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Researcher
Gert Matthijs
- Disciplines:Genetics, Systems biology, Medical imaging and therapy, Molecular and cell biology, Other paramedical sciences
Affiliations
- Laboratory for Molecular Diagnosis (Division)
Responsible
From1 Jan 2008 → Today - Department of Human Genetics (Department)
Member
From1 Oct 1999 → Today
Projects
1 - 10 of 34
- Dolichol: An overlooked lipid in human health and diseaseFrom1 Jan 2024 → TodayFunding: FWO research project (including WEAVE projects)
- Training the future generation of clinical and basic reseachers for Congenital Disorders of GlycosylationFrom1 Feb 2023 → TodayFunding: BOF - various
- Congenital Disorders of Glycosylation: new defects and mechanismsFrom1 Oct 2022 → TodayFunding: FWO senior postdoctoral fellowship
- Expanding the genetic landscape of Congenital Disorders of Glycosylation using genomic techniques - RNA-SeqFrom1 Oct 2021 → 30 Sep 2023Funding: BOF - projects
- DHRSX deficiency - A novel CDG and a new facet of dolichol metabolism?From1 Apr 2021 → 31 Mar 2022Funding: Foreign private sponsor - undefined
- Inborn Errors of GlycosylationFrom1 Jan 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- EU-Genomics: EU Infrastructure for Genome AnalysisFrom1 Jan 2021 → TodayFunding: FWO Large scale research infrastructure
- Deciphering the function(s) of SLC10A7 in Congenital Disorders of Glycosylation (CDG).From1 Oct 2020 → TodayFunding: BOF - doctoral mandates
- Untangling the pathophysiology of congenital disorders of glycosylation affecting the OST complexFrom1 Jul 2020 → 30 Jun 2022Funding: H2020-EU.1.3.- EXCELLEN SCIENCE - Marie Skłodowska-Curie actions
- Beyond 1M GenomesFrom1 Jun 2020 → 31 Aug 2023Funding: H2020-EU.3.1. - SOCIETAL CHALLENGES - Health, demographic change and wellbeing
Publications
211 - 220 of 226
- Inter-laboratory diagnostic validation of conformation sensitive capillary electrophoresis(2008)
Authors: Gert Matthijs
Pages: S66 - S66 - Patenting and licensing in genetic testing: ethical, legal, and social issues(2008)
Authors: Gert Matthijs
Pages: S10 - S50 - Deletion of C2orf34, PREPL and SLC3A1 causes atypical Hypotonia-Cystinuria Syndrome(2008)
Authors: Gert Matthijs, John Creemers
Pages: 314 - 318 - Introduction(2008)
Authors: Gert Matthijs
Pages: 398S - 400S - Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation(2008)
Authors: Florence Molinari, François Foulquier, Patrick S Tarpey, Willy Morelle, Sarah Boissel, Jon Teague, Sarah Edkins, P Andrew Futreal, Michael R Stratton, Gillian Turner, et al.
Pages: 1150 - 1157 - Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation(2008)
Authors: François Foulquier, Gert Matthijs
Pages: 1150 - 1157 - Patenting and licensing in genetic testing: recommendations of the European Society of Human Genetics(2008)
Authors: Gert Matthijs
Pages: 405 - 411 - Introduction(2008)
Authors: Gert Matthijs
Pages: S1 - S2 - Patenting and licensing in genetic testing(2008)
Authors: Gert Matthijs
Pages: 405 - 411 - Epilepsy as part of the phenotype associated with ATP1A2 mutations(2008)
Authors: Kristl Claeys, Gert Matthijs, Wim Van Paesschen
Pages: 500 - 508