Published in Epilepsy Res on October 03, 2005
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A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions. Arch Neurol (2002) 1.77
Association of a functional BDNF polymorphism and anxiety-related personality traits. Psychopharmacology (Berl) (2005) 1.77
Expression pattern and functional characteristics of two novel splice variants of the two-pore-domain potassium channel TREK-2. J Physiol (2002) 1.56
A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy. Ann Neurol (2006) 1.55
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Gender-dependent association of the functional catechol-O-methyltransferase Val158Met genotype with sensation seeking personality trait. Neuropsychopharmacology (2007) 1.05
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Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. Epilepsia (2012) 0.94
The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits. Neurobiol Dis (2005) 0.94
Metabolic consequences of a novel missense mutation of the mtDNA CO I gene. Hum Mol Genet (2002) 0.94
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests. Hum Hered (2010) 0.93
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Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta. BMC Med Genet (2011) 0.92
Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. Ann Neurol (2005) 0.91
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Met carriers of BDNF Val66Met genotype show increased N-acetylaspartate concentration in the anterior cingulate cortex. Neuroimage (2009) 0.88
Speech-induced aphasic seizures in epilepsy caused by LGI1 mutation. Epilepsia (2005) 0.88
Association of HTR2C, but not LEP or INSIG2, genes with antipsychotic-induced weight gain in a German sample. Pharmacogenomics (2010) 0.88
Toxicity-indicating structural patterns. J Chem Inf Model (2006) 0.87
Using gene-history and expression analyses to assess the involvement of LGI genes in human disorders. Mol Biol Evol (2005) 0.87
Neonatal seizures with tonic clonic sequences and poor developmental outcome. Epilepsy Res (2005) 0.87
A Korean kindred with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation. Arch Neurol (2003) 0.87
Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy. Neurobiol Dis (2007) 0.86
Linkage and mutational analysis of CLCN2 in childhood absence epilepsy. Epilepsy Res (2007) 0.86
Evaluation of CACNA1H in European patients with childhood absence epilepsy. Epilepsy Res (2006) 0.86
Allelic variants of the functional promoter polymorphism of the human serotonin transporter gene is associated with auditory cortical stimulus processing. Neuropsychopharmacology (2002) 0.86
A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsy. Epilepsia (2003) 0.86
Linkage and association analysis of CACNG3 in childhood absence epilepsy. Eur J Hum Genet (2007) 0.86
A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy. Epilepsia (2010) 0.85
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Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy. Epilepsy Res (2006) 0.83
Association analysis of exonic variants of the GABA(B)-receptor gene and alpha electroencephalogram voltage in normal subjects and alcohol-dependent patients. Behav Genet (2003) 0.83
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q. Epilepsy Res (2002) 0.83
Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy. Epilepsia (2014) 0.82
Association analysis between the human interleukin 1beta (-511) gene polymorphism and susceptibility to febrile convulsions. Neurosci Lett (2002) 0.82
COMT Val108/158Met genotype modulates human sensory gating. Neuroimage (2010) 0.82
Flexophore, a new versatile 3D pharmacophore descriptor that considers molecular flexibility. J Chem Inf Model (2008) 0.82
Failure to replicate an allelic association between an exon 8 polymorphism of the human alpha(1A) calcium channel gene and common syndromes of idiopathic generalized epilepsy. Epilepsy Res (2002) 0.82
Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia. Neurosci Lett (2006) 0.81
Association of EEG coherence and an exonic GABA(B)R1 gene polymorphism. Am J Med Genet B Neuropsychiatr Genet (2003) 0.81
Genetic variations of the NR3A subunit of the NMDA receptor modulate prefrontal cerebral activity in humans. J Cogn Neurosci (2007) 0.81
Polymorphisms in the NMDA subunit 2B are not associated with alcohol dependence and alcohol withdrawal-induced seizures and delirium tremens. Eur Arch Psychiatry Clin Neurosci (2004) 0.81
Role of GRM4 in idiopathic generalized epilepsies analysed by genetic association and sequence analysis. Epilepsy Res (2010) 0.81