Gert Van Goethem onbezoldigd medewerker Publicaties Gert Van Goethem Disturbed brain ether lipid metabolism and histology inSjogren-Larssonsyndrome Bron Journal of inherited metabolic disease - ISSN 0141-8955- () p. 1-14 Auteur(s) Pippa Staps, William B. Rizzo, Frederic M. Vaz, Marianna Bugiani, Mar…

Jasper Verwilt postdoc mandaat FWO Publicaties Jasper Verwilt Blood collection tube and RNA purification method recommendations for extracellular RNA transcriptome profiling Bron Nature communications - ISSN 2041-1723-16:1 (2025) p. 1-17 Auteur(s) Jasper Anckaert, Francisco Avila Cobos, Anneleen Dec…

Jasper Verwilt postdoc researcher FWO Publications Jasper Verwilt Blood collection tube and RNA purification method recommendations for extracellular RNA transcriptome profiling Source Nature communications - ISSN 2041-1723-16:1 (2025) p. 1-17 Author(s) Jasper Anckaert, Francisco Avila Cobos, Annele…

Gert Van Goethem unpaid staff Publications Gert Van Goethem Disturbed brain ether lipid metabolism and histology inSjogren-Larssonsyndrome Source Journal of inherited metabolic disease - ISSN 0141-8955- () p. 1-14 Author(s) Pippa Staps, William B. Rizzo, Frederic M. Vaz, Marianna Bugiani, Martin Gie…

Natacha Camacho Elizondo Publicaties Natacha Camacho Elizondo A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy Bron European journal of human genetics - ISSN 1018-4813-34 (2026) p. 45-52 Auteur(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Natacha Cam…

Mathijs van der Lei onderzoeker Publicaties Mathijs van der Lei From discovery to innovative translational approaches in 80 years of fragile X syndrome research Bron Biomedicines - ISSN 2227-9059-13:4 (2025) p. 1-27 Auteur(s) Mathijs van der Lei, Frank Kooy Citatielink Cognitive deficits in human Ap…

Natacha Camacho Elizondo Publications Natacha Camacho Elizondo A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy Source European journal of human genetics - ISSN 1018-4813- (2025) p. Author(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Natacha Camacho …

Ina Weber onbezoldigd medewerker Publicaties Ina Weber Who can say what? Testing the impact of interpersonal mechanisms and gender on fairness evaluations of content moderation Bron Social Media + Society - ISSN 2056-3051-10:4 (2024) p. 1-15 Auteur(s) Ina Weber, Joao Goncalves, Gina M. Masullo, Mari…

Luc Debaene onbezoldigd medewerker Publicaties Luc Debaene Klinisch redeneren : van model naar competentie Bron Leuven, Acco, 2022,163 p. Auteur(s) Jef van den Ende, Bert Aertgeerts, Jef Boeckx, Rudi Bruyninckx, Johan Buffels, Samuel Coenen, Luc Debaene, Jan Matthys, Jan Reniers, Jan Vandevoorde, We…

Katrien Janssens projectcoördinator Publicaties Katrien Janssens RNA sequencing offers new diagnostic opportunities in neurodevelopmental disorders : a systematic review Bron Genetics in medicine - ISSN 1098-3600-28:4 (2026) p. 1-12 Auteur(s) Jessica Rosenblum, Ellen Rijckmans, Randy Osei, Katrien …

Astrid Van den Branden Publicaties Astrid Van den Branden Intravenous iron treatment fuels chronic kidney disease-induced arterial media calcification in rats Bron The journal of pathology - ISSN 0022-3417-265:2 (2025) p. 172-183 Auteur(s) Astrid Van den Branden, Britt Opdebeeck, Saar Adriaensen, Pi…

Vincent Timmerman gewoon hoogleraar Publicaties Vincent Timmerman Axonal degeneration in peripheral neuropathies : from the molecular mechanisms to the therapeutic approach Bron Milan, University of Antwerp, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences,149 p. Auteur(s) Anke Claessen…

Mathijs van der Lei researcher Publications Mathijs van der Lei From discovery to innovative translational approaches in 80 years of fragile X syndrome research Source Biomedicines - ISSN 2227-9059-13:4 (2025) p. 1-27 Author(s) Mathijs van der Lei, Frank Kooy Citation link Cognitive deficits in huma…

Jonathan De Winter onbezoldigd medewerker Publicaties Jonathan De Winter Charcot-Marie-Tooth disease and related neuropathies Bron Nature reviews disease primers - ISSN 2056-676X-12:1 (2026) p. 1-20 Auteur(s) Joshua Burns, Vincent Timmerman, Matilde Laura, Eppie M. Yiu, Maurizio D'antonio, Bipasha M…

Willem De Ridder onbezoldigd medewerker Publicaties Willem De Ridder Gender differences in Myasthenia Gravis in a neuromuscular reference center in Belgium Bron Acta neurologica Belgica - ISSN 0300-9009- (2026) p. Auteur(s) Alicia Alonso Jimenez, Willem De Ridder, Paul van Schil, Jonathan Baets, Rud…

Ina Weber unpaid staff Publications Ina Weber Who can say what? Testing the impact of interpersonal mechanisms and gender on fairness evaluations of content moderation Source Social Media + Society - ISSN 2056-3051-10:4 (2024) p. 1-15 Author(s) Ina Weber, Joao Goncalves, Gina M. Masullo, Marisa Torr…

Luc Debaene unpaid staff Publications Luc Debaene Klinisch redeneren : van model naar competentie Source Leuven, Acco, 2022,163 p. Author(s) Jef van den Ende, Bert Aertgeerts, Jef Boeckx, Rudi Bruyninckx, Johan Buffels, Samuel Coenen, Luc Debaene, Jan Matthys, Jan Reniers, Jan Vandevoorde, Werner Va…

Wouter De Coster postdoc researcher FWO Research Wouter De Coster Research team VIB CMN - Applied and Translational Neurogenomics Expertise Genetics, nanopore, long-read sequencing, DNA, structural variation, human genome Investigation of the role of a TMEM106B AluYb8 insertion-deletion polymorphism…

Astrid Van den Branden Publications Astrid Van den Branden Intravenous iron treatment fuels chronic kidney disease-induced arterial media calcification in rats Source The journal of pathology - ISSN 0022-3417-265:2 (2025) p. 172-183 Author(s) Astrid Van den Branden, Britt Opdebeeck, Saar Adriaensen,…

Jonathan Baets hoogleraar - fundamenteel klinisch navorser Publicaties Jonathan Baets Gender differences in Myasthenia Gravis in a neuromuscular reference center in Belgium Bron Acta neurologica Belgica - ISSN 0300-9009- (2026) p. Auteur(s) Alicia Alonso Jimenez, Willem De Ridder, Paul van Schil, Jo…

Biljana Ermanoska postdoctoraal bursaal Publicaties Biljana Ermanoska A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy Bron European journal of human genetics - ISSN 1018-4813-34 (2026) p. 45-52 Auteur(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Nat…

Jarl Bastianen Laboratoriumtechnoloog Cardiogenetica 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 L…

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) …

Jonathan De Winter unpaid staff Publications Jonathan De Winter A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy Source European journal of human genetics - ISSN 1018-4813- (2025) p. Author(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Natacha Camacho…

Vincent Timmerman full professor Publications Vincent Timmerman Axonal degeneration in peripheral neuropathies : from the molecular mechanisms to the therapeutic approach Source Milan, University of Antwerp, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences,149 p. Author(s) Anke Claessen…