< Back to previous page
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
41 - 50 of 222
- Clinical Utility Gene Card For: GALNT3 defective congenital disorder of glycosylation(2018)
Authors: Gert Matthijs
Pages: 1230 - 1233 - Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer(2018)
Authors: Gert Matthijs, Erika Souche
Pages: 80 - 80 - Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical Experience(2018)
Authors: Simon Ardui, Thomy de Ravel de l'Argentière, Hilde Van Esch, Koenraad Devriendt, Gert Matthijs, Joris Vermeesch
- Patient with confirmed LEOPARD syndrome developing multiple melanoma(2018)
Authors: Gert Matthijs
Pages: 59 - 62 - Investigating the function of Gdt1p in yeast Golgi glycosylation(2018)
Authors: Marine Houdou, Gert Matthijs, François Foulquier
Pages: 394 - 402 - Protective BCL11A and HBS1L-MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia(2018)
Authors: Koenraad Devriendt, Gert Matthijs
- Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the 3.7 triplication in congolese patients than in worldwide series(2018)
Authors: Koenraad Devriendt, Gert Matthijs
- Všichni jsme GENiální: Lidská genetika slovem a obrazem(2018)
Authors: Pascal Borry, Gert Matthijs
- Mutations in ATP6AP2 are associated to Congenital Disorders of Glycosylation with autophagic defects(2017)
Authors: Romain Peanne, Magda Cannata Serio, Maria A Rujano, Ganna Panasyuk, Janine Reunert, Dulce Quelhas, Michael Schwake, Sandrine Duvet, Francois Foulquier, Gert Matthijs, et al.
Pages: 1215 - 1216 - Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects(2017)
Authors: Romain Péanne, Erika Souche, François Foulquier, Gert Matthijs
Pages: 3707 - 3729