Jesper Petersen

587 total citations
46 papers, 358 citations indexed

About

Jesper Petersen is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Jesper Petersen has authored 46 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 23 papers in Hematology and 10 papers in Molecular Biology. Recurrent topics in Jesper Petersen's work include Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (14 papers) and Erythrocyte Function and Pathophysiology (7 papers). Jesper Petersen is often cited by papers focused on Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (14 papers) and Erythrocyte Function and Pathophysiology (7 papers). Jesper Petersen collaborates with scholars based in Denmark, Netherlands and United Kingdom. Jesper Petersen's co-authors include Martin Dufva, Henrik Birgens, Andreas Glenthøj, Kristian Smistrup, Mikkel Fougt Hansen, Šarūnas Petronis, Detlef Snakenborg, David Sabourin, Claus Bo Vöge Christensen and David C. Rees and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Jesper Petersen

40 papers receiving 347 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jesper Petersen Denmark 11 159 119 76 74 42 46 358
Meichen Pan China 10 34 0.2× 134 1.1× 55 0.7× 42 0.6× 29 0.7× 36 310
Kexin Zou China 12 19 0.1× 80 0.7× 13 0.2× 16 0.2× 15 0.4× 36 357
James Kim United States 8 45 0.3× 36 0.3× 55 0.7× 51 0.7× 41 1.0× 10 263
Fabian Tölle Germany 9 101 0.6× 388 3.3× 5 0.1× 67 0.9× 7 0.2× 15 568
Tomoya Hayashi Japan 10 16 0.1× 36 0.3× 22 0.3× 150 2.0× 12 0.3× 34 291
Caio C. Quini Brazil 10 124 0.8× 185 1.6× 4 0.1× 11 0.1× 22 0.5× 17 392
Kanika Singh India 10 16 0.1× 130 1.1× 12 0.2× 10 0.1× 7 0.2× 22 285
Arkadiusz Pierzchalski Germany 10 213 1.3× 104 0.9× 3 0.0× 11 0.1× 13 0.3× 23 415
Cecilia Arfvidsson Sweden 11 36 0.2× 181 1.5× 11 0.1× 6 0.1× 11 0.3× 23 384

Countries citing papers authored by Jesper Petersen

Since Specialization
Citations

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

Fields of papers citing papers by Jesper Petersen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jesper Petersen

This figure shows the co-authorship network connecting the top 25 collaborators of Jesper Petersen. A scholar is included among the top collaborators of Jesper Petersen 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 Jesper Petersen. Jesper Petersen 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.
Hansen, Dennis Lund, et al.. (2024). 10‐Year Risk of Gallstones in Congenital Red Blood Cell Disorder Patients: A Nationwide Cohort Study. American Journal of Hematology. 100(2). 229–235.
2.
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Wijk, Richard van, et al.. (2024). Glucose phosphate isomerase deficiency demasked by whole-genome sequencing: a case report. Journal of Medical Case Reports. 18(1). 130–130.
4.
Jørgensen, Finn Stener, et al.. (2024). Optimisation of the Danish national haemoglobinopathy screening programme – A prospective intervention study. SHILAP Revista de lepidopterología. 6(3). e980–e980.
5.
Petersen, Jesper, Mathias Rathe, Charlotte Holm, et al.. (2023). The Danish national haemoglobinopathy screening programme: Report from 16 years of screening in a low‐prevalence, non‐endemic region. British Journal of Haematology. 204(1). 329–336. 6 indexed citations
6.
Karlsson, Linda, et al.. (2022). Acquired spherocytosis in the setting of myelodysplasia. Leukemia Research Reports. 17. 100332–100332. 1 indexed citations
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8.
Hansen, Dennis Lund, et al.. (2021). Priapism in patients with hemolytic disorders: a nationwide retrospective cohort study. Annals of Hematology. 100(8). 1947–1951. 5 indexed citations
9.
Glenthøj, Andreas, et al.. (2020). Improving the EMA Binding Test by Using Commercially Available Fluorescent Beads. Frontiers in Physiology. 11. 569289–569289. 8 indexed citations
10.
Hansen, Dennis Lund, Andreas Glenthøj, Sören Möller, et al.. (2020). <p>Prevalence of Congenital Hemolytic Disorders in Denmark, 2000–2016</p>. Clinical Epidemiology. Volume 12. 485–495. 11 indexed citations
11.
Køllgaard, Tania, Brian Kornblit, Jesper Petersen, et al.. (2016). (GT)n Repeat Polymorphism in Heme Oxygenase-1 (HO-1) Correlates with Clinical Outcome after Myeloablative or Nonmyeloablative Allogeneic Hematopoietic Cell Transplantation. PLoS ONE. 11(12). e0168210–e0168210. 4 indexed citations
12.
Rank, Cecilie Utke, et al.. (2015). Hereditary Hyperferritinemia-cataract Syndrome. European Oncology & Haematology. 11(2). 147–147. 2 indexed citations
13.
Lausen, Birgitte, et al.. (2015). Severe G6PD Deficiency Due to a New Missense Mutation in an Infant of Northern European Descent. Journal of Pediatric Hematology/Oncology. 37(8). e497–e499. 6 indexed citations
14.
Sabourin, David, Jesper Petersen, Detlef Snakenborg, et al.. (2010). Microfluidic DNA microarrays in PMMA chips: streamlined fabrication via simultaneous DNA immobilization and bonding activation by brief UV exposure. Biomedical Microdevices. 12(4). 673–681. 23 indexed citations
15.
Dufva, Martin, et al.. (2009). Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies. Analytical and Bioanalytical Chemistry. 395(3). 669–677. 14 indexed citations
16.
Petersen, Jesper, et al.. (2009). Genotyping of Mutations in the Beta-Globin Gene Using Allele Specific Hybridization. Methods in molecular biology. 529. 157–170. 1 indexed citations
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18.
Petersen, Jesper, et al.. (2007). Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays. Nucleic Acids Research. 36(2). e10–e10. 32 indexed citations
19.
Petersen, Jesper, Michael Stangegaard, Henrik Birgens, & Martin Dufva. (2006). Detection of mutations in the β-globin gene by colorimetric staining of DNA microarrays visualized by a flatbed scanner. Analytical Biochemistry. 360(1). 169–171. 11 indexed citations
20.
Smistrup, Kristian, et al.. (2005). On-chip magnetic bead microarray using hydrodynamic focusing in a passive magnetic separator. Lab on a Chip. 5(11). 1315–1315. 66 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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