Barely Significant
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Common and rare variant analyses implicate late-infancy cerebellar development and immune genes in ADHD.

J Neurodev Disord · 2025 · PMC12180188 · PMID 40542392

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closest p · 1.0× alpha
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nominally significantp < 0.05actually significant
For PGS showing nominally significant prediction (empirical p < 0.05 after 10000-replicate permutation test), we further conducted a pathway-based PGS analysis for each of the 7,763 GO BP terms from MsigDB [ 27 , 28 ] by PRset with a permutation procedure to take pathway size into account [ 39 ].

also in 7,732 other papers

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