Bjørn A. Nexø

4.1k citations
92 papers · 2.9k indexed · h-index 33

Bjørn A. Nexø

91 papers receiving 2.8k citations

Peers

Bjørn A. Nexø
Comparison fields: 5 of 110
  • Cancer Research 640
  • Pathology and Forensic Medicine 486
  • Molecular Biology 1.8k
  • Genetics 604
  • Immunology 428
Replace Harumi Suzuki with:
Harumi Suzuki Japan
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Enric Esplugues United States
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Citations per year

Countries citing papers authored by Bjørn A. Nexø

Since Specialization
Citations

This map shows the geographic impact of Bjørn A. Nexø'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 Bjørn A. Nexø with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bjørn A. Nexø more than expected).

Fields of papers citing papers by Bjørn A. Nexø

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bjørn A. Nexø. 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 Bjørn A. Nexø. The network helps show where Bjørn A. Nexø may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Bjørn A. Nexø, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bjørn A. Nexø Line = papers co-authored together Bjørn A. Nexø links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20183
2 201552
3 201533
4 201318
5 201319
6 201265
7 200776
8 200544
9 200529
10
No association between OGG1 Ser326Cys and risk of basal cell carcinoma.
20045
11 200423
12 200412
13 200454
14
No association between the DNA repair gene XRCC3 T241M polymorphism and risk of skin cancer and breast cancer.
200364
15
Multiple single nucleotide polymorphisms on human chromosome 19q13.2-3 associate with risk of Basal cell carcinoma.
200254
16 20007
17 200035
18 200088
19
Polymorphisms in the DNA repair gene XPD: correlations with risk and age at onset of basal cell carcinoma.
1999157
20
Inflammatory potential of organic dust components and chemicals measured by IL-8 secretion from human epithelial cell line A549 in vitro
199712

About Bjørn A. Nexø

Bjørn A. Nexø is a scholar working on Cancer Research, Genetics and Virology, having authored 92 papers that have together received 2.9k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (25 papers), Carcinogens and Genotoxicity Assessment (12 papers), Chromosomal and Genetic Variations (9 papers), Genetic factors in colorectal cancer (7 papers), Virus-based gene therapy research (7 papers), Genomics and Chromatin Dynamics (6 papers), T-cell and Retrovirus Studies (5 papers) and Indoor Air Quality and Microbial Exposure (5 papers). The work is most often cited by research in Cancer Research (640 citations), Pathology and Forensic Medicine (486 citations) and Molecular Biology (1.8k citations). Bjørn A. Nexø has collaborated with scholars based in Denmark, Norway and United States. Frequent co-authors include Ulla Vogel, Håkan Wallin, Anne Tjønneland, Kim Overvad, Marianne Dybdahl, Ole Raaschou‐Nielsen, G Frentz, Anja Olsen, Magdalena Janina Laska and Klaus Bahl Andersen. Their work appears in journals such as PLoS ONE, American Journal of Clinical Nutrition and Journal of Virology.

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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