Frequency / statistic
learning, speech and behaviour
1 supporting source
confidence 97%
novelty 60%
We performed the association analyses separately for each epilepsy subtype - including 1,938 individuals with a diagnosi
A source reports “938 individuals” in the context of neurodevelopment: “We performed the association analyses separately for each epilepsy subtype - including 1,938 individuals with a diagnosis of a DEE, 5,499 with GGE, and 9,219 with NAFE - as well as for all epilepsy-affected individuals combined (including an additional 4,323 w”
How this was derived
Numbers are quoted verbatim from the source; check the source before quoting onward.
Generated 2026-11-13, last changed
yesterday. Dedup key freq:938 individuals.
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Evidence (1 quote)
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
peer_reviewed
· published 2024-01-01
· live page
We performed the association analyses separately for each epilepsy subtype - including 1,938 individuals with a diagnosis of a DEE, 5,499 with GGE, and 9,219 with NAFE - as well as for all epilepsy-affected individuals combined (including an additional 4,323 with other epilepsy syndromes).
Supporting documents (1)
| Document | Source | Published | Seen | Relevance |
|---|---|---|---|---|
| Exome sequencing of 20,979 individuals with epilepsy reveals shared... | pmc | 2024-01-01 | yesterday | 1.00 |