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Genetics of Cerebral Small Vessel Disease.

作者信息

Marini Sandro, Anderson Christopher D, Rosand Jonathan

机构信息

From the Center for Genomic Medicine (S.M., C.D.A., J.R.), Massachusetts General Hospital, Boston.

Department of Neurology (S.M., C.D.A., J.R.), Massachusetts General Hospital, Boston.

出版信息

Stroke. 2020 Jan;51(1):12-20. doi: 10.1161/STROKEAHA.119.024151. Epub 2019 Nov 22.

DOI:10.1161/STROKEAHA.119.024151
PMID:31752611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7337039/
Abstract
摘要

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本文引用的文献

[1]
The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts.

Mol Genet Metab Rep. 2019-2-6

[2]
Association of Apolipoprotein E With Intracerebral Hemorrhage Risk by Race/Ethnicity: A Meta-analysis.

JAMA Neurol. 2019-4-1

[3]
Genetics of Vascular Cognitive Impairment.

Stroke. 2019-3

[4]
Genetic variation in is associated with white matter hyperintensities (n = 11,226).

Neurology. 2019-1-18

[5]
Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction.

Circulation. 2019-3-26

[6]
Genome-wide meta-analysis identifies 3 novel loci associated with stroke.

Ann Neurol. 2018-11-30

[7]
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.

Stroke. 2018-8

[8]
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.

Nat Genet. 2018-3-12

[9]
is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls.

Neurology. 2017-10-24

[10]
CADASIL: Treatment and Management Options.

Curr Treat Options Neurol. 2017-9

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