Genome-wide rare copy number variations potentially associated with drug resistance in epilepsy.

Sci Rep · 2026 · PMC13096472 · PMID 41807523

Europe PMC DOI

hedged sentence

—

closest p

—

boldest claim

The sentences

highly significantno p-value reported

Furthermore, although recent studies have indicated a highly significant role of non-coding genomic variants in epilepsy 36 , the interpretation and implications of these non-coding variants remain highly heterogeneous.

also in 132,142 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.