Rikke Katrine Jentoft Olsen

ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

Rikke Katrine Jentoft Olsen, S. E. Olpin, Brage Storstein Andresen et al. · Brain · 2007 · 326 citations

Metabolic Disorder, Genetics, Molecular Biology +25

Clear relationship betweenETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency

Rikke Katrine Jentoft Olsen, Brage Storstein Andresen, Ernst Christensen et al. · Human Mutation · 2003 · 233 citations

Residual Enzyme Activity, Developmental Biology, Autoimmune Disease +13

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency

Rikke Katrine Jentoft Olsen, Eliška Koňaříková, Teresa Anna Giancaspero et al. · The American Journal of Human Genetics · 2016 · 146 citations · Full text

Mitochondrial fatty acid oxidation defects—remaining challenges

Niels Gregersen, Brage Storstein Andresen, Christina B. Pedersen et al. · Journal of Inherited Metabolic Disease · 2008 · 139 citations

Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B

Gladys Ho, Atsushi Yonezawa, Satohiro Masuda et al. · Human Mutation · 2010 · 120 citations

Riboflavin Transport, Riboflavin Transporter, Developmental Biology +13