Barely Significant
← all excerpts

Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.

Nat Commun · 2025 · PMC12032271 · PMID 40280976

Europe PMCDOI
1
hedged sentence
0.0002
closest p · 0.0× alpha
0.0002
boldest claim

The sentences

nominally significantP = 1.72 × 10 −4actually significant
These loci were only nominally significant in the analysis including the svPPA patients ( LRP1B : P = 1.72 × 10 −4 ; OR = 4.66, COL22A1 : P = 0.03; OR = 5.32; TMEM135 : P = 1.68 × 10 −3 ; OR = 2.19, and TRPC4 P = 1.25 × 10 −4 ; OR = 2.91).

also in 7,732 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.