Lodewijk IJlst

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

Nadav Shai, Eden Yifrach, Carlo W.T. van Roermund et al. · Nature Communications · 2018 · 307 citations · Full text

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

Gerbert A. Jansen, Rob Oftnan, Sacha Ferdinandusse et al. · Nature Genetics · 1997 · 304 citations

Biology, Genetic Disorder, Natural Sciences +7

Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

Brage Storstein Andresen, S. E. Olpin, Ben J. H. M. Poorthuis et al. · The American Journal of Human Genetics · 1999 · 300 citations · Full text

Genetic Diseases, Disease Phenotype, Genetic Determinant +10

Brown‐Vialetto‐Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment

Annet M. Bosch, N. G. G. M. Abeling, Lodewijk IJlst et al. · Journal of Inherited Metabolic Disease · 2010 · 240 citations · Full text

The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters

Carlo W.T. van Roermund, Wouter F. Visser, Lodewijk IJlst et al. · The FASEB Journal · 2008 · 230 citations

Biochemistry, Lipid Metabolism, Fatty Acids +12