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Researcher
Kim Vancampenhout
- Keywords:Medicine
- Disciplines:Humanities and the arts, Engineering and technology, Natural sciences
Affiliations
- Clinical sciences (Department)
Member
From1 Jan 2014 → 31 Dec 2014 - Department of Embryology and Genetics (Department)
Member
From16 Nov 2013 → 31 Dec 2013 - Reproduction and Genetics (Research group)
Member
From21 Jun 2010 → 31 Dec 2014 - Department of Embryology and Genetics (Department)
Member
From16 Nov 2009 → 15 Nov 2013
Publications
1 - 4 of 4
- Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells(2017)
Authors: Filippo Zambelli, Kim Vancampenhout, Dorien Daneels, Daniel Brown, Joke Mertens, Sonia Van Dooren, Ben Caljon, Luca Gianaroli, Karen Sermon, Thierry Voet, et al.
Pages: 1229-1236 - Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?(2015)
Authors: Sara Seneca, Kim Vancampenhout, Rudy Van Coster, Joél Smet, Willy Lissens, A. Vanlander, Boel De Paepe, An Jonckheere, Katrien Stouffs, Linda De Meirleir
Pages: 41-48 - Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene(2014)
Authors: François-Guillaume Debray, M. Gonce, Kim Vancampenhout, F. Boemer, Laurent Weekers, Joel Smet, Rudy Van Coster
Pages: 101-105 - A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome(2014)
Authors: Kim Vancampenhout, Ben Caljon, Claudia Spits, Katrien Stouffs, An Jonckheere, Linda De Meirleir, Willy Lissens, A. Vanlander, Joél Smet, Boel De Paepe, et al.