Genetics of congenital heart disease: the glass half empty (Q26862793)

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B. D. Gelb

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15 February 2013

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112

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issue

4

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page(s)

707-20

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Evolution and development of the building plan of the vertebrate heart

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Endocardial and epicardial epithelial to mesenchymal transitions in heart development and disease

21 March 2017

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Coordinating tissue interactions: Notch signaling in cardiac development and disease

21 March 2017

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Transcription factor genes Smad4 and Gata4 cooperatively regulate cardiac valve development. [corrected]

21 March 2017

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Integration of a Notch-dependent mesenchymal gene program and Bmp2-driven cell invasiveness regulates murine cardiac valve formation.

21 March 2017

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New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle

21 March 2017

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Haploinsufficiency of TAB2 causes congenital heart defects in humans

21 March 2017

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Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis

21 March 2017

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Characterization and in vivo pharmacological rescue of a Wnt2-Gata6 pathway required for cardiac inflow tract development

21 March 2017

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Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

21 March 2017

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A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects

21 March 2017

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Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

21 March 2017

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Targeted deletion of Dicer in the heart leads to dilated cardiomyopathy and heart failure

21 March 2017

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α-cardiac actin mutations produce atrial septal defects

21 March 2017

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Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy

21 March 2017

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Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

21 March 2017

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NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway

21 March 2017

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Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

21 March 2017

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Mutations in NOTCH1 cause aortic valve disease

21 March 2017

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Mutation in myosin heavy chain 6 causes atrial septal defect

21 March 2017

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Common arterial trunk associated with a homeodomain mutation of NKX2.6

21 March 2017

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Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

21 March 2017

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Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects

21 March 2017

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Role of TBX1 in human del22q11.2 syndrome

21 March 2017

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GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

21 March 2017

1 reference

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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

21 March 2017

1 reference

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Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

21 March 2017

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Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations

21 March 2017

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Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development.

21 March 2017

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

21 March 2017

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Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

21 March 2017

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Mutations in the human Jagged1 gene are responsible for Alagille syndrome

21 March 2017

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Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

21 March 2017

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Gene regulatory networks in cardiac conduction system development

21 March 2017

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Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis

21 March 2017

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Establishment of vertebrate left-right asymmetry

21 March 2017

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Conserved and divergent mechanisms in left-right axis formation

21 March 2017

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Endothelial deletion of murine Jag1 leads to valve calcification and congenital heart defects associated with Alagille syndrome

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

α-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Dysregulation of cardiogenesis, cardiac conduction, and cell cycle in mice lacking miRNA-1-2

21 March 2017

1 reference

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Chromosome 21 and down syndrome: from genomics to pathophysiology

21 March 2017

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Modulation of morphogenesis by noncanonical Wnt signaling requires ATF/CREB family-mediated transcriptional activation of TGFbeta2

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Rescue of cardiac alpha-actin-deficient mice by enteric smooth muscle gamma-actin

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Nodal is a novel TGF-beta-like gene expressed in the mouse node during gastrulation

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Heart defects in X-linked heterotaxy: evidence for a genetic interaction of Zic3 with the nodal signaling pathway

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Smooth-muscle contraction without smooth-muscle myosin

21 March 2017

1 reference

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Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1

21 March 2017

1 reference

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Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

21 March 2017

1 reference

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Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis

7 April 2017

1 reference

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A copy number variation morbidity map of developmental delay

7 April 2017

1 reference

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Building the mammalian heart from two sources of myocardial cells

7 April 2017

1 reference

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The Congenital Heart Disease Genetic Network Study: rationale, design, and early results

7 April 2017

1 reference

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Phenotypic heterogeneity of genomic disorders and rare copy-number variants

28 September 2017

1 reference

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Rare copy number variants contribute to congenital left-sided heart disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Burden of Congenital Rubella Syndrome (CRS) in India: a systematic review

28 September 2017

1 reference

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Iroquois homeodomain transcription factors in heart development and function.

28 September 2017

1 reference

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NPHP4 variants are associated with pleiotropic heart malformations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

A new level of complexity: the role of microRNAs in cardiovascular development.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Tbx1 regulates oral epithelial adhesion and palatal development.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Human gene copy number spectra analysis in congenital heart malformations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Histone H3 phosphorylation, immediate-early gene expression, and the nucleosomal response: a historical perspective

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Notch activation of Jagged1 contributes to the assembly of the arterial wall.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Identification of dysfunctional modules and disease genes in congenital heart disease by a network-based approach

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Histone deacetylase 3 regulates smooth muscle differentiation in neural crest cells and development of the cardiac outflow tract

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Systems biology approaches to heart development and congenital heart disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Epigenetic regulation of cardiovascular differentiation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Chromatin remodeling in cardiovascular development and physiology

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Myocardial lineage development

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Birth defects among a cohort of infants born to HIV-infected women on antiretroviral medication

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Mortality resulting from congenital heart disease among children and adults in the United States, 1999 to 2006

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

The changing epidemiology of congenital heart disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Noonan syndrome: clinical features, diagnosis, and management guidelines

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

How to make a heart: the origin and regulation of cardiac progenitor cells

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Dissecting spatio-temporal protein networks driving human heart development and related disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Consanguinity mapping of congenital heart disease in a South Indian population

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Application of gene network analysis techniques identifies AXIN1/PDIA2 and endoglin haplotypes associated with bicuspid aortic valve

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Williams-Beuren syndrome.

28 September 2017

1 reference

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Overview of developmental heart defects by dioxins, PCBs, and pesticides

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Functional variant in microRNA-196a2 contributes to the susceptibility of congenital heart disease in a Chinese population

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Importance of gene-environment interactions in the etiology of selected birth defects.

28 September 2017

1 reference

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28 September 2017

Turner syndrome 2008.

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Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Prevalence of congenital heart defects in metropolitan Atlanta, 1998-2005.

28 September 2017

1 reference

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NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Taking microRNAs to heart

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene

28 September 2017

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Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia

28 September 2017

1 reference

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Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Making or breaking the heart: from lineage determination to morphogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

DiGeorge syndrome: new insights

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

CONCOR, an initiative towards a national registry and DNA-bank of patients with congenital heart disease in the Netherlands: rationale, design, and first results

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

T-box genes in early embryogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Cardiovascular malformations in infants of diabetic mothers

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Finding genetic contributions to sporadic disease: a recessive locus at 12q24 commonly contributes to patent ductus arteriosus

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Left-right asymmetry determination in vertebrates

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Elastin: mutational spectrum in supravalvular aortic stenosis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Mutations in MKKS cause Bardet-Biedl syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Congenital heart disease in adults. First of two parts

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Congenital heart disease at a tertiary care center in Lebanon.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Incidence of congenital heart disease: II. Prenatal incidence

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Evolutionary origin of cardiac malformations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Identification of downstream genetic pathways of Tbx1 in the second heart field

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Biomechanics of early cardiac development.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Altered microRNAs in bicuspid aortic valve: a comparison between stenotic and insufficient valves

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Regulation of muscle development by DPF3, a novel histone acetylation and methylation reader of the BAF chromatin remodeling complex

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Mutation in ankyrin repeats of the mouse Notch2 gene induces early embryonic lethality.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Parsing the heart: genetic modules for organ assembly

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Prepregnancy Body Mass Index and Congenital Heart Defects among Offspring: A Population-based Study

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Rare non-synonymous variations in the transcriptional activation domains of GATA5 in bicuspid aortic valve disease

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Rare copy number variants in isolated sporadic and syndromic atrioventricular septal defects.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Noncoding RNA expression in myocardium from infants with tetralogy of Fallot.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Consanguinity and the risk of congenital heart disease

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

A novel GATA6 mutation associated with congenital ventricular septal defect.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

GATA5 interacts with GATA4 and GATA6 in outflow tract development

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

A derangement of the maternal lipid profile is associated with an elevated risk of congenital heart disease in the offspring.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Chromatin remodeling in heart development.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Familial transposition of the great arteries caused by multiple mutations in laterality genes

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Frequency of Bicuspid Aortic Valve in Young Male Conscripts by Echocardiogram

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

NKX2.5mutations in patients with congenital heart disease

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

X-linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3827691

Congenital malformations among liveborn infants with trisomies 18 and 13

28 November 2018

1 reference

12 December 2020

Echocardiographic and color flow Doppler findings in military pilot applicants

1 reference

12 December 2020

Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly

1 reference

12 December 2020

First-cousin matings and congenital heart disease in Saudi Arabia

1 reference

12 December 2020

Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome

1 reference

12 December 2020

Recurrence of Congenital Heart Defects in Families

1 reference

12 December 2020

The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)

1 reference

12 December 2020

Investigation of the MYH11 gene in sporadic patients with an isolated persistently patent arterial duct

1 reference

12 December 2020

Balloon dilation of severe aortic stenosis in the fetus: potential for prevention of hypoplastic left heart syndrome: candidate selection, technique, and results of successful intervention

1 reference

12 December 2020

2010 Report from the ISPD Special Interest Group fetal therapy: fetal cardiac interventions

1 reference

12 December 2020

Two novel mutations of the IRX4 gene in patients with congenital heart disease

1 reference

12 December 2020

An echocardiographic survey of primary school children for bicuspid aortic valve

1 reference

12 December 2020

Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5

1 reference

12 December 2020

Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease

1 reference

12 December 2020