Matthew P Wilson

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 18

Top Venues

bioRxiv : the preprint server for biology

Journal of inherited metabolic disease

Analytical chemistry

JIMD reports

KU Leuven

This page only lists publications with an associated author ORCID identifier.

Affiliation History

KU Leuven Jul 02 2019

Belgium

Postdoctoral associate :: Laboratory for Molecular Diagnosis

University College London Jan 01 2015 - Jun 10 2019

United Kingdom

PhD Student :: Institute of Child Health, Genetics and Genomic Medicine

Publications

Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie Graff, Eline Pieters, Pamela Stanley, Joseph N Contessa, Emile Van Schaftingen, Gert Matthijs, François Foulquier, Guido T Bommer, Matthew P Wilson
The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene. bioRxiv : the preprint server for biology (2024)
Francisco Del Caño-Ochoa, Bobby George Ng, Antonio Rubio-Del-Campo, Sonal Mahajan, Matthew P Wilson, Marçal Vilar, Daisy Rymen, Paula Sánchez-Pintos, Janna Kenny, Myriam Ley Martos, Teresa Campos, Saskia B Wortmann, Hudson H Freeze, Santiago Ramón-Maiques
Beyond genetics: Deciphering the impact of missense variants in CAD deficiency. Journal of inherited metabolic disease (2023)
Matthew P Wilson, Zoé Durin, Özlem Unal, Bobby G Ng, Thomas Marrecau, Liesbeth Keldermans, Erika Souche, Daisy Rymen, Mehmet Gündüz, Gülşen Köse, Luisa Sturiale, Domenico Garozzo, Hudson H Freeze, Jaak Jaeken, François Foulquier, Gert Matthijs
CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking. Human molecular genetics 31 (15) (2022)
Matthew P Wilson, Dulce Quelhas, Elisa Leão-Teles, Luisa Sturiale, Daisy Rymen, Liesbeth Keldermans, Valérie Race, Erika Souche, Esmeralda Rodrigues, Teresa Campos, Emile Van Schaftingen, François Foulquier, Domenico Garozzo, Gert Matthijs, Jaak Jaeken
SLC37A4-CDG: Second patient. JIMD reports 58 (1) (2021)
Matthew P Wilson, Emma J Footitt, Apostolos Papandreou, Mari-Liis Uudelepp, Ronit Pressler, Danielle C Stevenson, Camila Gabriel, Mel McSweeney, Matthew Baggot, Derek Burke, Tommy Stödberg, Kate Riney, Manuel Schiff, Simon J R Heales, Kevin A Mills, Paul Gissen, Peter T Clayton, Philippa B Mills
An LC-MS/MS-Based Method for the Quantification of Pyridox(am)ine 5'-Phosphate Oxidase Activity in Dried Blood Spots from Patients with Epilepsy. Analytical chemistry 89 (17) (2017)

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Publication Activity (10 Years)

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Matthew P Wilson