Ulf Kristoffersson

6.9k total citations
156 papers, 4.2k citations indexed

About

Ulf Kristoffersson is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Ulf Kristoffersson has authored 156 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Genetics, 46 papers in Molecular Biology and 33 papers in Pathology and Forensic Medicine. Recurrent topics in Ulf Kristoffersson's work include BRCA gene mutations in cancer (43 papers), Genomic variations and chromosomal abnormalities (30 papers) and Chronic Lymphocytic Leukemia Research (18 papers). Ulf Kristoffersson is often cited by papers focused on BRCA gene mutations in cancer (43 papers), Genomic variations and chromosomal abnormalities (30 papers) and Chronic Lymphocytic Leukemia Research (18 papers). Ulf Kristoffersson collaborates with scholars based in Sweden, Germany and Switzerland. Ulf Kristoffersson's 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 and has published in prestigious journals such as JNCI Journal of the National Cancer Institute, Cancer and Stroke.

In The Last Decade

Ulf Kristoffersson

151 papers receiving 4.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ulf Kristoffersson Sweden 33 1.9k 1.3k 935 745 631 156 4.2k
Catherine Bonaïti‐Pellié France 35 2.7k 1.4× 2.1k 1.7× 543 0.6× 981 1.3× 538 0.9× 109 5.4k
Daynna J. Wolff United States 24 1.2k 0.6× 1.0k 0.8× 392 0.4× 511 0.7× 822 1.3× 80 2.8k
Judy Kirk Australia 30 1.3k 0.7× 579 0.5× 614 0.7× 826 1.1× 554 0.9× 107 3.1k
Marilyn M. Li United States 26 733 0.4× 997 0.8× 479 0.5× 589 0.8× 1.0k 1.6× 105 3.2k
Hagay Sobol France 33 1.5k 0.8× 859 0.7× 647 0.7× 733 1.0× 713 1.1× 113 2.8k
Dominique Plantaz France 39 385 0.2× 1.5k 1.2× 456 0.5× 898 1.2× 729 1.2× 173 4.7k
Maurizio Genuardi Italy 38 1.7k 0.9× 2.3k 1.8× 1.8k 1.9× 1.3k 1.8× 1.1k 1.8× 203 5.1k
Ingrid Winship Australia 36 1.4k 0.8× 1.4k 1.1× 1.4k 1.5× 1.3k 1.7× 829 1.3× 229 5.0k
Franck Bourdeaut France 33 341 0.2× 2.2k 1.8× 1.0k 1.1× 559 0.8× 603 1.0× 130 3.9k
Janusz Limon Poland 40 1.2k 0.6× 1.8k 1.4× 962 1.0× 1.2k 1.6× 968 1.5× 240 5.8k

Countries citing papers authored by Ulf Kristoffersson

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

20 of 20 papers shown
1.
Ilinca, Andreea, et al.. (2024). Diagnosing Monogenic Stroke at Younger Age. Stroke. 55(12). 2846–2855. 1 indexed citations
2.
Ilinca, Andreea, Andreas Puschmann, Jukka Putaala, et al.. (2022). Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of stroke. European Journal of Human Genetics. 31(2). 239–242. 5 indexed citations
3.
Augustinsson, Annelie, Martin Nilsson, Carolina Ellberg, et al.. (2021). Genetic testing in women with early-onset breast cancer: a Traceback pilot study. Breast Cancer Research and Treatment. 190(2). 307–315. 7 indexed citations
4.
Augustinsson, Annelie, Carolina Ellberg, Ulf Kristoffersson, Åke Borg, & Håkan Olsson. (2017). Accuracy of self-reported family history of cancer, mutation status and tumor characteristics in patients with early onset breast cancer. Acta Oncologica. 57(5). 595–603. 17 indexed citations
5.
Challen, Kirsty, Hilary Harris, Ulf Kristoffersson, et al.. (2010). General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices. Journal of Community Genetics. 1(2). 83–90. 6 indexed citations
6.
Kristoffersson, Ulf, Jörg Schmidtke, & J J Cassiman. (2010). Quality Issues in Clinical Genetic Services. DIAL (Catholic University of Leuven). 22 indexed citations
7.
Plass, Anne Marie, Marieke J.H. Baars, Martina C. Cornel, et al.. (2009). Testing the Children: Do Non-Genetic Health-Care Providers Differ in Their Decision to Advise Genetic Presymptomatic Testing on Minors? A Cross-Sectional Study in Five Countries in the European Union. Genetic Testing and Molecular Biomarkers. 13(3). 367–376. 6 indexed citations
8.
Kristoffersson, Ulf. (2009). The action of hexyl mercury bromide on Chinese hamster cells in vitro. Hereditas. 79(2). 306–308.
9.
Kristoffersson, Ulf. (2009). The effect of cyclamate and saccharin on the chromosomes of a Chinese hamster cell line. Hereditas. 70(2). 271–282. 3 indexed citations
10.
Kristoffersson, Ulf, Roland Berger, Bo Nilsson, et al.. (2008). Constitutional C-band polymorphism in lymphocytes from patients with chronic myeloid leukemia. Hereditas. 110(2). 145–148. 1 indexed citations
11.
Lövkvist, Håkan, Holger Luthman, Peter Höglund, et al.. (2008). Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region. European Journal of Human Genetics. 16(9). 1117–1125. 25 indexed citations
12.
Kristoffersson, Ulf, Sverre Heim, Håkan Olsson, Måns Åkerman, & Felix Mitelman. (2008). Cytogenetic studies in non-Hodgkin lymphomas-Results from surgical biopsies. Hereditas. 104(1). 1–13. 3 indexed citations
13.
Kristoffersson, Ulf, Roland Berger, Alain Bernheim, et al.. (2008). No abnormal C-band polymorphism in lung cancer patients. Hereditas. 110(3). 201–202.
14.
Kristoffersson, Ulf, Håkan Olsson, Måns Åkerman, & Felix Mitelman. (2008). Cytogenetic studies in non-Hodgkin lymphomas-Results from fineneedle aspiration samples. Hereditas. 103(1). 63–76. 4 indexed citations
15.
Challen, Kirsty, Hilary Harris, Claire Julian‐Reynier, et al.. (2005). Genetic education and nongenetic health professionals: Educational providers and curricula in Europe. Genetics in Medicine. 7(5). 302–310. 32 indexed citations
16.
Godard, Béatrice, Helena Kääriäinen, Ulf Kristoffersson, et al.. (2003). Provision of genetic services in Europe: current practices and issues. European Journal of Human Genetics. 11(S2). S13–S48. 76 indexed citations
17.
Bratt, Ola, Jan‐Erik Damber, Monica Emanuelsson, et al.. (2000). Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer. European Journal of Cancer. 36(2). 235–241. 101 indexed citations
18.
Bratt, Ola, Ulf Kristoffersson, Rolf Lundgren, & Håkan Olsson. (1999). Familial and hereditary prostate cancer in southern Sweden. A population-based case–control study. European Journal of Cancer. 35(2). 272–277. 69 indexed citations
19.
Panagopoulos, Ioannis, Nikos Pandis, Carl Petersson, et al.. (1996). The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14.. PubMed. 56(21). 4871–5. 59 indexed citations
20.
Gustavii, Björn, et al.. (1989). [Risk of miscarriage after chorionic biopsy is probably not higher than after amniocentesis].. PubMed. 86(48). 4221–2. 2 indexed citations

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.

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