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
111 - 120 of 171
- Congenital contractural arachnodactyly due to a novel splice site mutation in the FBN2 gene
Authors: Virendra Mehar, Dinesh Yadav, Ravindra Kumar, Summi Yadav, Kuldeep Singh, Bert Callewaert, Shahnawaz Parhan
Pages: 163 - 166 - Mowat-Wilson syndrome : growth charts
Authors: Ivan Ivanovski, Olivera Djuric, Serena Broccoli, Stefano Giuseppe Caraffi, Patrizia Accorsi, Margaret P. Adam, Kristina Avela, Magdalena Badura-Stronka, Allan Bayat, Jill Clayton-Smith, et al.
- An unusual presentation of congenital nephrotic syndrome caused by WT1 mutationVolume: 28
Authors: Ann Raes, SOFIE MAEBE, Bert Callewaert
Number of pages: 1 - Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndromeVolume: 30
Authors: Lore Pottie, Christin S. Adamo, Aude Beyens, Steffen Luetke, Piyanoot Tapaneeyaphan, Phil Salmon, Alper Gezdirici, Elif Yilmaz Gulec, Naz Khan, Jill E. Urquhart, et al.
Pages: 40 - 41 - Mutations in LTBP1 cause autosomal recessive cutis laxa syndrome
Authors: Lore Pottie, Alper Gezdirici, Christin Adamo, William Newman, Aude Beyens, Riet De Rycke, Adelbert De Clercq, Patrick Sips, Gerhard Sengle, Bert Callewaert
Number of pages: 1 - Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndrome
Authors: Dong Li, Michael E. March, Paola Fortugno, Liza L. Cox, Leticia S. Matsuoka, Rosanna Monetta, Christoph Seiler, Louise C. Pyle, Emma C. Bedoukian, María José Sánchez-Soler, et al.
Pages: 1061 - 1076 - The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
Authors: Claire Redin, Harrison Brand, Ryan L Collins, Tammy Kammin, Elyse Mitchell, Jennelle C Hodge, Carrie Hanscom, Vamsee Pillalamarri, Catarina M Seabra, Mary-Alice Abbott, et al.
Pages: 36 - 45 - Fibromuscular dysplasia : results of a multicentre study in FlandersVolume: 72
Authors: Marie De Groote, Dimitri Hemelsoet, Patricia Van der Niepen, Bert Callewaert, Frank Vermassen, Jean-Marie Billiouw, An De Vriese, Jan Donck, Tine De Backer
Pages: 113 - 113 - Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND)
Authors: Gabriella Vera, Arthur Sorlin, Geoffroy Delplancq, François Lecoquierre, Marie Brasseur-Daudruy, Florence Petit, Thomas Smol, Alban Ziegler, Dominique Bonneau, Estelle Colin, et al.
- Unusual 8p inverted duplication deletion with telomere capture from 8q
Authors: Karen Buysse, F Antonacci, Bert Callewaert, Bart Loeys, Ulrike Fränkel, Victoria Siu, Geert Mortier
Pages: 31 - 36