Genetic basis of hypertension for the development of tailored medicine (Q37526376)

20 August 2017

Genetic basis of hypertension for the development of tailored medicine (English)

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20 August 2017

3

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20 August 2017

Tomohiro Katsuya

1

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20 August 2017

Ryuichi Morishita

series ordinal

2

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20 August 2017

Toshio Ogihrara

series ordinal

4

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20 August 2017

19 June 2009

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20 August 2017

Hypertension Research

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20 August 2017

32

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20 August 2017

8

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20 August 2017

643-648

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https://scigraph.springernature.com/pub.10.1038/hr.2009.87

20 August 2017

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The causes of essential hypertension

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Heritability of cardiovascular and personality traits in 6,148 Sardinians

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Rare independent mutations in renal salt handling genes contribute to blood pressure variation

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Identification of 108 SNPs in TSC, WNK1, and WNK4 and their association with hypertension in a Japanese general population

21 January 2018

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G2736A polymorphism of thiazide-sensitive Na-Cl cotransporter gene predisposes to hypertension in young women.

21 January 2018

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The thiazide-sensitive Na(+)-Cl(-) cotransporter gene, C1784T, and adrenergic receptor-beta3 gene, T727C, may be gene polymorphisms susceptible to the antihypertensive effect of thiazide diuretics.

21 January 2018

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Molecular variants of the thiazide-sensitive Na+-Cl- cotransporter in hypertensive families

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Hypertension in a patient with Gitelman's syndrome.

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Human hypertension caused by mutations in WNK kinases

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Mechanism of regulation of renal ion transport by WNK kinases

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WNK3 and WNK4 amino-terminal domain defines their effect on the renal Na+-Cl- cotransporter

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From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

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Role of renin-angiotensin system in adipose tissue dysfunction

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Feasibility of treating prehypertension with an angiotensin-receptor blocker

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Metabolic disorders predict development of hypertension in normotensive Japanese subjects

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Hypoadiponectinemia is an independent risk factor for hypertension

21 January 2018

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The molecular sources of reactive oxygen species in hypertension

21 January 2018

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A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis

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Association of methylenetetrahydrofolate reductase gene polymorphism with carotid atherosclerosis depending on smoking status in a Japanese general population

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Beneficial effects of pioglitazone on hypertensive cardiovascular injury are enhanced by combination with candesartan

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Beta2- and beta3-adrenergic receptor polymorphisms are related to the onset of weight gain and blood pressure elevation over 5 years

21 January 2018

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High plasma norepinephrine levels associated with beta2-adrenoceptor polymorphisms predict future renal damage in nonobese normotensive individuals

21 January 2018

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Leptin-receptor polymorphisms relate to obesity through blunted leptin-mediated sympathetic nerve activation in a Caucasian male population

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beta2- and beta3-Adrenoceptor polymorphisms relate to subsequent weight gain and blood pressure elevation in obese normotensive individuals

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Haplotypic analysis of Wellcome Trust Case Control Consortium data

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

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Genetic effect on blood pressure is modulated by age: the Hypertension Genetic Epidemiology Network Study.

21 January 2018

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High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project

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Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

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T-cadherin is a receptor for hexameric and high-molecular-weight forms of Acrp30/adiponectin

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DNA methylation markers and early recurrence in stage I lung cancer

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Genomewide association analysis of coronary artery disease

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Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure

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Genome-wide association study identifies eight loci associated with blood pressure

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Genome-wide association study of blood pressure and hypertension

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Genotyping the future: scientists' expectations about race/ ethnicity after BiDil

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Hypertension and ethnic group

21 January 2018

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Diuretic therapy, the alpha-adducin gene variant, and the risk of myocardial infarction or stroke in persons with treated hypertension

21 January 2018

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

21 January 2018

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beta-adrenergic receptor gene polymorphisms and beta-blocker treatment outcomes in hypertension

21 January 2018

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Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic

21 January 2018

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Pharmacogenomics of antihypertensive drugs: rationale and design of the Pharmacogenomic Evaluation of Antihypertensive Responses (PEAR) study

21 January 2018

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

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7 January 2021

T+31C polymorphism of angiotensinogen gene and nocturnal blood pressure decline: the Ohasama study

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7 January 2021

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

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7 January 2021

High-resolution mapping for essential hypertension using microsatellite markers

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7 January 2021

Sex-specific effects of AGT-6 and ACE I/D on pulse pressure after 6 months on antihypertensive treatment: the GenHAT study

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7 January 2021

Progress report on The Hypertension Objective Treatment Based on Measurement by Electrical Devices of Blood Pressure (HOMED-BP) study: status at February 2004

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7 January 2021

Identifiers

DOI

10.1038/HR.2009.87

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Dimensions Publication ID

20 August 2017

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