Researcher
Bert Callewaert
- Keywords:connective tissue, cutis lax, mutation, mental retardation, zebrafish, arterial tortuosity syndrome, next generation sequencing, aneurysm, mouse model, congenital heart defect, Genetics
- Disciplines:Cardiac and vascular medicine not elsewhere classified, Cardiology, Paediatrics and neonatology not elsewhere classified, Neonatology, Paediatrics, Genetics, Vascular diseases
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 2004 → 30 Sep 2018
Projects
1 - 10 of 15
- Generation and analysis of zebrafish models for human pathologyFrom1 Oct 2023 → 31 Mar 2024Funding: BOF - doctoral mandates
- Identifying antifibrotic targets in complementary disease models for Myhre syndrome, a Mendelian multisystemic and profibrotic disorderFrom1 Oct 2023 → TodayFunding: BOF - doctoral mandates
- An appraisal of the contribution of neural crest lineages in a zebrafish model for aortic dissectionFrom1 Jul 2023 → TodayFunding: Foreign private sponsor - undefined
- Regulatory landscaping: towards improved genetic diagnosis and therapy for SATB2-associated syndromeFrom1 Nov 2022 → TodayFunding: FWO fellowships
- Genetic predictors of joint shape and cartilage mechanicsFrom1 Oct 2022 → TodayFunding: BOF - projects
- Steunfonds Marguerite-Marie Delacroix: Regulatory landscaping: towards improved genetic diagnosis and therapy for SATB2-associated syndrome (Lisa Hamerlinck)From1 Jan 2022 → 31 Dec 2023Funding: Foundations, funds and other with scientific goal
- An integrated translational platform to improve the management and outcome of rare heritable connective tissue diseaseFrom1 Jan 2021 → TodayFunding: BOF - projects
- Research equipment for behavior analysis in zebrafish disease models.From1 Dec 2020 → 30 Nov 2022Funding: BOF - scientific equipment program
- Integrating clinical data, ultrastructural imaging, and pathophysiology to unravel cutis laxa syndromesFrom1 Jan 2020 → 31 Dec 2023Funding: FWO research project (including WEAVE projects)
- CRISPR/Cas9-mediated knock-in for variant testing and disease modeling in the zebrafish model systemFrom1 Jan 2020 → 31 Dec 2023Funding: FWO research project (including WEAVE projects)
Publications
41 - 50 of 171
- Arterial tortuosity syndrome : 40 new families and literature review (vol 20, pg 1236, 2017)(2019)
Authors: Aude Beyens, Juliette Albuisson, Mazen Al-Essa, Waheed Al-Manea, Damien Bonnet, Ozlem Bostan, Odile Boute, Tiffany Busa, Nathalie Canham, Ergun Cil, et al.
Pages: 1894 - 1895 - Defining the clinical, molecular and ultrastructural characteristics in occipital horn syndrome : two new cases and review of the literature(2019)
Authors: Aude Beyens, Kyaran Van Meensel, Lore Pottie, Riet De Rycke, Michiel De Bruyne, Femke Baeke, Piet Hoebeke, Frank Plasschaert, Bart Loeys, Sofie De Schepper, et al.
- Myhre syndrome : a first familial recurrence and broadening of the phenotypic spectrum(2019)
Authors: Ilse Meerschaut, Aude Beyens, Wouter Steyaert, Riet De Rycke, Katrien Bonte, Tine De Backer, Sandra Janssens, Joseph Panzer, Frank Plasschaert, Daniël De Wolf, et al.
Pages: 2494 - 2499 - Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care(2018)
Authors: Ivan Ivanovski, Olivera Djuric, Stefano Giuseppe Caraffi, Daniela Santodirocco, Marzia Pollazzon, Simonetta Rosato, Duccio Maria Cordelli, Ebtesam Abdalla, Patrizia Accorsi, Margaret P Adam, et al.
Pages: 965 - 975 - Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology guidelines for the interpretation of sequenced variants in the FBN1 gene for Marfan syndrome : proposal for a disease- and gene-specific guideline(2018)
Authors: Felke Steijns, Tjorven Audenaert, Ilse Meerschaut, Wouter Steyaert, Bert Callewaert, Marjolijn Renard
- Arterial tortuosity syndrome : 40 new families and literature review(2018)
Authors: Aude Beyens, Juliette Albuisson, Mazen Al-Essa, Waheed Al-Manea, Damien Bonnet, Ozlem Bostan, Odile Boute, Tiffany Busa, Nathalie Canham, Ergun Cil, et al.
Pages: 1236 - 1245 - Genetic analysis of osteogenesis imperfecta in the Palestinian population : molecular screening of 49 affected families(2018)
Authors: Osama Essawi, Maha Fannana, Mohammad Darwish, Mohammad Farraj, Tamer Essawi, Bert Callewaert, Fransiska Malfait
Pages: 15 - 26 - 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
- De gevolgen van FOXP1-mutaties : meer dan verstandelijke beperking en taalontwikkelingsstoornissen alleen(2018)
Authors: Ilse Meerschaut, Bert Callewaert
Pages: 28 - 30 - 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