Christine Kretz
Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut de génétique et de biologie moléculaire et cellulaire(FR)
Publications by Year
Research Areas
Cellular transport and secretion, Muscle Physiology and Disorders, Ubiquitin and proteasome pathways, Microtubule and mitosis dynamics, Genetic Neurodegenerative Diseases
Most-Cited Works
- → Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome(1991)1,491 cited
- → Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation(1991)641 cited
- → A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast(1996)624 cited
- → Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy(2007)431 cited
- → The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein(1994)300 cited
- → Origin of the expansion mutation in myotonic dystrophy(1993)212 cited