Barely Significant
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Association of MAPT subhaplotypes with clinical and demographic features in Parkinson's disease.

Ann Clin Transl Neurol · 2020 · PMC7480915 · PMID 32767721

1
hedged sentence
0.0600
closest p · 1.2× alpha
0.0600
boldest claim

The sentences

a nonsignificant trendP = 0.06so close (0.05 < p ≤ 0.1)
Other than a nonsignificant trend toward an association between H1v and a lower risk of PSP (OR = 0.44, P = 0.06), the H1b, H1r, and H1v haplotypes have not been associated with other neurodegenerative disorders with a similar clinical or neuropathological phenotype to PD, such as PSP, MSA, or DLB. 12 , 13 , 28 Though it will be important to validate the findings of our study, future studies examination associations of H1 subhaplotypes with clinical features of other neurodegenerative diseases will also be important.

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