Dorien Schepers

1.9k citations

19 papers · 493 · h-index 7

Impact in

Genetics top 10%
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
Cardiology and Cardiovascular Medicine top 10%
- Cardiac electrophysiology and arrhythmias

Papers in

Molecular Biology 12
- Ion channel regulation and function 5
- Pluripotent Stem Cells Research 3
- RNA and protein synthesis mechanisms 2
Cardiology and Cardiovascular Medicine 10
- Cardiac electrophysiology and arrhythmias 9
- Cardiomyopathy and Myosin Studies 3
- Cardiovascular Effects of Exercise 2

Co-authors: Maaike Alaerts (16 shared papers)Bart Loeys (17 shared papers)Aline Verstraeten (6 shared papers)Lut Van Laer (10 shared papers)Josephina Meester (4 shared papers)Elke Guenther (1 shared paper)Ingrid E. Scheffer (1 shared paper)Peter De Jonghe (1 shared paper)
Journals: Reviews of physiology, biochemistry and pharmacology (1 paper)Scientific Reports (1 paper)Annals of Cardiothoracic Surgery (1 paper)Orphanet Journal of Rare Diseases (1 paper)European Journal of Medical Genetics (1 paper)
Partner nations: Belgium Netherlands Australia

In The Last Decade

Dorien Schepers

18 papers receiving 488 citations

Peers

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-authors

The 25 scholars most cited alongside Dorien Schepers, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dorien Schepers Line = papers co-authored together Dorien Schepers links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

19 of 19 papers shown

#	Work
1	Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome Annals of Cardiothoracic Surgery ·Josephina Meester, Aline Verstraeten, Dorien Schepers, Maaike Alaerts, Lut Van Laer, Bart Loeys	2017	178
2	Dominant‐negative effects of KCNQ2 mutations are associated with epileptic encephalopathy Annals of Neurology ·Gökce Orhan, Merle Bock, Dorien Schepers, Elena I. Ilina, Stephanie Nadine Reichel, Heidi Löffler, Nicole Jezutkovic, Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Timm Danker, Elke Guenther, Ingrid E. Scheffer, Peter De Jonghe, Holger Lerche, Snezana Maljevic	2013	166
3	Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease Clinical Genetics ·Josephina Meester, Aline Verstraeten, Maaike Alaerts, Dorien Schepers, Lut Van Laer, Bart Loeys	2018	45
4	Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: further delineation of the phenotype Journal of Medical Genetics ·Elyssa Cannaerts, Marlies Kempers, Alessandra Maugeri, Carlo Marcelis, Thatjana Gardeitchik, Julie Richer, Dimitra Micha, Luc Beauchesne, Janneke Timmermans, Paul Vermeersch, Nathalie Meyten, Sébastien Chénier, Gerarda van de Beek, Nils Peeters, Maaike Alaerts, Dorien Schepers, Lut Van Laer, Aline Verstraeten, Bart Loeys	2018	28
5	FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature BMC Medical Genetics ·Elyssa Cannaerts, Anju Shukla, Mensuda Hasanhodžić, Maaike Alaerts, Dorien Schepers, Lut Van Laer, Katta M. Girisha, Iva Hojsak, Bart Loeys, Aline Verstraeten	2018	19
6	iPSC-Cardiomyocyte Models of Brugada Syndrome—Achievements, Challenges and Future Perspectives International Journal of Molecular Sciences ·Aleksandra Nijak, Johan Saenen, Alain J. Labro, Dorien Schepers, Bart Loeys, Maaike Alaerts	2021	18
7	Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes Biology Open ·Aleksandra Nijak, Eline Simons, Benjamin Vandendriessche, Dieter Van de Sande, Erik Fransén, Ewa Sieliwończyk, Ilse Van Gucht, Emeline M. Van Craenenbroeck, Johan Saenen, Hein Heidbüchel, Peter Ponsaerts, Alain J. Labro, Dirk J. Snyders, Winnok H. De Vos, Dorien Schepers, Maaike Alaerts, Bart Loeys	2022	6
8	Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome ASVIDE ·Josephina Meester, Aline Verstraeten, Dorien Schepers, Maaike Alaerts, Lut Van Laer, Bart Loeys	2017	6
9	Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping Scientific Reports ·Ewa Sieliwończyk, Benjamin Vandendriessche, Charlotte Claes, Evy Mayeur, Maaike Alaerts, Philip Holmgren, Tycho Canter Cremers, Dirk J. Snyders, Bart Loeys, Dorien Schepers	2023	5
10	Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report Frontiers in Cardiovascular Medicine ·Aleksandra Nijak, Alain J. Labro, Hans De Wilde, Wendy Dewals, Steve Peigneur, Jan Tytgat, Dirk J. Snyders, Ewa Sieliwończyk, Eline Simons, Emeline M. Van Craenenbroeck, Dorien Schepers, Lut Van Laer, Johan Saenen, Bart Loeys, Maaike Alaerts	2020	4
11	Severe Phenotype of Cutis Laxa Type 1B with Antenatal Signs due to a Novel Homozygous Nonsense Mutation in EFEMP2 Molecular Syndromology ·Pascaline Létard, Dorien Schepers, Juliette Albuisson, Patrick Bruneval, Emmanuel Spaggiari, Gerarda van de Beek, Suonavy Khung‐Savatovsky, N. Belarbi, Yline Capri, Anne‐Lise Delezoide, Bart Loeys, Fabien Guimiot	2018	4
12	Inherited Ventricular Arrhythmia in Zebrafish: Genetic Models and Phenotyping Tools Reviews of physiology, biochemistry and pharmacology ·Ewa Sieliwończyk, Vladimir V. Matchkov, Benjamin Vandendriessche, Maaike Alaerts, Jeroen Bakkers, Bart Loeys, Dorien Schepers	2021	3
13	Clinical characterization of the first Belgian SCN5A founder mutation cohort EP Europace ·Ewa Sieliwończyk, Maaike Alaerts, Tomas Robyns, Dorien Schepers, Charlotte Claes, Anniek Corveleyn, Rik Willems, Emeline M. Van Craenenbroeck, Eline Simons, Aleksandra Nijak, Benjamin Vandendriessche, Geert Mortier, Christiaan Vrints, Pieter Koopman, Hein Heidbüchel, Lut Van Laer, Johan Saenen, Bart Loeys	2020	3
14	Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population Orphanet Journal of Rare Diseases ·Ewa Sieliwończyk, Maaike Alaerts, Eline Simons, Dirk J. Snyders, Aleksandra Nijak, Benjamin Vandendriessche, Dorien Schepers, Dogan Akdeniz, Emeline M. Van Craenenbroeck, Katleen Knaepen, Laura Rabaut, Hein Heidbüchel, Lut Van Laer, Johan Saenen, Alain J. Labro, Bart Loeys	2023	2
15	Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death European Journal of Medical Genetics ·Eline Simons, Alain J. Labro, Johan Saenen, Aleksandra Nijak, Ewa Sieliwończyk, Bert Vandendriessche, Małgorzata Dąbrowska, Emeline M. Van Craenenbroeck, Dorien Schepers, Lut Van Laer, Bart Loeys, Maaike Alaerts	2021	2
16	Optical Mapping in hiPSC-CM and Zebrafish to Resolve Cardiac Arrhythmias SHILAP Revista de lepidopterología ·Bert Vandendriessche, Ewa Sieliwończyk, Maaike Alaerts, Bart Loeys, Dirk J. Snyders, Dorien Schepers	2020	2
17	Cardiogeneticsbank@UZA: A Collection of DNA, Tissues, and Cell Lines as a Translational Tool Frontiers in Medicine ·Maaike Alaerts, Gerarda van de Beek, Ilse Luyckx, Josephina Meester, Dorien Schepers, Aline Verstraeten, Johan Saenen, Emeline M. Van Craenenbroeck, Inge Goovaerts, Inez Rodrigus, Steven Laga, Jeroen Hendriks, Sofie Goethals, Annemieke De Wilde, Elke Smits, Philippe G. Jorens, Manon Huizing, Lut Van Laer, Bart Loeys	2019	1
18	The sqstm1tmΔUBA zebrafish model, a proof-of-concept in vivo model for Paget’s disease of bone? Bone Reports ·Yentl Huybrechts, R. de Ridder, Björn De Samber, Eveline Boudin, Francesca Tonelli, Dries Knapen, Dorien Schepers, Jan De Beenhouwer, Jan Sijbers, Antonella Forlino, Geert Mortier, Paul Coucke, P. Eckhard Witten, Ronald Y. Kwon, Andy Willaert, Gretl Hendrickx, Wim Van Hul	2022	1
19	An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells Methods ·Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van Rossem, Tycho Canter Cremers, Kevin De Man, Ewa Sieliwończyk, Hanne M. Boen, Dogan Akdeniz, Laura Rabaut, Jolien Schippers, Peter Ponsaerts, R. Frank Kooy, Bart Loeys, Dorien Schepers, Maaike Alaerts	2025	0

About Dorien Schepers

Dorien Schepers is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Genetics, Cellular and Molecular Neuroscience and Pulmonary and Respiratory Medicine, having authored 19 papers that have together received 493 indexed citations. Recurring topics across this work include Cardiac electrophysiology and arrhythmias (9 papers), Connective tissue disorders research (5 papers), Ion channel regulation and function (5 papers), Neuroscience and Neural Engineering (3 papers), Cardiomyopathy and Myosin Studies (3 papers), Pluripotent Stem Cells Research (3 papers), Cardiovascular Effects of Exercise (2 papers) and RNA and protein synthesis mechanisms (2 papers). The work is most often cited by research in Genetics (232 citations), Cardiology and Cardiovascular Medicine (163 citations), Cellular and Molecular Neuroscience (97 citations), Psychiatry and Mental health (69 citations) and Pulmonary and Respiratory Medicine (132 citations). Dorien Schepers has collaborated with scholars based in Belgium, Netherlands and Australia. Frequent co-authors include Maaike Alaerts, Bart Loeys, Aline Verstraeten, Lut Van Laer, Josephina Meester, Elke Guenther, Ingrid E. Scheffer, Peter De Jonghe, Snezana Maljevic and Sarah Weckhuysen. Their work appears in journals such as Reviews of physiology, biochemistry and pharmacology, Scientific Reports, Annals of Cardiothoracic Surgery, Orphanet Journal of Rare Diseases and European Journal of Medical Genetics.

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.

Explore authors with similar magnitude of impact

Dorien Schepers

Impact in

Papers in i

In The Last Decade

Dorien Schepers

Peers

Countries citing papers authored by Dorien Schepers

Fields of papers citing papers by Dorien Schepers

All Works

About Dorien Schepers

Explore authors with similar magnitude of impact

Papers in