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- 2021
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Mark
The copy number variation and stroke (CaNVAS) risk and outcome study
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- Contribution to journal › Article
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Mark
Genetic basis of lacunar stroke : a pooled analysis of individual patient data and genome-wide association studies
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- Contribution to journal › Article
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Mark
Excessive White Matter Hyperintensity Increases Susceptibility to Poor Functional Outcomes After Acute Ischemic Stroke
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- Contribution to journal › Article
- 2020
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Mark
White matter hyperintensity burden in acute stroke patients differs by ischemic stroke subtype
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- Contribution to journal › Article
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Mark
Brain Volume : An Important Determinant of Functional Outcome After Acute Ischemic Stroke
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- Contribution to journal › Article
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Mark
Detailed phenotyping of posterior vs. anterior circulation ischemic stroke : a multi-center MRI study
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- Contribution to journal › Article
- 2019
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Mark
White matter hyperintensity quantification in large-scale clinical acute ischemic stroke cohorts – The MRI-GENIE study
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- Contribution to journal › Article
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Mark
Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke
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- Contribution to journal › Article
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Mark
Big Data Approaches to Phenotyping Acute Ischemic Stroke Using Automated Lesion Segmentation of Multi-Center Magnetic Resonance Imaging Data
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- Contribution to journal › Article
- 2017
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Mark
Genetic variants influencing elevated myeloperoxidase levels increase risk of stroke
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- Contribution to journal › Article
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Mark
Design and rationale for examining neuroimaging genetics in ischemic stroke : The MRI-GENIE study
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- Contribution to journal › Article
- 2016
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Mark
Low-frequency and common genetic variation in ischemic stroke : The METASTROKE collaboration
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- Contribution to journal › Article
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Mark
Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.
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- Contribution to journal › Article
- 2015
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Mark
Recommendations from the international stroke genetics consortium, part 2: biological sample collection and storage.
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- Contribution to journal › Debate/Note/Editorial
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Mark
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease
(
- Contribution to journal › Article