Elisabeth M. Lodder

2.7k total citations
40 papers, 1.0k citations indexed

About

Elisabeth M. Lodder is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Elisabeth M. Lodder has authored 40 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Cardiology and Cardiovascular Medicine, 19 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Elisabeth M. Lodder's work include Cardiac electrophysiology and arrhythmias (18 papers), Cardiomyopathy and Myosin Studies (14 papers) and Ion channel regulation and function (7 papers). Elisabeth M. Lodder is often cited by papers focused on Cardiac electrophysiology and arrhythmias (18 papers), Cardiomyopathy and Myosin Studies (14 papers) and Ion channel regulation and function (7 papers). Elisabeth M. Lodder collaborates with scholars based in Netherlands, United States and Germany. Elisabeth M. Lodder's co-authors include Arthur A.M. Wilde, Connie R. Bezzina, Christiaan C. Veerman, Arie O. Verkerk, Carol Ann Remme, Leander Beekman, Stefania Rizzo, Annelies de Klein, Dion Paridaens and Emine Kılıç and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and PLoS ONE.

In The Last Decade

Elisabeth M. Lodder

38 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabeth M. Lodder Netherlands 16 592 529 175 98 90 40 1.0k
Anna Pfenniger United States 17 524 0.9× 799 1.5× 20 0.1× 243 2.5× 53 0.6× 44 1.4k
Jakob Triebel Germany 15 127 0.2× 184 0.3× 84 0.5× 54 0.6× 46 0.5× 50 770
Yuuki Kaminoh United States 11 111 0.2× 463 0.9× 134 0.8× 23 0.2× 70 0.8× 12 757
Pier Luigi DiPatre United States 6 67 0.1× 201 0.4× 119 0.7× 152 1.6× 27 0.3× 8 630
Ryuichiro Anan Japan 14 1.3k 2.1× 668 1.3× 21 0.1× 8 0.1× 27 0.3× 28 1.6k
Takahito Nakama Japan 18 84 0.1× 235 0.4× 450 2.6× 35 0.4× 16 0.2× 35 819
Jiaxiang Qu United States 9 281 0.5× 431 0.8× 6 0.0× 41 0.4× 64 0.7× 11 660
Bente Kühn Madsen Denmark 13 265 0.4× 375 0.7× 5 0.0× 107 1.1× 42 0.5× 20 760
Tuncer Onay United States 15 58 0.1× 406 0.8× 120 0.7× 127 1.3× 119 1.3× 23 928
Igor Kovačević Netherlands 15 66 0.1× 284 0.5× 27 0.2× 28 0.3× 21 0.2× 21 643

Countries citing papers authored by Elisabeth M. Lodder

Since Specialization
Citations

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

Fields of papers citing papers by Elisabeth M. Lodder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elisabeth M. Lodder. 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 Elisabeth M. Lodder. The network helps show where Elisabeth M. Lodder may publish in the future.

Co-authorship network of co-authors of Elisabeth M. Lodder

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth M. Lodder. A scholar is included among the top collaborators of Elisabeth M. Lodder 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 Elisabeth M. Lodder. Elisabeth M. Lodder 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.
Postma, Alex V., Saskia N. van der Crabben, Leander Beekman, et al.. (2025). Sinus Bradycardia and Long QT Syndrome: Double Heterozygosity for Variants in KCNH2 and HCN4. Pure Amsterdam UMC. 15(4). 31–31.
2.
Koopmann, Tamara T., Jeffrey M. Vinocur, Nico A. Blom, et al.. (2024). Reduced kinase function in two ultra‐rare TNNI3K variants in families with congenital junctional ectopic tachycardia. Clinical Genetics. 106(1). 37–46. 2 indexed citations
3.
Glinge, Charlotte, L Oestergaard, Thomas Hadberg Lynge, et al.. (2023). Risk of Sudden Infant Death Syndrome Among Siblings of Children Who Died of Sudden Infant Death Syndrome in Denmark. JAMA Network Open. 6(1). e2252724–e2252724. 10 indexed citations
4.
5.
Bootsma, Marianne, Chai‐Ann Ng, Arthur A.M. Wilde, et al.. (2022). Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance. Human Molecular Genetics. 32(7). 1072–1082. 2 indexed citations
6.
Marchal, Gerard A., Maaike van Putten, Arie O. Verkerk, et al.. (2021). Low human dystrophin levels prevent cardiac electrophysiological and structural remodelling in a Duchenne mouse model. Scientific Reports. 11(1). 9779–9779. 11 indexed citations
7.
Glinge, Charlotte, Thomas Engstrøm, Sofie Midgley, et al.. (2020). Seasonality of ventricular fibrillation at first myocardial infarction and association with viral exposure. PLoS ONE. 15(2). e0226936–e0226936. 4 indexed citations
8.
Meijborg, Veronique M.F., et al.. (2020). From Genome-Wide Association Studies to Cardiac Electrophysiology: Through the Maze of Biological Complexity. Frontiers in Physiology. 11. 557–557. 5 indexed citations
9.
Verkerk, Arie O., Elisabeth M. Lodder, & Ronald Wilders. (2019). Aquaporin Channels in the Heart—Physiology and Pathophysiology. International Journal of Molecular Sciences. 20(8). 2039–2039. 30 indexed citations
10.
Veerman, Christiaan C., Rafik Tadros, Elisabeth M. Lodder, et al.. (2017). The Brugada Syndrome Susceptibility Gene HEY2 Modulates Cardiac Transmural Ion Channel Patterning and Electrical Heterogeneity. Circulation Research. 121(5). 537–548. 44 indexed citations
11.
Lahrouchi, Najim, Elisabeth M. Lodder, Rafik Tadros, et al.. (2017). Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death. European Journal of Human Genetics. 25(6). 783–787. 20 indexed citations
12.
Lieve, Krystien V.V., Arie O. Verkerk, Christian van der Werf, et al.. (2017). Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation. International Journal of Cardiology. 236. 187–193. 30 indexed citations
13.
Milano, Annalisa, Elisabeth M. Lodder, & Connie R. Bezzina. (2015). TNNI3K in cardiovascular disease and prospects for therapy. Journal of Molecular and Cellular Cardiology. 82. 167–173. 14 indexed citations
14.
Koopmann, Tamara T., Michiel Adriaens, Perry D. Moerland, et al.. (2014). Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart. PLoS ONE. 9(5). e97380–e97380. 27 indexed citations
15.
Milano, Annalisa, Alexa M.C. Vermeer, Elisabeth M. Lodder, et al.. (2014). HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy. Journal of the American College of Cardiology. 64(8). 745–756. 126 indexed citations
16.
Rizzo, Stefania, Elisabeth M. Lodder, Arie O. Verkerk, et al.. (2012). Intercalated disc abnormalities, reduced Na+ current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes. Cardiovascular Research. 95(4). 409–418. 150 indexed citations
17.
Lodder, Elisabeth M., Brendon P. Scicluna, Annalisa Milano, et al.. (2012). Dissection of a Quantitative Trait Locus for PR Interval Duration Identifies Tnni3k as a Novel Modulator of Cardiac Conduction. PLoS Genetics. 8(12). e1003113–e1003113. 36 indexed citations
18.
Lodder, Elisabeth M. & Stefania Rizzo. (2012). Mouse Models in Arrhythmogenic Right Ventricular Cardiomyopathy. Frontiers in Physiology. 3. 221–221. 15 indexed citations
19.
Milano, Annalisa, Elisabeth M. Lodder, Brendon P. Scicluna, et al.. (2011). Abstract 16031: Tnni3k is a Novel Modulator of Cardiac Conduction. Circulation. 124. 1 indexed citations
20.
Lodder, Elisabeth M., A. Jeannette M. Hoogeboom, J. Henk Coert, & Esther de Graaff. (2008). Deletion of 1 amino acid in Indian hedgehog leads to brachydactylyA1. American Journal of Medical Genetics Part A. 146A(16). 2152–2154. 16 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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