Andrew A.M. Morris

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 · 328 citations

Life Sciences, Biochemistry, Molecular Genetics +15

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 · 302 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

<i>IDH2</i> Mutations in Patients with <scp>d</scp> -2-Hydroxyglutaric Aciduria

Martijn Kranendijk, Eduard A. Struys, Emile Van Schaftingen et al. · Science · 2010 · 194 citations

Life Sciences, Molecular Biology, Molecular Genetics +13

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation

Robert McFarland, Kim M. Clark, Andrew A.M. Morris et al. · Nature Genetics · 2002 · 172 citations

Medicine, Genetics, Molecular Genetics +12

<i>LRPPRC</i>mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population

Monika Oláhová, Steven Hardy, Julie Hall et al. · Brain · 2015 · 107 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17