Sverre Heim
- Molecular Biology
- Pulmonary and Respiratory Medicine top 10%
- Hematology top 5%
- Cancer Research top 10%
- Genetics
- Co-authors
- Felix MitelmanRolf LundgrenNils MandahlJanusz LimonUlf KristofferssonNikos PandisGeorgia BardiRagnhild A. Lothe
- Topics
- Genomic variations and chromosomal abnormalities (4 papers)Cancer Genomics and Diagnostics (4 papers)Genetic factors in colorectal cancer (3 papers)
In The Last Decade
Sverre Heim
16 papers receiving 687 citations
Peers
Comparison fields: 5 of 50
- Molecular Biology 278
- Pulmonary and Respiratory Medicine 217
- Hematology 200
- Cancer Research 175
- Genetics 143
Countries citing papers authored by Sverre Heim
This map shows the geographic impact of Sverre Heim'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 Sverre Heim with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sverre Heim more than expected).
Fields of papers citing papers by Sverre Heim
This network shows the impact of papers produced by Sverre Heim. 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 Sverre Heim. The network helps show where Sverre Heim may publish in the future.
Co-authorship network of co-authors of Sverre Heim
This figure shows the co-authorship network connecting the top 25 collaborators of Sverre Heim. A scholar is included among the top collaborators of Sverre Heim 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 Sverre Heim. Sverre Heim is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 51 | |
| 2 | 23 | |
| 3 | 17 | |
| 4 | 20 | |
| 5 | 1 | |
| 6 | 16 | |
| 7 | 25 | |
| 8 | Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis. | 65 |
| 9 | 26 | |
| 10 | 17 | |
| 11 | 9 | |
| 12 | 104 | |
| 13 | 145 | |
| 14 | 81 | |
| 15 | 27 | |
| 16 | 79 |
About Sverre Heim
Sverre Heim is a scholar working on Hematology, Cancer Research and Pathology and Forensic Medicine, having authored 16 papers that have together received 706 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Cancer Genomics and Diagnostics (4 papers) and Genetic factors in colorectal cancer (3 papers). The work is most often cited by research in Hematology (200 citations), Cancer Research (175 citations) and Pathology and Forensic Medicine (139 citations). Sverre Heim has collaborated with scholars based in Sweden, Denmark and Norway. Frequent co-authors include Felix Mitelman, Rolf Lundgren, Nils Mandahl, Janusz Limon, Nils Mandahl, Ulf Kristoffersson, Nikos Pandis, Georgia Bardi, Ragnhild A. Lothe and A.L. Børresen-Dale. Their work appears in journals such as International Journal of Cancer, British Journal of Haematology and Genes Chromosomes and 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.