Rudy N. Van Coster

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 589 citations · Full text

High-dose statins and skeletal muscle metabolism in humans: A randomized, controlled trial

Hannu Päivä, Karin Thelen, Rudy N. Van Coster et al. · Clinical Pharmacology & Therapeutics · 2005 · 307 citations

A Novel Disorder Caused by Defective Biosynthesis of N-Linked Oligosaccharides Due to Glucosidase I Deficiency

Claudine M. De Praeter, Gerrit J. Gerwig, Ernst Bause et al. · The American Journal of Human Genetics · 2000 · 190 citations · Full text

Biosynthesis, Engineering, Cellular Enzymology +12

Aminoacylase I deficiency: A novel inborn error of metabolism

Rudy N. Van Coster, E. Gerlo, Thierry Giardina et al. · Biochemical and Biophysical Research Communications · 2005 · 59 citations

Metabolic Disorder, Biochemistry, Genetic Disorder +5

Dominant Inheritance of Sialuria, an Inborn Error of Feedback Inhibition

Jules G. Leroy, Raili Seppälä, Marjan Huizing et al. · The American Journal of Human Genetics · 2001 · 57 citations · Full text

Urology, Dominant Inheritance, Genetic Disorder +5