Genetic architecture and clinical features of Tourette syndrome in a child and adolescent cohort: an explorative clinical exome-based study.

Front Psychiatry · 2026 · PMC12946004 · PMID 41767149

Europe PMC DOI

hedged sentence

0.2450

closest p · 4.9× alpha

0.2450

boldest claim

The sentences

did not reach statistical significancep = 0.245not close (p > 0.1)

Despite these variations, the overall comparison did not reach statistical significance (p = 0.245), suggesting that EEG alterations are not systematically linked to variant type in this cohort. 3.4.4 MRI analysis Structural brain anomalies identified on MRI were relatively common but comparably distributed across groups.

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