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
1 - 10 of 171
- Beyond gene-disease validity : capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions(2023)
Authors: Katherine S. Josephs, Angharad M. Roberts, Pantazis Theotokis, Roddy Walsh, Philip J. Ostrowski, Matthew Edwards, Andrew Fleming, Courtney Thaxton, Jason D. Roberts, Melanie Care, et al.
- The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Authors: Michiel Vanhooydonck, Maxim Verlee, Lore Pottie, Annekatrien Boel, Piyanoot Tapaneeyaphan, Marta Guerreiro Santana Ramos Da Silva, Adelbert De Clercq, Lisa Caboor, Matthias Van Impe, Delfien Syx, et al.
Number of pages: 1 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Authors: Michiel Vanhooydonck, Lore Pottie, Annekatrien Boel, Piyanoot Tapaneeyaphan, Marta Guerreiro Santana Ramos Da Silva, Adelbert De Clercq, Matthias Van Impe, Delfien Syx, Andy Willaert, Lisa Caboor, et al.
Number of pages: 1 - Structural variants disrupt a critical regulatory region downstream of FOXG1(2023)Volume: 31
Authors: Eva D'haene, Lies Vantomme, Björn Menten, Bert Callewaert, Elfride De Baere, Sarah Vergult
Pages: 28 - 28 - HRAS-related epidermal nevus syndromes : expansion of the spectrum with first branchial arch defects(2023)
Authors: Aude Beyens, Charlotte Lietaer, Kathleen Claes, Elfride De Baere, Marleen Goeteyn, Bob Lerut, Hannes Syryn, Olivier Vanakker, Joni Van der Meulen, Lieve Vanwalleghem, et al.
Pages: 709 - 713 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Authors: Michiel Vanhooydonck, Maxim Verlee, Lore Pottie, Annekatrien Boel, Piyanoot Tapaneeyaphan, Marta Guerreiro Santana Ramos Da Silva, Adelbert De Clercq, Lisa Caboor, Matthias Van Impe, Delfien Syx, et al.
Number of pages: 1 - SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile(2022)
Authors: Reem Al-Jawahiri, Aidin Foroutan, Jennifer Kerkhof, Haley McConkey, Michael Levy, Sadegheh Haghshenas, Kathleen Rooney, Jasmin Turner, Debbie Shears, Muriel Holder, et al.
Pages: 1261 - 1273 - Apoptotic enteropathy, gluten intolerance, and IBD-like inflammation associated with lipotoxicity in DGAT1 deficiency–related diarrhea : a case report of a 17-year-old patient and literature review(2022)
Authors: Ellen Deolet, Bert Callewaert, Jeroen Geldof, Saskia Vande Velde, Myriam Van Winckel, Anne Hoorens
Pages: 785 - 791 - Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects(2022)
Authors: Gerarda Cappuccio, Nicola BrunettiU+2010Pierri, Paul Clift, Christopher Learn, John C. Dykes, Catherine L. Mercer, Bert Callewaert, Ilse Meerschaut, Alessandro Mauro Spinelli, Irene Bruno, et al.
Pages: 1384 - 1395 - Exploring the mutational landscape of isolated congenital heart defects : an exome sequencing study using cardiac DNA(2022)
Authors: Ilse Meerschaut, Wouter Steyaert, Thierry Bové, Katrien Francois, Thomas Martens, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera, Joseph Panzer, Kristof Vandekerckhove, et al.