Barely Significant
← all phrases

nominally significant

7,733 sentences · 7,733 papers · 9,414 search hits before verification · confirmed specimen

Sighted at

p=0.08

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

In the literature

nominally significantP = 0.04991.0× alphagold
Finally, we found significant differences in the frequencies of TAGA ( P = 0.005, OR = 3.187, 95% CI 1.376–7.382) containing rs4570625-rs11178997-rs1386494-rs7305115 between ODD and control groups (Tables 7 , 8 ). However, the further analysis by Haploview revealed the nominally significant finding for rs1386494 ( χ 2 = 3.846, P = 0.0499), and only one haplotypes (TAGA, χ 2 = 4.366, P = 0.0367) remained significant.
nominally significantP < 0.051.0× alphagold
Differences between groups were nominally significant (nominal P < 0.05) if the 95% confidence interval [CI] of the group difference did not include the null value (0 for mean differences and 1 for odds ratios), but for the sake of convenience, if the nominal P ‐value in the secondary analysis is less than 0.05, it is described as significant, and if it is 0.05 or more, it is described as non‐significant.
nominally significantP < 0.051.0× alphagold
In the hDRG, hPEP.PIEZOh, hNP1, and hTRPM8 were nominally significant ( P < 0.05) cell types among females, and hPEP.TRPV1/A1.2, hAδ.LTMR, and hTRPM8 were nominally significant among males, though none of these cell types was significantly enriched after correction for multiple testing ( Supplemental Figure 1B and Supplemental Table 12 ).
nominally significantP <0.051.0× alphagold
A total of 19 HLA alleles had nominally significant maternal and/or fetal effects on BW ( P <0.05; Supplementary Table S7 , available as Supplementary data at IJE online); 13 of the 19 alleles had evidence for a maternal effect only, four alleles primarily had evidence for a fetal effect only and two alleles had evidence of both.
nominally significantP < 0.051.0× alphagold
To verify the reliability of these polygenic associations, we repeated the analyses using PRS comprising only the 108 sentinel genome-wide significant schizophrenia variants 15 , based on the assumption that the effect size estimates of genome-wide significant variants should be less affected by population structure than non-significant variants; 77 of the 104 associated traits were nominally significant ( P < 0.05) based on the PRS comprising only genome-wide significant variants.
nominally significantp < 0.051.0× alphagold
Multivariable modelling and the relations between predictor variables All predictor variables having shown nominally significant (p < 0.05) effects on hand preference in univariable testing (i.e. all but maternal smoking) were then included in the multivariable analysis, using general linear modelling (Methods), with hand preference as the dependent variable.