Ulf Kristoffersson
- Genetics top 0.5%
- Molecular Biology top 5%
- Pathology and Forensic Medicine top 1%
- Oncology top 5%
- Cancer Research top 5%
- Co-authors
- Håkan OlssonFelix MitelmanSverre HeimÅke BorgNils MandahlRolf LundgrenNiklas LomanÓskar Þór Jóhannsson
- Topics
- BRCA gene mutations in cancer (43 papers)Genomic variations and chromosomal abnormalities (30 papers)Chronic Lymphocytic Leukemia Research (18 papers)
- Partner nations
- SwedenGermanySwitzerland
In The Last Decade
Ulf Kristoffersson
151 papers receiving 4.0k citations
Peers
Comparison fields: 5 of 114
- Genetics 1.9k
- Molecular Biology 1.3k
- Pathology and Forensic Medicine 935
- Oncology 745
- Cancer Research 631
Countries citing papers authored by Ulf Kristoffersson
This map shows the geographic impact of Ulf Kristoffersson'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 Ulf Kristoffersson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ulf Kristoffersson more than expected).
Fields of papers citing papers by Ulf Kristoffersson
This network shows the impact of papers produced by Ulf Kristoffersson. 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 Ulf Kristoffersson. The network helps show where Ulf Kristoffersson may publish in the future.
Co-authorship network of co-authors of Ulf Kristoffersson
This figure shows the co-authorship network connecting the top 25 collaborators of Ulf Kristoffersson. A scholar is included among the top collaborators of Ulf Kristoffersson 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 Ulf Kristoffersson. Ulf Kristoffersson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 5 | |
| 3 | 7 | |
| 4 | 17 | |
| 5 | 4 | |
| 6 | 21 | |
| 7 | 6 | |
| 8 | 0 | |
| 9 | 3 | |
| 10 | 1 | |
| 11 | 3 | |
| 12 | 0 | |
| 13 | 4 | |
| 14 | 3 | |
| 15 | 32 | |
| 16 | 26 | |
| 17 | 69 | |
| 18 | The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14. | 59 |
| 19 | 5 | |
| 20 | 17 |
About Ulf Kristoffersson
Ulf Kristoffersson is a scholar working on Genetics, Genetics and Hematology, having authored 156 papers that have together received 4.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (43 papers), Genomic variations and chromosomal abnormalities (30 papers) and Chronic Lymphocytic Leukemia Research (18 papers). The work is most often cited by research in Genetics (1.9k citations), Hematology (582 citations) and Pathology and Forensic Medicine (935 citations). Ulf Kristoffersson has collaborated with scholars based in Sweden, Germany and Switzerland. Frequent co-authors include Håkan Olsson, Felix Mitelman, Sverre Heim, Åke Borg, Nils Mandahl, Rolf Lundgren, Niklas Loman, Óskar Þór Jóhannsson, Ola Bratt and Fredrik Mertens. Their work appears in journals such as JNCI Journal of the National Cancer Institute, Cancer and Stroke.
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.