Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation (Q36464752)

14 August 2017

Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation (English)

1 reference

14 August 2017

1 reference

Julia B Winston

1

1 reference

14 August 2017

Claire E Schulkey

2

1 reference

14 August 2017

Iuan-Bor D Chen

3

1 reference

14 August 2017

Suk D Regmi

4

1 reference

14 August 2017

Maria Efimova

5

1 reference

14 August 2017

Jonathan M Erlich

6

1 reference

14 August 2017

Courtney A Green

7

1 reference

14 August 2017

Ashley Aluko

8

1 reference

14 August 2017

Patrick Y Jay

9

1 reference

14 August 2017

24 April 2012

1 reference

Circulation: Cardiovascular Genetics

14 August 2017

1 reference

14 August 2017

5

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14 August 2017

3

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14 August 2017

293-300

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Genetic factors in non-syndromic congenital heart malformations

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Functional modules, mutational load and human genetic disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Heterogeneity of genetic modifiers ensures normal cardiac development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Missing data analysis using multiple imputation: getting to the heart of the matter

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Genetic origins of pediatric heart disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

The role of secondary heart field in cardiac development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

A histone H3 lysine 36 trimethyltransferase links Nkx2-5 to Wolf-Hirschhorn syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Activation of Tolloid-like 1 gene expression by the cardiac specific homeobox gene Nkx2-5.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Mouse models of congenital cardiovascular disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Can recent insights into cardiac development improve our understanding of congenitally malformed hearts?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

R/qtlDesign: inbred line cross experimental design

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Review: a gentle introduction to imputation of missing values

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Identification and functional analysis of CITED2 mutations in patients with congenital heart defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

The epidemiology of cardiovascular defects, part I: a study based on data from three large registries of congenital malformations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

The combinatorial activities of Nkx2.5 and dHAND are essential for cardiac ventricle formation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

The cardiac homeobox gene Csx/Nkx2.5 lies genetically upstream of multiple genes essential for heart development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Congenital heart disease caused by mutations in the transcription factor NKX2-5

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Multifactorial inheritance hypothesis for the etiology of congenital heart diseases. The genetic-environmental interaction

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Parental age as a risk factor for isolated congenital malformations in a Polish population.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Maternal age and birth defects: a population study

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Maternal age-specific risk of non-chromosomal anomalies

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Descriptive epidemiology of selected congenital heart defects, Hawaii, 1986-1999.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Maternal age and non-chromosomal birth defects, Atlanta--1968-2000: teenager or thirty-something, who is at risk?

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

NKX2.5mutations in patients with congenital heart disease

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

The mammalian Tolloid-like 1 gene, Tll1, is necessary for normal septation and positioning of the heart.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Formation of the atrioventricular septal structures in the normal mouse.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

The incidence of congenital heart defects in the first year of life

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3521568

Maternal age and prevalence of isolated congenital heart defects in an urban area of the United States

21 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22534315

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Maternal age and malformations in singleton births

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22534315

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The spectrum of cardiovascular anomalies in CHF1/Hey2 deficient mice reveals roles in endocardial cushion, myocardial and vascular maturation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22534315

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1161/CIRCGENETICS.111.961136

1 reference

14 August 2017

1 reference

14 August 2017

PubMed publication ID

22534315

1 reference