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Profil bibliographique

Cathy R. Zhang

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

8Publications signalées
298Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Cerebrovascular and genetic disordersDementia and Cognitive Impairment ResearchAcute Ischemic Stroke ManagementAdvanced MRI Techniques and ApplicationsNeuroinflammation and Neurodegeneration Mechanisms

Les publications récentes

2016 conference-abstract OpenAlex

Abstract WP162: Shared Biological Pathways Among Genetic Variants Associated With White Matter Hyperintensity in CADASIL

Anne‐Katrin Giese, Cathy R. Zhang, Lisa Cloonan, Natalia S. Rost

Introduction: White matter hyperintensity (WMH) is a prominent neuroimaging phenotype commonly detected in patients with stroke as well as genetic disorders like cerebral autosomal dominant arteriopathy with subcortical infarcts and leukencephalopathy (CADASIL). We sought to identify biologically connected pathways between the genetic …

us (code pays fourni par la source)

0 citations Stroke
Accès ouvert 2015 review OpenAlex

Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke

Matthew Traylor, Cathy R. Zhang, Poneh Adib‐Samii, William J. Devan et autres

OBJECTIVE: For 3,670 stroke patients from the United Kingdom, United States, Australia, Belgium, and Italy, we performed a genome-wide meta-analysis of white matter hyperintensity volumes (WMHV) on data imputed to the 1000 Genomes reference dataset to provide insights into disease mechanisms. METHODS: …

us (code pays fourni par la source)

97 citations Neurology
Accès ouvert 2015 article OpenAlex

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease

Kristiina Rannikmäe, Gail Davies, Pippa A. Thomson, Steve Bevan et autres

OBJECTIVES: We hypothesized that common variants in the collagen genes COL4A1/COL4A2 are associated with sporadic forms of cerebral small vessel disease. METHODS: We conducted meta-analyses of existing genotype data among individuals of European ancestry to determine associations of 1,070 common single nucleotide …

us (code pays fourni par la source)

133 citations Neurology
Accès ouvert 2014 article OpenAlex

Genetic Architecture of White Matter Hyperintensities Differs in Hypertensive and Nonhypertensive Ischemic Stroke

Poneh Adib‐Samii, William J. Devan, Matthew Traylor, Silvia Lanfranconi et autres

BACKGROUND AND PURPOSE: Epidemiological studies suggest that white matter hyperintensities (WMH) are extremely heritable, but the underlying genetic variants are largely unknown. Pathophysiological heterogeneity is known to reduce the power of genome-wide association studies (GWAS). Hypertensive and nonhypertensive individuals with WMH might …

gb, it, us (code pays fourni par la source)

29 citations Stroke
2014 conference-abstract OpenAlex

Abstract T P130: Determinants of White Matter Hyperintensity Burden Differ at the Extremes of Age of Ischemic Stroke Onset

Cathy R. Zhang, Lisa Cloonan, Kaitlin Fitzpatrick, Allison Kanakis et autres

Background: White matter hyperintensity (WMH) detected on MRI scans of patients with acute ischemic stroke (AIS) is associated with greater risk of infarct progression, poor post-stroke outcomes, and recurrent stroke. Age is strongly linked to risk of stroke and WMH. We hypothesized …

us, Kenya (code pays fourni par la source)

0 citations Stroke

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