Stephanie Hampp
Impact in
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- PARP inhibition in cancer therapy
- Cancer-related Molecular Pathways
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- DNA Repair Mechanisms
- Epigenetics and DNA Methylation
- CRISPR and Genetic Engineering
- RNA modifications and cancer
Papers in
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- DNA Repair Mechanisms 5
- RNA regulation and disease 1
- Oncology 5
- Cancer-related Molecular Pathways 4
- PARP inhibition in cancer therapy 3
- Co-authors
- Lisa Wiesmüller (6 shared papers)Jürgen Thomale (1 shared paper)Vanesa Gottifredi (1 shared paper)Helmut Pospiech (1 shared paper)Sabrina F. Mansilla (1 shared paper)Galina Selivanova (2 shared papers)Alexander Bürkle (1 shared paper)Arthur Fischbach (1 shared paper)
- Journals
- Nucleic Acids Research (1 paper)Carcinogenesis (1 paper)The FASEB Journal (1 paper)Proceedings of the National Academy of Sciences (1 paper)Human Mutation (1 paper)
- Partner nations
- GermanyUnited StatesSweden
In The Last Decade
Stephanie Hampp
7 papers receiving 284 citations
Peers
Comparison fields: 5 of 54
- Oncology 152
- Molecular Biology 198
- Cancer Research 39
- Physiology 8
- Neurology 18
Countries citing papers authored by Stephanie Hampp
This map shows the geographic impact of Stephanie Hampp'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 Stephanie Hampp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie Hampp more than expected).
Fields of papers citing papers by Stephanie Hampp
This network shows the impact of papers produced by Stephanie Hampp. 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 Stephanie Hampp. The network helps show where Stephanie Hampp may publish in the future.
Co-authors
The 25 scholars most cited alongside Stephanie Hampp, 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 | 2017 | 88 | |
| 2 | 2016 | 80 | |
| 3 | 2019 | 32 | |
| 4 | 2014 | 31 | |
| 5 | 2011 | 23 | |
| 6 | 2019 | 20 | |
| 7 | 2016 | 12 |
About Stephanie Hampp
Stephanie Hampp is a scholar working on Molecular Biology, Oncology, Genetics, Public Health, Environmental and Occupational Health and Infectious Diseases, having authored 7 papers that have together received 286 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (5 papers), Cancer-related Molecular Pathways (4 papers), PARP inhibition in cancer therapy (3 papers), Genetics and Neurodevelopmental Disorders (1 paper), Acute Lymphoblastic Leukemia research (1 paper), BRCA gene mutations in cancer (1 paper), RNA regulation and disease (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Oncology (152 citations), Molecular Biology (198 citations), Cancer Research (39 citations), Physiology (8 citations) and Neurology (18 citations). Stephanie Hampp has collaborated with scholars based in Germany, United States and Sweden. Frequent co-authors include Lisa Wiesmüller, Jürgen Thomale, Vanesa Gottifredi, Helmut Pospiech, Sabrina F. Mansilla, Galina Selivanova, Alexander Bürkle, Arthur Fischbach, Elisa Ferrando‐May and Ján Fischer. Their work appears in journals such as Nucleic Acids Research, Carcinogenesis, The FASEB Journal, Proceedings of the National Academy of Sciences and Human Mutation.
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.