Schindler. (2009). Genotype–phenotype correlations in Fanconi anemia. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 668(1-2). 73–91. 99 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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