Laura Andreasen

1.0k total citations
25 papers, 533 citations indexed

About

Laura Andreasen is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Laura Andreasen has authored 25 papers receiving a total of 533 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Cardiology and Cardiovascular Medicine, 9 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Laura Andreasen's work include Cardiac electrophysiology and arrhythmias (8 papers), Atrial Fibrillation Management and Outcomes (7 papers) and Cardiomyopathy and Myosin Studies (7 papers). Laura Andreasen is often cited by papers focused on Cardiac electrophysiology and arrhythmias (8 papers), Atrial Fibrillation Management and Outcomes (7 papers) and Cardiomyopathy and Myosin Studies (7 papers). Laura Andreasen collaborates with scholars based in Denmark, Norway and United States. Laura Andreasen's co-authors include Morten S. Olesen, Jesper Hastrup Svendsen, Stig Haunsø, Jonas B. Nielsen, Lena Refsgaard, Ahmad Sajadieh, Anders G. Holst, Gustav Ahlberg, Charlotte Andreasen and Alex Hørby Christensen and has published in prestigious journals such as Nature Communications, Journal of the American College of Cardiology and European Heart Journal.

In The Last Decade

Laura Andreasen

23 papers receiving 527 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laura Andreasen Denmark 13 413 177 72 28 28 25 533
Karen McGuire United Kingdom 3 356 0.9× 230 1.3× 94 1.3× 41 1.5× 7 0.3× 4 475
Paul A. van der Zwaag Netherlands 19 854 2.1× 319 1.8× 96 1.3× 70 2.5× 17 0.6× 44 1.1k
Sean J. Jurgens United States 9 170 0.4× 111 0.6× 89 1.2× 55 2.0× 7 0.3× 33 358
Johanna C. Herkert Netherlands 12 160 0.4× 194 1.1× 156 2.2× 37 1.3× 9 0.3× 16 432
Michele Lioncino Italy 13 264 0.6× 194 1.1× 36 0.5× 102 3.6× 14 0.5× 39 438
Hervé Le Marec France 5 449 1.1× 370 2.1× 76 1.1× 54 1.9× 7 0.3× 6 574
Eline A. Nannenberg Netherlands 15 743 1.8× 422 2.4× 66 0.9× 34 1.2× 8 0.3× 21 890
Francesca Brun Italy 15 950 2.3× 276 1.6× 25 0.3× 41 1.5× 19 0.7× 25 1.1k
Annapaola Cirillo Italy 13 256 0.6× 119 0.7× 27 0.4× 93 3.3× 42 1.5× 40 369
Lien Lam Australia 13 554 1.3× 287 1.6× 40 0.6× 112 4.0× 5 0.2× 19 646

Countries citing papers authored by Laura Andreasen

Since Specialization
Citations

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

Fields of papers citing papers by Laura Andreasen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Andreasen

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Andreasen. A scholar is included among the top collaborators of Laura Andreasen 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 Laura Andreasen. Laura Andreasen 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.
Diederichsen, Søren Zöga, Lei Xing, Gustav Ahlberg, et al.. (2025). Atrial Fibrillation Screening According to Genetic Risk. Journal of the American College of Cardiology. 87(2). 143–153.
2.
Diederichsen, Søren Zöga, Pia R. Lundegaard, Litten Bertelsen, et al.. (2024). Genetic Determinants of Left Atrial Function Are Associated With Stroke. Journal of the American Heart Association. 13(23). e037490–e037490. 2 indexed citations
3.
Diederichsen, Søren Zöga, Laura Andreasen, Emil Loldrup Fosbøl, et al.. (2024). Atrial fibrillation: age at diagnosis, incident cardiovascular events, and mortality. European Heart Journal. 45(24). 2119–2129. 18 indexed citations
4.
Liss, Martin, Gustav Ahlberg, Laura Andreasen, et al.. (2023). Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation. JACC Basic to Translational Science. 9(2). 163–180. 7 indexed citations
5.
Ghouse, Jonas, Gustav Ahlberg, Laura Andreasen, et al.. (2021). Association of Variants Near the Bradykinin Receptor B2 Gene With Angioedema in Patients Taking ACE Inhibitors. Journal of the American College of Cardiology. 78(7). 696–709. 8 indexed citations
6.
Andreasen, Laura. (2021). Mendelian randomization—a powerful tool to study the causal effects of atrial fibrillation on loss of brain volume. BMC Medicine. 19(1). 70–70. 1 indexed citations
7.
Andreasen, Laura, et al.. (2020). Atrial fibrillation—a complex polygenetic disease. European Journal of Human Genetics. 29(7). 1051–1060. 43 indexed citations
8.
Ahlberg, Gustav, Jonas Ghouse, Laura Andreasen, et al.. (2020). Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation. Journal of Clinical Medicine. 9(2). 372–372. 16 indexed citations
9.
Bertelsen, Litten, Niels Vejlstrup, Laura Andreasen, Morten Olesen, & Jesper Hastrup Svendsen. (2020). Cardiac magnetic resonance systematically overestimates mitral regurgitations by the indirect method. Open Heart. 7(2). e001323–e001323. 6 indexed citations
10.
Bertelsen, Litten, Francisco Alarcón, Laura Andreasen, et al.. (2019). Verification of threshold for image intensity ratio analyses of late gadolinium enhancement magnetic resonance imaging of left atrial fibrosis in 1.5T scans. International journal of cardiac imaging. 36(3). 513–520. 20 indexed citations
11.
Andreasen, Laura, Gustav Ahlberg, Charlotte Andreasen, et al.. (2018). Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes. European Journal of Human Genetics. 26(5). 660–668. 9 indexed citations
12.
Andreasen, Laura, Jonas Ghouse, Morten W. Skov, et al.. (2018). Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest. Frontiers in Physiology. 9. 894–894. 3 indexed citations
13.
Ahlberg, Gustav, Lena Refsgaard, Pia R. Lundegaard, et al.. (2018). Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation. Nature Communications. 9(1). 4316–4316. 83 indexed citations
14.
Ahlberg, Gustav, Javad Jabbari, K. Henningsen, et al.. (2017). Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants. Heart Rhythm. 14(10). 1531–1538. 12 indexed citations
15.
Ghouse, Jonas, Morten W. Skov, Laura Andreasen, et al.. (2016). Numerous Brugada syndrome–associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality. Genetics in Medicine. 19(5). 521–528. 18 indexed citations
16.
Andreasen, Laura, Jonas B. Nielsen, & Morten S. Olesen. (2014). Genetic Aspects of Lone Atrial Fibrillation: What Do We Know?. Current Pharmaceutical Design. 21(5). 667–678. 13 indexed citations
17.
Andreasen, Laura, Jonas B. Nielsen, Ingrid E. Christophersen, et al.. (2014). Brugada syndrome risk loci seem protective against atrial fibrillation. European Journal of Human Genetics. 22(12). 1357–1361. 12 indexed citations
18.
Andreasen, Charlotte, Jonas B. Nielsen, Lena Refsgaard, et al.. (2013). New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants. European Journal of Human Genetics. 21(9). 918–928. 151 indexed citations
19.
Andreasen, Laura, Jonas B. Nielsen, Ingrid E. Christophersen, et al.. (2013). Genetic Modifier of the QTc Interval Associated With Early-Onset Atrial Fibrillation. Canadian Journal of Cardiology. 29(10). 1234–1240. 9 indexed citations
20.
Olesen, Morten S., Laura Andreasen, Javad Jabbari, et al.. (2013). Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation. Heart Rhythm. 11(2). 246–251. 45 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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