Per Guldberg

14.8k total citations · 1 hit paper
195 papers, 10.9k citations indexed

About

Per Guldberg is a scholar working on Molecular Biology, Clinical Biochemistry and Oncology. According to data from OpenAlex, Per Guldberg has authored 195 papers receiving a total of 10.9k indexed citations (citations by other indexed papers that have themselves been cited), including 124 papers in Molecular Biology, 54 papers in Clinical Biochemistry and 42 papers in Oncology. Recurrent topics in Per Guldberg's work include Metabolism and Genetic Disorders (54 papers), Epigenetics and DNA Methylation (34 papers) and Folate and B Vitamins Research (27 papers). Per Guldberg is often cited by papers focused on Metabolism and Genetic Disorders (54 papers), Epigenetics and DNA Methylation (34 papers) and Folate and B Vitamins Research (27 papers). Per Guldberg collaborates with scholars based in Denmark, United States and Germany. Per Guldberg's co-authors include Christina Dahl, Jesper Zeuthen, Jiří Bártek, Jiřina Bártková, Kirsten Grønbæk, Per thor Straten, Alexei F. Kirkin, Karen Koed, Jesper Worm and Alwin Krämer and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Per Guldberg

193 papers receiving 10.7k citations

Hit Papers

DNA damage response as a candidate anti-cancer barrier in... 2005 2026 2012 2019 2005 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Per Guldberg Denmark 53 7.3k 3.2k 1.5k 1.5k 1.3k 195 10.9k
John E.J. Rasko Australia 57 6.4k 0.9× 1.9k 0.6× 328 0.2× 1.8k 1.2× 1.1k 0.9× 238 11.1k
Richard A. Van Etten United States 51 7.0k 1.0× 3.3k 1.0× 340 0.2× 793 0.5× 1.6k 1.2× 144 15.1k
Ivan Gout United Kingdom 52 9.7k 1.3× 1.7k 0.5× 296 0.2× 592 0.4× 2.3k 1.8× 157 12.8k
Karl R. Clauser United States 49 7.2k 1.0× 2.2k 0.7× 277 0.2× 1.1k 0.8× 1.5k 1.2× 84 11.6k
Naohiko Seki Japan 70 12.1k 1.7× 2.1k 0.7× 292 0.2× 8.2k 5.6× 1.1k 0.9× 357 16.4k
Martin Eilers Germany 77 16.1k 2.2× 6.9k 2.2× 201 0.1× 3.1k 2.1× 2.2k 1.7× 193 20.6k
Reinhard Buettner Germany 60 8.9k 1.2× 3.4k 1.1× 120 0.1× 2.1k 1.5× 1.3k 1.0× 312 14.3k
Kenneth H. Kraemer United States 57 9.4k 1.3× 2.7k 0.9× 165 0.1× 3.3k 2.2× 835 0.7× 196 12.9k
Luisa Lanfrancone Italy 38 4.9k 0.7× 1.6k 0.5× 125 0.1× 813 0.6× 1.2k 1.0× 95 7.8k
Richard A. Gatti United States 58 8.7k 1.2× 3.2k 1.0× 101 0.1× 3.4k 2.4× 1.9k 1.5× 267 12.5k

Countries citing papers authored by Per Guldberg

Since Specialization
Citations

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

Fields of papers citing papers by Per Guldberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Per Guldberg. 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 Per Guldberg. The network helps show where Per Guldberg may publish in the future.

Co-authorship network of co-authors of Per Guldberg

This figure shows the co-authorship network connecting the top 25 collaborators of Per Guldberg. A scholar is included among the top collaborators of Per Guldberg 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 Per Guldberg. Per Guldberg 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.
Frías, Alex, Luca Di Leo, Asier Antoranz, et al.. (2023). Ambra1 modulates the tumor immune microenvironment and response to PD-1 blockade in melanoma. Journal for ImmunoTherapy of Cancer. 11(3). e006389–e006389. 5 indexed citations
2.
Dzhandzhugazyan, Karine N., Per Guldberg, & Alexei F. Kirkin. (2018). Adoptive T cell cancer therapy. Nature Materials. 17(6). 475–477. 18 indexed citations
3.
Eskelund, Christian Winther, Christina Dahl, Jakob Werner Hansen, et al.. (2017). TP53 mutations identify younger mantle cell lymphoma patients who do not benefit from intensive chemoimmunotherapy. Blood. 130(17). 1903–1910. 242 indexed citations
4.
Dahl, Christina, Claus Christensen, Göran Jönsson, et al.. (2013). Mutual Exclusivity Analysis of Genetic and Epigenetic Drivers in Melanoma Identifies a Link Between p14ARF and RARβ Signaling. Molecular Cancer Research. 11(10). 1166–1178. 21 indexed citations
5.
Lade‐Keller, Johanne, Per Guldberg, Rikke Riber‐Hansen, et al.. (2012). Evaluation of BRAF Mutation Testing Methodologies in Formalin-Fixed, Paraffin-Embedded Cutaneous Melanomas. Journal of Molecular Diagnostics. 15(1). 70–80. 57 indexed citations
6.
Møller, Henrik Devitt, Natascha Cremers, Mika Frankel, et al.. (2011). Role of Fibulin-5 in Metastatic Organ Colonization. Molecular Cancer Research. 9(5). 553–563. 23 indexed citations
7.
Cadwell, Kevin, Jeanette Falck Winther, E. Janet Tawn, et al.. (2010). The heritability of G2chromosomal radiosensitivity and its association with cancer in Danish cancer survivors and their offspring. International Journal of Radiation Biology. 86(11). 986–995. 26 indexed citations
8.
Dahl, Christina & Per Guldberg. (2007). A ligation assay for multiplex analysis of CpG methylation using bisulfite-treated DNA. Nucleic Acids Research. 35(21). e144–e144. 26 indexed citations
9.
Dahl, Christina, Karen Grønskov, Lars Allan Larsen, Per Guldberg, & Karen Brøndum‐Nielsen. (2007). A Homogeneous Assay for Analysis of FMR1 Promoter Methylation in Patients with Fragile X Syndrome. Clinical Chemistry. 53(4). 790–793. 27 indexed citations
10.
Christensen, Claus, Noona Ambartsumian, Giorgio F. Gilestro, et al.. (2005). Proteolytic Processing Converts the Repelling Signal Sema3E into an Inducer of Invasive Growth and Lung Metastasis. Cancer Research. 65(14). 6167–6177. 91 indexed citations
11.
Bártková, Jiřina, Zuzana Hořejšı́, Karen Koed, et al.. (2005). DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis. Nature. 434(7035). 864–870. 2117 indexed citations breakdown →
12.
Celis, Julio E., José M.A. Moreira, Irina Gromova, et al.. (2004). Towards discovery‐driven translational research in breast cancer. FEBS Journal. 272(1). 2–15. 43 indexed citations
13.
Straten, Per thor, Jürgen C. Becker, Jesper Zeuthen, & Per Guldberg. (2003). T-Cell Receptor Clonotype Mapping Using Denaturing Gradient Gel Electrophoresis: Analysis of Clonal T-Cell Responses in Melanoma. Humana Press eBooks. 61. 339–351. 3 indexed citations
14.
Koch, Richard, et al.. (1999). Long-Term Beneficial Effects of the Phenylalanine-Restricted Diet in Late-Diagnosed Individuals with Phenylketonuria. Molecular Genetics and Metabolism. 67(2). 148–155. 38 indexed citations
15.
Guldberg, Per, et al.. (1997). Single‐step DGGE‐based mutation scanning of the p53 gene: Application to genetic diagnosis of colorectal cancer. Human Mutation. 9(4). 348–355. 4 indexed citations
16.
Guldberg, Per, Alexei F. Kirkin, Kirsten Grønbæk, et al.. (1997). Complete scanning of theCDK4 gene by denaturing gradient gel electrophoresis: A novel missense mutation but low overall frequency of mutations in sporadic metastatic malignant melanoma. International Journal of Cancer. 72(5). 780–783. 23 indexed citations
17.
Koch, Richard, et al.. (1997). The Relationship of Genotype to Phenotype in Phenylalanine Hydroxylase Deficiency1. Biochemical and Molecular Medicine. 60(2). 92–101. 16 indexed citations
18.
Greber‐Platzer, Susanne, Per Guldberg, S Scheibenreiter, et al.. (1997). Molecular heterogeneity of classical and duarte galactosemia: Mutation analysis by denaturing gradient gel electrophoresis. Human Mutation. 10(1). 49–57. 44 indexed citations
19.
Guldberg, Per & Flemming Güttler. (1993). A simple method for identification of point mutations using denaturing gradient gel electrophoresis. Nucleic Acids Research. 21(9). 2261–2262. 50 indexed citations
20.
Guldberg, Per, et al.. (1993). A novel missense mutation in the phenylalanine hydroxylase gene of a homozygous Pakistani patient with non-PKU hyperphenylalaninemia. Human Molecular Genetics. 2(7). 1061–1062. 5 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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