ARIC Publications
Filters: Keyword is Cerebral Small Vessel Diseases [Clear All Filters]
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Genetic variation at 16q24.2 is associated with small vessel stroke." Ann Neurol. 2017;81(3):383-394.
"Cerebral small vessel disease genomics and its implications across the lifespan." Nat Commun. 2020;11(1):6285.
""Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies." Lancet Neurol. 2016;15(7):695-707.
Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects." Brain. 2019;142(4):1009-1023.
"Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate." Brain. 2022;145(6):1992-2007.
"Association of common genetic variants with brain microbleeds: A genome-wide association study." Neurology. 2020;95(24):e3331-e3343.
"Electrocardiographic left atrial abnormality and stroke subtype in the atherosclerosis risk in communities study." Ann Neurol. 2015;78(5):670-8.
"Genetic overlap between diagnostic subtypes of ischemic stroke." Stroke. 2015;46(3):615-9.
"Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities." Stroke. 2020;51(7):2111-2121.
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