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Ronald J. A. Wanders

Researcher Next ID · RN-029404

Researcher · Biochemistry, Genetics and Molecular Biology

Emma Kinderziekenhuis

Amsterdam, Netherlands

Not currently recruitingFunding unknown
Works count
1,147
Citation count
59,593
H-index
124
i10-index
752

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Metabolism and Genetic Disorders
Peroxisome Proliferator-Activated Receptors
Mitochondrial Function and Pathology
Adipose Tissue and Metabolism
Diet and metabolism studies

Publications

  • Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact

    Nature Communications · 2018 · 10.1038/s41467-018-03957-8

  • Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

    Reviews in Endocrine and Metabolic Disorders · 2018 · 10.1007/s11154-018-9448-1

  • Metabolic Interplay between Peroxisomes and Other Subcellular Organelles Including Mitochondria and the Endoplasmic Reticulum

    Frontiers in Cell and Developmental Biology · 2016 · 10.3389/fcell.2015.00083

  • Human disorders of peroxisome metabolism and biogenesis

    Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · 2015 · 10.1016/j.bbamcr.2015.11.015

  • The Biochemistry and Physiology of Mitochondrial Fatty Acid β-Oxidation and Its Genetic Disorders

    Annual Review of Physiology · 2015 · https://doi.org/10.1146/annurev-physiol-021115-105045

  • Rhabdomyolysis: Review of the literature

    Neuromuscular Disorders · 2014 · 10.1016/j.nmd.2014.05.005

  • Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies

    Nature Medicine · 2014 · https://doi.org/10.1038/nm.3545

  • X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management

    Orphanet Journal of Rare Diseases · 2012 · 10.1186/1750-1172-7-51

  • A general introduction to the biochemistry of mitochondrial fatty acid β‐oxidation

    Journal of Inherited Metabolic Disease · 2010 · https://doi.org/10.1007/s10545-010-9061-2

  • The Secret Life of NAD+: An Old Metabolite Controlling New Metabolic Signaling Pathways

    Endocrine Reviews · 2010 · https://doi.org/10.1210/er.2009-0026

  • Valproic acid metabolism and its effects on mitochondrial fatty acid oxidation: A review

    Journal of Inherited Metabolic Disease · 2008 · 10.1007/s10545-008-0841-x

  • Cardiolipin provides an essential activating platform for caspase-8 on mitochondria

    The Journal of Cell Biology · 2008 · https://doi.org/10.1083/jcb.200803129

  • A Lethal Defect of Mitochondrial and Peroxisomal Fission

    New England Journal of Medicine · 2007 · 10.1056/nejmoa064436

  • Biochemistry of Mammalian Peroxisomes Revisited

    Annual Review of Biochemistry · 2006 · https://doi.org/10.1146/annurev.biochem.74.082803.133329

  • Functions and biosynthesis of plasmalogens in health and disease

    Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · 2004 · 10.1016/j.bbalip.2003.12.010

  • Carnitine biosynthesis in mammals

    Biochemical Journal · 2002 · 10.1042/bj3610417

  • Carnitine biosynthesis in mammals

    Biochemical Journal · 2002 · 10.1042/0264-6021:3610417

  • Mutations in the 3β-Hydroxysterol Δ24-Reductase Gene Cause Desmosterolosis, an Autosomal Recessive Disorder of Cholesterol Biosynthesis

    The American Journal of Human Genetics · 2001 · 10.1086/323473

  • ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations

    Human Mutation · 2001 · 10.1002/humu.1227

  • Defective Remodeling of Cardiolipin and Phosphatidylglycerol in Barth Syndrome

    Biochemical and Biophysical Research Communications · 2000 · 10.1006/bbrc.2000.3952

  • Smith-Lemli-Opitz Syndrome Is Caused by Mutations in the 7-Dehydrocholesterol Reductase Gene

    The American Journal of Human Genetics · 1998 · 10.1086/301982

  • Refsum disease is caused by mutations in the phytanoyl–CoA hydroxylase gene

    Nature Genetics · 1997 · 10.1038/ng1097-190

  • The ABC transporter proteins Pat1 and Pat2 are required for import of long‐chain fatty acids into peroxisomes of Saccharomyces cerevisiae.

    The EMBO Journal · 1996 · 10.1002/j.1460-2075.1996.tb00755.x

  • The membrane of peroxisomes in Saccharomyces cerevisiae is impermeable to NAD(H) and acetyl‐CoA under in vivo conditions.

    The EMBO Journal · 1995 · 10.1002/j.1460-2075.1995.tb07354.x

  • Peroxisomal disorders: A newly recognised group of genetic diseases

    European Journal of Pediatrics · 1986 · 10.1007/bf00441734

Current projects

    No projects listed.