69 resultaten gevonden
Publicaties Gert Van Goethem | Gert Van Goethem | Universiteit Antwerpen
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…
Publicaties Jasper Verwilt | Jasper Verwilt | Universiteit Antwerpen
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…
Publications Jasper Verwilt | Jasper Verwilt | University of Antwerp
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…
Publications Gert Van Goethem | Gert Van Goethem | University of Antwerp
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…
Publicaties Natacha Camacho Elizondo | Natacha Camacho Elizondo | Universiteit Antwerpen
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- (2025) p. Auteur(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Natacha Camacho Eli…
Publicaties Mathijs van der Lei | Mathijs van der Lei | Universiteit Antwerpen
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…
Publicaties Ina Weber | Ina Weber | Universiteit Antwerpen
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…
Publications Natacha Camacho Elizondo | Natacha Camacho Elizondo | University of Antwerp
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 …
Publicaties Luc Debaene | Luc Debaene | Universiteit Antwerpen
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…
Publicaties Astrid Van den Branden | Astrid Van den Branden | Universiteit Antwerpen
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…
Publicaties Vincent Timmerman | Vincent Timmerman | Universiteit Antwerpen
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…
Publicaties Jonathan De Winter | Jonathan De Winter | Universiteit Antwerpen
Jonathan De Winter onbezoldigd medewerker Publicaties Jonathan De Winter A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy Bron European journal of human genetics - ISSN 1018-4813- (2025) p. Auteur(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Natacha …
Publications Mathijs van der Lei | Mathijs van der Lei | University of Antwerp
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…
Publicaties Katrien Janssens | Katrien Janssens | Universiteit Antwerpen
Katrien Janssens projectcoördinator Publicaties Katrien Janssens Diagnostic yield and clinical impact of prenatal whole exome sequencing (WES) : four-year single center experience Bron Journal of perinatal medicine - ISSN 0300-5577- (2025) p. Auteur(s) Katleen Janssens, Marjan De Rademaker, Joke Mu…
Publicaties Jonathan Baets | Jonathan Baets | Universiteit Antwerpen
Jonathan Baets hoogleraar - fundamenteel klinisch navorser Publicaties Jonathan Baets Asparaginyl-tRNA synthetase (NARS1) variants implicated in dominant neurological phenotypes display dominant-negative properties Bron Human genetics and genomics advances - ISSN 2666-2477-7:1 (2026) p. 1-12 Auteur(…
Publicaties Willem De Ridder | Willem De Ridder | Universiteit Antwerpen
Willem De Ridder onbezoldigd medewerker Publicaties Willem De Ridder A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy Bron European journal of human genetics - ISSN 1018-4813- (2025) p. Auteur(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Natacha Cama…
Publicaties Alice Monticelli | Alice Monticelli | Universiteit Antwerpen
Alice Monticelli Publicaties Alice Monticelli A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy Bron European journal of human genetics - ISSN 1018-4813- (2025) p. Auteur(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Natacha Camacho Elizondo, Tine Deco…
Publications Ina Weber | Ina Weber | University of Antwerp
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…
Publications Luc Debaene | Luc Debaene | University of Antwerp
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…
Research Wouter De Coster | Wouter De Coster | University of Antwerp
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…
Publicaties Biljana Ermanoska | Biljana Ermanoska | Universiteit Antwerpen
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- (2025) p. Auteur(s) Liedewei Van de Vondel, Jonathan De Winter, Alice Monticelli, Natacha Cam…
Publicaties Jarl Bastianen | Jarl Bastianen | Universiteit Antwerpen
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…
Publicaties Lut Van Laer | Lut Van Laer | Universiteit Antwerpen
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) …
Publications Astrid Van den Branden | Astrid Van den Branden | University of Antwerp
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,…
Publications Jonathan De Winter | Jonathan De Winter | University of Antwerp
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…