Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia

Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy

(2015) Emanuela Dazzo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in mammalian target of rapamycin regulatorDEPDC5cause focal epilepsy with brain malformations

(2014) Ingrid E. Scheffer et al.   ANNALS OF NEUROLOGY

Vestibular responses to direct stimulation of the human insular cortex

(2014) Laure Mazzola et al.   ANNALS OF NEUROLOGY

Seizure semiology in autosomal dominant epilepsy with auditory features, due to novel LGI1 mutations

(2013) Lynette G. Sadleir et al.   EPILEPSY RESEARCH

Familial KANK1 deletion that does not follow expected imprinting pattern

(2013) Rena J. Vanzo et al.   European Journal of Medical Genetics

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

(2013) Leanne M Dibbens et al.   NATURE GENETICS

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features

(2008) M. J. Rosanoff et al.   NEUROLOGY