Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Biochemistry, Genetics and Molecular Biology

• Exome Sequencing 100%
• Genetic Risk 100%
• Exome 66%
• Rare Variant 66%
• Candidate Gene 33%
• Genetic Architecture 33%
• Indel 33%
• Gene Discovery 33%
• Excitability 33%
• Ion Channel 33%

Neuroscience

• Exome Sequencing 100%
• Epilepsy Subtypes 100%
• Ion Channel 50%
• Neuronal Excitability 50%
• Focal Epilepsy 50%
• Indel Mutation 50%
• Risk Factor 50%