(Q37915080)

English

Stroke genetics

scientific article published on 10 August 2011

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scholarly article

1 reference

Europe PubMed Central

25 August 2017

1 reference

Europe PubMed Central

Stroke genetics (English)

1 reference

Europe PubMed Central

25 August 2017

author name string

Hugh S Markus

1

1 reference

Europe PubMed Central

25 August 2017

publication date

10 August 2011

1 reference

Europe PubMed Central

25 August 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

25 August 2017

20

1 reference

Europe PubMed Central

25 August 2017

R2

1 reference

Europe PubMed Central

25 August 2017

R124-31

1 reference

Europe PubMed Central

25 August 2017

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

1 reference

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

21 January 2018

Infarcts of undetermined cause: the NINCDS Stroke Data Bank

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Risk factor profile of cerebral small vessel disease and its subtypes

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Genetics of ischaemic stroke

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathy

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population

1 reference

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

21 January 2018

Role of COL4A1 in small-vessel disease and hemorrhagic stroke.

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Genomewide association studies of stroke

1 reference

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

21 January 2018

Failure to validate association between 12p13 variants and ischemic stroke

1 reference

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

21 January 2018

Common mitochondrial sequence variants in ischemic stroke

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Carotid intima-media thickness measurements: techniques and clinical relevance

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Genetic basis of variation in carotid artery wall thickness

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Carotid intima-media thickness is greater but carotid plaque prevalence is lower in black compared with white subjects

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

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

1 reference

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

21 January 2018

Identifiers

10.1093/HMG/DDR345

1 reference

Europe PubMed Central

25 August 2017

1 reference

Europe PubMed Central

25 August 2017

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