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

To assess our nominally significant findings we used three methods: (a) the gold standard Bonferroni correction to adjust p-values for multiple testing in our 12 main analyses [additive, dominant and recessive models of CLOCK SNP main effects and SNP × stress factor (CHA, RLE, or FINANC) interactions on migraineID in the total sample
Despite overall negative findings, this study unravelled nominally significant association between multifocal FMD and myosin light chain kinase ( MYLK ; previously involved in thoracic aortic aneurysms), dynein cytoplasmic heavy chain 1 gene ( DYNC2H1 ), obscurin ( OBSCN ; a sarcomeric protein) and RNF213 , previously associated with Moyamoya disease ( p = 0.01) [ 43 ].
Genomics of Fibromuscular Dysplasia.
Int J Mol Sci · 2018 · PMC5983654
Fourth, to evaluate whether the effect of DNA methylation on migraine is mediated through gene expression, we restricted the analysis to CpG sites that showed a significant causal association with migraine or its subtypes in the mQTL–MR analyses (used as exposures), and genes with nominally significant causal effects on migraine in the eQTL–MR analyses (used as mediators).
Results We failed to detect significant differences between genotypes in depression‐like behaviors, anxiety‐like behaviors, social behaviors, sensorimotor gaiting, or learning and memory, while 1473G mice exhibited a nominally significant impairment in gait analysis, which failed to reach study‐wide significance.