(Q34032512)

30 July 2017

1 reference

title

The genetics of white matter lesions (English)

1 reference

30 July 2017

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

John B Kwok

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

Perminder Sachdev

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

author name string

Arezoo Assareh

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

Karen A Mather

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

publication date

7 July 2010

1 reference

21951372

CNS Neuroscience & Therapeutics

30 July 2017

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

volume

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

page(s)

525-540

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

Periventricular lesions in the white matter on magnetic resonance imaging in the elderly. A morphometric correlation with arteriolosclerosis and dilated perivascular spaces.

14 May 2020

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Decline in intelligence is associated with progression in white matter hyperintensity volume

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Should we distinguish between periventricular and deep white matter hyperintensities?

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Silent brain infarcts and white matter lesions increase stroke risk in the general population: the Rotterdam Scan Study

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

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Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume

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

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Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis

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CADASIL: hereditary arteriopathy leading to multiple brain infarcts and dementia

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

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Stroke genomics: approaches to identify, validate, and understand ischemic stroke gene expression

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CADASIL: what component of the vessel wall is really a target for Notch 3 gene mutations?

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Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy: MR Imaging Findings at Different Ages—3rd–6th Decades

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

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Brain MRI white matter lesions in migraine patients: is there a relationship with antiphospholipid antibodies and coagulation parameters?

21 January 2018

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High molecular weight complex in human plasma between vitamin K-dependent protein S and complement component C4b-binding protein

21 January 2018

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Isolation of a protein Z-dependent plasma protease inhibitor

21 January 2018

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Frequency of protein Z deficiency in patients with ischaemic stroke.

21 January 2018

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Progressive cerebral vascular degeneration with mitochondrial encephalopathy.

21 January 2018

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The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct.

21 January 2018

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CT, MRI, and autopsy findings in brain of a patient with MELAS.

21 January 2018

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Serial brain imaging analysis of stroke-like episodes in MELAS.

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Selective arterial distribution of cerebral hyperperfusion in Fabry disease

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21 January 2018

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Magnetic resonance imaging changes in Fabry disease.

21 January 2018

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Voxel based analyses of diffusion tensor imaging in Fabry disease.

21 January 2018

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Quantitative analysis of cerebral vasculopathy in patients with Fabry disease

21 January 2018

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Cerebrovascular complications of Fabry's disease

21 January 2018

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Effect of genetic modifiers on cerebral lesions in Fabry disease.

21 January 2018

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Genome-wide scan for white matter hyperintensity: the Framingham Heart Study.

21 January 2018

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Apolipoprotein E, angiotensin-converting enzyme and kallikrein gene polymorphisms and the risk of Alzheimer's disease and vascular dementia.

21 January 2018

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

21 January 2018

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

21 January 2018

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The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

21 January 2018

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Finding the missing heritability of complex diseases

21 January 2018

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Interaction between hypertension, apoE, and cerebral white matter lesions

21 January 2018

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Imaging genetics of brain longevity and mental wellness: the next frontier?

21 January 2018

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Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

21 January 2018

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Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium

21 January 2018

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Apolipoprotein E and Alzheimer's disease: molecular mechanisms and therapeutic opportunities.

21 January 2018

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Apolipoprotein E genotype and cardiovascular disease in the Framingham Heart Study

21 January 2018

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Periventricular white matter hyperintensities increase the likelihood of progression from amnestic mild cognitive impairment to dementia

21 January 2018

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Impact of apolipoprotein E epsilon4 and vascular disease on brain morphology in men from the NHLBI twin study

21 January 2018

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Relationship of deep white matter hyperintensities and apolipoprotein E genotype to depressive symptoms in older adults without clinical depression.

21 January 2018

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Role of white matter lesions, cerebral atrophy, and APOE on cognition in older persons with and without dementia: the Cache County, Utah, study of memory and aging

21 January 2018

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Cerebral white matter lesions are not associated with apoE genotype but with age and female sex in Alzheimer's disease.

21 January 2018

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Apolipoprotein E polymorphism and silent microangiopathy-related cerebral damage. Results of the Austrian Stroke Prevention Study.

21 January 2018

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Association of apolipoprotein E epsilon2 with white matter disease but not with microbleeds.

21 January 2018

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Genetics of the human renin angiotensin system

21 January 2018

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The role of the brain renin-angiotensin system in neurodegenerative disorders

21 January 2018

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Angiotensinogen variants and human hypertension

21 January 2018

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M235T angiotensinogen gene polymorphism and cardiovascular renal risk.

21 January 2018

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Enhanced predictability of myocardial infarction in Japanese by combined genotype analysis

21 January 2018

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Angiotensinogen M235T polymorphism is associated with plasma angiotensinogen and cardiovascular disease.

21 January 2018

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Polymorphisms of the renin-angiotensin system are associated with blood pressure, atherosclerosis and cerebral white matter pathology

21 January 2018

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Evolution of white matter lesions

21 January 2018

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Renin-angiotensin system genetic polymorphisms and cerebral white matter lesions in essential hypertension.

21 January 2018

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Isolation of a cDNA encoding the vascular type-1 angiotensin II receptor

21 January 2018

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Are genetic factors important in the aetiology of leukoaraiosis? Results from a memory clinic population

21 January 2018

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Evaluation of the roles of common genetic mutations in leukoaraiosis

21 January 2018

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Polymorphism of angiotensin converting enzyme, angiotensinogen, and apolipoprotein E genes in a Japanese population with cerebrovascular disease.

21 January 2018

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Specific APO E genotypes in combination with the ACE D/D or MTHFR 677TT mutation yield an independent genetic risk of leukoaraiosis

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Correlation between left ventricular mass and urinary sodium excretion in specific genotypes of CYP11B2.

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Haplotype analysis of aldosterone synthase gene (CYP11B2) polymorphisms shows association with essential hypertension

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Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensities.

21 January 2018

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Biological and clinical implications of the MTHFR C677T polymorphism

21 January 2018

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Homocysteine and the brain in midadult life: evidence for an increased risk of leukoaraiosis in men.

21 January 2018

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Evaluation of genetic risk factors for silent brain infarction

21 January 2018

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MTHFR Gene Polymorphism as a Risk Factor for Silent Brain Infarcts and White Matter Lesions in the Japanese General Population

21 January 2018

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Association of genetic variants of methionine metabolism with methotrexate-induced CNS white matter changes in patients with primary CNS lymphoma

21 January 2018

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Influence of the MTHFR C677T polymorphism on magnetic resonance imaging hyperintensity volume and cognition in geriatric depression

21 January 2018

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White matter activated glial cells produce BDNF in a stroke model of monkeys.

21 January 2018

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The human BDNF gene maps between FSHB and HVBS1 at the boundary of 11p13-p14.

21 January 2018

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The brain-derived neurotrophic factor VAL66MET polymorphism and cerebral white matter hyperintensities in late-life depression

21 January 2018

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BDNF Val66Met polymorphism influences age differences in microstructure of the Corpus Callosum.

21 January 2018

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p66(Shc): at the crossroad of oxidative stress and the genetics of aging

21 January 2018

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Cloning, purification, and refolding of human paraoxonase-3 expressed in Escherichia coli and its characterization

21 January 2018

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Human paraoxonases (PON1, PON2, and PON3) are lactonases with overlapping and distinct substrate specificities

21 January 2018

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Paraoxonase PON1 polymorphism leu-Met54 is associated with carotid atherosclerosis: results of the Austrian Stroke Prevention Study.

21 January 2018

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Paraoxonase 1 gene polymorphisms in patients with osteonecrosis of the femoral head with and without cerebral white matter lesions.

21 January 2018

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Increased frequency of white matter lesions in patients with osteonecrosis (WMLeOn) of the femoral head

21 January 2018

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Isolation and chromosomal localization of the human endothelial nitric oxide synthase (NOS3) gene

21 January 2018

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Intracellular processing of endothelial nitric oxide synthase isoforms associated with differences in severity of cardiopulmonary diseases: cleavage of proteins with aspartate vs. glutamate at position 298.

21 January 2018

1 reference

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Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease.

21 January 2018

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Prevalence of cerebral white matter lesions in elderly people: a population based magnetic resonance imaging study. The Rotterdam Scan Study

21 January 2018

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Progression of white matter hyperintensities in elderly individuals over 3 years

21 January 2018

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Human CYP11B2 (Aldosterone Synthase) Maps To Chromosome 8q24.3

21 January 2018

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The deletion/insertion polymorphism of the angiotensin converting enzyme gene and cardiovascular-renal risk

21 January 2018

1 reference

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Magnetic Resonance Signal Abnormalities in Asymptomatic Individuals: Their Incidence and Functional Correlates

21 January 2018

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Extent and Distribution of White Matter Hyperintensities in Stroke Patients

21 January 2018

1 reference

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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

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Quantitative study of signal hyperintensities on T2-weighted magnetic resonance imaging in late-onset schizophrenia

21 January 2018

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12 December 2020

Characterization of six novel mutations in the methylenetetrahydrofolate reductase (MTHFR) gene in patients with homocystinuria

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12 December 2020

Relationship between the blood coagulation-fibrinolysis system and the subclinical indicators of arteriosclerosis in a healthy male population

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12 December 2020

Gene polymorphism of the renin-angiotensin system associates with risk for lacunar infarction. The Ohasama study

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12 December 2020

The cognitive correlates of white matter abnormalities in normal aging: a quantitative review

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12 December 2020

MRI cerebral white matter lesions and paraoxonase PON1 polymorphisms : three-year follow-up of the austrian stroke prevention study

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12 December 2020

APO E gene and gene-environment effects on plasma lipoprotein-lipid levels

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12 December 2020

Angiotensinogen gene promoter haplotype and microangiopathy-related cerebral damage: results of the Austrian Stroke Prevention Study

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12 December 2020

Angiotensinogen polymorphism M235T, carotid atherosclerosis, and small-vessel disease-related cerebral abnormalities

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12 December 2020

Silent cerebral infarcts in basal ganglia are advanced in congenital protein C-deficient heterozygotes with hypertension

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12 December 2020

Diagnostic strategies in CADASIL

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12 December 2020

Angiotensinogen gene haplotype and hypertension: interaction with ACE gene I allele

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12 December 2020

Congenital microcephaly in two infants with the factor V Leiden mutation

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12 December 2020

Genetic risk factors associated with thrombosis in children with congenital neurologic disorders

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12 December 2020

AIDS with acute cerebral infarct: a case report

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12 December 2020

Associations of the angiotensin II type 1 receptor A1166C and the endothelial NO synthase G894T gene polymorphisms with silent subcortical white matter lesions in essential hypertension

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12 December 2020

Genetics of cerebral venous thrombosis.

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12 December 2020

[Early diagnostic significance and dynamic pattern of DWI compared with conventional MRI in newborns with neonatal cerebral infarction].

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12 December 2020

Reversible leukoencephalopathy with acute neurological deterioration and permanent residua in classical homocystinuria: A case report

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12 December 2020

Linkage and association: basic concepts

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12 December 2020

The renin-angiotensin-aldosterone system in cerebral small vessel disease

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12 December 2020

Inherited protein C deficiency with acute ischemic stroke in a young adult: a case report

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12 December 2020

Ischaemic stroke patients with heterozygous factor V Leiden present with multiple brain infarctions and widespread atherothrombotic disease

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12 December 2020

Respiratory function decline and DNA mutation in mitochondria, oxidative stress and altered gene expression during aging

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12 December 2020

Two sisters with generalized dystonia associated with homocystinuria

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12 December 2020

Haplotype analysis of CYP11B2

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12 December 2020

Association of angiotensinogen gene T235 variant with increased risk of coronary heart disease

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12 December 2020

[Effect of folic acid for treatment of homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency]

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12 December 2020

Pathologic correlates of incidental MRI white matter signal hyperintensities

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12 December 2020

[An adult case of homocystinuria probably due to methylenetetrahydrofolate-reductase deficiency--treatment with folic acid and the course of coagulation-fibrinolysis parameters]

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12 December 2020

Associations between candidate loci angiotensin-converting enzyme and angiotensinogen with coronary heart disease and myocardial infarction: the NHLBI Family Heart Study

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12 December 2020

Human CYP11B2 (aldosterone synthase) maps to chromosome 8q24.3

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10.1111/J.1755-5949.2010.00181.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6493881&resulttype=core&format=json

14 May 2020

21951372

1 reference