Barely Significant
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CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment.

Mol Autism · 2015 · PMC4612430 · PMID 26491539

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hedged sentence
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closest p · 0.5× alpha
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boldest claim

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highly significantp = 0.023actually significant
6a ), the overlap of DEGs from ZNF804A knockdown and NRXN1 knockdown was highly significant (OR = 2.63, p = 0.023, Fisher’s exact test, one-tailed).

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