Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships (Q33689539)

28 July 2017

title

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

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28 July 2017

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7

Eric Boerwinkle

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Thomas H Mosley

series ordinal

4

object named as

Thomas H Mosley

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28 July 2017

5

David S Knopman

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28 July 2017

6

Sharon L R Kardia

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28 July 2017

2

Myriam Fornage

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28 July 2017

3

Clifford R Jack

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28 July 2017

8

Mariza de Andrade

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28 July 2017

Stephen T Turner

1

1 reference

28 July 2017

publication date

1 July 2009

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28 July 2017

published in

Archives of Neurology

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28 July 2017

volume

66

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28 July 2017

issue

7

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28 July 2017

page(s)

847-857

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Normalizing a large number of quantitative traits using empirical normal quantile transformation

28 July 2017

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Less atherosclerosis and lower blood pressure for a meaningful life perspective with more brain

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Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels

21 June 2018

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21 June 2018

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Association of 3'-UTR polymorphisms of the oxidised LDL receptor 1 (OLR1) gene with Alzheimer's disease

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Germ-line mutations in nonsyndromic pheochromocytoma

21 June 2018

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Age at onset in two common neurodegenerative diseases is genetically controlled

21 June 2018

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Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy

21 June 2018

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FLAIR histogram segmentation for measurement of leukoaraiosis volume

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 June 2018

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Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study

21 June 2018

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An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing

21 June 2018

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Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorder

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome.

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Brain structure in men remains highly heritable in the seventh and eighth decades of life

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Evidence of linkage of familial hypoalphalipoproteinemia to a novel locus on chromosome 11q23.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Ataxia and abnormal cerebellar microorganization in mice with ablated contactin gene expression

21 June 2018

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Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum

21 June 2018

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Midlife cardiovascular risk factors and brain morphology in identical older male twins

21 June 2018

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Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

21 June 2018

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An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

21 June 2018

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The P-selectin gene is highly polymorphic: reduced frequency of the Pro715 allele carriers in patients with myocardial infarction

21 June 2018

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 June 2018

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Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes

21 June 2018

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Pathogenesis of leukoaraiosis: a review

21 June 2018

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Quantitative genetics of dehydroepiandrosterone sulfate and its relation to possible cardiovascular disease risk factors in Mexican Americans

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Progression of coronary atherosclerosis is associated with a common genetic variant of the human stromelysin-1 promoter which results in reduced gene expression

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

A-IMilano apoprotein. Decreased high density lipoprotein cholesterol levels with significant lipoprotein modifications and without clinical atherosclerosis in an Italian family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Apolipoprotein C-III(Lys58----Glu). Identification of an apolipoprotein C-III variant in a family with hyperalphalipoproteinemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Analysis of the gene sequences of the insulin receptor and the insulin-sensitive glucose transporter (GLUT-4) in patients with common-type non-insulin-dependent diabetes mellitus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Frequency of LRRK2 mutations in early- and late-onset Parkinson disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Genome-wide linkage analysis for loci affecting pulse pressure: the Family Blood Pressure Program

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Control of platelet activation by cyclic AMP turnover and cyclic nucleotide phosphodiesterase type-3.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

CYP2D6 polymorphism, pesticide exposure, and Parkinson's disease

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Oxidized LDL receptor gene (OLR1) is associated with the risk of myocardial infarction.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Microsatellite polymorphism in promoter of heme oxygenase-1 gene is associated with susceptibility to coronary artery disease in type 2 diabetic patients

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Association between the PPARA L162V polymorphism and plasma lipid levels: the Framingham Offspring Study

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Multi-center genetic study of hypertension: The Family Blood Pressure Program (FBPP).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Cardiovascular risk assessment using pulse pressure in the first national health and nutrition examination survey (NHANES I).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Relationships of cerebral MRI findings to ultrasonographic carotid atherosclerosis in older adults : the Cardiovascular Health Study. CHS Collaborative Research Group

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Significance levels in complex inheritance

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Assessing linkage on chromosome 5 using components of variance approach: Univariate versus multivariate

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

A susceptibility gene for late-onset idiopathic Parkinson's disease

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2828902

Association found between the promoter region polymorphism in the apolipoprotein A-V gene and the serum triglyceride level in Japanese schoolchildren

30 October 2018

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12 December 2020

E-selectin polymorphism and atherosclerosis: an association study

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12 December 2020

Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?

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12 December 2020

Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12p

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12 December 2020

Extensions to pedigree analysis. IV. Covariance components models for multivariate traits

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12 December 2020

Comparison of Multivariate Tests for Genetic Linkage

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12 December 2020

A comparison of univariate and multivariate tests for genetic linkage

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12 December 2020

10.1001/ARCHNEUROL.2009.110

Identifiers

DOI

1 reference

release_fl5jkztquva7pe5ga5b3hr3bzq

28 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fl5jkztquva7pe5ga5b3hr3bzq

24 November 2022

mapped directly with Wikidata item

PMC publication ID

2828902

1 reference

28 July 2017

1 reference