Barely Significant
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Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.

Hum Mutat · 2019 · PMC6593842 · PMID 30763456

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marginal significanceno p-value reported
As a result, of eight comorbidities, only “epilepsy/tics” showed marginal significance (Table S11).

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By comparing the variant spectra between cases with and without specific features using Fisher's exact test with a 2 × m contingency table, where “ m ” indicates the number of genes, we selected the feature shown to be marginally statistically significant to investigate the correlation with the gene by Fisher's exact test with a 2 × 2 contingency table.

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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.