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
21 - 30 of 34
- Insights into Golgi stress response from a new glycosylation disorderFrom1 Jan 2015 → 31 Mar 2016Funding: Foreign foundations, funds with scientific view
- Molecular sequence-analysis to determine the variability and epigenetic signature of tandem repeats in the human genome.From1 Jan 2014 → 21 Dec 2018Funding: IWT personal funding - strategic basic research grants
- Human genetics in the Democratic Republic of Congo.From1 Oct 2013 → 31 Dec 2015Funding: VLIR-UOS International Conferences (INCO)
- Introducing diagnostic applications of '3Gb-testing' in human geneticsFrom1 Sep 2013 → 31 Aug 2015Funding: Health
- New insights into ER and Golgi N-linked glycosylation - Contribution of CDG patients.From1 Oct 2012 → 30 Sep 2018Funding: FWO fellowships
- PACBIO.From26 Apr 2012 → 1 Nov 2018Funding: Hercules - Large scale research infrastructure
- Systematic search for novel Congenital Disorders of Glycosylation (CDG): the identification of new defects in ER and Golgi and a functional study of TPARL, a new gene with a possible role in pH and Ca2+ homeostasis.From1 Jan 2012 → 31 Dec 2017Funding: FWO research project (including WEAVE projects)
- A systemic search for novel congenital disorders of Glycosylation type 1 (CDG-I), with a comprehensive evaluation of the clinical phenotypes.From1 Oct 2011 → 30 Sep 2017Funding: FWO fellowships
- A functional human genome project: integrated research of human congenital disorders.From1 Oct 2011 → 30 Sep 2016Funding: BOF - Concerted Research Project from 1994
- EuroGentest2: Genetic testing in Europe - Network for the further development, harmonization, validation and standardization of services.From1 Jan 2011 → 31 Dec 2013Funding: General Activities (Annex IV)
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