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
11 - 20 of 34
- Deep familial phenotyping and genotyping to resolve phenotypic variability of inherited pathogenic genetic variantsFrom1 Oct 2019 → 30 Sep 2023Funding: BOF - projects
- An integrated 'omics' approach for identifying and characterizing congenital glycosylation defectsFrom1 Feb 2019 → 31 Dec 2022Funding: FWO research project (including WEAVE projects)
- European Joint Programme on Rare DiseasesFrom1 Jan 2019 → 31 Dec 2023Funding: H2020-EU.3.2. - SOCIETAL CHALLENGES - Food security, sustainable agriculture, marine and maritime research and the bio-economy
- EUROGLYCAN-omics: congenital errors of glycosylation.From1 May 2018 → 30 Apr 2020Funding: BOF - Bilateral scientific cooperation
- Genomic Medicine: Translation of Whole Genome Analyses to Health GenomicsFrom1 May 2018 → TodayFunding: IOF - mandates, IOF - Industrial Research Fund
- Implementation of an expanded carrier screening offer for couplesFrom1 Jan 2018 → 31 Dec 2021Funding: FWO research project (including WEAVE projects)
- A comprehensive study of genetic determinants of motor neuron vulnerabilityFrom1 Oct 2017 → 2 May 2022Funding: FWO fellowships
- HBOC (Hereditary Breast and Ovarian Cancer), a paradigm shift for counseling and treatment of patients with defects in homologous recombination - an explorative studyFrom1 Jan 2017 → 31 Dec 2018Funding: Nonprofit institution or equivalents
- GENETIC MODULATORS OF SICKLE CELL DISEASE IN THE DEMOCRATIC REPUBLIC OF CONGOFrom1 Jan 2017 → 25 Mar 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- European research network aimed at improving the diagnosis and treatment of congenital glycosylation defects.From1 Jan 2016 → 31 Dec 2020Funding: FWO research project (including WEAVE projects)
Publications
1 - 10 of 222
- 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
- Knowledge, attitudes and preferences regarding reproductive genetic carrier screening among reproductive-aged men and women in Flanders (Belgium)(2022)
Authors: Eva Van Steijvoort, Hilde Peeters, Karen Peeraer, Gert Matthijs, Pascal Borry
Pages: 1255 - 1261 - Exploring informed choice in preconception reproductive genetic carrier screening by using a modified Multidimensional Measure of Informed Choice(2022)
Authors: Eva Van Steijvoort, Hilde Peeters, Karen Peeraer, Gert Matthijs, Pascal Borry
Pages: 3313 - 3318 - A PMM2-CDG caused by an A108V mutation associated with a heterozygous 70 kilobases deletion case report(2022)
Authors: Gert Matthijs
- Reasons affecting the uptake of reproductive genetic carrier screening among nonpregnant reproductive-aged women in Flanders (Belgium)(2022)
Authors: Eva Van Steijvoort, Hilde Peeters, Karen Peeraer, Gert Matthijs, Pascal Borry
Pages: 1043 - 1053