(Q35202339)

7 August 2017

title

Progress and future aspects in genetics of human hypertension (English)

1 reference

7 August 2017

2

Tanika N Kelly

1 reference

7 August 2017

Qi Zhao

1

1 reference

7 August 2017

Changwei Li

series ordinal

3

1 reference

7 August 2017

Jiang He

series ordinal

4

1 reference

7 August 2017

language of work or name

1 reference

1 December 2013

1 reference

Current Hypertension Reports

7 August 2017

published in

1 reference

7 August 2017

volume

15

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7 August 2017

issue

6

1 reference

7 August 2017

page(s)

676-686

1 reference

Finding the sources of missing heritability in a yeast cross

7 August 2017

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Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase

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13 July 2018

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13 July 2018

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13 July 2018

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13 July 2018

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Cardiovascular epigenetics: basic concepts and results from animal and human studies

13 July 2018

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Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program

13 July 2018

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13 July 2018

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Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension

13 July 2018

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13 July 2018

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13 July 2018

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Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations

13 July 2018

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

13 July 2018

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Genome-wide association study of blood pressure and hypertension

13 July 2018

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Genetics of hypertensive syndrome

13 July 2018

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

13 July 2018

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

13 July 2018

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13 July 2018

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13 July 2018

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Ethnic differences in cardiovascular drug response: potential contribution of pharmacogenetics

13 July 2018

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

13 July 2018

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

13 July 2018

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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

13 July 2018

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

13 July 2018

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

13 July 2018

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13 July 2018

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Genomewide association analysis of coronary artery disease

13 July 2018

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

13 July 2018

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Heritability of blood pressure responses to dietary sodium and potassium intake in a Chinese population

13 July 2018

1 reference

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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

13 July 2018

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A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

13 July 2018

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Heritability of blood pressure traits and the genetic contribution to blood pressure variance explained by four blood-pressure-related genes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4368442

Monogenic forms of low-renin hypertension

13 July 2018

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Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data

13 July 2018

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Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

13 July 2018

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Genetic determinants of blood pressure regulation

13 July 2018

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Mendelian forms of human hypertension and mechanisms of disease

13 July 2018

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Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

13 July 2018

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Global burden of hypertension: analysis of worldwide data

13 July 2018

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

13 July 2018

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Beta 1-adrenergic receptor polymorphisms and antihypertensive response to metoprolol

13 July 2018

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13 July 2018

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Heritability of blood pressure in Nigerian families

13 July 2018

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Monogenic forms of human hypertension

13 July 2018

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13 July 2018

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Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

13 July 2018

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QTL influencing blood pressure maps to the region of PPH1 on chromosome 2q31-34 in Old Order Amish

13 July 2018

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Maximum-likelihood generalized heritability estimate for blood pressure in Nigerian families

13 July 2018

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Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome.

13 July 2018

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Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

13 July 2018

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Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

13 July 2018

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Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

13 July 2018

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Molecular genetics of human blood pressure variation

13 July 2018

1 reference

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Disorders of aldosterone biosynthesis and action

13 July 2018

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Heritability of conventional and ambulatory blood pressures. A study in twins

13 July 2018

1 reference

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Evidence that a single gene with gender- and age-dependent effects influences systolic blood pressure determination in a population-based sample

13 July 2018

1 reference

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National, regional, and global trends in systolic blood pressure since 1980: systematic analysis of health examination surveys and epidemiological studies with 786 country-years and 5·4 million participants

13 July 2018

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Different inactivating mutations of the mineralocorticoid receptor in fourteen families affected by type I pseudohypoaldosteronism

21 January 2018

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Heritability of daytime ambulatory blood pressure in an extended twin design

21 January 2018

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High heritability of ambulatory blood pressure in families of East African descent

21 January 2018

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Meta-analysis of genome-wide scans for blood pressure in African American and Nigerian samples. The National Heart, Lung, and Blood Institute GeneLink Project

21 January 2018

1 reference

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A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany.

21 January 2018

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A navigator for human genome epidemiology.

21 January 2018

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Reevaluation of the association of seven candidate genes with blood pressure and hypertension: a replication study and meta-analysis with a larger sample size

21 January 2018

1 reference

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A genome-wide association study of hypertension-related phenotypes in a Japanese population

21 January 2018

1 reference

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A meta-analysis of association between C677T polymorphism in the methylenetetrahydrofolate reductase gene and hypertension.

21 January 2018

1 reference

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Comparing methods for performing trans-ethnic meta-analysis of genome-wide association studies

21 January 2018

1 reference

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Transethnic meta-analysis of genomewide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-013-0388-6

Epigenetic control of 11 beta-hydroxysteroid dehydrogenase 2 gene promoter is related to human hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-013-0388-6

Catecholamine release-inhibitory peptide catestatin (chromogranin A(352-372)): naturally occurring amino acid variant Gly364Ser causes profound changes in human autonomic activity and alters risk for hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-013-0388-6

Prediction of blood pressure changes over time and incidence of hypertension by a genetic risk score in Swedes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-013-0388-6

beta1-Adrenergic receptor polymorphisms influence the response to metoprolol monotherapy in patients with essential hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-013-0388-6

Global DNA methylation changes in blood of patients with essential hypertension.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4368442

Heritability and stability of resting blood pressure in Australian twins.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4368442

Heritability and stability of resting blood pressure.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4368442

Segregation analysis reveals a major gene effect controlling systolic blood pressure and BMI in an Israeli population.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4368442

Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3

26 September 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-013-0388-6

Use of genome-wide association studies for drug repositioning

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-013-0388-6

Physiological Interaction Between α-Adducin and WNK1-NEDD4L Pathways on Sodium-Related Blood Pressure Regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11906-013-0388-6

Evidence for genetic heterogeneity of pseudohypoaldosteronism type 1: identification of a novel mutation in the human mineralocorticoid receptor in one sporadic case and no mutations in two autosomal dominant kindreds

21 January 2018

1 reference

12 December 2020

Blood pressure QTLs identified by genome-wide linkage analysis and dependence on associated phenotypes

1 reference

12 December 2020

Where are all the blood-pressure genes?

1 reference

12 December 2020

Heritability of ambulatory and office blood pressure phenotypes in Swedish families

1 reference

12 December 2020

Genome scan for hypertension in nonobese African Americans: the National Heart, Lung, and Blood Institute Family Blood Pressure Program

1 reference

12 December 2020

Elevated Plasma Membrane and Sarcoplasmic Reticulum Ca2+Pump mRNA Levels in Cultured Aortic Smooth Muscle Cells from Spontaneously Hypertensive Rats

1 reference

12 December 2020

10.1007/S11906-013-0388-6

Identifiers

DOI

1 reference

7 August 2017

1 reference

7 August 2017

1 reference