Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. - Wikidata - awgldk - TriplyDB

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

http://www.wikidata.org/entity/Q36041812

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Down syndrome: searching for the genetic culprits Study on Environmental Causes and SNPs of MTHFR, MS and CBS Genes Related to Congenital Heart Disease Risk factors for Down syndrome.Rare de novo copy number variants in patients with congenital pulmonary atresia.Genetic polymorphism of methylenetetrahydrofolate reductase as a potential risk factor for congenital heart disease: A meta-analysis in Chinese pediatric population The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome.Association between 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and congenital heart disease: A meta-analysis Molecular signatures of cardiac defects in Down syndrome lymphoblastoid cell lines suggest altered ciliome and Hedgehog pathways.Chromosome 21 scan in Down syndrome reveals DSCAM as a predisposing locus in Hirschsprung disease.Genetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease: an integrated meta-analysis Contribution of copy-number variation to Down syndrome-associated atrioventricular septal defects.Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects.The use of mouse models for understanding the biology of down syndrome and aging Vitamin D-related genetic variation, plasma vitamin D, and risk of lethal prostate cancer: a prospective nested case-control study Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.[Turner syndrome and genetic polymorphism: a systematic review]DNA methylation abnormalities in congenital heart disease.Systematic Tracking of Disrupted Modules Identifies Altered Pathways Associated with Congenital Heart Defects in Down Syndrome.An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects A functional variant in the cystathionine β-synthase gene promoter significantly reduces congenital heart disease susceptibility in a Han Chinese population.Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier.Possible selection of host folate pathway gene polymorphisms in patients with malaria from a malaria endemic region in North East India.The reduced folate carrier (RFC-1) 80A>G polymorphism and maternal risk of having a child with Down syndrome: a meta-analysis.Kernel machine SNP-set testing under multiple candidate kernels.Association between methionine synthase reductase A66G polymorphism and the risk of congenital heart defects: evidence from eight case-control studies.Role of folate-homocysteine pathway gene polymorphisms and nutritional cofactors in Down syndrome: A triad study.The MTR 2756A>G polymorphism and maternal risk of birth of a child with Down syndrome: a case-control study and a meta-analysis.Gender differences in the prevalence of congenital heart disease in Down's syndrome: a brief meta-analysis.Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects.DNMT3B promoter polymorphisms and maternal risk of birth of a child with Down syndrome.MTHFR A1298C polymorphisms reduce the risk of congenital heart defects: a meta-analysis from 16 case-control studies.Folate, vitamin B12, homocysteine and polymorphisms in folate metabolizing genes in children with congenital heart disease and their mothers.Genetic polymorphisms modulate the folate metabolism of Brazilian individuals with Down syndrome.Survey of Human Chromosome 21 Gene Expression Effects on Early Development in Danio rerio.

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Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

http://www.wikidata.org/entity/Q36041812

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2010年论文

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2010年论文

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Variation in folate pathway ge ...... ndividuals with Down syndrome.

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Genetic Epidemiology

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Variation in folate pathway ge ...... ndividuals with Down syndrome.

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Claudine P Torfs

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Emily G Allen

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George Capone

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Kenneth J Dooley

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Lora J H Bean

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Michael P Epstein

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Sallie B Freeman

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Soo Yeon Cheong

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Stephanie L Sherman

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Stuart W Tinker

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P2860

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

dbSNP: the NCBI database of genetic variation

Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

A haplotype map of the human genome

Haploview: analysis and visualization of LD and haplotype maps

Homocysteine metabolism in children with Down syndrome: in vitro modulation

Genomic control for association studies

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

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613-623

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10.1002/GEPI.20518

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6

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34

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Clifford L. Cua

Eleanor Feingold

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2010-09-01T00:00:00Z

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