Dorien Schepers
Universiteit Antwerpen
H-index: 12
Europe-Belgium
Top articles of Dorien Schepers
A Novel in Vivo Model for Paget's Disease of Bone: The sqstm1tmΔUBA Zebrafish Line
JOURNAL OF BONE AND MINERAL RESEARCH
2023/2/1
Dries Knapen
H-Index: 31
Dorien Schepers
H-Index: 9
Jan Sijbers
H-Index: 42
Chrissy Hammond
H-Index: 20
Ronald Kwon
H-Index: 15
Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population
Orphanet Journal of Rare Diseases
2023/1/31
Dorien Schepers
H-Index: 9
Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping
Scientific Reports
2023/1/27
Philip Holmgren
H-Index: 8
Dorien Schepers
H-Index: 9
The sqstm1tmΔUBA zebrafish model, a proof-of-concept in vivo model for Paget’s disease of bone
Bone Rep
2022/5/1
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes
Biology Open
2022/2/15
Erik Fransen
H-Index: 13
Dorien Schepers
H-Index: 9
Modeling of an SCN5A founder mutation in iPSC-derived cardiomyocytes
Cardiovascular Research
2022/6/1
Molecular autopsy and subsequent functional analysis reveal de novo DSG2 mutation as cause of sudden death
European Journal of Medical Genetics
2021/11/1
Dorien Schepers
H-Index: 9
Inherited ventricular arrhythmia in zebrafish: Genetic models and phenotyping tools
2021/9/18
Dorien Schepers
H-Index: 9
A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8
The American Journal of Human Genetics
2021/6/3
Clinical characterization of the first Belgian SCN5A founder mutation cohort
EP Europace
2021/6/1
iPSC-cardiomyocyte models of Brugada syndrome—achievements, challenges and future perspectives
2021/3/10
Dorien Schepers
H-Index: 9
Optical mapping in hiPSC-CM and Zebrafish to resolve cardiac arrhythmias
2020/12/21
Dorien Schepers
H-Index: 9
Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report
Frontiers in Cardiovascular Medicine
2020/7/24
Electrophysiological characterization of a Brugada syndrome SCN5A Belgian founder mutation in induced pluripotent stem cell cardiomyocytes
2020
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