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
21 - 30 of 171
- Clinical characteristics of Galloway-Mowat syndrome and mutations in the TPRKB gene(2021)Volume: 23
Authors: Lieselot Peremans, Bert Callewaert, Ann Raes, Evelien Snauwaert, agnieszka Prytula
Number of pages: 1 - Loss-of-function variants in EFEMP1 cause a recognizable connective tissue disorder characterized by cutis laxa and multiple herniations(2021)
Authors: Maxim Verlee, Aude Beyens, Alper Gezdirici, Elif Gulec, Lore Pottie, Silke De Feyter, Michiel Vanhooydonck, Piyanoot Tapaneeyaphan, Bert Callewaert
- Clinical and molecular delineation of cutis laxa syndromes : paradigms for elastic fiber homeostasis(2021)Edition: 2Series: Advances in Experimental Medicine and Biology (AEMB)
Authors: Aude Beyens, Lore Pottie, Patrick Sips, Bert Callewaert, Jaroslava Halper
Pages: 273 - 309 - Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome(2021)
Authors: Lore Pottie, Christin S. Adamo, Aude Beyens, Steffen Lütke, Piyanoot Tapaneeyaphan, Phil L. Salmon, Alper Gezdirici, Elif Yilmaz Gulec, Naz Khan, Jill E. Urquhart, et al.
Pages: 1095 - 1114 - A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 gene (ZFHX3)(2021)
Authors: Maria del Rocio Pérez Baca, Eva Jacobs, Mareike Bauer, Melissa Bellini, Claire Beneteau, Natasha Brown, David Coman, Annelies Dheedene, Tine Duelund Hjortshøj, Maria Lascone, et al.
Number of pages: 1 - Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders(2021)
Authors: Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema, Jill Rosenfeld, Pengfei Liu, Hui Guo, Chang N. Kim, Bert B. A. De Vries, Lisenka E. L. M. Vissers, Magnus Nordenskjold, et al.
- A reassessment of copy number variations in congenital heart defects : picturing the whole genome(2021)
Authors: Ilse Meerschaut, Sarah Vergult, Annelies Dheedene, Katya De Groote, Hans De Wilde, Laura Muiño Mosquera, Joseph Panzer, Daniël De Wolf, Bert Callewaert
- Two cases of DCDC2U+2010related neonatal sclerosing cholangitis with developmental delay and literature review(2021)
Authors: Hannes Syryn, Anne Hoorens, Tassos Grammatikopoulos, Maesha Deheragoda, Saskia Vande Velde, Myriam Van Winckel, Patrick Verloo, Bert Callewaert, Ruth De Bruyne
Pages: 447 - 452 - Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures(2021)
Authors: Lore Pottie, Wouter Van Gool, Michiel Vanhooydonck, Franz-Georg Hanisch, Geert Goeminne, Andreja Rajkovic, Bert Callewaert, Zsolt Urban
- IQSEC2 disorder : a new disease entity or a Rett spectrum continuum?(2021)
Authors: Diego Lopergolo, Flavia Privitera, Giuseppe Castello, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Anna Maria Pinto, Francesca Ariani, Aurora Currò, Vittoria Lamacchia, Roberto Canitano, et al.
Pages: 462 - 474