Åke Borg
Impact in
- Cancer Research top 0.02%
- Cancer Genomics and Diagnostics
- Breast Cancer Treatment Studies
- Genetics top 0.05%
- BRCA gene mutations in cancer
Papers in
- Genetics 138
- BRCA gene mutations in cancer 123
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- Breast Cancer Treatment Studies 39
- Cancer Genomics and Diagnostics 32
- Co-authors
- Hakan Lars Olsson (56 shared papers)Mårten Fernö (35 shared papers)Markus Ringnér (27 shared papers)Johan Vallon‐Christersson (53 shared papers)Lao H. Saal (30 shared papers)Johan Staaf (53 shared papers)Jorma J Isola (19 shared papers)Sofia K. Gruvberger-Saal (15 shared papers)
- Journals
- Breast Cancer Research (21 papers)Nature Communications (21 papers)Genes Chromosomes and Cancer (14 papers)European Journal of Cancer (13 papers)British Journal of Cancer (12 papers)
- Partner nations
- SwedenUnited StatesUnited Kingdom
In The Last Decade
Åke Borg
388 papers receiving 58.9k citations
Åke Borg's Hit Papers
Peers
Comparison fields: 5 of 144
- Cancer Research 10.3k
- Genetics 11.4k
- Oncology 6.2k
- Molecular Biology 8.8k
- Reproductive Medicine 817
Countries citing papers authored by Åke Borg
This map shows the geographic impact of Åke Borg'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 Åke Borg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Åke Borg more than expected).
Fields of papers citing papers by Åke Borg
This network shows the impact of papers produced by Åke Borg. 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 Åke Borg. The network helps show where Åke Borg may publish in the future.
Co-authors
The 25 scholars most cited alongside Åke Borg, 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 394 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Signatures of mutational processes in human cancer Hit paper breakdown → | 2013 | 7666 |
| 2 | Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies Hit paper breakdown → | 2003 | 2873 |
| 3 | Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer Families Hit paper breakdown → | 1998 | 2443 |
| 4 | Visualization and analysis of gene expression in tissue sections by spatial transcriptomics Hit paper breakdown → | 2016 | 2435 |
| 5 | The repertoire of mutational signatures in human cancer Hit paper breakdown → | 2020 | 2401 |
| 6 | Pan-cancer analysis of whole genomes Hit paper breakdown → | 2020 | 2169 |
| 7 | International network of cancer genome projects Hit paper breakdown → | 2010 | 1844 |
| 8 | Landscape of somatic mutations in 560 breast cancer whole-genome sequences Hit paper breakdown → | 2016 | 1681 |
| 9 | Mutational Processes Molding the Genomes of 21 Breast Cancers Hit paper breakdown → | 2012 | 1487 |
| 10 | The Life History of 21 Breast Cancers Hit paper breakdown → | 2012 | 1111 |
| 11 | High-definition spatial transcriptomics for in situ tissue profiling Hit paper breakdown → | 2019 | 836 |
| 12 | HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures Hit paper breakdown → | 2017 | 798 |
| 13 | 2005 | 760 | |
| 14 | The evolutionary history of 2,658 cancers Hit paper breakdown → | 2020 | 730 |
| 15 | 2006 | 628 | |
| 16 | Estrogen receptor status in breast cancer is associated with remarkably distinct gene expression patterns. | 2001 | 577 |
| 17 | Patterns of somatic structural variation in human cancer genomes Hit paper breakdown → | 2020 | 564 |
| 18 | Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing Hit paper breakdown → | 2020 | 489 |
| 19 | 2008 | 476 | |
| 20 | Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer Hit paper breakdown → | 2013 | 468 |
About Åke Borg
Åke Borg is a scholar working on Genetics, Cancer Research, Oncology, Pathology and Forensic Medicine and Molecular Biology, having authored 394 papers that have together received 60.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (123 papers), Breast Cancer Treatment Studies (39 papers), Cancer Genomics and Diagnostics (32 papers), Genetic factors in colorectal cancer (9 papers), HER2/EGFR in Cancer Research (9 papers), Epigenetics and DNA Methylation (7 papers), Acute Myeloid Leukemia Research (6 papers) and Cutaneous Melanoma Detection and Management (6 papers). The work is most often cited by research in Cancer Research (10.3k citations), Genetics (11.4k citations), Oncology (6.2k citations), Molecular Biology (8.8k citations) and Reproductive Medicine (817 citations). Åke Borg has collaborated with scholars based in Sweden, United States and United Kingdom. Frequent co-authors include Hakan Lars Olsson, Mårten Fernö, Markus Ringnér, Johan Vallon‐Christersson, Lao H. Saal, Johan Staaf, Jorma J Isola, Sofia K. Gruvberger-Saal, Óskar Þór Jóhannsson and Pär‐Ola Bendahl. Their work appears in journals such as Breast Cancer Research, Nature Communications, Genes Chromosomes and Cancer, European Journal of Cancer and British Journal of Cancer.
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.