Dale Annear postdoc researcher FWO Research Dale Annear Research team Medical Genetics (MEDGEN) Validation of Novel AI-Predicted Treatments for Fragile X Syndrome Through Next Generation Mouse Phenotyping. 01/01/2025 - 31/12/2025 Abstract Fragile X syndrome is a frequent form of genetic autism and i…

Eleesha Annear doctoral scholarship holder About Eleesha Annear Eleesha Annear Contact Campus Drie Eiken Show email address Universteitsplein 1 2610 Wilrijk, BEL Department Department of Biology Statute & functions Bijzonder academisch personeel doctoral scholarship holder Cookie prreferences Strict…

Dale Annear postdoc researcher FWO About Dale Annear Dale Annear Contact Campus Drie Eiken Show email address Tel. +3232759756 Prins Boudewijnlaan 43 2650 Edegem, BEL Department Department of Biomedical Sciences Statute & functions Bijzonder academisch personeel postdoc researcher FWO Cookie prrefer…

Dale Annear postdoc researcher FWO Publications Dale Annear A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome Source European journal of human genetics - ISSN 1018-4813- (2025) p. Author(s) Claudio D' Incal, Bram Die…

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Dale Annear postdoc mandaat FWO Over Dale Annear Dale Annear Contact Campus Drie Eiken Toon e-mailadres Tel. +3232759756 Prins Boudewijnlaan 43 2650 Edegem, BEL Afdeling Departement Biomedische Wetenschappen Statuut & functies Bijzonder academisch personeel postdoc mandaat FWO Cookie-voorkeuren Stri…

Dale Annear postdoc mandaat FWO Publicaties Dale Annear A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome Bron European journal of human genetics - ISSN 1018-4813- (2025) p. Auteur(s) Claudio D' Incal, Bram Dierickx,…

Eleesha Annear doctoraatsbursaal Over Eleesha Annear Eleesha Annear Contact Campus Drie Eiken Toon e-mailadres Universteitsplein 1 2610 Wilrijk, BEL Afdeling Departement Biologie Statuut & functies Bijzonder academisch personeel doctoraatsbursaal Cookie-voorkeuren Strikt noodzakelijke cookies Ze zij…

Eleesha Annear doctoraatsbursaal Onderzoek Eleesha Annear Onderzoeksgroep Functionele morfologie Cookie-voorkeuren Strikt noodzakelijke cookies Ze zijn noodzakelijk voor de goede werking van de website en kunnen niet worden uitgeschakeld. Ze worden over het algemeen enkel gedefinieerd naar aanleidin…

Dale Annear postdoc mandaat FWO Onderzoek Dale Annear Onderzoeksgroep Medische Genetica (MEDGEN) Validatie van nieuwe, door AI voorspelde behandelingen voor het fragiele X-syndroom via next generation muisfenotypering 01/01/2025 - 31/12/2025 Abstract Fragiele X-syndroom is een veelvoorkomende vorm v…

Ellen Elinck Publicaties Ellen Elinck The ADNP-mediated transcriptome response to ketamine impairs the cytoskeletal protein axis Bron Journal of molecular neuroscience - ISSN 0895-8696-75:4 (2025) p. 1-17 Auteur(s) Claudio D' Incal, Ligia Mateiu, Kevin De Man, Ellen Elinck, Illana Gozes, Frank Kooy …

Frank Kooy emeritus met opdracht Publicaties Frank Kooy Understanding the functional consequences of mutations in the Helsmoortel-Van der Aa and fragile X syndromes Bron Antwerp, University of Antwerp, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Department of Biomedical Sciences,4…

Ellen Elinck Publications Ellen Elinck The ADNP-mediated transcriptome response to ketamine impairs the cytoskeletal protein axis Source Journal of molecular neuroscience - ISSN 0895-8696-75:4 (2025) p. 1-17 Author(s) Claudio D' Incal, Ligia Mateiu, Kevin De Man, Ellen Elinck, Illana Gozes, Frank Ko…

Frank Kooy emeritus with assignment Publications Frank Kooy Understanding the functional consequences of mutations in the Helsmoortel-Van der Aa and fragile X syndromes Source Antwerp, University of Antwerp, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Department of Biomedical Scie…

Bregje Christiaenssen predoc mandaat FWO Publicaties Bregje Christiaenssen Paracentric inversion disrupting the SHANK2 gene Bron European journal of medical genetics - ISSN 1769-7212-75 (2025) p. 1-11 Auteur(s) Jolien Huyghebaert, Bregje Christiaenssen, Marjan De Rademaker, Jenneke van den Ende, Gee…

Bregje Christiaenssen predoc researcher FWO Publications Bregje Christiaenssen Paracentric inversion disrupting the SHANK2 gene Source European journal of medical genetics - ISSN 1769-7212-75 (2025) p. 1-11 Author(s) Jolien Huyghebaert, Bregje Christiaenssen, Marjan De Rademaker, Jenneke van den End…

Jolien Huyghebaert onbezoldigd medewerker Publicaties Jolien Huyghebaert 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 H…

Marjan De Rademaker onbezoldigd medewerker Publicaties Marjan De Rademaker 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…

Functional Morphology search menu search content Members Spokesperson Raoul Van Damme Member Tim Andries Eleesha Annear Simon Baeckens Pim Boute Tim De Ridder Leonard Dewaele Genevieve Diedericks Ioanna Gavriilidi Lukas Hageneder Katleen Huyghe Cas Jorissen Ilias Kotoulas Jamie Maclaren Maja Mielke …

Medical Genetics search menu search content Members Spokesperson Bart Loeys Member Dogan Akdeniz Maaike Alaerts Dale Annear Reihaneh Asadi Bettina Blaumeiser Amira Bousbaa Lucia Buccioli Ana Regina de Abreu Pauline De Kinderen Katrien De Roeck Ivanna Fedoryshchenko Erik Fransen Anne Hebert Tammy Huy…

Jolien Huyghebaert unpaid staff Publications Jolien Huyghebaert 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 Huygheba…

Marjan De Rademaker unpaid staff Publications Marjan De Rademaker Diagnostic yield and clinical impact of prenatal whole exome sequencing (WES) : four-year single center experience Source Journal of perinatal medicine - ISSN 0300-5577- (2025) p. Author(s) Katleen Janssens, Marjan De Rademaker, Joke …

Claudio D'Incal senior onderzoeker Publicaties Claudio D'Incal Understanding the functional consequences of mutations in the Helsmoortel-Van der Aa and fragile X syndromes Bron Antwerp, University of Antwerp, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Department of Biomedical Sci…

Mathijs van der Lei onderzoeker Onderzoek Mathijs van der Lei Onderzoeksgroep Medische Genetica (MEDGEN) Validatie van nieuwe, door AI voorspelde behandelingen voor het fragiele X-syndroom via next generation muisfenotypering 01/01/2025 - 31/12/2025 Abstract Fragiele X-syndroom is een veelvoorkomend…

Geert Vandeweyer onbezoldigd medewerker Publicaties Geert Vandeweyer Leveraging patient-driven research to improve rational therapy selection in ROS1+ non-small cell lung cancer Bron Antwerp, University of Antwerp, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Department of Medical …