Leo A. J. Kluijtmans
Radboud University Nijmegen(NL)Radboud University Medical Center(NL)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Folate and B Vitamins Research, Metabolomics and Mass Spectrometry Studies, Esophageal and GI Pathology, Mitochondrial Function and Pathology
Most-Cited Works
- → A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase(1995)5,697 cited
- Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.(1996)
- → FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study(2011)419 cited
- → Exome Sequencing and the Management of Neurometabolic Disorders(2016)279 cited
- → Cystathionine ?-synthase mutations in homocystinuria(1999)279 cited
- → The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations(2001)274 cited