/manager/Index ${session.getAttribute("locale")} 5 Common NOTCH3 variants and cerebral small-vessel disease /manager/Repository/uon:28335 0.01 were included in the analysis. A significance level of P<0.0015 was used, adjusted for the effective number of independent SNPs in the region using the Galwey method. Results: We found no association of any common variants in NOTCH3 (including rs10404382, rs1043994, rs10423702, and rs1043997) with lacunar stroke or white matter hyperintensity volume. We repeated our analysis stratified for hypertension but again found no association. Conclusions: Our study does not support a role for common NOTCH3 variation in the risk of sporadic small-vessel disease.]]> Tue 21 Jul 2020 09:43:47 AEST ]]> Genetic associations with white matter hyperintensities confer risk of lacunar stroke /manager/Repository/uon:24807 Tue 21 Jul 2020 09:42:31 AEST ]]> Association of MTHFR C677T genotype with ischemic stroke is confined to cerebral small vessel disease subtype /manager/Repository/uon:24521 Tue 21 Jul 2020 09:42:08 AEST ]]> Differences in common genetic predisposition to ischemic stroke by age and sex /manager/Repository/uon:22678 Sat 24 Mar 2018 07:12:09 AEDT ]]>