Wanders, Ronald J.A.

Factors determining the relative contribution of the adenine-nucleotide translocator and the ADP-regenerating system to the control of oxidative phosphorylation in isolated rat-liver mitochondria

WANDERS, R. J. A., GROEN, A. K., VAN ROERMUND, C. W. T., & TAGER, J. M. (1984) · European Journal of Biochemistry

Mitochondrial Function and PathologyATP Synthase and ATPases Research

Cited by 93

X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism, ABC half-transporters and the complicated route to treatment

Kemp, S., & Wanders, R. J. A. (2007) · Molecular Genetics and Metabolism

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 82

A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform

Barøy, T., Koster, J., Strømme, P., Ebberink, M. S., Misceo, D., Ferdinandusse, S., Holmgren, A., Hughes, T., Merckoll, E., Westvik, J., et al. (2015) · Human Molecular Genetics

Metabolism and Genetic DisordersGenomics and Rare Diseases

Cited by 81

Aberrant protein acylation is a common observation in inborn errors of acyl-CoA metabolism

Pougovkina, O., te Brinke, H., Wanders, R. J. A., Houten, S. M., & de Boer, V. C. J. (2014) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersNeurological diseases and metabolism

Cited by 80

Comparison of C26:0-carnitine and C26:0-lysophosphatidylcholine as diagnostic markers in dried blood spots from newborns and patients with adrenoleukodystrophy

Huffnagel, I. C., van de Beek, M.-C., Showers, A. L., Orsini, J. J., Klouwer, F. C. C., Dijkstra, I. M. E., Schielen, P. C., van Lenthe, H., Wanders, R. J. A., Vaz, F. M., et al. (2017) · Molecular Genetics and Metabolism

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 71

Peroxisomal D-bifunctional protein deficiency

Lines, M. A., Jobling, R., Brady, L., Marshall, C. R., Scherer, S. W., Rodriguez, A. R., Lee, L., Lang, A. E., Mestre, T. A., Wanders, R. J. A., et al. (2014) · Neurology

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 70

Bile acid treatment alters hepatic disease and bile acid transport in peroxisome-deficient PEX2 Zellweger mice

Keane, M. H., Overmars, H., Wikander, T. M., Ferdinandusse, S., Duran, M., Wanders, R. J. A., & Faust, P. L. (2007) · Hepatology

Metabolism and Genetic DisordersDrug Transport and Resistance Mechanisms

Cited by 68

Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene

Sevin, C., Ferdinandusse, S., Waterham, H. R., Wanders, R. J., & Aubourg, P. (2011) · Orphanet Journal of Rare Diseases

Metabolism and Genetic DisordersGenetic Neurodegenerative Diseases

Cited by 66

Peroxisomal very long-chain fatty acid β-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders

Wanders, R. J. A., van Roermund, C. W. T., van Wijland, M. J. A., Heikoop, J., Schutgens, R. B. H., Schram, A. W., Tager, J. M., van den Bosch, H., Poll-Thé, B. T., Saudubray, J. M., et al. (1987) · Clinica Chimica Acta

Metabolism and Genetic DisordersGenetic and rare skin diseases.

Cited by 58

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

Herzog, K., Pras‐Raves, M. L., Ferdinandusse, S., Vervaart, M. A. T., Luyf, A. C. M., van Kampen, A. H. C., Wanders, R. J. A., Waterham, H. R., & Vaz, F. M. (2018) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

Cited by 57

C26:0-Carnitine Is a New Biomarker for X-Linked Adrenoleukodystrophy in Mice and Man

van de Beek, M.-C., Dijkstra, I. M. E., van Lenthe, H., Ofman, R., Goldhaber-Pasillas, D., Schauer, N., Schackmann, M., Engelen-Lee, J.-Y., Vaz, F. M., Kulik, W., et al. (2016) · PLOS ONE

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 48

Developmental changes of bile acid composition and conjugation in L- and D-bifunctional protein single and double knockout mice

Ferdinandusse, S., Denis, S., Overmars, H., Van Eeckhoudt, L., Van Veldhoven, P. P., Duran, M., Wanders, R. J. A., & Baes, M. (2005) · Journal of Biological Chemistry

Cholesterol and Lipid MetabolismMetabolism and Genetic Disorders

Cited by 47

Role of peroxisomes in human lipid metabolism and its importance for neurological development

Wanders, R. J. A., & Poll-The, B. T. (2017) · Neuroscience Letters

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

Cited by 46

Conservation of targeting but divergence in function and quality control of peroxisomal ABC transporters: An analysis using cross-kingdom expression

Zhang, X., De Marcos Lousa, C., Schutte-Lensink, N., Ofman, R., Wanders, R. J., Baldwin, S. A., Baker, A., Kemp, S., & Theodoulou, F. L. (2011) · Biochemical Journal

Metabolism and Genetic DisordersDrug Transport and Resistance Mechanisms

Cited by 43

Neuroimaging of peroxisome biogenesis disorders (Zellweger spectrum) with prolonged survival

Barth, P. G., Majoie, C. B. L. M., Gootjes, J., Wanders, R. J. A., Waterham, H. R., van der Knaap, M. S., de Klerk, J. B. C., Smeitink, J., & Poll-The, B. T. (2004) · Neurology

Metabolism and Genetic DisordersHereditary Neurological Disorders

Cited by 43

Adult Refsum disease: A form of tapetoretinal dystrophy accessible to therapy.

Rüether, K., Baldwin, E., Casteels, M., Feher, M. D., Horn, M., Kuranoff, S., Leroy, B. P., Wanders, R. J., & Wierzbicki, A. S. (2010) · Survey of Ophthalmology

Metabolism and Genetic DisordersRetinal Development and Disorders

Cited by 42

Peroxisomal acyl‐CoA‐oxidase deficiency: Two new cases

Carrozzo, R., Bellini, C., Lucioli, S., Deodato, F., Cassandrini, D., Cassanello, M., Caruso, U., Rizzo, C., Rizza, T., Napolitano, M. L., et al. (2008) · American Journal of Medical Genetics Part A

Metabolism and Genetic DisordersNeurological diseases and metabolism

Cited by 40

Method for measurement of peroxisomal very-long-chain fatty acid β-oxidation in human skin fibroblasts using stable-isotope-labeled tetracosanoic acid

Kemp, S., Valianpour, F., Mooyer, P. A. W., Kulik, W., & Wanders, R. J. A. (2004) · Clinical Chemistry

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

Cited by 40

Syndromic retinitis pigmentosa.

Karuntu, J. S., Almushattat, H., Nguyen, X.-T.-A., Plomp, A. S., Wanders, R. J. A., Hoyng, C. B., van Schooneveld, M. J., Schalij-Delfos, N. E., Brands, M. M., Leroy, B. P., et al. (2025) · Progress in Retinal and Eye Research

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 39

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy

Kemp, S., Mooyer, P. A. W., Bolhuis, P. A., van Geel, B. M., Mandel, J. L., Barth, P. G., Aubourg, P., & Wanders, R. J. A. (1996) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 37

A new type of chondrodysplasia punctata associated with peroxisomal dysfunction

Poll‐The, B. T., Maroteaux, P., Narcy, C., Quetin, P., Guesnu, M., Wanders, R. J. A., Schutgens, R. B. H., & Saudubray, J. M. (1991) · Journal of Inherited Metabolic Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 32

Peroxisomes and their central role in metabolic interaction networks in humans.

Wanders, R. J. A., Waterham, H. R., & Ferdinandusse, S. (2018) · Subcellular Biochemistry

Metabolism and Genetic DisordersLipid metabolism and biosynthesis

Cited by 31

CYP4F2 affects phenotypic outcome in adrenoleukodystrophy by modulating the clearance of very long-chain fatty acids

van Engen, C. E., Ofman, R., Dijkstra, I. M. E., van Goethem, T. J., Verheij, E., Varin, J., Vidaud, M., Wanders, R. J. A., Aubourg, P., Kemp, S., et al. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 26

Delay in diagnosis of X-linked adrenoleukodystrophy

van Geel, B. M., Assies, J., Haverkort, E. B., Barth, P. G., Wanders, R. J. A., Schutgens, R. B. H., Keyser, A., & Zwetsloot, C. P. (1993) · Clinical Neurology and Neurosurgery

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 26