Barely Significant
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Genetic diagnostic outcomes from a 10-year research programme in autism in Aotearoa New Zealand.

J R Soc N Z · 2025 · PMC12315138 · PMID 40756852

Europe PMCDOI
2
hedged sentences
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantP < 0.0001actually significant
Furthermore, there was a highly significant difference when comparing participants with co-occurring GDD/ID to those without GDD/ID (43.8% and 8.2% respectively, P < 0.0001).

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an established trendno p-value reported
A ‘causal’ or ‘likely causal’ category variant was more likely to be discovered in participants who also presented with GDD/ID than those who did not, following an established trend (Stefanski et al. 2021 ).

also in 56 other papers

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.