Barely Significant
← all excerpts

Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain.

Am J Med Genet B Neuropsychiatr Genet · 2016 · PMC4988385 · PMID 27004590

1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantP = 1.03 × 10 −4actually significant
Expression of the NT5C2 allele in phase with the ch10_104957618_I risk allele was also reduced in all assayed adult brain regions (mean DLPFC: 15%, hippocampus: 12%, caudate: 13%), with highly significant differences in allele ratios observed between cDNA and genomic DNA that survived Bonferroni correction in all areas (DLPFC: P = 1.03 × 10 −4 , corrected P = 0.003; hippocampus: P = 2.64 × 10 −6 , corrected P = 8.46 × 10 −5 ; caudate P = 8.11 × 10 −5 , corrected P = 0.0025).

also in 132,142 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.