- Translational research in genomics of Alzheimer's disease: A review of current practice and future perspectives
- Phenotypic and molecular characterization of Bruck syndrome (Osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2
- Genetic analysis of indicators of cholesterol synthesis and absorption: Lathosterol and phytosterols in Dutch twins and their parents
- An amino acid polymorphism in histidine-rich glycoprotein (HRG) explains 59% of the variance in plasma HRG levels
- Identification and genetic analysis of a common molecular variant of histidine-rich glycoprotein with a difference of 2KD in apparent molecular weight
- Triglyceride-rich lipoproteins of subjects heterozygous for apolipoprotein E2(Lys146 → Gln) are inefficiently converted to cholesterol-rich lipoproteins