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Researcher
Matthew Wilson
- Disciplines:Clinical genetics and molecular diagnostics, Genetics
Affiliations
- Laboratory for Molecular Diagnosis (Division)
Member
From1 Jul 2019 → 30 Sep 2022
Projects
1 - 2 of 2
- Congenital Disorders of Glycosylation: new defects and mechanismsFrom1 Oct 2022 → TodayFunding: FWO senior postdoctoral fellowship
- Untangling the pathophysiology of congenital disorders of glycosylation affecting the OST complexFrom1 Jul 2020 → 30 Jun 2022Funding: H2020 - Skills and Career Development (Marie Skłodowska-Curie) actions
Publications
1 - 7 of 7
- CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking(2022)
Authors: Matthew Wilson, Erika Souche, Daisy Rymen, Gert Matthijs
Pages: 2571 - 2581 - Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation(2022)
Authors: Frederik Staels, Matthew Wilson, Rik Schrijvers, Gert Matthijs
Pages: 1279 - 1286 - Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings(2021)
Authors: Matthew Wilson, Erika Souche, Daisy Rymen, Peter Witters, Gert Matthijs
Pages: 2130 - 2144 - The evolving genetic landscape of congenital disorders of glycosylation(2021)
Authors: Matthew Wilson, Gert Matthijs
- SLC37A4-CDG: Second patient(2021)
Authors: Matthew Wilson, Daisy Rymen, Erika Souche, Gert Matthijs
Pages: 122 - 128 - Disorders affecting vitamin B-6 metabolism(2019)
Authors: Matthew Wilson, Barbara Plecko, Philippa B Mills, Peter T Clayton
Pages: 629 - 646 - PDXK mutations cause polyneuropathy responsive to pyridoxal 5 '-phosphate supplementation(2019)
Authors: Viorica Chelban, Matthew Wilson, Jodi Warman Chardon, Jana Vandrovcova, M Natalia Zanetti, Eleni Zamba-Papanicolaou, Stephanie Efthymiou, Simon Pope, Maria R Conte, Giancarlo Abis, et al.
Pages: 225 - 240