Barely Significant
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Chromosome 11q13.5 variant as a risk factor for atopic dermatitis in children.

Postepy Dermatol Alergol · 2020 · PMC7247065 · PMID 32467693

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highly significantno p-value reported
Our former study and data presented here also provided highly significant replication of the previously-reported association of the 4 nonsense FLG mutations with atopic dermatitis [ 21 , 22 ].

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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.