(Q37367970)

20 August 2017

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. (English)

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genome-wide association study

20 August 2017

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genome-wide association study

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Second-generation PLINK: rising to the challenge of larger and richer datasets

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Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations

6 September 2017

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Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data

6 September 2017

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6 September 2017

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6 September 2017

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Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

6 September 2017

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A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations

6 September 2017

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Temporal trends in survival among infants with critical congenital heart defects

6 September 2017

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Cathepsin K knockout alleviates pressure overload-induced cardiac hypertrophy

6 September 2017

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Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

6 September 2017

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Heart Disease and Stroke Statistics--2013 Update: A Report From the American Heart Association

6 September 2017

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An integrated map of genetic variation from 1,092 human genomes

6 September 2017

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

6 September 2017

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6 September 2017

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

6 September 2017

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Congenital heart disease: current knowledge about causes and inheritance

6 September 2017

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Neurodevelopmental outcomes in children with congenital heart disease: evaluation and management: a scientific statement from the American Heart Association

6 September 2017

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Direct and indirect involvement of microRNA-499 in clinical and experimental cardiomyopathy

6 September 2017

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Myh7b/miR-499 gene expression is transcriptionally regulated by MRFs and Eos

6 September 2017

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Role for cysteine protease cathepsins in heart disease: focus on biology and mechanisms with clinical implication

6 September 2017

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Developmental expression and cardiac transcriptional regulation of Myh7b, a third myosin heavy chain in the vertebrate heart

6 September 2017

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6 September 2017

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Hypoplastic left heart syndrome: current considerations and expectations

6 September 2017

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A linear complexity phasing method for thousands of genomes

6 September 2017

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Clan genomics and the complex architecture of human disease

6 September 2017

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Estimating missing heritability for disease from genome-wide association studies

6 September 2017

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Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects

6 September 2017

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6 September 2017

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NOTCH1 missense alleles associated with left ventricular outflow tract defects exhibit impaired receptor processing and defective EMT.

6 September 2017

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Robust relationship inference in genome-wide association studies

6 September 2017

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6 September 2017

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LocusZoom: regional visualization of genome-wide association scan results

6 September 2017

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6 September 2017

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Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

6 September 2017

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Uncoupling of expression of an intronic microRNA and its myosin host gene by exon skipping

6 September 2017

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A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance

6 September 2017

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Common regulatory variation impacts gene expression in a cell type-dependent manner

6 September 2017

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

6 September 2017

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Hypoplastic left heart syndrome links to chromosomes 10q and 6q and is genetically related to bicuspid aortic valve

6 September 2017

1 reference

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Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome).

6 September 2017

1 reference

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

6 September 2017

1 reference

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Hypoplastic left heart syndrome is heritable

6 September 2017

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6 September 2017

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Mutations in NOTCH1 cause aortic valve disease

6 September 2017

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Epidemiology of noncomplex left ventricular outflow tract obstruction malformations (aortic valve stenosis, coarctation of the aorta, hypoplastic left heart syndrome) in Texas, 1999-2001

6 September 2017

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Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions

6 September 2017

1 reference

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The allelic architecture of human disease genes: common disease-common variant... or not?

6 September 2017

1 reference

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The incidence of congenital heart disease

6 September 2017

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Are rare variants responsible for susceptibility to complex diseases?

6 September 2017

1 reference

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Association analysis identifies new risk loci for congenital heart disease in Chinese populations

6 September 2017

1 reference

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Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies

14 September 2017

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Functional annotation of noncoding sequence variants.

14 September 2017

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Psychosocial profile of adults with complex congenital heart disease

28 September 2017

1 reference

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Pathogenetic mechanisms of congenital cardiovascular malformations revisited

28 September 2017

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Lifetime prevalence of congenital heart disease in the general population from 2000 to 2010.

28 September 2017

1 reference

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Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.

2 September 2018

1 reference

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Deaths: leading causes for 2010.

2 September 2018

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Risk factors in the origin of congenital left-ventricular outflow-tract obstruction defects of the heart: a population-based case-control study

2 September 2018

1 reference

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Association between maternal chronic conditions and congenital heart defects: a population-based cohort study.

2 September 2018

1 reference

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Genetic abnormalities in FOXP1 are associated with congenital heart defects

2 September 2018

1 reference

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Mortality in adult congenital heart disease.

2 September 2018

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Congenital heart disease in the general population: changing prevalence and age distribution.

2 September 2018

1 reference

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Blocking expression of AHR2 and ARNT1 in zebrafish larvae protects against cardiac toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin

2 September 2018

1 reference

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Increased expression of elastolytic cathepsins S, K, and V and their inhibitor cystatin C in stenotic aortic valves.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5081047

Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5081047

A family-based association study of congenital left-sided heart malformations and 5,10 methylenetetrahydrofolate reductase

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5081047

Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease

2 September 2018

1 reference

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

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDW071

Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations

21 January 2018

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12 December 2020

Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies

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12 December 2020

Left ventricular outflow tract obstruction: should cardiac screening be offered to first-degree relatives?

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12 December 2020

Recurrence of Congenital Heart Defects in Families

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12 December 2020

Identifiers

DOI

10.1093/HMG/DDW071

1 reference

20 August 2017

1 reference

20 August 2017

1 reference