Sverre Heim
Impact in
- Cancer Research top 0.2%
- Cancer Genomics and Diagnostics
- Pathology and Forensic Medicine top 0.2%
- Genetic factors in colorectal cancer
Papers in
-
- Genomics and Chromatin Dynamics 32
-
- Genetic factors in colorectal cancer 37
- Lymphoma Diagnosis and Treatment 35
- Co-authors
- Felix Mitelman (172 shared papers)Nils Mandahl (130 shared papers)Ioannis Panagopoulos (115 shared papers)Ludmila Gorunova (99 shared papers)Francesca Micci (94 shared papers)Bodil Bjerkehagen (44 shared papers)Nikos Pandis (56 shared papers)Helena Willén (34 shared papers)
- Journals
- Genes Chromosomes and Cancer (73 papers)Cancer Genomics & Proteomics (34 papers)International Journal of Cancer (14 papers)Oncology Reports (11 papers)Hereditas (10 papers)
- Partner nations
- NorwaySwedenSwitzerland
In The Last Decade
Sverre Heim
428 papers receiving 11.4k citations
Peers
Comparison fields: 5 of 140
- Cancer Research 2.7k
- Pathology and Forensic Medicine 2.3k
- Obstetrics and Gynecology 904
- Hematology 1.3k
- Pulmonary and Respiratory Medicine 3.0k
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-authors
The 25 scholars most cited alongside Sverre Heim, 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 432 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Cancer risk in humans predicted by increased levels of chromosomal aberrations in lymphocytes: Nordic study group on the health risk of chromosome damage. | 1994 | 419 |
| 2 | 1992 | 238 | |
| 3 | 1990 | 187 | |
| 4 | 2006 | 180 | |
| 5 | 1993 | 150 | |
| 6 | 2006 | 128 | |
| 7 | 1992 | 120 | |
| 8 | Chromosome abnormalities in eighty-three head and neck squamous cell carcinomas: influence of culture conditions on karyotypic pattern. | 1993 | 115 |
| 9 | 2013 | 113 | |
| 10 | 1991 | 110 | |
| 11 | 1988 | 106 | |
| 12 | 1995 | 103 | |
| 13 | 2008 | 101 | |
| 14 | 2009 | 100 | |
| 15 | 1989 | 99 | |
| 16 | 1991 | 99 | |
| 17 | 1991 | 96 | |
| 18 | 1994 | 96 | |
| 19 | 1992 | 90 | |
| 20 | 2012 | 89 |
About Sverre Heim
Sverre Heim is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Pulmonary and Respiratory Medicine, Genetics and Cancer Research, having authored 432 papers that have together received 11.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (85 papers), Sarcoma Diagnosis and Treatment (84 papers), Cancer Genomics and Diagnostics (65 papers), Acute Myeloid Leukemia Research (53 papers), Genetic factors in colorectal cancer (37 papers), Lymphoma Diagnosis and Treatment (35 papers), Acute Lymphoblastic Leukemia research (32 papers) and Genomics and Chromatin Dynamics (32 papers). The work is most often cited by research in Cancer Research (2.7k citations), Pathology and Forensic Medicine (2.3k citations), Obstetrics and Gynecology (904 citations), Hematology (1.3k citations) and Pulmonary and Respiratory Medicine (3.0k citations). Sverre Heim has collaborated with scholars based in Norway, Sweden and Switzerland. Frequent co-authors include Felix Mitelman, Nils Mandahl, Ioannis Panagopoulos, Ludmila Gorunova, Francesca Micci, Bodil Bjerkehagen, Nikos Pandis, Helena Willén, Georgia Bardi and Manuel R. Teixeira. Their work appears in journals such as Genes Chromosomes and Cancer, Cancer Genomics & Proteomics, International Journal of Cancer, Oncology Reports and Hereditas.
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.