Dorien Schepers

1.9k total citations
19 papers, 493 citations indexed

About

Dorien Schepers is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Dorien Schepers has authored 19 papers receiving a total of 493 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Cardiology and Cardiovascular Medicine and 5 papers in Genetics. Recurrent topics in Dorien Schepers's work include Cardiac electrophysiology and arrhythmias (9 papers), Ion channel regulation and function (5 papers) and Connective tissue disorders research (5 papers). Dorien Schepers is often cited by papers focused on Cardiac electrophysiology and arrhythmias (9 papers), Ion channel regulation and function (5 papers) and Connective tissue disorders research (5 papers). Dorien Schepers collaborates with scholars based in Belgium, Netherlands and Denmark. Dorien Schepers's co-authors include Maaike Alaerts, Bart Loeys, Aline Verstraeten, Lut Van Laer, Josephina Meester, Timm Danker, Heidi Löffler, Ingrid E. Scheffer, Holger Lerche and Simone Mandelstam and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Scientific Reports.

In The Last Decade

Dorien Schepers

18 papers receiving 488 citations

Peers

Dorien Schepers

GENET

MB

CCM

PRM

CMN

Gina O’Grady New Zealand

Junko Kanno Japan

Yu Abe Japan

Teresa Giugliano Italy

Marta Szybowska Canada

HG Brunner Netherlands

Luis Rohena United States

Shoko Komatsuzaki Germany

Emanuela Dazzo Italy

Yalda Nilipour Iran

Gina O’Grady New Zealand

Dorien Schepers

137 ×0.6

GENET

282 ×1.4

MB

106 ×0.7

CCM

13 ×0.1

PRM

97 ×1.0

CMN

Citations per year, relative to Dorien Schepers Dorien Schepers (= 1×) peers Gina O’Grady

Countries citing papers authored by Dorien Schepers

Since Specialization

Citations

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

Fields of papers citing papers by Dorien Schepers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorien Schepers

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

All Works

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19 of 19 papers shown

1.

Ponsaerts, Peter, et al.. (2025). An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells. Methods. 241. 33–42.

2.

Vandendriessche, Benjamin, Charlotte Claes, Maaike Alaerts, et al.. (2023). Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping. Scientific Reports. 13(1). 1491–1491. 5 indexed citations

3.

Alaerts, Maaike, Dirk J. Snyders, Benjamin Vandendriessche, et al.. (2023). Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population. Orphanet Journal of Rare Diseases. 18(1). 23–23. 2 indexed citations

4.

Vandendriessche, Benjamin, Erik Fransén, Emeline M. Van Craenenbroeck, et al.. (2022). Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes. Biology Open. 11(2). 6 indexed citations

5.

Ridder, R. de, Björn De Samber, Eveline Boudin, et al.. (2022). The sqstm1tmΔUBA zebrafish model, a proof-of-concept in vivo model for Paget’s disease of bone?. Bone Reports. 16. 101483–101483. 1 indexed citations

6.

Matchkov, Vladimir V., Benjamin Vandendriessche, Maaike Alaerts, et al.. (2021). Inherited Ventricular Arrhythmia in Zebrafish: Genetic Models and Phenotyping Tools. Reviews of physiology, biochemistry and pharmacology. 184. 33–68. 3 indexed citations

7.

Labro, Alain J., Johan Saenen, Emeline M. Van Craenenbroeck, et al.. (2021). Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death. European Journal of Medical Genetics. 64(11). 104322–104322. 2 indexed citations

8.

Saenen, Johan, et al.. (2021). iPSC-Cardiomyocyte Models of Brugada Syndrome—Achievements, Challenges and Future Perspectives. International Journal of Molecular Sciences. 22(6). 2825–2825. 18 indexed citations

9.

Labro, Alain J., Hans De Wilde, Wendy Dewals, et al.. (2020). Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report. Frontiers in Cardiovascular Medicine. 7. 117–117. 4 indexed citations

10.

Alaerts, Maaike, et al.. (2020). Optical Mapping in hiPSC-CM and Zebrafish to Resolve Cardiac Arrhythmias. SHILAP Revista de lepidopterología. 1(3). 181–199. 2 indexed citations

11.

Alaerts, Maaike, Tomas Robyns, Dorien Schepers, et al.. (2020). Clinical characterization of the first Belgian SCN5A founder mutation cohort. EP Europace. 23(6). 918–927. 3 indexed citations

12.

Alaerts, Maaike, Gerarda van de Beek, Ilse Luyckx, et al.. (2019). Cardiogeneticsbank@UZA: A Collection of DNA, Tissues, and Cell Lines as a Translational Tool. Frontiers in Medicine. 6. 198–198. 1 indexed citations

13.

Shukla, Anju, Maaike Alaerts, Dorien Schepers, et al.. (2018). FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature. BMC Medical Genetics. 19(1). 140–140. 19 indexed citations

14.

Schepers, Dorien, Juliette Albuisson, Patrick Bruneval, et al.. (2018). Severe Phenotype of Cutis Laxa Type 1B with Antenatal Signs due to a Novel Homozygous Nonsense Mutation in EFEMP2. Molecular Syndromology. 9(4). 190–196. 4 indexed citations

15.

Kempers, Marlies, Alessandra Maugeri, Carlo Marcelis, et al.. (2018). Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: further delineation of the phenotype. Journal of Medical Genetics. 56(4). 220–227. 28 indexed citations

16.

Meester, Josephina, Aline Verstraeten, Maaike Alaerts, et al.. (2018). Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease. Clinical Genetics. 95(1). 85–94. 45 indexed citations

17.

Meester, Josephina, Aline Verstraeten, Dorien Schepers, et al.. (2017). Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome. ASVIDE. 4. 544–544. 6 indexed citations

18.

Meester, Josephina, Aline Verstraeten, Dorien Schepers, et al.. (2017). Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome. Annals of Cardiothoracic Surgery. 6(6). 582–594. 178 indexed citations

19.

Schepers, Dorien, Elena I. Ilina, Stephanie Nadine Reichel, et al.. (2013). Dominant‐negative effects of KCNQ2 mutations are associated with epileptic encephalopathy. Annals of Neurology. 75(3). 382–394. 166 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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