Browsing Universitätsbibliographie by Author "Becker, Felicitas"

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A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsy

Becker, Felicitas; Lerche, Holger; Weber, Yvonne G. (2014)
Analysis of shared heritability in common disorders of the brain

Lerche, Holger; Becker, Felicitas; Gasser, Thomas; Heutink, Peter; Sharma, Manu; Freilinger, Tobias Maximilian (2018)
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation

Becker, Felicitas; Schubert, Julian; Biskup, Saskia; Lerche, Holger; Weber, Yvonne G. (2016)
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

Becker, Felicitas; Lerche, Holger (2020)
Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis

Becker, Felicitas; Wolking, Stefan; Lerche, Holger (2017)
DEPDC5 Mutations in Genetic Focal Epilepsies of Childhood

Schubert, Julian; Becker, Felicitas; Lerche, Holger; Weber, Yvonne G. (2014)
Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?

Becker, Felicitas; Schubert, Julian; Lerche, Holger; Weber, Yvonne G.; Grüninger, Steffen (2015)
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

Becker, Felicitas; Weber, Yvonne G.; Lerche, Holger (2013)
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes

Becker, Felicitas; Weber, Yvonne G.; Lerche, Holger (2016)
Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy

Becker, Felicitas; Lerche, Holger; Weber, Yvonne G. (2015)
Focal epilepsy in Glucose transporter type 1 (Glut1) defects: case reports and a review of literature

Wolking, Stefan; Becker, Felicitas; Lerche, Holger; Weber, Yvonne G. (2014)
Galanin pathogenic mutations in temporal lobe epilepsy

Weber, Yvonne G.; Becker, Felicitas (2015)
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger (2012)
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger (2012)
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

Becker, Felicitas; Hengsbach, Christian; Lerche, Holger; Rau, Sarah; Weber, Yvonne G.; Wolff, Markus; Wolking, Stefan (2018)
In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising during Neurodevelopment

Rosa, Filip; Dhingra, Ashutosh; Elsen, Gina; Schwarz, Niklas; Castillo-Lizardo, Melissa; Becker, Felicitas; Heutink, Peter; Lerche, Holger; Maljevic, Snezana; Uysal, Betül; Löffler, Heidi; Müller, Stephan Tobias (2020)
Investigation of GRIN2A in common epilepsy phenotypes

Schubert, Julian; Becker, Felicitas; Weber, Yvonne G.; Lerche, Holger (2015)
Mutation in the mitochondrial tRNA(Ile) gene causes progressive myoclonus epilepsy

Becker, Felicitas; Lerche, Holger; Weber, Yvonne G. (2013)
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Alber, Michael Wolfgang Hans-Peter; Ruf, Susanne; Wolff, Markus; Becker, Felicitas; Weber, Yvonne G.; Lerche, Holger; Biskup, Saskia (2013)
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes

Schubert, Julian; Becker, Felicitas; Riesch, Erik; Biskup, Saskia; Weber, Yvonne G.; Lerche, Holger (2014)

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