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

Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes

(2013) Nathan D. VanderKraats et al.   NUCLEIC ACIDS RESEARCH

LINE-1 methylation status and its association with tetralogy of fallot in infants

(2012) Wei Sheng et al.   BMC Medical Genomics

Intermediate- and Low-Methylation Epigenotypes Do Not Correspond to CpG Island Methylator Phenotype (Low and -Zero) in Colorectal Cancer

(2012) P. Karpinski et al.   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION

CpG Island Methylator Phenotype-Positive Tumors in the Absence of MLH1 Methylation Constitute a Distinct Subset of Duodenal Adenocarcinomas and Are Associated with Poor Prognosis

(2012) T. Fu et al.   CLINICAL CANCER RESEARCH

A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot

(2012) Valentina Guida et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease

(2012) Scott Smemo et al.   HUMAN MOLECULAR 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

Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects

(2011) Marleny Salazar et al.   European Journal of Medical Genetics

Maternal Genome-Wide DNA Methylation Patterns and Congenital Heart Defects

(2011) Shimul Chowdhury et al.   PLoS One

Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects

(2010) Li Wang et al.   AMERICAN JOURNAL OF CLINICAL NUTRITION

New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle

(2010) A De Luca et al.   CLINICAL GENETICS

5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects

(2010) Eiki Nakamura et al.   European Journal of Medical Genetics

DNA methylation analysis of multiple tissues from newborn twins reveals both genetic and intrauterine components to variation in the human neonatal epigenome

(2010) Miina Ollikainen et al.   HUMAN MOLECULAR GENETICS

Jagged1 (JAG1) mutations in patients with tetralogy of fallot or pulmonic stenosis

(2010) Robert C. Bauer et al.   HUMAN MUTATION

Epigenetic modifications and human disease

(2010) Anna Portela et al.   NATURE BIOTECHNOLOGY

A role for DNA methylation in regulation of EphA5 receptor expression in the mouse retina

(2010) Tihomira D. Petkova et al.   VISION RESEARCH

CFC1 mutations in Chinese children with congenital heart disease

(2009) Binbin Wang et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Structural Abnormalities of the Pulmonary Trunk in Tetralogy of Fallot and Potential Clinical Implications

(2009) Elisabeth Bédard et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Differential methylation of tissue- and cancer-specific CpG island shores distinguishes human induced pluripotent stem cells, embryonic stem cells and fibroblasts

(2009) Akiko Doi et al.   NATURE GENETICS

The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores

(2009) Rafael A Irizarry et al.   NATURE GENETICS

Insulin Gene Expression Is Regulated by DNA Methylation

(2009) Akio Kuroda et al.   PLoS One

Tetralogy of Fallot as a Model to Study Cardiac Progenitor Cell Migration and Differentiation During Heart Development

(2009) Valentina Di Felice et al.   TRENDS IN CARDIOVASCULAR MEDICINE

Tetralogy of Fallot: Yesterday and Today

(2009) Joanne P. Starr   WORLD JOURNAL OF SURGERY

Chromosomal abnormalities among children born with conotruncal cardiac defects

(2008) Edward J. Lammer et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

DNA methylation profile of tissue-dependent and differentially methylated regions (T-DMRs) in mouse promoter regions demonstrating tissue-specific gene expression

(2008) S. Yagi et al.   GENOME RESEARCH

NFATc2 Is a Necessary Mediator of Calcineurin-dependent Cardiac Hypertrophy and Heart Failure

(2008) Meriem Bourajjaj et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Cytosine methylation profiling of cancer cell lines

(2008) M. Ehrich et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA