Markus Kreuz
Impact in
- Cancer Research top 0.2%
- Cancer Genomics and Diagnostics
- Pathology and Forensic Medicine top 0.5%
- Lymphoma Diagnosis and Treatment
- Genetic factors in colorectal cancer
Papers in
-
- Lymphoma Diagnosis and Treatment 39
- Genetic factors in colorectal cancer 12
-
- Cancer Genomics and Diagnostics 22
- Co-authors
- Inga Vater (6 shared papers)Lorenz H. P. Trümper (12 shared papers)Reiner Siebert (12 shared papers)Stefan Gesk (6 shared papers)Markus W. Loeffler (12 shared papers)Reiner Siebert (3 shared papers)Astrid Jeibmann (1 shared paper)Reinhard Schneppenheim (1 shared paper)
- Journals
- Nature Communications (16 papers)Haematologica (7 papers)Nature Genetics (6 papers)Nature (6 papers)Leukemia (5 papers)
- Partner nations
- GermanyUnited StatesCanada
In The Last Decade
Markus Kreuz
104 papers receiving 12.4k citations
Markus Kreuz's Hit Papers
Peers
Comparison fields: 5 of 155
- Cancer Research 4.6k
- Pathology and Forensic Medicine 2.6k
- Genetics 1.3k
- Oncology 2.9k
- Molecular Biology 6.0k
Countries citing papers authored by Markus Kreuz
This map shows the geographic impact of Markus Kreuz'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 Markus Kreuz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Markus Kreuz more than expected).
Fields of papers citing papers by Markus Kreuz
This network shows the impact of papers produced by Markus Kreuz. 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 Markus Kreuz. The network helps show where Markus Kreuz may publish in the future.
Co-authors
The 25 scholars most cited alongside Markus Kreuz, 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 107 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2339 |
| 2 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2109 |
| 3 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 705 |
| 4 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 550 |
| 5 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 476 |
| 6 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes Hit paper breakdown → | 2020 | 419 |
| 7 | 2020 | 317 | |
| 8 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition Hit paper breakdown → | 2020 | 309 |
| 9 | 2020 | 301 | |
| 10 | 2020 | 293 | |
| 11 | 2010 | 273 | |
| 12 | 2015 | 259 | |
| 13 | 2011 | 218 | |
| 14 | 2015 | 205 | |
| 15 | 2020 | 184 | |
| 16 | 2014 | 170 | |
| 17 | 2020 | 160 | |
| 18 | 2020 | 159 | |
| 19 | 2012 | 154 | |
| 20 | 2020 | 152 |
About Markus Kreuz
Markus Kreuz is a scholar working on Pathology and Forensic Medicine, Cancer Research, Genetics, Oncology and Molecular Biology, having authored 107 papers that have together received 12.5k indexed citations. Recurring topics across this work include Lymphoma Diagnosis and Treatment (39 papers), Cancer Genomics and Diagnostics (22 papers), Chronic Lymphocytic Leukemia Research (19 papers), Viral-associated cancers and disorders (18 papers), Genetic factors in colorectal cancer (12 papers), CAR-T cell therapy research (9 papers), RNA modifications and cancer (8 papers) and RNA Research and Splicing (6 papers). The work is most often cited by research in Cancer Research (4.6k citations), Pathology and Forensic Medicine (2.6k citations), Genetics (1.3k citations), Oncology (2.9k citations) and Molecular Biology (6.0k citations). Markus Kreuz has collaborated with scholars based in Germany, United States and Canada. Frequent co-authors include Inga Vater, Lorenz H. P. Trümper, Reiner Siebert, Stefan Gesk, Markus W. Loeffler, Reiner Siebert, Astrid Jeibmann, Reinhard Schneppenheim, Michael G. Pfreundschuh and Tobias Obser. Their work appears in journals such as Nature Communications, Haematologica, Nature Genetics, Nature and Leukemia.
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.