Barely Significant
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Genetic Variants Associated With Subjective Cognitive Decline in Patients With Migraine.

Front Aging Neurosci · 2022 · PMC9248861 · PMID 35783123

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However, all replicating variants, including the rs7412 in the APOE gene, did not reach statistical significance in the migraine group ( Table 4 ).

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a clear trendno p-value reported
In addition, two other SNPs were identified in non-migraineurs with SCD (rs2352564 on chromosome 7, rs6089473 in CDH4), and there was a clear trend associated with the underlying pathogenesis of SCD based on migraineur status, as explored below.

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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.