Related references
Note: Only part of the references are listed.Folate, vitamin B12, homocysteine and polymorphisms in folate metabolizing genes in children with congenital heart disease and their mothers
K. E. Elizabeth et al.
EUROPEAN JOURNAL OF CLINICAL NUTRITION (2017)
A66G and C524T polymorphisms of methionine synthase reductase gene are linked to the development of acyanotic congenital heart diseases in Egyptian children
Fahima M. Hassan et al.
GENE (2017)
Components of the folate metabolic pathway and ADHD core traits: an exploration in eastern Indian probands
Tanusree Saha et al.
JOURNAL OF HUMAN GENETICS (2017)
Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect
Qian-nan Guo et al.
BIOMED RESEARCH INTERNATIONAL (2017)
MTHFD1 regulates nuclear de novo thymidylate biosynthesis and genome stability
Martha S. Field et al.
BIOCHIMIE (2016)
Effect of Folic Acid Food Fortification in Canada on Congenital Heart Disease Subtypes
Shiliang Liu et al.
CIRCULATION (2016)
Genetic and Developmental Basis of Cardiovascular Malformations
Mohamad Azhar et al.
CLINICS IN PERINATOLOGY (2016)
Illustrated Imaging Essay on Congenital Heart Diseases: Multimodality Approach Part II: Acyanotic Congenital Heart Disease and Extracardiac Abnormalities
Venkatraman Bhat et al.
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH (2016)
Illustrated Imaging Essay on Congenital Heart Diseases: Multimodality Approach Part III: Cyanotic Heart Diseases and Complex Congenital Anomalies
Venkatraman Bhat et al.
JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH (2016)
Profile and risk factors for congenital heart defects: A study in a tertiary care hospital
Shaad Abqari et al.
ANNALS OF PEDIATRIC CARDIOLOGY (2016)
Maternal Folic Acid Supplementation and the Risk of Congenital Heart Defects in Offspring: A Meta-Analysis of Epidemiological Observational Studies
Yu Feng et al.
SCIENTIFIC REPORTS (2015)
MTHFD1 polymorphism as maternal risk for neural tube defects: a meta-analysis
Jinyu Zheng et al.
NEUROLOGICAL SCIENCES (2015)
STRING v10: protein-protein interaction networks, integrated over the tree of life
Damian Szklarczyk et al.
NUCLEIC ACIDS RESEARCH (2015)
Nuclear Enrichment of Folate Cofactors and Methylenetetrahydrofolate Dehydrogenase 1 (MTHFD1) Protect de Novo Thymidylate Biosynthesis during Folate Deficiency
Martha S. Field et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Associations of Common Variants in Methionine Metabolism Pathway Genes with Plasma Homocysteine and the Risk of Type 2 Diabetes in Han Chinese
Tao Huang et al.
JOURNAL OF NUTRIGENETICS AND NUTRIGENOMICS (2014)
Association Between Methionine Synthase Reductase A66G Polymorphism and the Risk of Congenital Heart Defects: Evidence From Eight Case-Control Studies
Di Yu et al.
PEDIATRIC CARDIOLOGY (2014)
Genetic Variant in MTRR, but Not MTR, Is Associated with Risk of Congenital Heart Disease: An Integrated Meta-Analysis
Bingxi Cai et al.
PLOS ONE (2014)
Rare De Novo Copy Number Variants in Patients with Congenital Pulmonary Atresia
Li Xie et al.
PLOS ONE (2014)
Association Between MTHFR Polymorphisms and Congenital Heart Disease: A Meta-analysis based on 9,329 cases and 15,076 controls
Chao Xuan et al.
SCIENTIFIC REPORTS (2014)
RISK AND PROTECTIVE FACTORS IN THE ORIGIN OF ATRIAL SEPTAL DEFECT SECUNDUM - NATIONAL POPULATION-BASED CASE-CONTROL STUDY
Melinda Csaky-Szunyogh et al.
CENTRAL EUROPEAN JOURNAL OF PUBLIC HEALTH (2014)
MTHFR rs1801133 C>T polymorphism is associated with an increased risk of tetralogy of Fallot
Jianbing Huang et al.
BIOMEDICAL REPORTS (2014)
Isolated atrioventricular canal defects: Birth outcomes and risk factors: A population-based hungarian case-control study, 1980-1996
Attila Vereczkey et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2013)
Association analysis of complex diseases using triads, parent-child dyads and singleton monads
Ruzong Fan et al.
BMC GENETICS (2013)
Risk of congenital heart defects is influenced by genetic variation in folate metabolism
Karen E. Christensen et al.
CARDIOLOGY IN THE YOUNG (2013)
A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development
K. E. Christensen et al.
HUMAN MOLECULAR GENETICS (2013)
Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease
Benjing Wang et al.
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE (2013)
Methylenetetrahydrofolate reductase C677T and reduced folate carrier 80 G>A polymorphisms are associated with an increased risk of conotruncal heart defects
Dingxu Gong et al.
CLINICAL CHEMISTRY AND LABORATORY MEDICINE (2012)
Mthfd1 is a modifier of chemically induced intestinal carcinogenesis
Amanda J. MacFarlane et al.
CARCINOGENESIS (2011)
A66G and C524T polymorphisms of the methionine synthase reductase gene are associated with congenital heart defects in the Chinese Han population
W. Zeng et al.
GENETICS AND MOLECULAR RESEARCH (2011)
Birth Prevalence of Congenital Heart Disease Worldwide A Systematic Review and Meta-Analysis
Denise van der Linde et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2011)
Variants of Folate Metabolism Genes and Risk of Left-Sided Cardiac Defects
Laura E. Mitchell et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2010)
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects
Gary M. Shaw et al.
BMC MEDICAL GENETICS (2009)
The MTHFD1 p.Arg653Gln Variant Alters Enzyme Function and Increases Risk for Congenital Heart Defects
Karen E. Christensen et al.
HUMAN MUTATION (2009)
Variants of Folate Metabolism Genes and the Risk of Conotruncal Cardiac Defects
Elizabeth Goldmuntz et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2008)
Association of polymorphisms in one-carbon metabolizing genes and lung cancer risk: a case-control study in Chinese population
Hongliang Liu et al.
LUNG CANCER (2008)
Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies
Lorenzo D. Botto et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2007)
Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial defects and congenital heart defects in China
Lijun Pei et al.
ANNALS OF EPIDEMIOLOGY (2006)
Share Paper
