Faculty, Staff and Student Publications
Language
English
Publication Date
10-24-2017
Journal
Neurology
DOI
10.1212/WNL.0000000000004560
PMID
28954878
PMCID
PMC5664302
PubMedCentral® Posted Date
October 2017
PubMedCentral® Full Text Version
Post-print
Abstract
OBJECTIVE: To determine whether common variants in familial cerebral small vessel disease (SVD) genes confer risk of sporadic cerebral SVD.
METHODS: We meta-analyzed genotype data from individuals of European ancestry to determine associations of common single nucleotide polymorphisms (SNPs) in 6 familial cerebral SVD genes (
RESULTS: A locus in
CONCLUSIONS: These results provide evidence of shared genetic determinants and suggest common pathophysiologic mechanisms of distinct ischemic and hemorrhagic cerebral SVD stroke phenotypes, offering new insights into the causal mechanisms of cerebral SVD.
Keywords
Cerebral Hemorrhage, Collagen Type IV, Europe, Genetic Association Studies, Humans, Polymorphism, Single Nucleotide, Stroke, Lacunar
Published Open-Access
yes
Recommended Citation
Rannikmäe, Kristiina; Sivakumaran, Vhinoth; Millar, Henry; et al., "COL4A2 Is Associated With Lacunar Ischemic Stroke and Deep Ich: Meta-Analyses Among 21,500 Cases and 40,600 Controls" (2017). Faculty, Staff and Student Publications. 382.
https://digitalcommons.library.tmc.edu/uthmed_docs/382