Barely Significant
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“nominally significant”

7,733 sentences · 7,733 papers · 10,034 search hits before verification · confirmed specimen

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p=0.08

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

In the literature

3 SNPs were nominally significant with the most statistically significant difference observed for rs514659 in the ABO gene determining the ABO blood group (frequency of the minor allele C in STEMI patients 48.06% and in NSTEMI patients 43.26%; X 2 P = 0.0066), originally reported to be specifically associated with MI in presence of CAD [ 20 ].
These data are presented in Tables S1 and S2.Of these tests, the majority showed no association with either fluid or crystallized intelligence, but one test, total CNV counts for deletions in the range 200–500 kb, showed a nominally significant p-value of 0.039 with g f , although this is not robust to multiple testing correction.
Over-Representation Analysis (ORA) maps interesting genes within the transcriptome profiles to curated pathways or functional categories (Reactome and Gene Ontology were used) and assesses the statistical significance of the overlap; transcripts undergoing nominally significant changes were used.
Analysis of the transcriptomic datasets Pre-normalized public circadian transcriptomic microarray (GEO accession: GSE54650 7 ) and aging transcriptomic data sets (GEO accession: GSE57809 26 and GSE6591 27 for the liver and lung, respectively) were used for detection of circadian (see “Detection and analysis of circadian epigenetic oscillations”) and nominally significant aging mRNAs (see “Aging analysis for the mouse tissue DNA samples”).
Credibility and quality of the evidence assessment The credibility of the evidence of each association will be assessed on the basis of the following criteria: (1) associations with the number of participants of more than 1000, the P value of < 1 × 10 − 6 , the 95% PIs excluding the null, the largest study indicating a nominally significant effect size, the I 2 statistic of < 50%, no evidence of small-study effects and excess significance biases will be classified as convincing evidence (class I); (2) associations with the number of participants of more than 1000, the P value of < 1 × 10 − 6 , and the I 2 statistic of < 50% will be cl
Although the current nominally significant findings should be interpreted with caution and need replication in independent cohorts, this study supports the strategy to combine genetic approaches to determine the molecular mechanisms underlying bipolar disorder. status released display-pdf yes is-olf no is-manuscript no is-preprint no is-journal-matter no is-scanned no is-retracted no Received 2013 Jul 29; Accepted 2014 Jul 11; Collection date 2014.
Large-scale GWASs for regional cortical surface area and thickness have identified 369 genome-wide nominally significant loci related to cortical structures [ 18 ]. 26% of the variation in average cortical thickness and 34% of the variation in total surface area can be explained by common single-nucleotide polymorphisms (SNPs) [ 18 ].