E. Jill Dahle

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

Ruthie E. Amir, Ignatia B. Van den Veyver, Rebecca Schultz et al. · Annals of Neurology · 2000 · 345 citations

Mendelian Disorder, Genetic Disorder, Genetics +15

A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome

Nanda A. Singh, Chris Pappas, E. Jill Dahle et al. · PLoS Genetics · 2009 · 263 citations · Full text

Neurogenomics, Genetics, Molecular Genetics +23

Mouse models of human <i>KCNQ2</i> and <i>KCNQ3</i> mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization

Nanda A. Singh, James F. Otto, E. Jill Dahle et al. · The Journal of Physiology · 2008 · 143 citations · Full text

A New Rett Syndrome Family Consistent with X-Linked Inheritance Expands the X Chromosome Exclusion Map

N. Carolyn Schanen, E. Jill Dahle, Fiorentino Capozzoli et al. · The American Journal of Human Genetics · 1997 · 115 citations · Full text

Hippocampal TNFα Signaling Contributes to Seizure Generation in an Infection-Induced Mouse Model of Limbic Epilepsy

Dipan C. Patel, Glenna J. Wallis, E. Jill Dahle et al. · eNeuro · 2017 · 110 citations · Full text