Ortrud K. Steinlein

A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

Ortrud K. Steinlein, John C. Mulley, Peter Propping et al. · Nature Genetics · 1995 · 1.1K citations

Synaptic Plasticity, Molecular Neuroscience, Neurobiology Of Disease +12

A Potassium Channel Mutation in Neonatal Human Epilepsy

Christian Biervert, Björn C. Schroeder, Christian Kubisch et al. · Science · 1998 · 1.1K citations

An Insertion Mutation of the CHRNA4 Gene in a Family With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

Ortrud K. Steinlein, Andrés Magnússon, Jens Stoodt et al. · Human Molecular Genetics · 1997 · 360 citations

Benign familial neonatal‐infantile seizures: Characterization of a new sodium channelopathy

Samuel F. Berkovic, Sarah E. Heron, Lucio Giordano et al. · Annals of Neurology · 2004 · 276 citations

A Splice-Site Mutation in GABRG2 Associated With Childhood Absence Epilepsy and Febrile Convulsions

Colette Kananura, Karsten Haug, Thomas Sander et al. · Archives of Neurology · 2002 · 276 citations