Thomas J. Corydon

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

Rare versus common variants in pharmacogenetics: <i>SLCO1B1</i> variation and methotrexate disposition

Laura B. Ramsey, Gitte Hoffmann Bruun, Wenjian Yang et al. · Genome Research · 2011 · 258 citations · Full text

Seemingly Neutral Polymorphic Variants May Confer Immunity to Splicing-Inactivating Mutations: A Synonymous SNP in Exon 5 of MCAD Protects from Deleterious Mutations in a Flanking Exonic Splicing Enhancer

Karsten Nielsen, Suzette Sørensen, Luca Cartegni et al. · The American Journal of Human Genetics · 2007 · 148 citations · Full text

Synonymous Snp, Allelic Variant, Genetics +8

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

Alterations of the cytoskeleton in human cells in space proved by life-cell imaging

Thomas J. Corydon, Sascha Kopp, Markus Wehland et al. · Scientific Reports · 2016 · 125 citations · Full text

Dlr Pfc, Engineering, Cytoskeleton +20