Related references
Note: Only part of the references are listed.Intermediate- and Low-Methylation Epigenotypes Do Not Correspond to CpG Island Methylator Phenotype (Low and -Zero) in Colorectal Cancer
Pawel Karpinski et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2013)
A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot
Valentina Guida et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2013)
Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes
Nathan D. VanderKraats et al.
NUCLEIC ACIDS RESEARCH (2013)
LINE-1 methylation status and its association with tetralogy of fallot in infants
Wei Sheng et al.
BMC MEDICAL GENOMICS (2012)
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
Tao Fu et al.
CLINICAL CANCER RESEARCH (2012)
Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease
Scott Smemo et al.
HUMAN MOLECULAR GENETICS (2012)
Association of Common Variants in ERBB4 with Congenital Left Ventricular Outflow Tract Obstruction Defects
Kim L. McBride et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2011)
New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle
A. De Luca et al.
CLINICAL GENETICS (2011)
5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects
Eiki Nakamura et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2011)
Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects
Marleny Salazar et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2011)
CFC1 mutations in Chinese children with congenital heart disease
Binbin Wang et al.
INTERNATIONAL JOURNAL OF CARDIOLOGY (2011)
Maternal Genome-Wide DNA Methylation Patterns and Congenital Heart Defects
Shimul Chowdhury et al.
PLOS ONE (2011)
A role for DNA methylation in regulation of EphA5 receptor expression in the mouse retina
Tihomira D. Petkova et al.
VISION RESEARCH (2011)
Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects
Li Wang et al.
AMERICAN JOURNAL OF CLINICAL NUTRITION (2010)
DNA methylation analysis of multiple tissues from newborn twins reveals both genetic and intrauterine components to variation in the human neonatal epigenome
Miina Ollikainen et al.
HUMAN MOLECULAR GENETICS (2010)
Jagged1 (JAG1) Mutations in Patients with Tetralogy of Fallot or Pulmonic Stenosis
Robert C. Bauer et al.
HUMAN MUTATION (2010)
Epigenetic modifications and human disease
Anna Portela et al.
NATURE BIOTECHNOLOGY (2010)
Tetralogy of Fallot: Yesterday and Today
Joanne P. Starr
WORLD JOURNAL OF SURGERY (2010)
Chromosomal Abnormalities among Children Born with Conotruncal Cardiac Defects
Edward J. Lammer et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2009)
Structural Abnormalities of the Pulmonary Trunk in Tetralogy of Fallot and Potential Clinical Implications A Morphological Study
Elisabeth Bedard et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2009)
Differential methylation of tissue- and cancer-specific CpG island shores distinguishes human induced pluripotent stem cells, embryonic stem cells and fibroblasts
Akiko Doi et al.
NATURE GENETICS (2009)
The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores
Rafael A. Irizarry et al.
NATURE GENETICS (2009)
Insulin Gene Expression Is Regulated by DNA Methylation
Akio Kuroda et al.
PLOS ONE (2009)
Tetralogy of Fallot as a Model to Study Cardiac Progenitor Cell Migration and Differentiation During Heart Development
Valentina Di Felice et al.
TRENDS IN CARDIOVASCULAR MEDICINE (2009)
DNA methylation profile of tissue-dependent and differentially methylated regions (T-DMRs) in mouse promoter regions demonstrating tissue-specific gene expression
Shintaro Yagi et al.
GENOME RESEARCH (2008)
NFATc2 is a necessary mediator of calcineurin-dependent cardiac hypertrophy and heart failure
Meriem Bourajjaj et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Cytosine methylation profiling of cancer cell lines
Mathias Ehrich et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
CpG island methylator phenotype association with elevated serum α-fetoprotein level in hepatocellular carcinoma
Changsong Zhang et al.
CLINICAL CANCER RESEARCH (2007)
CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer
Daniel J. Weisenberger et al.
NATURE GENETICS (2006)
Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry
M Ehrich et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Ablation of the secondary heart field leads to tetralogy of Fallot and pulmonary atresia
C Ward et al.
DEVELOPMENTAL BIOLOGY (2005)
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies
LM Beauchesne et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2005)
The incidence of congenital heart disease
JIE Hoffman et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2002)
NKX2.5 mutations in patients with tetralogy of Fallot
E Goldmuntz et al.
CIRCULATION (2001)
Familial Tetralogy of Fallot caused by mutation in the jagged1 gene
ZA Eldadah et al.
HUMAN MOLECULAR GENETICS (2001)
Aberrant CpG-island methylation has non-random and tumour-type-specific patterns
JF Costello et al.
NATURE GENETICS (2000)