Maja Steinlin

Targeted next generation sequencing as a diagnostic tool in epileptic disorders

Johannes R. Lemke, Erik Riesch, Tim Scheurenbrand et al. · Epilepsia · 2012 · 324 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

Steffen Syrbe, Ulrike B. S. Hedrich, Erik Riesch et al. · Nature Genetics · 2015 · 275 citations · Full text

Medicine, Genetics, Molecular Genetics +14

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

Birgit Budde, Yasmin Namavar, P. G. Barth et al. · Nature Genetics · 2008 · 256 citations

Life Sciences, Genetics, Molecular Genetics +2

The First Three Years of the Swiss Neuropaediatric Stroke Registry (SNPSR): A Population-Based Study of Incidence, Symptoms and Risk Factors

Maja Steinlin, I. Pfister, J. Pavlovic et al. · Neuropediatrics · 2005 · 196 citations

Medicine, Neurology, Pediatrics +17

Strengthening of laterality of verbal and visuospatial functions during childhood and adolescence

Regula Everts, Karen Lidzba, Marko Wilke et al. · Human Brain Mapping · 2008 · 192 citations · Full text

Life Sciences, Human Development, Neuroscience +16