Eva M. Reinthaler

A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease

Alexander Zimprich, Anna Benet‐Pagès, Walter Struhal et al. · The American Journal of Human Genetics · 2011 · 876 citations · Full text

Late-onset Parkinson Disease, Retromer Complex, Neurodegenerative Diseases +8

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek et al. · Nature Communications · 2018 · 493 citations · Full text

Epilepsy Therapies, Genetics, Genetic Epidemiology +22

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Johannes R. Lemke, Dennis Lal, Eva M. Reinthaler et al. · Nature Genetics · 2013 · 436 citations

Neurobiology Of Disease, Neurophysiology, Genetics +10

RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy

Dennis Lal, Eva M. Reinthaler, Janine Altmüller et al. · PLoS ONE · 2013 · 117 citations · Full text

Exon Deletions, Neurophysiology, Neurological Disorder +13

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

Dennis Lal, Eva M. Reinthaler, Julian Schubert et al. · Annals of Neurology · 2014 · 113 citations