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A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability
Genetic ancestry and monogenic disease risk in the Scottish Traveller founder population.
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.
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