Association of maternal hypertension and diabetes with variants of the NKX2-5, LEFTY1 and LEFTY2 genes in children with congenital heart defects: a case-control study from Pakistani Population-Reference-Cited by-同舟云学术

Association of maternal hypertension and diabetes with variants of the NKX2-5, LEFTY1 and LEFTY2 genes in children with congenital heart defects: a case-control study from Pakistani Population

Published:2023-04-25 Issue:6 Volume:50 Page:5013-5020
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Ashiq Sana^ORCID,Sabar Muhammad Farooq^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s11033-023-08418-0.pdf

Reference24 articles.

1. Martin LJ, Benson DW (2021) Focused strategies for defining the genetic architecture of congenital heart defects. Genes 2021;12:827

2. Ashiq S, Ashiq K, Sabar MF (2021) The role of NKX2-5 gene polymorphisms in congenital heart disease (CHD): a systematic review and meta-analysis. Egypt Heart J 73:1–9

3. Nie X, Liu X, Wang C, Wu Z, Sun Z, Su J et al (2022) Assessment of evidence on reported non-genetic risk factors of congenital heart defects: the updated umbrella review. BMC Pregnancy Childbirth 22:1–7

4. Zuhlke L, Lawrenson J, Comitis G, De Decker R, Brooks A, Fourie B et al (2019) Congenital heart disease in low-and lower-middle–income countries: current status and new opportunities. Curr Cardiol Rep 21:163

5. Liu Y, Chen S, Zuhlke L, Black GC, Choy MK, Li N et al (2019) Global birth prevalence of congenital heart defects 1970–2017: updated systematic review and meta-analysis of 260 studies. Int J Epidemiol 48:455–463

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