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Pharmacogenetics and Genomics|May 6, 2009
Non-response to antiepileptic pharmacotherapy is associated with the ABCC2 -24C>T polymorphism in young and adult patients with epilepsyMike Ufer, Igor Mosyagin, Hiltrud Muhle, et al.Epilepsia|February 19, 2015
Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysisCorinna Hartmann, Sarah von Spiczak, Arvid Suls, et al.Pediatric Neurology|February 7, 2006
Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancyJennifer A Kearney, Anna K Wiste, Ulrich Stephani, et al.Plos One|September 17, 2013
RBFOX1 and RBFOX3 mutations in rolandic epilepsyDennis Lal, Eva M Reinthaler, Janine Altmüller, et al.Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2012
Exome sequencing in a family with restless legs syndromeAnne Weissbach, Katharina Siegesmund, Norbert Brüggemann, et al.Annals of Neurology|June 2, 2005
Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsyUlrike Tauer, Susanne Lorenz, Kirsten P Lenzen, et al.Epilepsy Research|March 27, 2010
Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysisHiltrud Muhle, Sarah von Spiczak, Verena Gaus, et al.Epilepsy Research|January 12, 2013
The role of SLC2A1 in early onset and childhood absence epilepsiesHiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, et al.Journal of Child Neurology|October 12, 2013
Atypical vitamin B6 deficiency: a rare cause of unexplained neonatal and infantile epilepsiesAnna Baumgart, Sarah von Spiczak, Nanda M Verhoeven-Duif, et al.Plos Genetics|May 27, 2010
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsiesHeather C Mefford, Hiltrud Muhle, Philipp Ostertag, et al.Pageof 11