Barely Significant
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nominally significant

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p=0.08

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

In the literature

nominally significantp = 0.0370.7× alphagold
A nominally significant association with bleeding risk persisted only for rosuvastatin (OR = 2.189; 95% CI: 1.039–4.612; p = 0.037), but this finding should be interpreted with caution and regarded as exploratory. 3.4.
nominally significantp = .0370.7× alphagold
An initial synthesis of the volume data from the left and right habenula using a paired samples t ‐test also supported this point: no significant interhemispheric differences for either the healthy samples ( t (24) = 1.443, p = .162, Cohen d = 0.289), or the patients with SCZ ( t (4) = −0.550, p = .612, d = −0.246); there appeared to be a nominally significant difference in MDD subgroup ( t (10) = 2.403, p = .037, d = 0.725), but it did not survive correction of multiple testing.
nominally significantp = 0.0380.8× alphagold
Among diabetic patients, a nominally significant difference in unadjusted event rates was observed (12% vs. 35%, p = 0.038), though this exploratory subgroup analysis requires cautious interpretation given the small sample and absence of adjustment for confounders. 4.1.
nominally significantp -value = 0.0380.8× alphagold
Longitudinal stratification of the CIPN phenotypes to examine links for neuropathy, identified nominally significant protective associations with the GSTM* null allele ( p -value = 0.038, OR = 0.55) and the presence of pain at month 2 of treatment, as well as a risk factor for pain related month 2 of treatment for individuals with the GSTT1* null allele ( p -value = 0.030, OR = 1.64).
nominally significantp = 0.0380.8× alphagold
PERMANOVA analyses identified nominally significant effects of Age within the ONT dataset at the phylum (R2 = 0.204, p = 0.038), family (R2 = 0.154, p = 0.020), and genus (R2 = 0.139, p = 0.029) levels, whereas no nominally significant effects were detected in the Illumina dataset (Supplementary Table S2).
nominally significantp = 0.0380.8× alphagold
Additional sensitivity analyses showed that the cML-MA-BIC-DP method (OR 0.60, 95% CI 0.53–0.69, p = 3.85 × 10 −11 ) yielded a similar result to IVW and weighted median methods ( Table 5 ), while the association from MR-APSS method was nominally significant (OR 0.20, 95% CI 0.05–0.92, p = 0.038) ( Table 5 ; Supplementary Figure S2 ).
nominally significantp = 0.0390.8× alphagold
For the hyperactivity/impulsivity subscale, no significant group × time interaction effects were observed at any assessment point except T2, where a nominally significant group × time effect was found ( b = -1.766, t = -2.066, p = 0.039); however, this result did not remain significant after FDR correction.
nominally significantP = 0.0390.8× alphagold
Reverse MR suggested nominally significant associations: higher genetically predicted heel BMD was associated with lower POI risk ( OR = 0.792, 95% CI : 0.635–0.988, P = 0.039), while genetic susceptibility to wrist fracture ( OR = 1.44, 95% CI : 1.038–1.986, P =0.025) and pelvic fracture ( OR =1.177, 95% CI :1.056–1.312, P =0.003) were associated with increased POI risk.