Mutations in folate transporter genes and risk for human myelomeningocele-Reference-Cited by-同舟云学术

Mutations in folate transporter genes and risk for human myelomeningocele

Published:2017-09-26 Issue:11 Volume:173 Page:2973-2984
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Findley Tina O.¹^ORCID,Tenpenny Joy C.¹,O'Byrne Michelle R.²,Morrison Alanna C.³,Hixson James E.³,Northrup Hope²⁴,Au Kit Sing²^ORCID

Affiliation:

1. Division of Neonatology; The University of Texas Health Science Center at Houston; Houston Texas

2. Division of Medical Genetics, Department of Pediatrics, McGovern Medical School; The University of Texas Health Science Center at Houston; Houston Texas

3. Department of Epidemiology, Human Genetics and Environmental Sciences, School of Public Health; The University of Texas Health Science Center at Houston; Houston Texas

4. Shriners Hospital for Children; Houston Texas

Funder

National Institutes of Health

Richard W. Mithoff Professorship Fund

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference63 articles.

1. Fetal surgery for myelomeningocele: Trials and tribulations;Adzick;Journal of Pediatric Surgery,2012

2. Proportion of neural tube defects attributable to known risk factors;Agopian;Birth Defects Research Part A, Clinical and Molecular Teratology,2013

3. Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele;Aneji;Birth Defects Research Part A, Clinical and Molecular Teratology,2012

4. In utero physiology: Role of folic acid in nutrient delivery and fetal development;Antony;American Journal of Clinical Nutrition,2007

5. Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals;Au;Birth Defects Research Part A, Clinical and Molecular Teratology,2008

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1. Mutational analysis of FOLR1 and FOLR2 genes in children with Myelomeningocele;Acta Biochimica Polonica;2023-10-26

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3. Association of polymorphisms of FOLR1 gene and FOLR2 gene and maternal folic acid supplementation with risk of ventricular septal defect: a case-control study;European Journal of Clinical Nutrition;2022-03-10

4. Maternal folic acid and multivitamin supplementation: International clinical evidence with considerations for the prevention of folate-sensitive birth defects;Preventive Medicine Reports;2021-12

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