Kirsten Geider

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

Sabine Endele, Georg Rosenberger, Kirsten Geider et al. · Nature Genetics · 2010 · 509 citations

Life Sciences, Genetics, Neuroscience +16

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Johannes R. Lemke, Dennis Lal, Eva M. Reinthaler et al. · Nature Genetics · 2013 · 440 citations

Medicine, Neurology, Neuroscience +14

<i>GRIN2B</i> mutations in west syndrome and intellectual disability with focal epilepsy

Johannes R. Lemke, Rik Hendrickx, Kirsten Geider et al. · Annals of Neurology · 2013 · 211 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Delineating the <i>GRIN1</i> phenotypic spectrum

Johannes R. Lemke, Kirsten Geider, Katherine L. Helbig et al. · Neurology · 2016 · 207 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The N-terminal domain of the GluN3A subunit determines the efficacy of glycine-activated NMDA receptors

Ivana Mesic, Christian Madry, Kirsten Geider et al. · Neuropharmacology · 2016 · 16 citations

Life Sciences, Neurobiology, Neuroscience +15