Folate and vitamin B12-related genes and risk for omphalocele (Q36029889)

11 August 2017

Folate and vitamin B12-related genes and risk for omphalocele (English)

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11 August 2017

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11 August 2017

Marilyn L Browne

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Aiyi Liu

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Aiyi Liu

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James L. Mills

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James L Mills

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Paul Romitti

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object named as

Paul A Romitti

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11 August 2017

Tonia C Carter

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11 August 2017

Lawrence C Brody

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11 August 2017

Michele Caggana

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11 August 2017

Charlotte M Druschel

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11 August 2017

25 November 2011

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131

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5

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739-746

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https://scigraph.springernature.com/pub.10.1007/s00439-011-1117-3

11 August 2017

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cites work

Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374579

Chromosomal abnormalities associated with omphalocele

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374579

Haploview: analysis and visualization of LD and haplotype maps

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374579

Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374579

Validation of birth certificate data in New York State

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374579

An evaluation of congenital malformations surveillance in New York State: an application of Centers for Disease Control and Prevention (CDC) guidelines for evaluating surveillance systems

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374579

Risk factors in congenital abdominal wall defects (omphalocele and gastroschisi): a study in a series of 265,858 consecutive births

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3374579

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

2 October 2017

1 reference

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Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

2 October 2017

1 reference

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Genetic-epidemiologic study of omphalocele and gastroschisis: evidence for heterogeneity

2 October 2017

1 reference

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Occurrence of omphalocele in relation to maternal multivitamin use: a population-based study

11 July 2018

1 reference

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Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects

21 January 2018

1 reference

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Changes in the birth prevalence of selected birth defects after grain fortification with folic acid in the United States: findings from a multi-state population-based study

21 January 2018

1 reference

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Clinical risk factors for gastroschisis and omphalocele in humans: a review of the literature

21 January 2018

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The impact of BRCA1 on spina bifida meningomyelocele lesions.

21 January 2018

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Gastroschisis and omphalocele

21 January 2018

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Homocysteine metabolism in pregnancies complicated by neural-tube defects.

21 January 2018

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Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects

21 January 2018

1 reference

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Birth defects surveillance: assessing the "gold standard"

21 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22116453

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Folate-related genes and omphalocele

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22116453

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00439-011-1117-3

1 reference

11 August 2017

1 reference

11 August 2017

PubMed publication ID

22116453

1 reference