Barely Significant
← all excerpts

The genetic spectrum of LRRK2 variants in Parkinson's disease: findings from a large Chinese cohort.

NPJ Parkinsons Dis · 2026 · PMC13194747 · PMID 41904258

Europe PMCDOI
1
hedged sentence
0.0580
closest p · 1.2× alpha
0.0580
boldest claim

The sentences

borderline significantP = 0.058so close (0.05 < p ≤ 0.1)
The burden of low-frequency non-synonymous variants remained borderline significant ( P = 0.058), pointing to the contribution of additional, novel pathogenic variants in LRRK2 (Supplementary Table 2 ).

also in 11,409 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.