Laura E. Warner

Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

Laura E. Warner, Pedro Mancías, Ian J. Butler et al. · Nature Genetics · 1998 · 491 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination

Laura E. Warner, Max J. Hilz, Stanley H. Appel et al. · Neuron · 1996 · 362 citations · Full text

Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype

Vincent Timmerman, Peter De Jonghe, C. Ceuterick et al. · Neurology · 1999 · 153 citations

Functional consequences of mutations in the early growth response 2 gene (EGR2) correlate with severity of human myelinopathies

Laura E. Warner · Human Molecular Genetics · 1999 · 138 citations

Human Myelinopathies, Genetics, Peripheral Nerve +16

Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease

Amparo Gutierrez, John D. England, Austin J. Sumner et al. · Muscle & Nerve · 2000 · 95 citations