Researcher
Rudy Van Coster
- Disciplines:Endocrinology and metabolic diseases, Paediatrics and neonatology, Nursing
Affiliations
- Department of Internal Medicine and Pediatrics (Department)
Member
From1 Oct 2018 → 30 Sep 2020 - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 1996 → 30 Sep 2018
Projects
1 - 3 of 3
- Bridging the gap in mitochondrial disorder diagnosis and treatment by using human embryos and pluripotent stem cellsFrom1 Jan 2017 → 31 Dec 2020Funding: FWO research project (including WEAVE projects)
- The role of mitochondrial dysfunctions in the pathogenesis of autism spectrum disorderFrom1 Oct 2014 → 31 Jul 2019Funding: BOF - Doctoral projects
- Characterization of novel genetic causes of combined OXPHOS deficienciesFrom1 Sep 2014 → 31 Aug 2015Funding: BOF - Doctoral projects
Publications
1 - 10 of 110
- Clinical, biochemical, and histopathological diagnosis of Egyptian paediatric patients with suspected mitochondrial diseases : a hospital-based study(2023)
Authors: D. M. Abdou, L. A. Selim, Rudy Van Coster, Joél Smet, G. A. Nakhla, D. A. Mehaney
Pages: 31 - 36 - Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy(2021)
Authors: Sarah Duerinckx, Julie Désir, Camille Perazzolo, Cindy Badoer, Valérie Jacquemin, Julie Soblet, Isabelle Maystadt, Yusuf Tunca, Bettina Blaumeiser, Berten Ceulemans, et al.
- Prolyl endopeptidase-like is a (thio)esterase involved in mitochondrial respiratory chain function(2021)
Authors: Karen Rosier, Molly T. McDevitt, Joél Smet, Brendan J. Floyd, Maxime Verschoore, Maria J. Marcaida, Craig A. Bingman, Irma Lemmens, Matteo Dal Peraro, Jan Tavernier, et al.
- Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features(2021)
Authors: Candy Kumps, Erika D'haenens, Sarah Vergult, Jasmine Leus, Rudy Van Coster, Anna Jansen, Koen Devriendt, Anna Oostra, Olivier Vanakker
Pages: 449 - 456 - Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in TK2 gene(2020)
Authors: George K. Papadimas, Efthimia Vargiami, Pinelopi Dragoumi, Rudy Van Coster, Joél Smet, Sara Seneca, Constantinos Papadopoulos, Evangelia Kararizou, Dimitrios Zafeiriou
Pages: 94 - 97 - Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrest(2020)
Authors: Maoxing Tang, Mina Popovic, Margot Van der Jeught, Rudy Van Coster, Dieter Deforce, Dominic Stoop
Pages: 1562 - 1577 - Functional characterization of novel MFSD8 pathogenic variants anticipates neurological involvement in juvenile isolated maculopathy(2020)
Authors: Miriam Bauwens, Stephan Storch, Nicole Weisschuh, Chantal Ceuterick-de Groote, Brecht Guillemyn, Sarah De Jaegere, Rudy Van Coster
Pages: 426 - 436 - Comparative analysis of different nuclear transfer techniques to prevent the transmission of mitochondrial DNA variants(2019)
Authors: Maoxing Tang, Ramesh Guggilla, Yannick Gansemans, Margot Van der Jeught, Annekatrien Boel, Mina Popovic, Panagiotis Stamatiadis, Minerva Ferrer Buitrago, Vanessa Thys, Rudy Van Coster, et al.
Pages: 797 - 810 - A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation(2019)
Authors: Simon Tavernier, V Athanasopoulos, PATRICK VERLOO, G Behrens, Jens Staal, Delfien Bogaert, Leslie Naesens, Marieke De Bruyne, Sofie Van Gassen, Eef Parthoens, et al.
- Comparative analysis of different nuclear transfer techniques to prevent the transmission of mitochondrial DNA variants(2019)Volume: 34
Authors: Maoxing Tang, R Reddy, Yannick Gansemans, Margot Van der Jeught, Rudy Van Coster, Dieter Deforce, Filip Van Nieuwerburgh
Pages: 222 - 223