Jean Rey

A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype

Per Guldberg, Françoise Rey, Johannes Zschocke et al. · The American Journal of Human Genetics · 1998 · 352 citations · Full text

Metabolic Syndrome, Mendelian Disorder, Biochemistry +11

Neuropsychologic Functions of Early Treated Patients with Phenylketonuria, on and off Diet: Results of a Cross-National and Cross-Sectional Study

Peter Burgard, Françoise Rey, André Rupp et al. · Pediatric Research · 1997 · 92 citations · Full text

Nutrition, Neuropsychology, Psychiatry +8

CpG dinucleotides are mutation hot spots in phenylketonuria

Véronique Abadie, Stanislas Lyonnet, Nicole Maurin et al. · Genomics · 1989 · 86 citations

Genetic Disorder, Natural Sciences, Genetics +6

Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.

Stanislas Lyonnet, Catherine Caillaud, F. Rey et al. · PubMed · 1989 · 71 citations

Histochemical Localization of Intestinal Disaccharidases: Application to Peroral Biopsy Specimens

Jos J, J Frézal, Jean Rey et al. · Nature · 1967 · 42 citations

Histopathology, Gastroenterology, Pathology +6