Barely Significant
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De novo genic mutations among a Chinese autism spectrum disorder cohort.

Nat Commun · 2016 · PMC5105161 · PMID 27824329

2
hedged sentences
0.0000
closest p · 0.0× alpha
0.0026
boldest claim

The sentences

highly significantP =1.17 × 10 −5actually significant
We repeated this analysis removing the 19 known ASD/ID genes ( Supplementary Data 1 ) and observed a reduced but still highly significant signal ( P =1.17 × 10 −5 ) corresponding to an odds ratio of 4.1 (95% CI=2.2–7.0).

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nominally significantP =2.6 × 10 −3actually significant
This difference was nominally significant ( P =2.6 × 10 −3 , two-tailed Fisher's exact test, OR=6.7, 95% CI=1.7–31.1) but did not withstand multiple testing correction for all 189 candidate genes.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.