(Q37998525)

26 August 2017

Genetics of ischemic stroke, stroke-related risk factors, stroke precursors and treatments (English)

1 reference

26 August 2017

Patrizia Ferroni

9

0 references

Raffaele Palmirotta

Raffaele Palmirotta

3

0 references

Pasquale Abete

Pasquale Abete

7

0 references

Franco Rengo

Franco Rengo

8

0 references

Tatjana Rundek

11

Tatjana Rundek

1 reference

26 August 2017

10

Ralph L Sacco

1 reference

26 August 2017

6

Maurizio Paciaroni

1 reference

26 August 2017

5

Valeria Caso

1 reference

26 August 2017

David Della-Morte

1

1 reference

PubMed ID

22462751

26 August 2017

Fiorella Guadagni

2

1 reference

PubMed ID

22462751

26 August 2017

Gianluca Testa

4

1 reference

26 August 2017

1 April 2012

1 reference

26 August 2017

1 reference

26 August 2017

13

1 reference

26 August 2017

5

1 reference

26 August 2017

595-613

1 reference

Genetic studies in rat models: insights into cardiovascular disease

26 August 2017

1 reference

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

21 January 2018

1 reference

21 January 2018

1 reference

Heritability of ischemic stroke in relation to age, vascular risk factors, and subtypes of incident stroke in population-based studies

21 January 2018

1 reference

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

21 January 2018

1 reference

The genetics of ischaemic stroke

21 January 2018

1 reference

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.

21 January 2018

1 reference

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

21 January 2018

1 reference

Many hypotheses but no replication for the association between PDE4D and stroke.

21 January 2018

1 reference

Candidate gene polymorphisms for ischemic stroke

21 January 2018

1 reference

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

21 January 2018

1 reference

Genomewide association studies of stroke

21 January 2018

1 reference

Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Transla

21 January 2018

1 reference

Individual progression of carotid intima media thickness as a surrogate for vascular risk (PROG-IMT): Rationale and design of a meta-analysis project

21 January 2018

1 reference

Carotid plaque, a subclinical precursor of vascular events: the Northern Manhattan Study.

21 January 2018

1 reference

Genetics of carotid atherosclerosis

21 January 2018

1 reference

CADASIL: pathogenesis, clinical and radiological findings and treatment

21 January 2018

1 reference

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

21 January 2018

1 reference

The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland

21 January 2018

1 reference

The role of genetics in stroke

21 January 2018

1 reference

Genetics and genomics of stroke: novel approaches

21 January 2018

1 reference

Genetics of ischaemic stroke

21 January 2018

1 reference

Stroke-related translational research.

21 January 2018

1 reference

Carotid atherosclerotic markers in CADASIL.

21 January 2018

1 reference

Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension

21 January 2018

1 reference

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

21 January 2018

1 reference

Natural history of Fabry disease in females in the Fabry Outcome Survey.

21 January 2018

1 reference

Monogenic vessel diseases related to ischemic stroke: a clinical approach

21 January 2018

1 reference

Moyamoya: epidemiology, presentation, and diagnosis

21 January 2018

1 reference

Loss of BRCC3 deubiquitinating enzyme leads to abnormal angiogenesis and is associated with syndromic moyamoya

21 January 2018

1 reference

Prediction of Coronary Heart Disease Using Risk Factor Categories

21 January 2018

1 reference

Molecular genetic insights into cardiovascular disease

21 January 2018

1 reference

Relative familial clustering of cerebral versus coronary ischemic events.

21 January 2018

1 reference

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

21 January 2018

1 reference

An extreme-sib-pair genome scan for genes regulating blood pressure

21 January 2018

1 reference

The human obesity gene map: the 1999 update.

21 January 2018

1 reference

Human pedigree-based quantitative-trait-locus mapping: localization of two genes influencing HDL-cholesterol metabolism

21 January 2018

1 reference

Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) Study

21 January 2018

1 reference

Lifetime risk for development of atrial fibrillation: the Framingham Heart Study

21 January 2018

1 reference

Prolonged signal-averaged P-wave duration as an intermediate phenotype for familial atrial fibrillation

21 January 2018

1 reference

Sodium channel mutations and arrhythmias

21 January 2018

1 reference

Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation

21 January 2018

1 reference

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

21 January 2018

1 reference

A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation

21 January 2018

1 reference

Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing

21 January 2018

1 reference

Cardiac sodium channel mutation in atrial fibrillation.

21 January 2018

1 reference

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

21 January 2018

1 reference

The role of blood pressure lowering before and after stroke

21 January 2018

1 reference

KCNQ1 gain-of-function mutation in familial atrial fibrillation

21 January 2018

1 reference

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation

21 January 2018

1 reference

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

21 January 2018

1 reference

Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation

21 January 2018

1 reference

Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Chromosome 9p21 in ischemic stroke: population structure and meta-analysis

21 January 2018

1 reference

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

21 January 2018

1 reference

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice

21 January 2018

1 reference

Genetic predisposition to stroke in relatives of hypertensives.

21 January 2018

1 reference

A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

21 January 2018

1 reference

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

21 January 2018

1 reference

Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome

21 January 2018

1 reference

Linkage of essential hypertension to chromosome 18q.

21 January 2018

1 reference

Two point mutations within the adducin genes are involved in blood pressure variation

21 January 2018

1 reference

Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study.

21 January 2018

1 reference

The ACE I/D polymorphism in US adults: limited evidence of association with hypertension-related traits and sex-specific effects by race/ethnicity

21 January 2018

1 reference

Cholesterol, stroke risk, and stroke prevention

21 January 2018

1 reference

Genetics of familial combined hyperlipidemia and risk of coronary heart disease

21 January 2018

1 reference

Linkage and association between distinct variants of the APOA1/C3/A4/A5 gene cluster and familial combined hyperlipidemia

21 January 2018

1 reference

Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families

21 January 2018

1 reference

Mechanisms linking apolipoprotein E isoforms with cardiovascular and neurological diseases

21 January 2018

1 reference

Apolipoproteins and carotid artery atherosclerosis in an elderly multiethnic population: the Northern Manhattan stroke study

21 January 2018

1 reference

Genetic loci for blood lipid levels identified by linkage and association analyses in Caribbean Hispanics

21 January 2018

1 reference

Reducing the risk of stroke in diabetes: what have we learned that is new?

21 January 2018

1 reference

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)

21 January 2018

1 reference

A genome-wide search for human type 1 diabetes susceptibility genes

21 January 2018

1 reference

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

21 January 2018

1 reference

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

21 January 2018

1 reference

TCF7L2 single nucleotide polymorphisms, cardiovascular disease and all-cause mortality: the Atherosclerosis Risk in Communities (ARIC) study

21 January 2018

1 reference

White matter lesions in the elderly

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships

21 January 2018

1 reference

Carotid plaque compared with intima-media thickness as a predictor of coronary and cerebrovascular disease

21 January 2018

1 reference

Carotid-artery intima and media thickness as a risk factor for myocardial infarction and stroke in older adults. Cardiovascular Health Study Collaborative Research Group

21 January 2018

1 reference

Measurement of intima-media thickness vs. carotid plaque: uses in patient care, genetic research and evaluation of new therapies.

21 January 2018

1 reference

Intimal plus medial thickness of the arterial wall: a direct measurement with ultrasound imaging

21 January 2018

1 reference

Carotid atherosclerosis measured by B-mode ultrasound in populations: associations with cardiovascular risk factors in the ARIC study

21 January 2018

1 reference

Carotid artery atherosclerosis, MRI indices of brain ischemia, aging, and cognitive impairment: the Framingham study

21 January 2018

1 reference

Common carotid artery intima-media thickness progression as a predictor of stroke in multi-ethnic study of atherosclerosis

21 January 2018

1 reference

Heritability and linkage analysis for carotid intima-media thickness: the family study of stroke risk and carotid atherosclerosis

21 January 2018

1 reference

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

21 January 2018

1 reference

Genomewide linkage analysis for internal carotid artery intimal medial thickness: evidence for linkage to chromosome 12.

21 January 2018

1 reference

A genome-wide scan for carotid artery intima-media thickness: the Mexican-American Coronary Artery Disease family study

21 January 2018

1 reference

Segment-specific genetic effects on carotid intima-media thickness: the Northern Manhattan study

21 January 2018

1 reference

Carotid intima-media thickness is associated with allelic variants of stromelysin-1, interleukin-6, and hepatic lipase genes: the Northern Manhattan Prospective Cohort Study

21 January 2018

1 reference

Multi-ethnic genetic association study of carotid intima-media thickness using a targeted cardiovascular SNP microarray

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetics of ultrasonographic carotid atherosclerosis

21 January 2018

1 reference

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

21 January 2018

1 reference

Genomewide linkage and peakwide association analyses of carotid plaque in Caribbean Hispanics

21 January 2018

1 reference

Familial Aggregation and Genome-Wide Linkage Analysis of Carotid Artery Plaque: The NHLBI Family Heart Study

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetic epidemiology of subclinical cardiovascular disease in the diabetes heart study

21 January 2018

1 reference

Carotid plaque and candidate genes related to inflammation and endothelial function in Hispanics from northern Manhattan

21 January 2018

1 reference

A candidate gene study revealed sex-specific association between the OLR1 gene and carotid plaque

21 January 2018

1 reference

Association of the sirtuin and mitochondrial uncoupling protein genes with carotid plaque

21 January 2018

1 reference

Genetic mapping of vascular calcified plaque loci on chromosome 16p in European Americans from the diabetes heart study.

21 January 2018

1 reference

Novel candidate genes in unstable areas of human atherosclerotic plaques.

21 January 2018

1 reference

Pharmacology and management of the vitamin K antagonists: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (8th Edition).

21 January 2018

1 reference

Anticoagulation intensity and outcomes among patients prescribed oral anticoagulant therapy: a systematic review and meta-analysis

21 January 2018

1 reference

Pharmacogenetics-based coumarin therapy

21 January 2018

1 reference

Equal proportion of adult male and female homozygous for the 677C ? T mutation in the methylenetetrahydrofolate reductase polymorphism

21 January 2018

1 reference

Association of warfarin dose with genes involved in its action and metabolism

21 January 2018

1 reference

Pharmacogenetics of oral anticoagulants

21 January 2018

1 reference

The risk of overanticoagulation in patients with cytochrome P450 CYP2C9*2 or CYP2C9*3 alleles on acenocoumarol or phenprocoumon

21 January 2018

1 reference

Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

21 January 2018

1 reference

Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose

21 January 2018

1 reference

Pharmacogenetics of coumarinic oral anticoagulants

21 January 2018

1 reference

Estimation of the warfarin dose with clinical and pharmacogenetic data

21 January 2018

1 reference

Warfarin genotyping reduces hospitalization rates results from the MM-WES (Medco-Mayo Warfarin Effectiveness study).

21 January 2018

1 reference

Prospective evaluation of a pharmacogenetics-guided warfarin loading and maintenance dose regimen for initiation of therapy

21 January 2018

1 reference

Role of warfarin pharmacogenetic testing in clinical practice

21 January 2018

1 reference

Identification of the platelet ADP receptor targeted by antithrombotic drugs

21 January 2018

1 reference

Reduced-function CYP2C19 genotype and risk of adverse clinical outcomes among patients treated with clopidogrel predominantly for PCI: a meta-analysis

21 January 2018

1 reference

2007 Focused Update of the ACC/AHA/SCAI 2005 Guideline Update for Percutaneous Coronary Intervention: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines: 2007 Writing Group to Review New Evide

21 January 2018

1 reference

Genetic susceptibility to ischemic stroke

21 January 2018

1 reference

Tailoring antiplatelet therapy based on pharmacogenomics: how well do the data fit?

21 January 2018

1 reference

Effects of CYP2C19 genotype on outcomes of clopidogrel treatment

21 January 2018

1 reference

Genetic determinants of response to clopidogrel and cardiovascular events

21 January 2018

1 reference

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

21 January 2018

1 reference

Effect of CYP2C19 and ABCB1 single nucleotide polymorphisms on outcomes of treatment with ticagrelor versus clopidogrel for acute coronary syndromes: a genetic substudy of the PLATO trial

21 January 2018

1 reference

Clinical pharmacogenetics and potential application in personalized medicine

21 January 2018

1 reference

Effects of clopidogrel in addition to aspirin in patients with acute coronary syndromes without ST-segment elevation

21 January 2018

1 reference

Effect of clopidogrel added to aspirin in patients with atrial fibrillation

21 January 2018

1 reference

The effect of elinogrel on high platelet reactivity during dual antiplatelet therapy and the relation to CYP2C19*2 genotype: first experience in patients

21 January 2018

1 reference

Clinical application of blood biomarkers in cerebrovascular disease

21 January 2018

1 reference

Relationship of Family History Scores for Stroke and Hypertension to Quantitative Measures of White-Matter Hyperintensities and Stroke Volume in Elderly Males

21 January 2018

1 reference

Letter by Rundek et al Regarding Article, “Prediction of Clinical Cardiovascular Events With Carotid Intima-Media Thickness: A Systematic Review and Meta-Analysis”

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.2217/PGS.12.14

1 reference

26 August 2017

1 reference

PubMed ID

22462751