Publications by authors named "Martin Vervaart"

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Discovery of novel diagnostic biomarkers for Sjögren-Larsson syndrome by untargeted lipidomics.
Frédéric M Vaz, Pippa Staps, Jan Bert van Klinken, Henk van Lenthe, Martin Vervaart

Biochim Biophys Acta Mol Cell Biol Lipids· March 2024

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An improved functional assay in blood spot to diagnose Barth syndrome using the monolysocardiolipin/cardiolipin ratio.
Frédéric M Vaz, Henk van Lenthe, Martin A T Vervaart, Femke S Stet, Johanne H Klinkspoor

J Inherit Metab Dis· January 2022

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Metabolomics and lipidomics in Caenorhabditis elegans using a single-sample preparation.
Marte Molenaars, Bauke V Schomakers, Hyung L Elfrink, Arwen W Gao, Martin A T Vervaart

Dis Model Mech· April 2021

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Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia.
Frédéric M Vaz, John H McDermott, Mariëlle Alders, Saskia B Wortmann, Stefan Kölker, Martin A T Vervaart

Brain· November 2019

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Functional characterisation of peroxisomal β-oxidation disorders in fibroblasts using lipidomics.
Katharina Herzog, Mia L Pras-Raves, Sacha Ferdinandusse, Martin A T Vervaart, Angela C M Luyf

J Inherit Metab Dis· May 2018

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Plasma lipidomics as a diagnostic tool for peroxisomal disorders.
Katharina Herzog, Mia L Pras-Raves, Sacha Ferdinandusse, Martin A T Vervaart, Angela C M Luyf

J Inherit Metab Dis· May 2018

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A sensitive mass spectrometry platform identifies metabolic changes of life history traits in C. elegans.
Arwen W Gao, Iliana A Chatzispyrou, Rashmi Kamble, Yasmine J Liu, Katharina Herzog, Martin A T Vervaart

Sci Rep· May 2017

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Lipidomic analysis of fibroblasts from Zellweger spectrum disorder patients identifies disease-specific phospholipid ratios.
Katharina Herzog, Mia L Pras-Raves, Martin A T Vervaart, Angela C M Luyf, Antoine H C van Kampen

J Lipid Res· August 2016

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Defining functional classes of Barth syndrome mutation in humans.
Ya-Wen Lu, Laura Galbraith, Jenny D Herndon, Ya-Lin Lu, Mia Pras-Raves, Martin Vervaart

Hum Mol Genet· May 2016

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