Barely Significant
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“nominally significant”

7,733 sentences · 7,733 papers · 10,034 search hits before verification · confirmed specimen

Sighted at

p=0.08

Listed by Hankins (2013) · Otte et al. (2022)

In the literature

Despite not meeting secondary endpoints (risk of acute exacerbation, hospitalization for respiratory cause, or death), a pooled analysis of the FIBRONEER trials showed that Nerandomilast 18 mg was associated with a nominally significant reduction in the risk of death by 43% overall, by 59% in patients without background therapy, and by 41% in patients with background Nintedanib [ 41 ].
In addition, to the extent that we can rely on ICEA results that were nominally significant, although not at standard levels after false discovery rate adjustment, to indicate possible interesting signals to investigate in future work, the standard subsequent memory effect was not particularly correlated with ICEA results.
Identifying causal subsequent memory effects.
Proc Natl Acad Sci U S A · 2023 · PMC10068819
Finally, to this reduced model, they separately added a household variance component for siblings representing “early life shared environment” and one for parents representing “later life shared environment,” and then screened for nominally significant cis -acting and trans -acting single-nucleotide polymorphisms (SNPs).
A nominally significant interaction of p‐tau217 levels and CEE/MPA versus placebo was observed, although dementia HRs for p‐tau217 in both the CEE/MPA and placebo groups were elevated. 25 The different BBMs associated with risk of MCI/probable dementia for CEE versus CEE/MPA suggest that there are different pathways and mechanisms that lead to dementia and dementia type for women who use estrogen alone versus estrogen plus progestin.
performed a case-control study in a group of 121 American case families (mother, father, and proband with DS and AVSD) and 122 American control families (mother, father, and proband with DS and no CHD), all genotyped for 45 polymorphisms in MTHFR, MTR, MTRR, RFC1 , and CBS genes, observing that several RFC1 polymorphisms, all in strong linkage with the RFC1 80G>A one, showed nominally significant associations with AVSD, with ORs of between 1.34 and 3.78.