Publications by authors named "D Schepers"

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Generation of a homozygous and heterozygous iPSC line carrying a variant of uncertain significance in CACNA1C, associated with Brugada syndrome.
Bert Vandendriessche, Jolien Schippers, Laura Rabaut, Peter Ponsaerts, Bart Loeys, Dorien Schepers

Stem Cell Res· December 2025

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An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells.
Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van Rossem, Tycho Canter Cremers, Kevin De Man, Dorien Schepers

Methods· September 2025

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Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone.
Yentl Huybrechts, Raphaël De Ridder, Dylan Bergen, Björn De Samber, Eveline Boudin, Dorien Schepers

Calcif Tissue Int· March 2025

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Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping.
Ewa Sieliwonczyk, Bert Vandendriessche, Charlotte Claes, Evy Mayeur, Maaike Alaerts, Dorien Schepers

Sci Rep· January 2023

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Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population.
Ewa Sieliwonczyk, Maaike Alaerts, Eline Simons, Dirk Snyders, Aleksandra Nijak, Dorien Schepers

Orphanet J Rare Dis· January 2023

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