No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.

PLoS Genet · 2015 · PMC4306541 · PMID 25621974

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hedged sentence

0.0100

closest p · 0.2× alpha

0.0100

boldest claim

The sentences

nominally significantp = 0.01actually significant

CNTN1 was found to show nominally significant association (12 in cases, 2 in controls, Fisher exact one-tailed p = 0.01) but this was not significant after correcting for the 10 genes studied.

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