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

nominally significantP < 0.051.0× alphagold
Plasma NFL alone (Pathway 3) showed nominally significant mediation effects for ADAS13, CDRSB, MEM, and LAN (total indirect effect: all uncorrected P < 0.05) ( Figure 2IV .A, B; Table S9); however, after FDR correction, only the mediation effect on MEM remained significant ( P < 0.05).
nominally significantP < 0.051.0× alphagold
Furthermore, a weighted polygenic risk score (PRS) made from the 18 SNPs common between the two datasets showed a nominally significant association ( P < 0.05) with the oral glucose tolerance test derived variables area under the curve (AUC) for insulin, AUC for insulin/AUC for glucose, insulin at 30 minutes and insulin sensitivity index ( S6 Table ).
nominally significantP < 0.051.0× alphagold
We provided detailed RegulomeDB annotations in relevant cell types (e.g., hematopoietic multipotent progenitor cells, CD34+ hematopoietic progenitor cells, any primary B-cell, lymphoblastoid cell lines from 1000 Genomes [i.e., GM19238], K562, NAMALWA, BLaER1) for: (a) all index variants; and (b) credible set variants with nominally significant ( P < 0.05) functional probability scores.
nominally significantP < 0.051.0× alphagold
Moreover, sensitivity gene-burden tests considering only those additional carriers identified by WGS (that is, not identified by WES data), 16 of the 23 gene masks with at least five carriers showed a nominally significant association ( P < 0.05) with the target phenotype, indicating that the additional coding variants identified by WGS are likely to be functionally relevant.
nominally significantp ≤ 0.051.0× alphagold
When Li treatment response phenotypes in bipolar patients was screened by a large (1,693 sequence) genome-wide association study of pre-miRNA genes plus 20 kb flanking sequence, only one pre-miRNA gene had a nominally significant (p ≤ 0.05) sequence variation association, but when corrected for multiple comparisons, no polymorphisms in pre-miRNA plus flanking sequence showed any association with Li treatment phenotypes 91 .
nominally significantp < .051.0× alphagold
Although autism GWASs currently provide limited statistical power for these analyses, we observed nominally significant ( p < .05) enrichment of associations in the deep layer excitatory neuron FC-ExN-4 of the frontal cortex and oligodendrocyte precursor Thal-OPC of the thalamus by both MAGMA and SLDSR ( Figure S11 in Supplement 2 ).
nominally significantP > 0.051.0× alphagold
For the probe annotated to GABBR1 among the top 1000 DMPs associated with MCI to AD conversion status in the AddNeuroMed study (cg06512249, β = − 0.03, P = 0.003), the direction was consistent with multiple probes in the same region from this study (cg03316098, β = − 0.05, P = 0.01; cg10234998, β = − 0.10, P = 0.005; cg12061917, β = − 0.07, P = 0.001; cg21481950, β = − 0.06 P = 0.007) even though cg06512249 did not reach the nominally significant threshold in this study ( P > 0.05) (Additional file 1 : Fig. 8E).
nominally significantP < 0.051.0× alphagold
We considered a SNP-lipid association to be validated if (i) the SNP was significantly associated ( P < 5 × 10 −8 ) in the unadjusted BHS discovery GWAS; (ii) the direction of effect was concordant between the validation meta-analysis and the BHS discovery analysis; and (iii) the association was nominally significant ( P < 0.05; less conservative) or reached the Bonferroni significance threshold ( P < 2.34 × 10 −5 ) in the validation meta-analysis.