Eva Hellstrom-Lindberg
Impact in
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
- Oncology top 2%
Papers in
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- Cancer Genomics and Diagnostics 9
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- Genetic factors in colorectal cancer 3
- Journals
- Nature (5 papers)Nature Communications (3 papers)Nature Genetics (2 papers)Cancer Research (1 paper)Nature Biotechnology (1 paper)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
Eva Hellstrom-Lindberg
12 papers receiving 7.0k citations
Eva Hellstrom-Lindberg's Hit Papers
Peers
Comparison fields: 5 of 132
- Cancer Research 3.3k
- Oncology 1.5k
- Molecular Biology 3.8k
- Pathology and Forensic Medicine 852
- Genetics 1.1k
Countries citing papers authored by Eva Hellstrom-Lindberg
This map shows the geographic impact of Eva Hellstrom-Lindberg'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 Eva Hellstrom-Lindberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eva Hellstrom-Lindberg more than expected).
Fields of papers citing papers by Eva Hellstrom-Lindberg
This network shows the impact of papers produced by Eva Hellstrom-Lindberg. 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 Eva Hellstrom-Lindberg. The network helps show where Eva Hellstrom-Lindberg may publish in the future.
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All Works
| # | 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 | Analyses of non-coding somatic drivers in 2,658 cancer whole genomes Hit paper breakdown → | 2020 | 419 |
| 6 | 2020 | 317 | |
| 7 | Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition Hit paper breakdown → | 2020 | 309 |
| 8 | 2020 | 160 | |
| 9 | 2020 | 77 | |
| 10 | 2017 | 71 | |
| 11 | 2020 | 30 | |
| 12 | 2020 | 9 |
About Eva Hellstrom-Lindberg
Eva Hellstrom-Lindberg is a scholar working on Cancer Research, Pathology and Forensic Medicine, Molecular Biology, Genetics and Oncology, having authored 12 papers that have together received 7.1k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (9 papers), Genomics and Phylogenetic Studies (3 papers), Genetic factors in colorectal cancer (3 papers), Cancer-related Molecular Pathways (2 papers), Bioinformatics and Genomic Networks (2 papers), RNA Research and Splicing (2 papers), Genomics and Chromatin Dynamics (2 papers) and Evolution and Genetic Dynamics (2 papers). The work is most often cited by research in Cancer Research (3.3k citations), Oncology (1.5k citations), Molecular Biology (3.8k citations), Pathology and Forensic Medicine (852 citations) and Genetics (1.1k citations). Eva Hellstrom-Lindberg has collaborated with scholars based in United States, Canada and Germany. Their work appears in journals such as Nature, Nature Communications, Nature Genetics, Cancer Research and Nature Biotechnology.
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.