Ulf Kristoffersson
- Genetics top 0.5%
- BRCA gene mutations in cancer 43
- Genomic variations and chromosomal abnormalities 30
- Chronic Lymphocytic Leukemia Research 18
- Genomics and Rare Diseases 16
- Hematology top 2%
- Acute Myeloid Leukemia Research 16
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- Lymphoma Diagnosis and Treatment 18
- Cancer Research top 5%
- Cancer Genomics and Diagnostics 15
- Genetics top 2%
- BRCA gene mutations in cancer 43
- Genomic variations and chromosomal abnormalities 30
- Chronic Lymphocytic Leukemia Research 18
- Genomics and Rare Diseases 16
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- Prenatal Screening and Diagnostics 15
- Co-authors
- Håkan OlssonFelix MitelmanSverre HeimÅke BorgNils MandahlRolf LundgrenNiklas LomanÓskar Þór Jóhannsson
- Partner nations
- SwedenGermanySwitzerland
In The Last Decade
Ulf Kristoffersson
151 papers receiving 4.0k citations
Peers
Comparison fields: 5 of 114
- Genetics 1.9k
- Hematology 582
- Pathology and Forensic Medicine 935
- Cancer Research 631
- Genetics 413
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
The 25 scholars most cited alongside Ulf Kristoffersson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 1 | |
| 2 | 2022 | 5 | |
| 3 | 2021 | 7 | |
| 4 | 2017 | 17 | |
| 5 | 2017 | 4 | |
| 6 | 2014 | 21 | |
| 7 | 2009 | 6 | |
| 8 | 2009 | 0 | |
| 9 | 2009 | 3 | |
| 10 | 2008 | 1 | |
| 11 | 2008 | 3 | |
| 12 | 2008 | 0 | |
| 13 | 2008 | 4 | |
| 14 | 2008 | 3 | |
| 15 | 2005 | 32 | |
| 16 | 2005 | 26 | |
| 17 | 1999 | 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. | 1996 | 59 |
| 19 | 1991 | 5 | |
| 20 | 1990 | 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), Chronic Lymphocytic Leukemia Research (18 papers), Lymphoma Diagnosis and Treatment (18 papers), Genomics and Rare Diseases (16 papers), Acute Myeloid Leukemia Research (16 papers), Cancer Genomics and Diagnostics (15 papers) and Prenatal Screening and Diagnostics (15 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.