Similar articles for PMID: 29399948

Year	Number of Results
1992	1
1994	1
1996	2
1997	1
2001	1
2002	1
2003	2
2004	2
2005	3
2006	4
2007	1
2008	3
2009	2
2010	2
2011	3
2012	7
2013	6
2014	9
2015	11
2016	8
2017	9
2018	11
2019	11
2020	12
2021	8
2022	1
2023	3
2024	0

1

A parent-of-origin analysis of paternal genetic variants and increased risk of conotruncal heart defects.

Nembhard WN, Tang X, Li J, MacLeod SL, Levy J, Schaefer GB, Hobbs CA; National Birth Defects Prevention Study. Nembhard WN, et al. Am J Med Genet A. 2018 Mar;176(3):609-617. doi: 10.1002/ajmg.a.38611. Epub 2018 Feb 5. Am J Med Genet A. 2018. PMID: 29399948 Free PMC article.

2

Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach.

Patel J, Bircan E, Tang X, Orloff M, Hobbs CA, Browne ML, Botto LD, Finnell RH, Jenkins MM, Olshan A, Romitti PA, Shaw GM, Werler MM, Li J, Nembhard WN; National Birth Defects Prevention Study. Patel J, et al. PLoS Genet. 2021 Mar 8;17(3):e1009413. doi: 10.1371/journal.pgen.1009413. eCollection 2021 Mar. PLoS Genet. 2021. PMID: 33684136 Free PMC article.

3

Maternal and infant genetic variants, maternal periconceptional use of selective serotonin reuptake inhibitors, and risk of congenital heart defects in offspring: population based study.

Nembhard WN, Tang X, Hu Z, MacLeod S, Stowe Z, Webber D; National Birth Defects Prevention Study. Nembhard WN, et al. BMJ. 2017 Mar 6;356:j832. doi: 10.1136/bmj.j832. BMJ. 2017. PMID: 28264803 Free PMC article.

4

Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways.

Hobbs CA, Cleves MA, Macleod SL, Erickson SW, Tang X, Li J, Li M, Nick T, Malik S; National Birth Defects Prevention Study. Hobbs CA, et al. Birth Defects Res A Clin Mol Teratol. 2014 Feb;100(2):116-26. doi: 10.1002/bdra.23225. Epub 2014 Feb 18. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24535845 Free PMC article.

5

Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes.

Shaw GM, Iovannisci DM, Yang W, Finnell RH, Carmichael SL, Cheng S, Lammer EJ. Shaw GM, et al. Am J Med Genet A. 2005 Sep 15;138(1):21-6. doi: 10.1002/ajmg.a.30924. Am J Med Genet A. 2005. PMID: 16100725

6

The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population.

Koshy T, Venkatesan V, Perumal V, Hegde S, Paul SF. Koshy T, et al. Pediatr Cardiol. 2015 Oct;36(7):1470-5. doi: 10.1007/s00246-015-1188-3. Epub 2015 May 17. Pediatr Cardiol. 2015. PMID: 25981563

7

Gene variants in the folate-mediated one-carbon metabolism (FOCM) pathway as risk factors for conotruncal heart defects.

Zhu H, Yang W, Lu W, Etheredge AJ, Lammer EJ, Finnell RH, Carmichael SL, Shaw GM. Zhu H, et al. Am J Med Genet A. 2012 May;158A(5):1124-34. doi: 10.1002/ajmg.a.35313. Epub 2012 Apr 11. Am J Med Genet A. 2012. PMID: 22495907 Free PMC article.

8

Genetic polymorphisms in MTR are associated with non-syndromic congenital heart disease from a family-based case-control study in the Chinese population.

Deng C, Deng Y, Xie L, Yu L, Liu L, Liu H, Dai L. Deng C, et al. Sci Rep. 2019 Mar 25;9(1):5065. doi: 10.1038/s41598-019-41641-z. Sci Rep. 2019. PMID: 30911047 Free PMC article.

9

Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects.

van Beynum IM, Mooij C, Kapusta L, Heil S, den Heijer M, Blom HJ. van Beynum IM, et al. Clin Chem Lab Med. 2008;46(10):1369-75. doi: 10.1515/CCLM.2008.271. Clin Chem Lab Med. 2008. PMID: 18844489

10

Rare copy number variants in patients with congenital conotruncal heart defects.

Xie HM, Werner P, Stambolian D, Bailey-Wilson JE, Hakonarson H, White PS, Taylor DM, Goldmuntz E. Xie HM, et al. Birth Defects Res. 2017 Mar 1;109(4):271-295. doi: 10.1002/bdra.23609. Epub 2017 Feb 13. Birth Defects Res. 2017. PMID: 28398664 Free PMC article.

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