Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.

Hum Mol Genet · 2016 · PMC5418836 · PMID 27798102

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failed to reach significanceno p-value reported

Similarly, the observed enrichment of additional alleles in the NeuroX (OR = 1.49, 95% CI: 0.90–2.46) and exome cohorts (OR = 1.51, 95% CI: 0.65–3.51; Table 2 ) failed to reach significance.

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