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

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

(2015) Yuan Lin et al.   Nature Communications

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

(2015) Christopher C Chang et al.   GigaScience

Pediatric inpatient hospital resource use for congenital heart defects

(2014) Regina M. Simeone et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Lifetime Prevalence of Congenital Heart Disease in the General Population From 2000 to 2010

(2014) Ariane J. Marelli et al.   CIRCULATION

Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data

(2014) Joseph T. Glessner et al.   CIRCULATION RESEARCH

Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations

(2014) Laura E. Mitchell et al.   HUMAN MOLECULAR GENETICS

Cardiac-specific ablation of ARNT leads to lipotoxicity and cardiomyopathy

(2014) Rongxue Wu et al.   JOURNAL OF CLINICAL INVESTIGATION

Functional annotation of noncoding sequence variants

(2014) Graham R S Ritchie et al.   NATURE METHODS

Replication of the 4p16 Susceptibility Locus in Congenital Heart Disease in Han Chinese Populations

(2014) Bijun Zhao et al.   PLoS One

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

(2014) Thor Thorsson et al.   Congenital Heart Disease

Association Between Maternal Chronic Conditions and Congenital Heart Defects

(2013) Shiliang Liu et al.   CIRCULATION

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

(2013) H. J. Cordell et al.   HUMAN MOLECULAR GENETICS

Genetic Abnormalities inFOXP1Are Associated with Congenital Heart Defects

(2013) Sheng-Wei Chang et al.   HUMAN MUTATION

Cathepsin K Knockout Alleviates Pressure Overload–Induced Cardiac Hypertrophy

(2013) Yinan Hua et al.   HYPERTENSION

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

(2013) Zhibin Hu et al.   NATURE GENETICS

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

(2013) Heather J Cordell et al.   NATURE GENETICS

Risk Factors in the Origin of Congenital Left-Ventricular Outflow-Tract Obstruction Defects of the Heart: A Population-Based Case–Control Study

(2013) Melinda Csáky-Szunyogh et al.   PEDIATRIC CARDIOLOGY

Temporal Trends in Survival Among Infants With Critical Congenital Heart Defects

(2013) M. E. Oster et al.   PEDIATRICS

Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease

(2012) Rachel Soemedi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Role for Cysteine Protease Cathepsins in Heart Disease

(2012) Xian Wu Cheng et al.   CIRCULATION

Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management

(2012) Bradley S. Marino et al.   CIRCULATION

Heart Disease and Stroke Statistics—2013 Update

(2012) Alan S. Go et al.   CIRCULATION

Direct and Indirect Involvement of MicroRNA-499 in Clinical and Experimental Cardiomyopathy

(2012) Scot J. Matkovich et al.   CIRCULATION RESEARCH

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

(2012) Andrew S. Warkman et al.   Cytoskeleton

Annotation of functional variation in personal genomes using RegulomeDB

(2012) A. P. Boyle et al.   GENOME RESEARCH

Congenital heart disease: current knowledge about causes and inheritance

(2012) Gillian M Blue et al.   MEDICAL JOURNAL OF AUSTRALIA

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

(2012)   NATURE

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

(2012) F. Yeung et al.   NUCLEIC ACIDS RESEARCH

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

(2012) Ashleigh R. Payne et al.   PEDIATRIC CARDIOLOGY

Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease

(2012) Marc-Phillip Hitz et al.   PLoS Genetics

Estimating Missing Heritability for Disease from Genome-wide Association Studies

(2011) Sang Hong Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

(2011) Kim L. McBride et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Clan Genomics and the Complex Architecture of Human Disease

(2011) James R. Lupski et al.   CELL

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

(2011) W. S. Kerstjens-Frederikse et al.   HEART

Hypoplastic Left Heart Syndrome

(2011) Jeffrey A. Feinstein et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

A linear complexity phasing method for thousands of genomes

(2011) Olivier Delaneau et al.   NATURE METHODS

Genotype Imputation with Thousands of Genomes

(2011) Bryan Howie et al.   G3-Genes Genomes Genetics

GCTA: A Tool for Genome-wide Complex Trait Analysis

(2010) Jian Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

(2010) Maurisa F. Riley et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

LocusZoom: regional visualization of genome-wide association scan results

(2010) R. J. Pruim et al.   BIOINFORMATICS

Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies

(2010) T.-P. Yang et al.   BIOINFORMATICS

Robust relationship inference in genome-wide association studies

(2010) Ani Manichaikul et al.   BIOINFORMATICS

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

(2010) William McLaren et al.   BIOINFORMATICS

METAL: fast and efficient meta-analysis of genomewide association scans

(2010) C. J. Willer et al.   BIOINFORMATICS

Mortality in adult congenital heart disease

(2010) C. L. Verheugt et al.   EUROPEAN HEART JOURNAL

Uncoupling of Expression of an Intronic MicroRNA and Its Myosin Host Gene by Exon Skipping

(2010) M. L. Bell et al.   MOLECULAR AND CELLULAR BIOLOGY

Recurrence of Congenital Heart Defects in Families

(2009) Nina Øyen et al.   CIRCULATION

A Family of microRNAs Encoded by Myosin Genes Governs Myosin Expression and Muscle Performance

(2009) Eva van Rooij et al.   DEVELOPMENTAL CELL

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

(2009) Kim L McBride et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Hypoplastic Left Heart Syndrome Links to Chromosomes 10q and 6q and Is Genetically Related to Bicuspid Aortic Valve

(2009) Robert B. Hinton et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Common Regulatory Variation Impacts Gene Expression in a Cell Type-Dependent Manner

(2009) A. S. Dimas et al.   SCIENCE

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics

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

(2008) K. L. McBride et al.   HUMAN MOLECULAR GENETICS