Laura E. Warner
Sarepta Therapeutics (United States)(US)
Publications by Year
Research Areas
Hereditary Neurological Disorders, RNA Research and Splicing, Genetic Neurodegenerative Diseases, RNA regulation and disease, Cellular Mechanics and Interactions
Most-Cited Works
- → Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies(1998)491 cited
- → Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination(1996)362 cited
- → Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype(1999)153 cited
- → Functional consequences of mutations in the early growth response 2 gene (EGR2) correlate with severity of human myelinopathies(1999)138 cited
- → Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease(2000)95 cited
- → Hereditary Peripheral Neuropathies: Clinical Forms, Genetics, and Molecular Mechanisms(1999)79 cited
- → Expression of Dp260 in muscle tethers the actin cytoskeleton to the dystrophin-glycoprotein complex and partially prevents dystrophy(2002)76 cited
- → Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease(1996)66 cited
- → Congenital hypomyelinating neuropathy: two patients with long-term follow-up(1999)52 cited
- → Molecular Mechanisms for CMT1A Duplication and HNPP Deletion(1999)41 cited