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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
11 - 20 of 222
- Recommendations for whole genome sequencing in diagnostics for rare diseases(2022)
Authors: Erika Souche, Gert Matthijs
Pages: 1017 - 1021 - CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking(2022)
Authors: Matthew Wilson, Erika Souche, Daisy Rymen, Gert Matthijs
Pages: 2571 - 2581 - Value of DNA testing in the diagnosis of sickle-cell anemia in childhood in an environment with a high prevalence of other causes of anemia(2022)
Authors: Gloire Mbayabo, Gert Matthijs, Koenraad Devriendt, Chris Van Geet
- Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation(2022)
Authors: Frederik Staels, Matthew Wilson, Rik Schrijvers, Gert Matthijs
Pages: 1279 - 1286 - CDG or not CDG(2022)
Authors: Gert Matthijs
Pages: 383 - 385 - DNA testing for sickle cell anemia in Africa: Implementation choices for the Democratic Republic of Congo(2022)
Authors: Gloire Mbayabo, Koenraad Devriendt, Gert Matthijs
- COG6-CDG: Novel variants and novel malformation(2022)
Authors: Gert Matthijs
Pages: 165 - 174 - Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings(2021)
Authors: Matthew Wilson, Erika Souche, Daisy Rymen, Peter Witters, Gert Matthijs
Pages: 2130 - 2144 - The evolving genetic landscape of congenital disorders of glycosylation(2021)
Authors: Matthew Wilson, Gert Matthijs
- MAN1B1-CDG: novel patients and novel variant(2021)
Authors: Gert Matthijs
Pages: 1207 - 1209