Barely Significant
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“marginally significant”

26,083 sentences · 26,083 papers · 36,483 search hits before verification · confirmed specimen

Sighted at

p>=0.1

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

In the literature

marginally significantP =0.0070.1× alphagold
Ileum tissue showed a significantly differential increase in InsP to inositol (LMM post hoc: Control − Inositol t 227 = 5.593, P <0.001) and a marginally significant decrease in InsP to phytase (LMM post hoc : Control − Phytase 6000 FTU/kg t 227 = 3.267, P =0.007).
marginally significantp = 0.0070.1× alphagold
A main effect of Stereotype was found in the by-participants analysis, along with a marginally significant effect in the by-items analysis, F 1 (2,56) = 5.50, p = 0.007; F 2 (2,32) = 3.00, p = 0.064, with faster RTs to word pairs that contained a neutral role term ( M = 828 ms), than those that contained male-biased ( M = 850 ms) or female-biased terms ( M = 889 ms).
marginally significantp = 0.0070.1× alphagold
Importantly, similar to the behavioral results, pairwise comparisons showed no difference between sequence and random trials in block 1 ( p = 0.53) and block 2 ( p = 0.94) but did show higher levels of caudate activation for sequence versus random trials in block 3 ( p = 0.040; marginally significant after Bonferroni correction for the four comparisons) and block 4 ( p = 0.007; full significance after Bonferroni correction).
The neural basis of implicit perceptual sequence learning.
Front Hum Neurosci · 2011 · PMC3213531
marginally significantp = 0.0080.2× alphagold
A 2 (rater gender) × 2 (partner type) mixed-factors ANOVA on rater accuracy showed a significant main effect for partner type, in addition to a marginally significant interaction ( p = 0.008). 2 See Table 2 for means, standard error, and two-way ANOVA statistics for the ratings from Study 3.
marginally significantP = 0.0080.2× alphagold
Clinically, these variants are associated with increased cardiovascular disease (CVD) risk; a 2023 meta-analysis of 66 studies ( n = 37,263) demonstrated that C677T carriers have a 13–20% higher odds of myocardial infarction (MI) under dominant (OR = 1.16, 95% CI:1.06–1.28, P = 0.008) and recessive (OR = 1.20, 95% CI:1.12–1.28, P < 0.001) models, with similar but marginally significant associations for A1298C (recessive OR = 1.27, 95% CI:1.06–1.51, P = 0.008), underscoring the need for genetic screening in CVD prevention [ 44 ].