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
31 - 34 of 34
- A functional human genome project: integrated research of human congenital disorders.From1 Oct 2010 → 30 Sep 2012Funding: BOF - Concerted Research Project from 1994
- Zebrafish as a Model for Glycosylation Defects. Fishing for the Role of TMEM165From1 Oct 2009 → 25 Jun 2014Funding: Own budget, for example: patrimony, inscription fees, gifts
- High throughput molecular diagnostics in individual patients for genetic diseases with heterogeneous clinical presentation (TECHGENE).From1 Feb 2009 → 31 Jan 2012Funding: General Activities (Annex IV)
- Novel causes of "Congenital Disorders of Glycosylation" (CDG): exploration of potential, new links to (the regulation of) mitosis and to an intracellular (ion) transporter.From1 Jan 2008 → 31 Dec 2013Funding: FWO research project (including WEAVE projects)
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