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A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability
Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin
Postictal Psychosis in Epilepsy: A Clinicogenetic Study.
Somatic variants as a cause of drug-resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis
Novel risk loci in LGI1-antibody encephalitis: genome-wide association study discovery and validation cohorts.
Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients
De-novo mutations in patients with chronic ultra-refractory epilepsy withonset after age five years
Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications
Polygenic risk score analysis reveals shared genetic burden between epilepsy and psychiatric comorbidities
Development of a genomics module within an epilepsy-specific electronic health record: Toward genomic medicine in epilepsy care.
Similarity of Phenotype in Three Male Patients With the c.320A>G Variant in ALG13: Possible Genotype-Phenotype Correlation
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