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
1 - 10 of 226
- Natural history of three late-diagnosed classic Galactosemia patients(2024)
Authors: Gert Matthijs
- N-glycosylation as a eukaryotic protective mechanism against protein aggregation.(2024)
Authors: Bert Houben, Matthias De Vleeschouwer, Matthew Wilson, Gert Matthijs, Joost Schymkowitz, Frederic Rousseau
Pages: eadk8173 - Exploring attitudes and experiences with reproductive genetic carrier screening among couples seeking medically assisted reproduction: a longitudinal survey study(2024)
Authors: Eva Van Steijvoort, Hilde Peeters, Karen Peeraer, Gert Matthijs, Pascal Borry
- Perspectives of parents of children with genetic conditions on reproductive genetic carrier screening(2024)
Authors: Eva Van Steijvoort, Gert Matthijs, Pascal Borry
Pages: 757 - 757 - Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa(2023)
Authors: Gloire Mbayabo, Gert Matthijs, Koenraad Devriendt, Chris Van Geet
- Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa.(2023)
Authors: Gert Matthijs, Chris Van Geet, Koenraad Devriendt
Pages: 595 - 601 - Experiences of nonpregnant couples after receiving reproductive genetic carrier screening results in Belgium(2023)
Authors: Eva Van Steijvoort, Hilde Peeters, Karen Peeraer, Gert Matthijs, Pascal Borry
Pages: 696 - 702 - BeSolveRD: The Belgian genome resource to resolve rare diseases(2023)
Authors: Koenraad Devriendt, Jeroen Luyten, Gert Matthijs
Pages: 573 - 574 - GENETIC MODULATORS OF SICKLE CELL DISEASE IN THE DEMOCRATIC REPUBLIC OF CONGO(2023)
Authors: Mamy Ngole Zita, Gert Matthijs, Prosper Lukusa-Tshilobo, Aimé Lumaka Zola
- Clinical and laboratory characterization of adult sickle cell anemia patients in Kinshasa(2022)
Authors: Gloire Mbayabo, Gert Matthijs, Chris Van Geet, Koenraad Devriendt