R. J. A. Wanders

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

Sander M. Houten, Wietse Kuis, Marinus Duran et al. · Nature Genetics · 1999 · 520 citations

Cause Hyperimmunoglobulinaemia D, Periodic Fever Syndrome, Autoimmune Disease +11

Defective peroxisomal catabolism of branched fatty acyl coenzyme A in mice lacking the sterol carrier protein-2/sterol carrier protein-x gene function

U. Seedorf, M. Raabe, Peter Ellinghaus et al. · Genes & Development · 1998 · 261 citations · Full text

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the α-subunit of the mitochondrial trifunctional protein

Lodewijk IJlst, R. J. A. Wanders, S. Ushikubo et al. · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · 1994 · 158 citations

Mitochondrial Biogenesis, Biochemistry, Mitochondrial Function +15

Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorder

R. J. A. Wanders, Herbert Schumacher, J. Heikoop et al. · Journal of Inherited Metabolic Disease · 1992 · 130 citations

Mendelian Disorder, Biochemistry, Genetic Disorder +8

Plasmalogens participate in very-long-chain fatty acid-induced pathology

Pedro Brites, P. A. W. Mooyer, L. el Mrabet et al. · Brain · 2008 · 110 citations · Full text

Lipid Peroxidation, Pathology, Cell Death +20