Martin A. T. Vervaart

Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia

Frédéric M. Vaz, John McDermott, Mariëlle Alders et al. · Brain · 2019 · 108 citations · Full text

Biology, Neurodegenerative Diseases, Etherlipid Homeostasis +15

Lipidomic analysis of fibroblasts from Zellweger spectrum disorder patients identifies disease-specific phospholipid ratios

Katharina Herzog, Mia L. Pras‐Raves, Martin A. T. Vervaart et al. · Journal of Lipid Research · 2016 · 84 citations · Full text

A sensitive mass spectrometry platform identifies metabolic changes of life history traits in C. elegans

Arwen W. Gao, Iliana A. Chatzispyrou, Rashmi Kamble et al. · Scientific Reports · 2017 · 79 citations · Full text

Defining functional classes of Barth syndrome mutation in humans

Ya‐Wen Lu, Laura C.A. Galbraith, Jenny D. Herndon et al. · Human Molecular Genetics · 2016 · 72 citations · Full text

Mendelian Disorder, Mitochondrial Biogenesis, Mitochondrial Function +14

Functional characterisation of peroxisomal β‐oxidation disorders in fibroblasts using lipidomics

Katharina Herzog, Mia L. Pras‐Raves, Sacha Ferdinandusse et al. · Journal of Inherited Metabolic Disease · 2017 · 55 citations · Full text

Lipid Analysis, Metabolic Pathways, Health Sciences +15