(Q37311436)

19 August 2017

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title

Genetic determinants of hypertension: an update (English)

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19 August 2017

main subject

arterial hypertension

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author name string

Michael Harrison

series ordinal

1

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19 August 2017

Karen Maresso

series ordinal

2

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19 August 2017

Ulrich Broeckel

series ordinal

3

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19 August 2017

publication date

1 December 2008

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Current Hypertension Reports

19 August 2017

published in

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19 August 2017

volume

10

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19 August 2017

issue

6

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19 August 2017

page(s)

488-495

1 reference

https://scigraph.springernature.com/pub.10.1007/s11906-008-0091-1

19 August 2017

exact match

0 references

cites work

Familial correlation and heritability for cardiovascular risk factors

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11906-008-0091-1

Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase

21 January 2018

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12 December 2020

Masked hypertension definition, impact, outcomes: a critical review

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12 December 2020

Worldwide prevalence of hypertension: a systematic review

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12 December 2020

Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness

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12 December 2020

Liddle disease caused by a missense mutation of beta subunit of the epithelial sodium channel gene

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12 December 2020

Role of Genetic Factors in Susceptibility to Experimental Hypertension due to Chronic Excess Salt Ingestion

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12 December 2020

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

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12 December 2020

Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population

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Elevated systolic blood pressure as a cardiovascular risk factor

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12 December 2020

The genetic dissection of essential hypertension

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12 December 2020

Identification of hypertension-susceptibility genes and pathways by a systemic multiple candidate gene approach: the millennium genome project for hypertension

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12 December 2020

A de novo missense mutation of the beta subunit of the epithelial sodium channel causes hypertension and Liddle syndrome, identifying a proline-rich segment critical for regulation of channel activity

1 reference

12 December 2020

Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program

1 reference

12 December 2020

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

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12 December 2020

Familial resemblance for resting blood pressure with particular reference to racial differences: preliminary analyses from the HERITAGE Family Study

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12 December 2020

The complete genome of an individual by massively parallel DNA sequencing

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12 December 2020

Functional genomics in hypertension

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12 December 2020

Further observations of the development of a strain of spontaneously hypertensive rats

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12 December 2020

Polymorphisms of ACE2 gene are associated with essential hypertension and antihypertensive effects of Captopril in women

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Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase

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Genetic analysis of inherited hypertension in the rat.

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Trends in prevalence, awareness, treatment, and control of hypertension in the United States, 1988-2000.

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High-resolution mapping for essential hypertension using microsatellite markers

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Mapping determinants of human gene expression by regional and genome-wide association

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12 December 2020

Multiple blood pressure loci on rat chromosome 13 attenuate development of hypertension in the Dahl S hypertensive rat.

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12 December 2020

Pharmacogenetic association of the NPPA T2238C genetic variant with cardiovascular disease outcomes in patients with hypertension

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Familial correlations, cohabitation effects, and heritability for cardiovascular risk factors.

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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Interactions between the adducin 2 gene and antihypertensive drug therapies in determining blood pressure in people with hypertension

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Angiotensin-converting enzyme gene polymorphism predicts the time-course of blood pressure response to angiotensin converting enzyme inhibition in the AASK trial

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A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism

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White-coat hypertension in adults

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12 December 2020

Broad and narrow heritabilities of quantitative traits in a founder population

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12 December 2020

Genetic dissection of a blood pressure quantitative trait locus on rat chromosome 1 and gene expression analysis identifies SPON1 as a novel candidate hypertension gene.

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12 December 2020

Cross-talk of expression quantitative trait loci within 2 interacting blood pressure quantitative trait loci.

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12 December 2020

Linkage mapping for hypertension susceptibility genes

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12 December 2020

High-density rat radiation hybrid maps containing over 24,000 SSLPs, genes, and ESTs provide a direct link to the rat genome sequence.

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Use of a panel of congenic strains to evaluate differentially expressed genes as candidate genes for blood pressure quantitative trait loci

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12 December 2020

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

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Brown Norway chromosome 13 confers protection from high salt to consomic Dahl S rat.

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12 December 2020

The clinical significance of white-coat and masked hypertension

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Candidate Genes That Determine Response to Salt in the Stroke-Prone Spontaneously Hypertensive Rat

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A high-density integrated genetic linkage and radiation hybrid map of the laboratory rat.

1 reference

12 December 2020

10.1007/S11906-008-0091-1

Identifiers

DOI

1 reference

19 August 2017

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