Birgit Neophytou

CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia

Francisco J. Arjona, Jeroen H. F. de Baaij, Karl P. Schlingmann et al. · PLoS Genetics · 2014 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

<i>DEPDC5</i> mutations in genetic focal epilepsies of childhood

Dennis Lal, Eva M. Reinthaler, Julian Schubert et al. · Annals of Neurology · 2014 · 115 citations

Medicine, Genetics, Neurology +17

Central nervous system‐related permanent consequences in patients with Langerhans cell histiocytosis

Edda Mittheisz, Rainer Seidl, Daniela Prayer et al. · Pediatric Blood & Cancer · 2006 · 72 citations

Medicine, Neurology, Neuroscience +17

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

Eva M. Reinthaler, Dennis Lal, Sébastien Lebon et al. · Human Molecular Genetics · 2014 · 70 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Rare variants in γ‐aminobutyric acid type <scp>A</scp> receptor genes in rolandic epilepsy and related syndromes

Eva M. Reinthaler, Borislav Dejanovic, Dennis Lal et al. · Annals of Neurology · 2015 · 64 citations

Life Sciences, Genetics, Neuroscience +17