Flemming Güttler
Kennedy Center(DK)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Mitochondrial Function and Pathology, Folate and B Vitamins Research, Pulmonary Hypertension Research and Treatments, Neonatal Health and Biochemistry
Most-Cited Works
- → A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype(1998)353 cited
- → Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria(1983)336 cited
- → Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria(1986)247 cited
- → Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria(1991)237 cited
- → What do doctors know about statistics?(1987)162 cited
- → The Maternal Phenylketonuria International Study: 1984–2002(2003)152 cited
- → Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenyl-alaninemia in Southern Europe