(Q37436202)

English

Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations

scientific article published on 09 February 2009

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scholarly article

1 reference

Europe PubMed Central

20 August 2017

Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations (English)

1 reference

Europe PubMed Central

20 August 2017

0 references

Eric Boerwinkle

9

object named as

Eric Boerwinkle

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12

object named as

Josef Coresh

1 reference

Europe PubMed Central

20 August 2017

David S Siscovick

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object named as

David S Siscovick

1 reference

Europe PubMed Central

20 August 2017

10

object named as

Bruce M Psaty

1 reference

Europe PubMed Central

20 August 2017

3

object named as

Wendy Post

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Europe PubMed Central

20 August 2017

author name string

W H Linda Kao

1

1 reference

Europe PubMed Central

20 August 2017

Dan E Arking

2

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Europe PubMed Central

20 August 2017

Thomas D Rea

4

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Europe PubMed Central

20 August 2017

Nona Sotoodehnia

5

1 reference

Europe PubMed Central

20 August 2017

Ronald J Prineas

6

1 reference

Europe PubMed Central

20 August 2017

Bryan Bishe

7

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Europe PubMed Central

20 August 2017

Betty Q Doan

8

1 reference

Europe PubMed Central

20 August 2017

Gordon F Tomaselli

11

1 reference

Europe PubMed Central

20 August 2017

Eduardo Marbán

14

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Europe PubMed Central

20 August 2017

Peter M Spooner

15

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Europe PubMed Central

20 August 2017

Gregory L Burke

16

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Europe PubMed Central

20 August 2017

Aravinda Chakravarti

17

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Europe PubMed Central

20 August 2017

language of work or name

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publication date

9 February 2009

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Europe PubMed Central

20 August 2017

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Europe PubMed Central

20 August 2017

119

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Europe PubMed Central

20 August 2017

7

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20 August 2017

940-951

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Europe PubMed Central

20 August 2017

CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Association of NOS1AP genetic variants with QT interval duration in families from the Diabetes Heart Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Emerging paradigms of the epidemiology and demographics of sudden cardiac arrest

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

A haplotype map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Efficiency and power in genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Current burden of sudden cardiac death: multiple source surveillance versus retrospective death certificate-based review in a large U.S. community

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Genomics in sudden cardiac death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Sudden cardiac death in the United States, 1989 to 1998.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Estimation of failure probabilities in the presence of competing risks: new representations of old estimators

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

Family history as a risk factor for primary cardiac arrest

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

The Cardiovascular Health Study: design and rationale

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

23 August 2017

QT interval is a heritable quantitative trait with evidence of linkage to chromosome 3 in a genome-wide linkage analysis: The Framingham Heart Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

14 September 2017

Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

14 September 2017

Methods of assessing prevalent cardiovascular disease in the Cardiovascular Health Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

28 September 2017

Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

2 September 2018

Common variation in NOS1AP and KCNH2 genes and QT interval duration in young adults. The Cardiovascular Risk in Young Finns Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

2 September 2018

Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

2 September 2018

Prolonged QTc interval and risk of sudden cardiac death in a population of older adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

2 September 2018

Prolonged QTc interval and high B-type natriuretic peptide levels together predict mortality in patients with advanced heart failure.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

2 September 2018

Sample-size formula for the proportional-hazards regression model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

2 September 2018

Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782762

3 December 2018

Linkage disequilibrium structure and its impact on the localization of a candidate functional mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19204306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of cerebrovascular disease in the Cardiovascular Health Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19204306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surveillance and ascertainment of cardiovascular events. The Cardiovascular Health Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19204306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Novacode criteria for classification of ECG abnormalities and their clinically significant progression and regression

1 reference

https://pubmed.ncbi.nlm.nih.gov/19204306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting sudden death in the population: the Paris Prospective Study I

1 reference

https://pubmed.ncbi.nlm.nih.gov/19204306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beta2-adrenergic receptor genetic variants and risk of sudden cardiac death

1 reference

https://pubmed.ncbi.nlm.nih.gov/19204306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events

1 reference

https://pubmed.ncbi.nlm.nih.gov/19204306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1161/CIRCULATIONAHA.108.791723

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

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