A genome‐wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study

Global birth prevalence of congenital heart defects 1970–2017: updated systematic review and meta-analysis of 260 studies

(2019) Yingjuan Liu et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

The Missing Diversity in Human Genetic Studies

(2019) Giorgio Sirugo et al.   CELL

Association between the 4p16 genomic locus and different types of congenital heart disease: results from adult survivors in the UK Biobank

(2019) Aldo Córdova-Palomera et al.   Scientific Reports

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

(2018) Mary Ella Pierpont et al.   CIRCULATION

Genome-Wide Association Studies and Meta-Analyses for Congenital Heart DefectsCLINICAL PERSPECTIVE

(2017) A. J. Agopian et al.   Circulation-Cardiovascular Genetics

Trends in Congenital Heart Disease

(2016) John K. Triedman et al.   CIRCULATION

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

(2016) Neil A. Hanchard et al.   HUMAN MOLECULAR GENETICS

The national birth defects prevention study: A review of the methods

(2015) Jennita Reefhuis et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Silencing of nodal modulator 1 inhibits the differentiation of P19 cells into cardiomyocytes

(2015) Hao Zhang et al.   EXPERIMENTAL CELL RESEARCH

Association Between the 4p16 Susceptibility Locus and the Risk of Atrial Septal Defect in Population from Southeast China

(2015) Kaiyan Pei et al.   PEDIATRIC CARDIOLOGY

Association between the European GWAS-Identified Susceptibility Locus at Chromosome 4p16 and the Risk of Atrial Septal Defect: A Case-Control Study in Southwest China and a Meta-Analysis

(2015) Li Zhao et al.   PLoS One

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

(2015) J. Homsy et al.   SCIENCE

The national birth defects prevention study: A review of the methods

(2015) Jennita Reefhuis et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

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

(2015) Christopher C Chang et al.   GigaScience

Prenatal Alcohol Exposure and Congenital Heart Defects: A Meta-Analysis

(2015) Jiaomei Yang et al.   PLoS One

Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways

(2014) Charlotte A. Hobbs et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Congenital Heart Disease: The Crossroads of Genetics, Epigenetics and Environment

(2014) Cecilia Vecoli et al.   CURRENT GENOMICS

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

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

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

(2014) Bijun Zhao et al.   PLoS One

The global burden of congenital heart disease : review article

(2013) Julien I.E. Hoffman   Cardiovascular Journal of Africa

Genetics of Congenital Heart Disease

(2013) Akl C. Fahed et al.   CIRCULATION RESEARCH

Prenatal diagnosis of de novo interstitial deletions involving 5q23.1–q23.3 and 18q12.1–q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect

(2013) Chih-Ping Chen et al.   GENE

De novo mutations in histone-modifying genes in congenital heart disease

(2013) Samir Zaidi et al.   NATURE

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

The Genotype-Tissue Expression (GTEx) project

(2013) John Lonsdale et al.   NATURE GENETICS

Associations between maternal genotypes and metabolites implicated in congenital heart defects

(2012) Shimul Chowdhury et al.   MOLECULAR GENETICS AND METABOLISM

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

Charting a course for genomic medicine from base pairs to bedside

(2011) Eric D. Green et al.   NATURE

Low dietary choline and low dietary riboflavin during pregnancy influence reproductive outcomes and heart development in mice

(2010) Jessica Chan et al.   AMERICAN JOURNAL OF CLINICAL NUTRITION

Robust relationship inference in genome-wide association studies

(2010) Ani Manichaikul et al.   BIOINFORMATICS

Mortality Resulting From Congenital Heart Disease Among Children and Adults in the United States, 1999 to 2006

(2010) Suzanne M. Gilboa et al.   CIRCULATION

Maternal Folate-Related Gene Environment Interactions and Congenital Heart Defects

(2010) Charlotte A. Hobbs et al.   OBSTETRICS AND GYNECOLOGY

Association between prepregnancy body mass index and congenital heart defects

(2009) Suzanne M. Gilboa et al.   AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY

National time trends in congenital heart defects, Denmark, 1977-2005

(2008) Nina Øyen et al.   AMERICAN HEART JOURNAL

Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature

(2008) Bert L. Callewaert et al.   HUMAN MUTATION