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

The analysis of Belgian CD trios revealed only nominally significant associations with the major alleles (i.e. allele frequency in controls >50%) of four SNPs, three of which are located in the haplotype block encompassing the region covering the MEFV promoter to intron 2 and its 5′ flanking region (rs182674( A ): p = 0.029; rs224217( G ): p = 0.052; rs224231( G ); p = 0.039; rs6501170( T ): p = 0.016; the risk nucleotides are indicated in brackets) ( Figure 2A , Table S1 ).
The overall omnibus p-value for surgical approach was p = 0.125 (non-significant); nominally significant individual contrasts for specific approach categories reflect sparse-data instability in the reference group and should not be interpreted as independent effects.
In order to identify novel associated loci, we considered the following steps (Figure 2 ): (1) we identified all loci that were statistically significant in the multi‐phenotype analysis ( p ‐value multivariate <1.85 x 10 −9 ) (significant loci); (2) among these, we identified all loci with a lead variant that was at least nominally significant for two of the individual datasets used in each combination of phenotypes (lead variant p ‐value univariate <.005) 30 , 31 , 32 (significant loci driven by more than one phenotype); (3) among the loci from step 2, we then narrowed it down to loci that were new for at least one of the ph
For plasma pTau217, post-hoc analysis of the change from baseline with ACI-35.030 treatment, when compared to the corresponding change from baseline for the pooled placebo group, was nominally significant at weeks 31, 36, and 74 for the 900 μg dose and 10, 15, and 36 for the 1800 μg dose ( Fig. 3 and Table 6 ).