Heidi Erlandsen

A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome

Frank Rutsch, Mary MacDougall, Changming Lu et al. · The American Journal of Human Genetics · 2015 · 222 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +3

Three-Dimensional Structure of Human Tryptophan Hydroxylase and Its Implications for the Biosynthesis of the Neurotransmitters Serotonin and Melatonin^,

Lin Wang, Heidi Erlandsen, Jan Haavik et al. · Biochemistry · 2002 · 178 citations

Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations

Heidi Erlandsen, Ángel L. Pey, Alejandra Gámez et al. · Proceedings of the National Academy of Sciences · 2004 · 169 citations · Full text

Protein Chemistry, Aldehyde Dehydrogenase, Aldo-keto Reductase +10

Structure of Tetrameric Human Phenylalanine Hydroxylase and Its Implications for Phenylketonuria

Fabrizia Fusetti, Heidi Erlandsen, Torgeir Flatmark et al. · Journal of Biological Chemistry · 1998 · 148 citations · Full text

Mechanisms underlying responsiveness to tetrahydrobiopterin in mild phenylketonuria mutations

Ángel L. Pey, Belén Pérez, Lourdes R. Desviat et al. · Human Mutation · 2004 · 122 citations