Daniela Endt
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Blood disorders and treatments
- Genomics and Rare Diseases
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- DNA Repair Mechanisms
- Epigenetics and DNA Methylation
Papers in
- Genetics 4
- BRCA gene mutations in cancer 3
- Blood disorders and treatments 1
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- DNA Repair Mechanisms 2
- Epigenetics and DNA Methylation 1
- Co-authors
- Detlev Schindler (4 shared papers)Kornelia Neveling (2 shared papers)Holger Hoehn (1 shared paper)Shehla N. Mohammed (1 shared paper)Beatrice Schuster (1 shared paper)Karen T. Barker (1 shared paper)Nazneen Rahman (1 shared paper)Heiner Schaal (1 shared paper)
- Journals
- Nature Genetics (2 papers)Human Molecular Genetics (2 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (1 paper)
- Partner nations
- GermanySpainUnited States
In The Last Decade
Daniela Endt
5 papers receiving 602 citations
Peers
Comparison fields: 5 of 35
- Genetics 302
- Molecular Biology 357
- Oncology 35
- Hematology 19
- Cancer Research 16
Countries citing papers authored by Daniela Endt
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
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-authors
The 25 scholars most cited alongside Daniela Endt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 335 | |
| 2 | 2009 | 115 | |
| 3 | 2012 | 90 | |
| 4 | 2012 | 78 | |
| 5 | 2012 | 4 |
About Daniela Endt
Daniela Endt is a scholar working on Genetics, Molecular Biology, Nuclear Energy and Engineering, Waste Management and Disposal and Infectious Diseases, having authored 5 papers that have together received 622 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (3 papers), DNA Repair Mechanisms (2 papers), Blood disorders and treatments (1 paper) and Epigenetics and DNA Methylation (1 paper). The work is most often cited by research in Genetics (302 citations), Molecular Biology (357 citations), Oncology (35 citations), Hematology (19 citations) and Cancer Research (16 citations). Daniela Endt has collaborated with scholars based in Germany, Spain and United States. Frequent co-authors include Detlev Schindler, Kornelia Neveling, Holger Hoehn, Shehla N. Mohammed, Beatrice Schuster, Karen T. Barker, Nazneen Rahman, Heiner Schaal, Marcel Freund and David J. Grimwade. Their work appears in journals such as Nature Genetics, Human Molecular Genetics and Mutation research. Fundamental and molecular mechanisms of mutagenesis.
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.