Barely Significant
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Proteome-Wide Mendelian Randomisation Study of Adverse Perinatal Outcomes.

Behav Genet · 2025 · PMC12494647 · PMID 40991151

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

The sentences

nominally significantp < 0.05actually significant
Causal estimates produced by the different methods had consistent direction of effect compared to the IVW estimate and all save MR-Egger were nominally significant (i.e. p < 0.05).

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