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. 2012 Feb 1;169(2):186–194. doi: 10.1176/appi.ajp.2011.11040551

TABLE 3.

Pathways Showing Nominally Significant Enrichment (p<0.05) in Both the Single-Nucleotide Polymorphism Data and the Copy Number Variant (CNV) Data in a Genome-Wide Association Study of ADHD

Pathway Numbera Number of Genes Gene Hits (Cases) Gene Hits (Comparison) p (CNV) p (corr)b p (GWAS) Description
MGI:5278 188 14 0 1.47E-05 0.002 0.030 Abnormal cholesterol homeostasis
MGI:3947 182 13 0 2.61E-05 0.004 0.023 Abnormal cholesterol level
MGI:180 169 13 0 2.61E-05 0.004 0.026 Abnormal circulating cholesterol level
GO:16746 214 14 0 1.42E-04 0.009 0.004 Transferase activity, transferring acyl groups
GO:8415 203 13 0 1.43E-04 0.009 0.003 Acyltransferase activity
GO:16747 205 13 0 1.43E-04 0.008 0.004 Transferase activity, transferring acyl groups other than amino-acyl groups
GO:51298 11 8 0 6.95E-04 0.050 0.033 Centrosome duplication
GO:32680 34 7 1 8.83E-03 0.341 0.014 Regulation of tumor necrosis factor production
GO:5261 271 17 6 1.84E-02 0.547 0.042 Cation channel activity
GO:7417 441 28 10 2.77E-02 0.683 0.002 Central nervous system development
GO:16247 56 8 2 3.07E-02 0.719 0.026 Channel regulator activity
GO:8233 572 25 8 4.89E-02 0.848 0.037 Peptidase activity
GO:70011 553 25 8 4.89E-02 0.848 0.038 Peptidase activity, acting on L-amino acid peptides

a GO=Gene Ontology; MGI=Mouse Genome Informatics

b Represents the probability of obtaining by chance at least one pathway with a pathway-specific p value for enrichment of case CNV hits at least as significant as that observed in the actual data. Note that genes <1 Mb apart in the same pathway were collapsed into one signal.