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

Maternal Variation inEPHX1, a Xenobiotic Metabolism Gene, Is Associated with Childhood Medulloblastoma: An Exploratory Case-Parent Triad Study

(2016) Philip J. Lupo et al.   PEDIATRIC HEMATOLOGY AND ONCOLOGY

Functional annotation of noncoding sequence variants

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

Effect of Copy Number Variants on Outcomes for Infants With Single Ventricle Heart Defects

(2013) Abigail S. Carey et al.   Circulation-Cardiovascular Genetics

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease

(2013) Dorothy Warburton et al.   HUMAN GENETICS

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

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

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

(2013) Samir Zaidi et al.   NATURE

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

Diabetes and Obesity-Related Genes and the Risk of Neural Tube Defects in the National Birth Defects Prevention Study

(2012) P. J. Lupo et al.   AMERICAN JOURNAL OF EPIDEMIOLOGY

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

Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts

(2012) Min Shi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

INRICH: interval-based enrichment analysis for genome-wide association studies

(2012) Phil H. Lee et al.   BIOINFORMATICS

Association between reported venlafaxine use in early pregnancy and birth defects, national birth defects prevention study, 1997-2007

(2012) Kara N. D. Polen et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Association between MTHFR polymorphisms and orofacial clefts risk: A meta-analysis

(2012) Ya L. Luo et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Association between MTR A2756G and MTRR A66G polymorphisms and maternal risk for neural tube defects: A meta-analysis

(2012) Shengrong Ouyang et al.   GENE

Exploration of Gene-Environment Interactions, Maternal Effects and Parent of Origin Effects in the Etiology of Hypospadias

(2012) Loes F.M. van der Zanden et al.   JOURNAL OF UROLOGY

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

(2012) Marc-Phillip Hitz et al.   PLoS 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

MI-GWAS: a SAS platform for the analysis of inherited and maternal genetic effects in genome-wide association studies using log-linear models

(2011) AJ Agopian et al.   BMC BIOINFORMATICS

Identification of de novo mutations and rare variants in hypoplastic left heart syndrome

(2011) M Iascone et al.   CLINICAL GENETICS

New evidence for the role of cystathionine beta-synthase in non-syndromic cleft lip with or without cleft palate

(2011) Marcella Martinelli et al.   EUROPEAN JOURNAL OF ORAL SCIENCES

Maternal Alcohol Consumption, Alcohol Metabolism Genes, and the Risk of Oral Clefts: A Population-based Case-Control Study in Norway, 1996-2001

(2010) A. L. Boyles et al.   AMERICAN JOURNAL OF EPIDEMIOLOGY

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

The changing epidemiology of congenital heart disease

(2010) Teun van der Bom et al.   Nature Reviews Cardiology

Maternal Folate-Related Gene Environment Interactions and Congenital Heart Defects

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

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

(2009) Paweł Stankiewicz et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

(2009) H Zhu et al.   CLINICAL GENETICS

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

Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: Roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature

(2009) Charles Shaw-Smith   European Journal of Medical Genetics

Trends in Hospitalizations for Adults With Congenital Heart Disease in the U.S.

(2009) Alexander R. Opotowsky et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

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

Genome-Wide Association Study Implicates Chromosome 9q21.31 as a Susceptibility Locus for Asthma in Mexican Children

(2009) Dana B. Hancock et al.   PLoS Genetics

Congenital heart disease in 111 225 births in Belgium: birth prevalence, treatment and survival in the 21st century

(2008) Philip Moons et al.   ACTA PAEDIATRICA