Stroke genetics (Q37915080)

25 August 2017

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title

Stroke genetics (English)

1 reference

25 August 2017

Hugh S Markus

1

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25 August 2017

publication date

10 August 2011

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25 August 2017

published in

Human Molecular Genetics

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25 August 2017

volume

20

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25 August 2017

issue

R2

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25 August 2017

page(s)

R124-31

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Heart disease and stroke statistics--2011 update: a report from the American Heart Association

25 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Infarcts of undetermined cause: the NINCDS Stroke Data Bank

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Risk factor profile of cerebral small vessel disease and its subtypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

A computerized algorithm for etiologic classification of ischemic stroke: the Causative Classification of Stroke System.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetics of ischaemic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Role of COL4A1 in small-vessel disease and hemorrhagic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

COL4A1 mutations as a monogenic cause of cerebral small vessel disease: a systematic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Do in vivo experimental models reflect human cerebral small vessel disease? A systematic review.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Systematic review of methods and results of studies of the genetic epidemiology of ischemic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Evaluating the genetic component of ischemic stroke subtypes: a family history study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Parental occurrence of stroke and risk of stroke in their children: the Framingham study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetics of ischaemic stroke among persons of non-European descent: a meta-analysis of eight genes involving approximately 32,500 individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetic association studies in stroke: methodological issues and proposed standard criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Variation in the PDE4D gene and ischemic stroke risk: a systematic review and meta-analysis on 5200 cases and 6600 controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Variants of the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) gene and risk of stroke: a HuGE gene-disease association review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetic variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke: a replication study in two independent populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

The association of the 4q25 susceptibility variant for atrial fibrillation with stroke is limited to stroke of cardioembolic etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

The 1425G/A SNP in PRKCH is associated with ischemic stroke and cerebral hemorrhage in a Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genomewide association studies of stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Failure to validate association between 12p13 variants and ischemic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Common mitochondrial sequence variants in ischemic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Carotid intima-media thickness measurements: techniques and clinical relevance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Prediction of clinical cardiovascular events with carotid intima-media thickness: a systematic review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetic basis of variation in carotid artery wall thickness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Population-Based Twin Study of the Effects of Migration From Finland to Sweden on Endothelial Function and Intima-Media Thickness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Heritability of carotid artery atherosclerotic lesions: an ultrasound study in 154 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetic and environmental contributions to carotid intima-media thickness and obesity phenotypes in the Northern Manhattan Family Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Carotid Intima-Media Thickness is Greater but Carotid Plaque Prevalence is Lower in Black Compared with White Subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

The clinical importance of white matter hyperintensities on brain magnetic resonance imaging: systematic review and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Evidence for genetic variance in white matter hyperintensity volume in normal elderly male twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetic variation in white matter hyperintensity volume in the Framingham Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genomic susceptibility loci for brain atrophy in hypertensive sibships from the GENOA study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetic risk factors for stroke and carotid atherosclerosis: insights into pathophysiology from candidate gene approaches

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

Genetic and Acquired Inflammatory Conditions Are Synergistically Associated With Early Carotid Atherosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR345

21 January 2018

Identifiers

DOI

10.1093/HMG/DDR345

1 reference

25 August 2017

1 reference