Moritz Gerstung
Impact in
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
- Health Informatics top 2%
Papers in
-
- DNA Repair Mechanisms 6
- Single-cell and spatial transcriptomics 6
- Epigenetics and DNA Methylation 5
-
- Cancer Genomics and Diagnostics 27
- Co-authors
- Peter J. Campbell (15 shared papers)Iñigo Martincorena (6 shared papers)Peter Van Loo (5 shared papers)Michael R. Stratton (6 shared papers)Niko Beerenwinkel (10 shared papers)Artem Shmatko (5 shared papers)Philip H. Jones (6 shared papers)Kerstin Haase (1 shared paper)
- Journals
- Nature Communications (9 papers)PLoS ONE (5 papers)Blood (5 papers)Nature Genetics (5 papers)Nature (3 papers)
- Partner nations
- United KingdomGermanySwitzerland
In The Last Decade
Moritz Gerstung
56 papers receiving 6.1k citations
Moritz Gerstung's Hit Papers
Peers
Comparison fields: 5 of 150
- Cancer Research 2.1k
- Health Informatics 66
- Molecular Biology 3.3k
- Aging 73
- Oncology 996
Countries citing papers authored by Moritz Gerstung
This map shows the geographic impact of Moritz Gerstung'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 Moritz Gerstung with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Moritz Gerstung more than expected).
Fields of papers citing papers by Moritz Gerstung
This network shows the impact of papers produced by Moritz Gerstung. 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 Moritz Gerstung. The network helps show where Moritz Gerstung may publish in the future.
Co-authors
The 25 scholars most cited alongside Moritz Gerstung, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | High burden and pervasive positive selection of somatic mutations in normal human skin Hit paper breakdown → | 2015 | 1151 |
| 2 | Universal Patterns of Selection in Cancer and Somatic Tissues Hit paper breakdown → | 2017 | 828 |
| 3 | Cell2location maps fine-grained cell types in spatial transcriptomics Hit paper breakdown → | 2022 | 550 |
| 4 | Pan-cancer computational histopathology reveals mutations, tumor composition and prognosis Hit paper breakdown → | 2020 | 386 |
| 5 | 2007 | 307 | |
| 6 | Artificial intelligence in histopathology: enhancing cancer research and clinical oncology Hit paper breakdown → | 2022 | 257 |
| 7 | 2014 | 227 | |
| 8 | 2016 | 200 | |
| 9 | 2012 | 175 | |
| 10 | 2017 | 163 | |
| 11 | 2015 | 148 | |
| 12 | 2020 | 142 | |
| 13 | 2010 | 131 | |
| 14 | 2022 | 120 | |
| 15 | 2020 | 111 | |
| 16 | 2021 | 108 | |
| 17 | 2018 | 89 | |
| 18 | 2014 | 85 | |
| 19 | Single-cell and spatial transcriptomics analysis of non-small cell lung cancer Hit paper breakdown → | 2024 | 82 |
| 20 | 2020 | 81 |
About Moritz Gerstung
Moritz Gerstung is a scholar working on Molecular Biology, Cancer Research, Genetics, Oncology and Hematology, having authored 59 papers that have together received 6.2k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (27 papers), Acute Myeloid Leukemia Research (8 papers), DNA Repair Mechanisms (6 papers), Single-cell and spatial transcriptomics (6 papers), Epigenetics and DNA Methylation (5 papers), Evolution and Genetic Dynamics (4 papers), AI in cancer detection (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Cancer Research (2.1k citations), Health Informatics (66 citations), Molecular Biology (3.3k citations), Aging (73 citations) and Oncology (996 citations). Moritz Gerstung has collaborated with scholars based in United Kingdom, Germany and Switzerland. Frequent co-authors include Peter J. Campbell, Iñigo Martincorena, Peter Van Loo, Michael R. Stratton, Niko Beerenwinkel, Artem Shmatko, Philip H. Jones, Kerstin Haase, Helen Davies and Kevin J. Dawson. Their work appears in journals such as Nature Communications, PLoS ONE, Blood, Nature Genetics and Nature.
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.