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Researcher
Andy Willaert
- Disciplines:Other basic sciences, Genetics
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today - Department of Pediatrics and medical genetics (Department)
Member
From15 Apr 2003 → 30 Sep 2018
Projects
1 - 3 of 3
- Cofunding core facility - Core Zebrafish Facility Ghent (Core ZFG)From1 Jul 2022 → TodayFunding: BOF - research organisations
- In vivo functional evaluation of unclassified variants, found in the breast cancer gene BRCA2, using CRISPR-mediated genome editing in zebrafishFrom15 Nov 2021 → TodayFunding: BOF - doctoral mandates
- Study of the pathogenesis of arterial tortuosity by using zebrafish as a model organismFrom1 Oct 2011 → 30 Sep 2015Funding: BOF - Other initiatives
Publications
21 - 25 of 25
- CRISPR/Cas9-mediated homology-directed repair by ssODNs in zebrafish induces complex mutational patterns resulting from genomic integration of repair-template fragments(2018)
Authors: Annekatrien Boel, Hanna De Saffel, Wouter Steyaert, Bert Callewaert, Anne De Paepe, Paul Coucke, Andy Willaert
- 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 - Zebrafish modeling of the β4GalT7-deficient type of Ehlers-Danlos syndrome(2017)
Authors: Sarah Delbaere, Tim Van Damme, Paul Coucke, Sofie Symoens, Delfien Syx, Andy Willaert, Fransiska Malfait
Number of pages: 1 - A hotspot splicing mutation in LEPREI affects prolyl 3-hydroxylation and causes recessive osteogenesis imperfecta(2008)Volume: 58
Authors: Fransiska Malfait, Andy Willaert, Sofie Symoens, Paul Coucke, Anne De Paepe
Pages: S223 - S223 - A Hotspot Splicing Mutation in LEPREI Affects Prolyl 3-hydroxylation and Causes Recessive Osteogenesis Imperfecta(2008)Volume: 23
Authors: Andy Willaert, Sofie Symoens, Fransiska Malfait, Kris Gevaert, Paul Coucke, Anne De Paepe
Pages: S294 - S294