Barely Significant
← all excerpts

Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders.

Sci Rep · 2024 · PMC11018828 · PMID 38622173

1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

nominally significantp < 0.05actually significant
Results from PrediXcan 30 (in blood) supported our hypothesis that parents would have higher predicted gene expression than their children when testing dominant and recessive DD genes containing putatively damaging PTVs, but this result was only nominally significant and did not pass multiple testing correction ( p < 0.05) (Supplementary Fig. 9 ).

also in 4,806 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.