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 -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 = 0.0380.8× 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 = 0.0390.8× alphagold
Subgroup analysis showed that patients with cN2‐3 had a significant survival benefit with NAC‐DCF (HR 0.51; 95% CI, 0.34–0.76) in the IPW analysis, whereas no clear association was observed in those with cN0–1 (HR 0.93; 95% CI, 0.62–1.34), with a nominally significant interaction by clinical N stage ( p = 0.039).
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.
nominally significantp = 0.0390.8× alphagold
Linear regression analysis using age, sex and intracranial volume as a priori predictors revealed that MAPT diplotype was a predictor of left insula and right cerebellar Crus II lobar volumes at a nominally significant level ( p = 0.039 and p = 0.033, respectively), with the H1 haplotype predicting lower grey matter volumes.
nominally significantp = 0.03990.8× alphagold
Progression-free survival (PFS) was also significant ( p = 6.730 × 10 −3 ; q = 0.0143), disease-specific survival (DSS) was nominally significant but borderline after FDR correction ( p = 0.0399; q = 0.0532), and disease-free survival (DFS) was not significant ( p = 0.0903; q = 0.0903) ( Figure 4 , Table S3 ).