Barely Significant
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Analysis of 470,000 exome-sequenced cases and controls fails to identify any genes impacting risk of developing affective disorder.

Acta Neuropsychiatr · 2025 · PMC13130275 · PMID 40583353

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highly significantno p-value reported
Then the genes producing the most highly significant results overall would be carried forward to be analysed in the second sample, using for each gene only the predictor which had yielded the most significant result.

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