Genome-Wide DNA Methylation Analysis and Epigenetic Variations Associated with Congenital Aortic Valve Stenosis (AVS)

Impact of SNPs on methylation readouts by Illumina Infinium HumanMethylation450 BeadChip Array: implications for comparative population studies

(2015) Patrycja Daca-Roszak et al.   BMC GENOMICS

Epigenetic markers for newborn congenital heart defect (CHD)

(2015) Ray O. Bahado-Singh et al.   Journal of Maternal-Fetal & Neonatal Medicine

Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes

(2014) Louise E Docherty et al.   JOURNAL OF MEDICAL GENETICS

Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot

(2014) Wei Sheng et al.   Journal of Translational Medicine

Evaluation of Links Between High-Density Lipoprotein Genetics, Functionality, and Aortic Valve Stenosis Risk in Humans

(2013) Benoit J. Arsenault et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array

(2013) JiHoon E Joo et al.   BMC BIOTECHNOLOGY

Review of processing and analysis methods for DNA methylation array data

(2013) C S Wilhelm-Benartzi et al.   BRITISH JOURNAL OF CANCER

Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray

(2013) Yi-an Chen et al.   Epigenetics

Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis

(2013) Yun Liu et al.   NATURE BIOTECHNOLOGY

Nongenetic Risk Factors and Congenital Heart Defects

(2013) Sonali S. Patel et al.   PEDIATRIC CARDIOLOGY

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

Helicase-Like Transcription Factor (Hltf) Regulates G2/M Transition, Wt1/Gata4/Hif-1a Cardiac Transcription Networks, and Collagen Biogenesis

(2013) Rebecca A. Helmer et al.   PLoS One

Prenatal diagnosis of nonsyndromic congenital heart defects

(2013) Elizabeth C. Ailes et al.   PRENATAL DIAGNOSIS

Exome Analysis of a Family With Pleiotropic Congenital Heart Disease

(2012) Cammon B. Arrington et al.   Circulation-Cardiovascular Genetics

Measuring the methylome in clinical samples: Improved processing of the Infinium Human Methylation450 BeadChip Array

(2012) Hong Pan et al.   Epigenetics

Prevalence, timing of diagnosis and mortality of newborns with congenital heart defects: a population-based study

(2012) Babak Khoshnood et al.   HEART

Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene

(2011) Eleanor S. Click et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Consanguinity Mapping of Congenital Heart Disease in a South Indian Population

(2010) Tracy L. McGregor et al.   PLoS One

Detailed molecular and clinical characterization of three patients with 21q deletions

(2009) A Lindstrand et al.   CLINICAL GENETICS

Hypercholesterolemia Association with Aortic Stenosis of Various Etiologies

(2009) Murat Bülent Rabuş et al.   JOURNAL OF CARDIAC SURGERY

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

(2009) Da Wei Huang et al.   Nature Protocols

Archived Guthrie blood spots as a novel source for quantitative DNA methylation analysis

(2008) Nicholas C. Wong et al.   BIOTECHNIQUES

Prevalence of Congenital Heart Defects in Metropolitan Atlanta, 1998-2005

(2008) Mark D. Reller et al.   JOURNAL OF PEDIATRICS

Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists

(2008) Da Wei Huang et al.   NUCLEIC ACIDS RESEARCH

APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia

(2008) Jian Wang et al.   Nature clinical practice. Cardiovascular medicine