Barely Significant
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The oxytocin receptor gene polymorphism rs2268491 and serum oxytocin alterations are indicative of autism spectrum disorder: A case-control paediatric study in Iraq with personalized medicine implications.

PLoS One · 2022 · PMC8939799 · PMID 35316293

2
hedged sentences
closest p
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The sentences

a marked trendno p-value reported
A marked trend for higher OXT was observed in the three genotypes of CC, CT, and TT in ASD patients relative to control.

also in 422 other papers

highly significantno p-value reported
A p-value of <0.001 was considered highly significant.

also in 132,142 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.