Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

Am J Psychiatry · 2012 · PMC3601404 · PMID 22420046

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nominally significantno p-value reported

Analysis was carried out using ALIGATOR ( 28 ), which converts a list of significant and nominally significant SNPs into a list of significant genes and tests this list for enrichment for genes within the gene sets, allowing for variable numbers of SNPs per gene.

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highly significantno p-value reported

Contrary to what some might expect, we found a highly significant overlap of biological pathways hit by both CNVs and SNPS.

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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.