Corroborating written history with ancient DNA: The case of the Well-man described in an Old Norse saga
Characterization of Y chromosome diversity in newfoundland and labrador: evidence for a structured founding population.
Novel risk loci in LGI1-antibody encephalitis: genome-wide association study discovery and validation cohorts.
WONOEP appraisal: Genetic insights into early onset epilepsies
Similarity of Phenotype in Three Male Patients With the c.320A>G Variant in ALG13: Possible Genotype-Phenotype Correlation
Do germline genetic variants influence surgical outcomes in drug-resistant epilepsy?
WONOEP 2022: Neurotechnology for the diagnosis of epilepsy
Somatic variants as a cause of drug-resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis
Reply: De novo mutations in CLDN5: alternating hemiplegia of childhood or not?
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
Polygenic risk score analysis reveals shared genetic burden between epilepsy and psychiatric comorbidities
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