Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation (Q24625036)

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English	Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation	scientific article

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scholarly article

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Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation (English)

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Hakon Hakonarson

11

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Scot J Matkovich

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Scot J Matkovich

2

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Muredach P. Reilly

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Muredach P Reilly

10

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author name string

Thomas P Cappola

1

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Wei Wang

3

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Derek van Booven

4

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Mingyao Li

5

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Xuexia Wang

6

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Liming Qu

7

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Nancy K Sweitzer

8

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James C Fang

9

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Jeanne M Nerbonne

12

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Gerald W Dorn

13

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language of work or name

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publication date

8 February 2011

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Proceedings of the National Academy of Sciences of the United States of America

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108

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6

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2456-61

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Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy

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7 April 2017

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

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7 April 2017

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

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7 April 2017

Barttin modulates trafficking and function of ClC-K channels

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

7 April 2017

A map of human genome variation from population-scale sequencing

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7 April 2017

Heart disease and stroke statistics--2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

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7 April 2017

Transcriptional genomics associates FOX transcription factors with human heart failure

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

7 April 2017

Salt wasting and deafness resulting from mutations in two chloride channels

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

7 April 2017

Barttin increases surface expression and changes current properties of ClC-K channels

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

7 April 2017

Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

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7 April 2017

Rare variants create synthetic genome-wide associations

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7 April 2017

Genotype imputation

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7 April 2017

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

7 April 2017

Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

27 September 2017

Common variants in HSPB7 and FRMD4B associated with advanced heart failure

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

27 September 2017

Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

27 September 2017

Clinical and genetic modifiers of long-term survival in heart failure

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

27 September 2017

Neuregulin-1 beta is associated with disease severity and adverse outcomes in chronic heart failure.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

27 September 2017

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

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27 September 2017

An improved terminology and classification of Bartter-like syndromes

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27 September 2017

A GRK5 polymorphism that inhibits beta-adrenergic receptor signaling is protective in heart failure

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

27 September 2017

Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes

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27 September 2017

HFSA 2006 Comprehensive Heart Failure Practice Guideline.

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27 September 2017

Incidence and epidemiology of heart failure

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27 September 2017

Heart failure in African Americans

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3038744

27 September 2017

No positive association between adrenergic receptor variants of alpha2cDel322-325, beta1Ser49, beta1Arg389 and the risk for heart failure in the Japanese population

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27 September 2017

The severe cardiorenal syndrome: 'Guyton revisited'.

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27 September 2017

Synergistic polymorphisms of beta1- and alpha2C-adrenergic receptors and the risk of congestive heart failure

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27 September 2017

Cardiomyopathy in an adult with Bartter's syndrome and hypokalemia. Hemodynamic, angiographic and metabolic studies

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27 September 2017

Heritability of left ventricular mass: the Framingham Heart Study.

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30 May 2018

Bartter's syndrome: a disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis

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30 May 2018

Association of Parental Heart Failure with Risk of Heart Failure in Offspring

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21 January 2018

Alpha2cDel322-325 and beta1Arg389 adrenergic polymorphisms are not associated with reduced left ventricular ejection fraction or increased left ventricular volume

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21 January 2018

Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

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21 January 2018

Evidence for cardiovascular remodeling in a patient with Bartter's syndrome.

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21 January 2018

A new tubular disorder with hypokalaemic metabolic alkalosis, severe hypermagnesuric hypomagnesaemia, hypercalciuria and cardiomyopathy.

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21 January 2018

Racial differences in the outcome of left ventricular dysfunction

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21 January 2018

Mixed messages: transcription patterns in failing and recovering human myocardium.

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21 January 2018

Salt sensitivity, pulse pressure, and death in normal and hypertensive humans

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Some observations on the pathogenesis of Bartter's syndrome

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium sensitivity and cardiovascular events in patients with essential hypertension

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.1017494108

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2011PNAS..108.2456C

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