Barely Significant
← all phrases

“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

Strikingly, this BMI signal colocalizes with 15 BMI MR trans -eQTLs ( PP median = 0.67 [range 0.49–0.98]) and 64 BMI MR trans -aQTLs ( PP median = 0.89 [range 0.49–1.00]), though among these nominally significant, colocalized trans -QTL signals, only 8 trans -aQTLs ( ANG , CSNK2A2 , ID2 , PIM1 , PTPRJ , TENM4 , TNFRSF10C and ZFAT ) were significant at FDR < 0.05 ( Fig 4 , and Tables 1 , S11 – S15 and S17 ).
17 This suggests that abnormalities in long-chain acylcarnitines reflect a common signature associated with myocardial mitochondrial dysfunction. The other nominally significant results included results for factor 2, comprised of long-chain dicarboxylacylcarnitines, unique in being the only factor which was only different in CpcPH compared to controls.
However, by examining the nominally significant genetic locus associated with the metabolite on chromosome 10 (BP 60,794,328-61,050,339), nearby genes and phenotypes associated with those genes were identified (genes included PHYHIPL , TRAF6P1 , LINC00844 , and FAM13C ; phenotypes included DNA methylation, sleep duration, and QT-interval duration in Trypanosoma cruzi seropositivity).
Regardless of reading performance, subjects with READ1d showed nominally significant lower global efficiency, local efficiency, and clustering coefficient compared to subjects without READ1d, with consistent effect directions across metrics; the nodal analysis revealed a significant effect of READ1d on a network spanning lateral, occipital and frontal cortex.
Cumulative effect of rs1801274, rs3818298, rs2736340 and rs4813003 on KD risk Next, we examined the cumulative effect of the 4 nominally significant SNPs by counting the number of non-risk genotypes associated with KD risk in each subject according to the potential inheritance models presumed by the results of dominant and recessive models from individual SNP analysis.