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UnknownSub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
Not available
S-EPMC8206159 | biostudies-literature
UnknownGenome-wide association meta-analyses of drug-resistant epilepsy.
Not available
S-EPMC12143209 | biostudies-literature
UnknownExome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC9980234 | biostudies-literature
UnknownExome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Not available
S-EPMC11646479 | biostudies-literature
UnknownUltra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals.
Not available
S-EPMC6698801 | biostudies-literature
UnknownEpilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
Not available
S-EPMC7364765 | biostudies-literature
UnknownPolygenic burden in focal and generalized epilepsies.
Not available
S-EPMC6821205 | biostudies-literature
UnknownGenome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
Not available
S-EPMC10359300 | biostudies-literature
UnknownGWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture.
Not available
S-EPMC10484785 | biostudies-literature
UnknownDistinct gene-set burden patterns underlie common generalized and focal epilepsies.
Not available
S-EPMC8479647 | biostudies-literature
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