Bert Vandendriessche
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Explore the profile of Bert Vandendriessche including associated specialties, affiliations and a list of published articles.
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7
Citations
13
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Recent Articles
1.
Boen H, Vandendriessche B, Schippers J, Rabaut L, Nijak-Paeske A, Ponsaerts P, et al.
Stem Cell Res
. 2024 Aug;
81:103536.
PMID: 39167847
Truncating variants in TTN (TTNtv) are present in 15-25 % of patients with idiopathic dilated cardiomyopathy. Interestingly, the pathogenicity of TTNtv seems to be linked to their location within the...
2.
Sieliwonczyk E, Alaerts M, Simons E, Snyders D, Nijak A, Vandendriessche B, et al.
Orphanet J Rare Dis
. 2023 Feb;
18(1):23.
PMID: 36721196
Background: The c.1124_1127delTTCA p.(Ile375Argfs*43) pathogenic variant is the most frequently identified molecular defect in the KCNQ1 gene in the cardiogenetics clinic of the Antwerp University Hospital. This variant was observed...
3.
Sieliwonczyk E, Vandendriessche B, Claes C, Mayeur E, Alaerts M, Holmgren P, et al.
Sci Rep
. 2023 Jan;
13(1):1491.
PMID: 36707549
Despite numerous prior attempts to improve knock-in (KI) efficiency, the introduction of precise base pair substitutions by the CRISPR-Cas9 technique in zebrafish remains challenging. In our efforts to generate KI...
4.
Nijak A, Simons E, Vandendriessche B, Van de Sande D, Fransen E, Sieliwonczyk E, et al.
Biol Open
. 2022 Feb;
11(2).
PMID: 35195246
Cardiomyocytes derived from induced pluripotent stem cells (iPSC-CMs) offer an attractive platform for cardiovascular research. Patient-specific iPSC-CMs are very useful for studying disease development, and bear potential for disease diagnostics,...
5.
Sieliwonczyk E, Matchkov V, Vandendriessche B, Alaerts M, Bakkers J, Loeys B, et al.
Rev Physiol Biochem Pharmacol
. 2021 Sep;
184:33-68.
PMID: 34533615
In the last years, the field of inheritable ventricular arrhythmia disease modelling has changed significantly with a push towards the use of novel cellular cardiomyocyte based models. However, there is...
6.
Simons E, Labro A, Saenen J, Nijak A, Sieliwonczyk E, Vandendriessche B, et al.
Eur J Med Genet
. 2021 Aug;
64(11):104322.
PMID: 34438094
Sudden cardiac death (SCD) is a common cause of death in young adults. In up to 80% of cases a genetic cause is suspected. Next-generation sequencing of candidate genes can...
7.
Sieliwonczyk E, Alaerts M, Robyns T, Schepers D, Claes C, Corveleyn A, et al.
Europace
. 2020 Nov;
23(6):918-927.
PMID: 33221854
Aims: We identified the first Belgian SCN5A founder mutation, c.4813 + 3_4813 + 6dupGGGT. To describe the clinical spectrum and disease severity associated with this mutation, clinical data of 101...