Markus Ringnér
Impact in
- Cancer Research top 0.1%
- Cancer Genomics and Diagnostics
- Breast Cancer Treatment Studies
- Oncology top 0.5%
- Cancer Immunotherapy and Biomarkers
- Cancer Cells and Metastasis
Papers in
-
- Cancer Genomics and Diagnostics 30
- Breast Cancer Treatment Studies 19
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- Gene expression and cancer classification 17
- Epigenetics and DNA Methylation 14
- Melanoma and MAPK Pathways 6
- Co-authors
- Åke Borg (27 shared papers)Lao H. Saal (7 shared papers)Carsten Peterson (9 shared papers)Paul S. Meltzer (9 shared papers)Johan Staaf (31 shared papers)Javed Iqbal Khan (3 shared papers)Mårten Fernö (10 shared papers)Erik Fredlund (4 shared papers)
- Journals
- Nature Communications (16 papers)Breast Cancer Research (9 papers)Nature (7 papers)Clinical Cancer Research (7 papers)Nature Genetics (5 papers)
- Partner nations
- SwedenUnited StatesUnited Kingdom
In The Last Decade
Markus Ringnér
124 papers receiving 24.7k citations
Markus Ringnér's Hit Papers
Peers
Comparison fields: 5 of 199
- Cancer Research 7k
- Oncology 4.2k
- Molecular Biology 8.6k
- Genetics 2.8k
- Genetics 411
Countries citing papers authored by Markus Ringnér
This map shows the geographic impact of Markus Ringnér'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 Ringnér with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Markus Ringnér more than expected).
Fields of papers citing papers by Markus Ringnér
This network shows the impact of papers produced by Markus Ringnér. 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 Ringnér. The network helps show where Markus Ringnér may publish in the future.
Co-authors
The 25 scholars most cited alongside Markus Ringnér, 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 125 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 | 2401 |
| 2 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2169 |
| 3 | Classification and diagnostic prediction of cancers using gene expression profiling and artificial neural networks Hit paper breakdown → | 2001 | 2136 |
| 4 | What is principal component analysis? Hit paper breakdown → | 2008 | 1855 |
| 5 | Landscape of somatic mutations in 560 breast cancer whole-genome sequences Hit paper breakdown → | 2016 | 1681 |
| 6 | Exosomes reflect the hypoxic status of glioma cells and mediate hypoxia-dependent activation of vascular cells during tumor development Hit paper breakdown → | 2013 | 825 |
| 7 | A Molecular Taxonomy for Urothelial Carcinoma Hit paper breakdown → | 2012 | 734 |
| 8 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 730 |
| 9 | Spatially and functionally distinct subclasses of breast cancer-associated fibroblasts revealed by single cell RNA sequencing Hit paper breakdown → | 2018 | 661 |
| 10 | Estrogen receptor status in breast cancer is associated with remarkably distinct gene expression patterns. | 2001 | 577 |
| 11 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 564 |
| 12 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 489 |
| 13 | 2008 | 476 | |
| 14 | 2007 | 445 | |
| 15 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes Hit paper breakdown → | 2020 | 428 |
| 16 | Impact of DNA amplification on gene expression patterns in breast cancer. | 2002 | 386 |
| 17 | 2017 | 373 | |
| 18 | 2011 | 347 | |
| 19 | Comprehensive molecular characterization of mitochondrial genomes in human cancers Hit paper breakdown → | 2020 | 319 |
| 20 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition Hit paper breakdown → | 2020 | 315 |
About Markus Ringnér
Markus Ringnér is a scholar working on Cancer Research, Molecular Biology, Oncology, Genetics and Neurology, having authored 125 papers that have together received 25.1k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (30 papers), Breast Cancer Treatment Studies (19 papers), Gene expression and cancer classification (17 papers), Epigenetics and DNA Methylation (14 papers), Genomic variations and chromosomal abnormalities (12 papers), Melanoma and MAPK Pathways (6 papers), Cutaneous Melanoma Detection and Management (6 papers) and Cancer Cells and Metastasis (5 papers). The work is most often cited by research in Cancer Research (7k citations), Oncology (4.2k citations), Molecular Biology (8.6k citations), Genetics (2.8k citations) and Genetics (411 citations). Markus Ringnér has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Åke Borg, Lao H. Saal, Carsten Peterson, Paul S. Meltzer, Johan Staaf, Javed Iqbal Khan, Mårten Fernö, Erik Fredlund, Frank Westermann and Frank Berthold. Their work appears in journals such as Nature Communications, Breast Cancer Research, Nature, Clinical Cancer Research and Nature Genetics.
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.