Rune Frank-Hansen

831 total citations
24 papers, 606 citations indexed

About

Rune Frank-Hansen is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Rune Frank-Hansen has authored 24 papers receiving a total of 606 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Cardiology and Cardiovascular Medicine and 9 papers in Genetics. Recurrent topics in Rune Frank-Hansen's work include Molecular Biology Techniques and Applications (10 papers), Forensic and Genetic Research (9 papers) and Cardiac electrophysiology and arrhythmias (7 papers). Rune Frank-Hansen is often cited by papers focused on Molecular Biology Techniques and Applications (10 papers), Forensic and Genetic Research (9 papers) and Cardiac electrophysiology and arrhythmias (7 papers). Rune Frank-Hansen collaborates with scholars based in Denmark and United Kingdom. Rune Frank-Hansen's co-authors include Niels Morling, Anders J. Hansen, Laura Ferrero‐Miliani, Michael Christiansen, Paal Skytt Andersen, Sofie Lindgren Christiansen, Gyda Lolk Ottesen, Morten Dahl, Petros Syrris and William J. McKenna and has published in prestigious journals such as Clinica Chimica Acta, Human Mutation and BioTechniques.

In The Last Decade

Rune Frank-Hansen

24 papers receiving 594 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rune Frank-Hansen Denmark	13	341	316	167	66	36	24	606
Xiaoming Chen China	10	59 0.2×	83 0.3×	82 0.5×	6 0.1×	41 1.1×	21	375
Joshua A. Keefe United States	9	270 0.8×	84 0.3×	103 0.6×	20 0.3×	27 0.8×	20	434
Emily A. Rex United States	7	148 0.4×	31 0.1×	28 0.2×	10 0.2×	15 0.4×	13	259
Jiří Beneš Czechia	11	146 0.4×	135 0.4×	18 0.1×	7 0.1×	31 0.9×	23	332
Ondřej Šebesta Czechia	11	163 0.5×	23 0.1×	35 0.2×	22 0.3×	18 0.5×	15	300
Mauro Pesaresi Italy	11	180 0.5×	28 0.1×	250 1.5×	43 0.7×	25 0.7×	35	448
Baerbel Klauke Germany	8	155 0.5×	232 0.7×	37 0.2×	36 0.5×	5 0.1×	10	388
Petra W. Oosthoek Netherlands	9	309 0.9×	375 1.2×	34 0.2×	12 0.2×	160 4.4×	10	576
Neil Green United States	13	253 0.7×	36 0.1×	84 0.5×	10 0.2×	29 0.8×	19	459
David Angeles-Albores United States	8	158 0.5×	87 0.3×	34 0.2×	28 0.4×	11 0.3×	12	406

Countries citing papers authored by Rune Frank-Hansen

Since Specialization

Citations

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

Fields of papers citing papers by Rune Frank-Hansen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rune Frank-Hansen. 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 Rune Frank-Hansen. The network helps show where Rune Frank-Hansen may publish in the future.

Co-authorship network of co-authors of Rune Frank-Hansen

This figure shows the co-authorship network connecting the top 25 collaborators of Rune Frank-Hansen. A scholar is included among the top collaborators of Rune Frank-Hansen 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 Rune Frank-Hansen. Rune Frank-Hansen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Christiansen, Sofie Lindgren, et al.. (2019). Targeted molecular genetic testing in young sudden cardiac death victims from Western Denmark. International Journal of Legal Medicine. 134(1). 111–121. 11 indexed citations

Christiansen, Sofie Lindgren, Laura Ferrero‐Miliani, Morten Dahl, et al.. (2016). Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting. European Journal of Human Genetics. 24(12). 1797–1802. 53 indexed citations

HERTZ, CHRISTIN L., Sofie Lindgren Christiansen, Morten Dahl, et al.. (2015). Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases. European Journal of Human Genetics. 24(6). 817–822. 48 indexed citations

Mogensen, Helle Smidt, Rune Frank-Hansen, & Niels Morling. (2015). Test of Investigator ESSPLEX SE QS with quality sensors. Forensic science international. Genetics supplement series. 5. e490–e491. 1 indexed citations

HERTZ, CHRISTIN L., Sofie Lindgren Christiansen, Laura Ferrero‐Miliani, et al.. (2015). Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart. International Journal of Legal Medicine. 130(1). 91–102. 44 indexed citations

Mikkelsen, Martin, Rune Frank-Hansen, Anders J. Hansen, & Niels Morling. (2014). Massively parallel pyrosequencing of the mitochondrial genome with the 454 methodology in forensic genetics. Forensic Science International Genetics. 12. 30–37. 35 indexed citations

HERTZ, CHRISTIN L., Sofie Lindgren Christiansen, Laura Ferrero‐Miliani, et al.. (2014). Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases. International Journal of Legal Medicine. 129(4). 793–800. 47 indexed citations

HERTZ, CHRISTIN L., Laura Ferrero‐Miliani, Rune Frank-Hansen, Niels Morling, & Henning Bundgaard. (2014). A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification. EP Europace. 17(3). 350–357. 14 indexed citations

Mogensen, Helle Smidt, Rune Frank-Hansen, Brandi Simonsen, & Niels Morling. (2013). Performance of the RapidHIT™200. Forensic science international. Genetics supplement series. 4(1). e286–e287. 10 indexed citations

10.

Rockenbauer, Eszter, Anders Buchard, Helle Smidt Mogensen, et al.. (2013). Non-uniform phenotyping of D12S391 resolved by second generation sequencing. Forensic Science International Genetics. 8(1). 195–199. 29 indexed citations

11.

Stangegaard, Michael, Claus Børsting, Laura Ferrero‐Miliani, et al.. (2013). Evaluation of Four Automated Protocols for Extraction of DNA from FTA Cards. SLAS TECHNOLOGY. 18(5). 404–410. 23 indexed citations

12.

Page, Stephen P, Stavros P. Kounas, Petros Syrris, et al.. (2012). Cardiac Myosin Binding Protein-C Mutations in Families With Hypertrophic Cardiomyopathy. Circulation Cardiovascular Genetics. 5(2). 156–166. 107 indexed citations

13.

Stangegaard, Michael, Tobias Guldberg Frøslev, Rune Frank-Hansen, Anders J. Hansen, & Niels Morling. (2011). Automated Extraction of DNA from Blood and PCR Setup using a Tecan Freedom EVO Liquid Handler for Forensic Genetic STR Typing of Reference Samples. JALA Journal of the Association for Laboratory Automation. 16(2). 134–140. 11 indexed citations

14.

Rockenbauer, Eszter, Sarah L. Fordyce, María C. Ávila‐Arcos, et al.. (2011). Sequences of microvariant/“off-ladder” STR alleles. Forensic science international. Genetics supplement series. 3(1). e204–e205. 3 indexed citations

15.

Kounas, Stavros P., Paal Skytt Andersen, Rune Frank-Hansen, et al.. (2010). 069 Cardiac myosin binding protein C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome. A40.2–A40. 7 indexed citations

16.

Stangegaard, Michael, Tobias Guldberg Frøslev, Rune Frank-Hansen, et al.. (2009). Automated extraction of DNA and PCR setup using a Tecan Freedom EVO® liquid handler. Forensic science international. Genetics supplement series. 2(1). 74–76. 5 indexed citations

17.

Stangegaard, Michael, Carmen Tomàs, Anders J. Hansen, et al.. (2008). Biomek-3000 and GenPlex SNP Genotyping in Forensic Genetics. JALA Journal of the Association for Laboratory Automation. 13(5). 297–303. 5 indexed citations

18.

Frank-Hansen, Rune, Stephen P Page, Petros Syrris, et al.. (2008). Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations. European Journal of Human Genetics. 16(9). 1062–1069. 22 indexed citations

19.

Frank-Hansen, Rune, Lars Allan Larsen, Paal Skytt Andersen, Cathrine Jespersgaard, & Michael Christiansen. (2004). Mutations in the genes KCND2 and KCND3 encoding the ion channels Kv4.2 and Kv4.3, conducting the cardiac fast transient outward current (ITO,f), are not a frequent cause of long QT syndrome. Clinica Chimica Acta. 351(1-2). 95–100. 15 indexed citations

20.

Larsen, Lars Allan, Martin R. Johnson, C. Brown, et al.. (2001). Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis. Human Mutation. 18(5). 451–457. 17 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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