Lynne Rumping unpaid guest prof. Publications Lynne Rumping Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci Source European journal of human genetics - ISSN 1018-4813- (2025) p. Author(s) Mathis Hildonen,…

Lynne Rumping onbezoldigd gastprofessor Publicaties Lynne Rumping Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci Bron European journal of human genetics - ISSN 1018-4813- (2025) p. Auteur(s) Mathis Hildo…

Aline Verstraeten associate research professor Publications Aline Verstraeten The complex heritability in thoracic aortic aneurysm and dissection : from clinical insights to stem cell disease modelling Source Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2025,233 p. Author…

Laura Rabaut Publications Laura Rabaut An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells Source Methods: a companion to methods in enzymology - ISSN 1046-2023-241 (2025) p. 33-42 Author(s) Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van Rossem, …

Laura Rabaut Publicaties Laura Rabaut An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells Bron Methods: a companion to methods in enzymology - ISSN 1046-2023-241 (2025) p. 33-42 Auteur(s) Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van Rossem, Tyc…

Aline Verstraeten hoofddocent Publicaties Aline Verstraeten The complex heritability in thoracic aortic aneurysm and dissection : from clinical insights to stem cell disease modelling Bron Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2025,233 p. Auteur(s) Joe Davis Velche…

Lut Van Laer associate professor Publications Lut Van Laer Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Source Genome medicine - ISSN 1756-994X-16:1 (2024) p. 1-14…

Maaike Bastiaansen Publications Maaike Bastiaansen Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome Source Npj genomic medicine - ISSN 2056-7944-9:1 (2024) p. 1-9 Author(s) Josephina Meester, Anne Hebert, Maaike Bastiaansen, Laura Rabaut, Jarl Bastianen, Nele Boeckx, Kathry…

Anne Hebert predoc researcher FWO Publications Anne Hebert Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomalies Source Genome medicine - ISSN 1756-994X-17:1 (2025) p. 1-16 Author(s) Francesca Mattioli, Rún Friðriksdóttir, Anne Hebert, Sissy Bassani, Nazia Ibr…

Jarl Bastianen Publications Jarl Bastianen Phenotypic spectrum of the first Belgian MYBPC3 founder : a large multi-exon deletion with a varying phenotype Source Frontiers in genetics - ISSN 1664-8021-15 (2024) p. 1-15 Author(s) Hanne Boen, Maaike Alaerts, Lut Van Laer, Johan Saenen, Inge Goovaerts, …

Diane Beysen unpaid guest prof. Publications Diane Beysen RORA-neurodevelopmental disorder : a unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizures Source Genetics in medicine - ISSN 1098-3600-27:4 (2025) p. 1-13 Author(s) Mariagrazia Talarico, Julitta de Bellesci…

Josephina Meester assistant professor - postdoc researcher FWO Publications Josephina Meester Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Source Genome medicine -…

Josephina Meester docent - postdoc mandaat FWO Publicaties Josephina Meester Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Bron Genome medicine - ISSN 1756-994X-16:…

Anne Hebert predoc mandaat FWO Publicaties Anne Hebert Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomalies Bron Genome medicine - ISSN 1756-994X-17:1 (2025) p. 1-16 Auteur(s) Francesca Mattioli, Rún Friðriksdóttir, Anne Hebert, Sissy Bassani, Nazia Ibrahim, …

Jarl Bastianen Publicaties Jarl Bastianen Phenotypic spectrum of the first Belgian MYBPC3 founder : a large multi-exon deletion with a varying phenotype Bron Frontiers in genetics - ISSN 1664-8021-15 (2024) p. 1-15 Auteur(s) Hanne Boen, Maaike Alaerts, Lut Van Laer, Johan Saenen, Inge Goovaerts, Jar…

Lut Van Laer hoofddocent Publicaties Lut Van Laer Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Bron Genome medicine - ISSN 1756-994X-16:1 (2024) p. 1-14 Auteur(s) …

Maaike Bastiaansen Publicaties Maaike Bastiaansen Expanding the clinical spectrum of biglycan-related Meester-Loeys syndrome Bron Npj genomic medicine - ISSN 2056-7944-9:1 (2024) p. 1-9 Auteur(s) Josephina Meester, Anne Hebert, Maaike Bastiaansen, Laura Rabaut, Jarl Bastianen, Nele Boeckx, Kathryn A…

Diane Beysen onbezoldigd gastprofessor Publicaties Diane Beysen RORA-neurodevelopmental disorder : a unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizures Bron Genetics in medicine - ISSN 1098-3600-27:4 (2025) p. 1-13 Auteur(s) Mariagrazia Talarico, Julitta de Bell…

μNEURO search menu search content Translational Neurosciences Recent publications Antigen-specific treatment modalities in MS : the past, the present, and the future Source Frontiers in immunology - ISSN 1664-3224-12 (2021) p. Author(s) Judith Derdelinckx, Patrick Cras, Zwi Nisan Berneman, Nathalie…