Lovise Mæhle
- Genetics top 2%
- Cancer Research top 5%
- Oncology top 5%
- Pathology and Forensic Medicine top 5%
- Molecular Biology
- Co-authors
- Pål MøllerJaran ApoldKetil HeimdalAnne Irene HagenNeal ClarkEli Marie GrindedalAnita VabøAstrid Stormorken
- Topics
- BRCA gene mutations in cancer (43 papers)Cancer Genomics and Diagnostics (22 papers)Genomic variations and chromosomal abnormalities (19 papers)
- Partner nations
- NorwayUnited KingdomNetherlands
In The Last Decade
Lovise Mæhle
59 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 94
- Genetics 918
- Cancer Research 525
- Oncology 474
- Pathology and Forensic Medicine 441
- Molecular Biology 424
Countries citing papers authored by Lovise Mæhle
This map shows the geographic impact of Lovise Mæhle'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 Lovise Mæhle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lovise Mæhle more than expected).
Fields of papers citing papers by Lovise Mæhle
This network shows the impact of papers produced by Lovise Mæhle. 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 Lovise Mæhle. The network helps show where Lovise Mæhle may publish in the future.
Co-authorship network of co-authors of Lovise Mæhle
This figure shows the co-authorship network connecting the top 25 collaborators of Lovise Mæhle. A scholar is included among the top collaborators of Lovise Mæhle based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lovise Mæhle. Lovise Mæhle is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 28 | |
| 2 | 32 | |
| 3 | 11 | |
| 4 | 3 | |
| 5 | 13 | |
| 6 | 14 | |
| 7 | 60 | |
| 8 | 4 | |
| 9 | 57 | |
| 10 | 11 | |
| 11 | 12 | |
| 12 | 11 | |
| 13 | 35 | |
| 14 | 33 | |
| 15 | 88 | |
| 16 | 24 | |
| 17 | [European guidelines for health care in hereditary breast cancer]. | 0 |
| 18 | 22 | |
| 19 | 21 | |
| 20 | 16 |
About Lovise Mæhle
Lovise Mæhle is a scholar working on Genetics, Cancer Research and Reproductive Medicine, having authored 61 papers that have together received 1.6k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (43 papers), Cancer Genomics and Diagnostics (22 papers) and Genomic variations and chromosomal abnormalities (19 papers). The work is most often cited by research in Cancer Research (525 citations), Genetics (918 citations) and Pathology and Forensic Medicine (441 citations). Lovise Mæhle has collaborated with scholars based in Norway, United Kingdom and Netherlands. Frequent co-authors include Pål Møller, Jaran Apold, Ketil Heimdal, Anne Irene Hagen, Neal Clark, Eli Marie Grindedal, Anita Vabø, Astrid Stormorken, D. Gareth Evans and Eivind Hovig. Their work appears in journals such as PLoS ONE, Clinical Cancer Research and Environmental Health Perspectives.
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.