Researcher
Wouter Steyaert
- Disciplines:Palliative care and end-of-life care, Laboratory medicine, Other translational sciences, Regenerative medicine, Nursing, Other clinical sciences, Other basic sciences, Other paramedical sciences, Other health sciences, Other medical and health sciences
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 2011 → 30 Sep 2018
Publications
11 - 20 of 32
- BATCH-GE : analysis of NGS data for genome editing assessment(2018)Series: Methods in Molecular Biology
Authors: Wouter Steyaert, Annekatrien Boel, Paul Coucke, Andy Willaert, Kris Vleminckx
Pages: 83 - 90 - Delineation of a clinical scoring system and diagnostic criteria for CCA(2018)
Authors: Ilse Meerschaut, Shana De Coninck, Annelies Matthys, Bjorn Tuytens, Wouter Steyaert, Daniël De Wolf, Frank Plasschaert, Bert Callewaert
Number of pages: 1 - arrEYE : a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs(2017)
Authors: Kristof Van Schil, Miriam Bauwens, Sarah De Jaegere, Wouter Steyaert, Tom Sante
Pages: 457 - 466 - Tissue-specific mosaicism for a lethal osteogenesis imperfecta COL1A1 mutation causes mild OI/EDS overlap syndrome(2017)
Authors: Wouter Steyaert, Lynn Demuynck, Karin EM Diderich, Fransiska Malfait
Pages: 1047 - 1050 - Mutations in ATP6V1E1 or ATP6V1A cause autosomal-recessive cutis laxa(2017)
Authors: Tim Van Damme, Thatjana Gardeitchik, Miski Mohamed, Sergio Guerrero-Castillo, Peter Freisinger, Brecht Guillemyn, Ariana Kariminejad, Daisy Dalloyaux, Sanne van Kraaij, Dirk J Lefeber, et al.
Pages: 216 - 227 - A homozygous B3GAT3 mutation causes a multisystemic cutis laxa-like syndrome, expanding the phenotype of linkeropathies(2016)
Authors: Brecht Guillemyn, Tim Van Damme, Wouter Steyaert, Sheela Nampoothiri, Fransiska Malfait
Number of pages: 1 - CRISPR/Cas9 mediated knockout of rb1 and rbl1 leads to rapid and penetrant retinoblastoma development in Xenopus tropicalis(2016)
Authors: Thomas Naert, Tom Van Nieuwenhuysen, Dionysia Dimitrakopoulou, Jannick Leoen, Jurgen Haustraete, Wouter Steyaert, Trees Lepez, Dieter Deforce, Kris Vleminckx
- Efficiency of exome sequencing for the molecular diagnosis of Pseudoxanthoma Elasticum(2015)
Authors: Mohammad Jakir Hosen, Filip Van Nieuwerburgh, Wouter Steyaert, Dieter Deforce, Ludovic Martin, Georges Leftheriotis, Olivier Vanakker
Pages: 992 - 998 - Tissue specific mosaicism for a lethal COL1A1 mutation causes mild Ehlers-Danlos syndrome(2015)
Authors: Wouter Steyaert, Lynn Demuynck, Fransiska Malfait, Karin EM Diderich
Number of pages: 1 - Genetic defects in TAPT1 disrupt ciliogenesis and cause a complex lethal osteochondrodysplasia(2015)
Authors: Aileen M Barnes, Charlotte Gistelinck, Fransiska Malfait, Brecht Guillemyn, Wouter Steyaert, Sanne D'hondt, Martine Biervliet, Paul Witten, Sergey Leikin, Elena Makareeva, et al.
Pages: 521 - 534