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. Author manuscript; available in PMC: 2014 Apr 20.
Published in final edited form as: Lancet. 2013 Feb 28;381(9875):1371–1379. doi: 10.1016/S0140-6736(12)62129-1

Table 3.

Expression quantitative trait loci enrichment analysis for single-nucleotide polymorphisms (SNPs) from primary meta-analysis by p-value cutoffs

Cis-regulatory eQTL datasets (enrichment p value)
Prefrontal cortex Cortex Cortex Liver (Schadt Skin (Ding LPL (Stranger
(Colantuoni et al27) (Myers et al21) (Webster et al22) et al23) et al24) et al25)
p<0·01 0·41 0·020 0·0028 0·37 0·22 0·11
p<0·1 0·11 0·020 0·000027 0·39 0·15 0·28
p<0·2 0·19 0·0030 0·000061 0·069 0·21 0·12
p<0·3 0·012 0·012 0·00034 0·013 0·02 0·066
p<0·4 0·023 0·0071 0·00030 0·045 0·044 0·10
p<0·5 0·023 0·043 0·0071 0·22 0·078 0·0068

Cross-disorder risk SNPs were defined as those meeting the p-value cutoffs shown in the left column in the primary meta-analysis of five disorders, and residing within 1 M bases from human reference hg18 genes.

LPL=lymphoblastoid cell lines.