Wang B - Search Results

1

Methylenetetrahydrofolate reductase polymorphisms at 3'-untranslated region are associated with susceptibility to preterm birth.

Zhu Q, Chen Y, Dai J, Wang B, Liu M, Wang Y, Tao J, Li H. Zhu Q, et al. Among authors: wang y, wang b. Transl Pediatr. 2015 Jan;4(1):57-62. doi: 10.3978/j.issn.2224-4336.2015.01.02. Transl Pediatr. 2015. PMID: 26835361 Free PMC article.

2

[Folic acid metabolism gene polymorphism and congenital heart disease].

Wang BJ, Chen Y. Wang BJ, et al. Zhonghua Er Ke Za Zhi. 2012 Aug;50(8):630-3. Zhonghua Er Ke Za Zhi. 2012. PMID: 23158745 Review. Chinese. No abstract available.

3

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.

Wang B, Liu M, Yan W, Mao J, Jiang D, Li H, Chen Y. Wang B, et al. J Matern Fetal Neonatal Med. 2013 Dec;26(18):1768-77. doi: 10.3109/14767058.2013.799648. Epub 2013 Jun 10. J Matern Fetal Neonatal Med. 2013. PMID: 23701284 Free article.

4

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y. Mao J, et al. Clin Chim Acta. 2014 Jun 10;433:190-3. doi: 10.1016/j.cca.2014.03.011. Epub 2014 Mar 22. Clin Chim Acta. 2014. PMID: 24667696

5

[Multicenter investigation on the impact of newborn infants' gestational age and birth weight on the level of 17α-hydroxyprogesterone].

Zhang Q, Wang B, Chen Y, Jiang D, Chen Y. Zhang Q, et al. Among authors: wang b. Zhonghua Er Ke Za Zhi. 2014 Sep;52(9):706-9. Zhonghua Er Ke Za Zhi. 2014. PMID: 25476436 Chinese.

6

SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.

Li H, Wang B, Liu D, Wang T, Li Q, Wang W, Li H. Li H, et al. Among authors: wang w, wang t, wang b. Genomics. 2015 Aug;106(2):83-7. doi: 10.1016/j.ygeno.2015.05.004. Epub 2015 May 22. Genomics. 2015. PMID: 26004784 Free article.

7

Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.

Chen Y, Liu Y, Wang B, Mao J, Wang T, Ye K, Ye Y, Cram DS, Li H. Chen Y, et al. Among authors: wang t, wang b. Prenat Diagn. 2016 Dec;36(13):1233-1241. doi: 10.1002/pd.4962. Epub 2016 Dec 9. Prenat Diagn. 2016. PMID: 27862068

8

New Ratios for Performance Improvement for Identifying Acyl-CoA Dehydrogenase Deficiencies in Expanded Newborn Screening: A Retrospective Study.

Wang B, Zhang Q, Gao A, Wang Q, Ma J, Li H, Wang T. Wang B, et al. Among authors: wang t, wang q. Front Genet. 2019 Sep 18;10:811. doi: 10.3389/fgene.2019.00811. eCollection 2019. Front Genet. 2019. PMID: 31620161 Free PMC article.

9

Expanded Newborn Screening for Inborn Errors of Metabolism by Tandem Mass Spectrometry in Suzhou, China: Disease Spectrum, Prevalence, Genetic Characteristics in a Chinese Population.

Wang T, Ma J, Zhang Q, Gao A, Wang Q, Li H, Xiang J, Wang B. Wang T, et al. Among authors: wang b, wang q. Front Genet. 2019 Oct 29;10:1052. doi: 10.3389/fgene.2019.01052. eCollection 2019. Front Genet. 2019. PMID: 31737040 Free PMC article.

10

Investigating the Metabolic Model in Preterm Neonates by Tandem Mass Spectrometry: A Cohort Study.

Wang B, Zhang Q, Wang Q, Ma J, Cao X, Chen Y, Pan Y, Li H, Xiang J, Wang T. Wang B, et al. Among authors: wang t, wang q. Horm Metab Res. 2021 Feb;53(2):112-123. doi: 10.1055/a-1300-2294. Epub 2020 Nov 27. Horm Metab Res. 2021. PMID: 33246344

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