Zeng D - Search Results

1

The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation.

Luo S, Chen X, Zeng D, Tang N, Yuan D, Zhong Q, Mao A, Xu R, Yan T. Luo S, et al. Among authors: zeng d. J Hum Genet. 2022 Apr;67(4):183-195. doi: 10.1038/s10038-021-00983-1. Epub 2021 Oct 25. J Hum Genet. 2022. PMID: 34690349 Free PMC article.

2

Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease.

Li Z, Huang J, Liang B, Zeng D, Luo S, Yan T, Liao F, Huang J, Li J, Cai R, Deng X, Tang N. Li Z, et al. Among authors: zeng d. J Clin Lab Anal. 2019 Feb;33(2):e22660. doi: 10.1002/jcla.22660. Epub 2018 Sep 17. J Clin Lab Anal. 2019. PMID: 30221396 Free PMC article.

3

Analysis of Copy Number Variations by Low-Depth Whole-Genome Sequencing in Fetuses with Congenital Cardiovascular Malformations.

Huang J, Deng X, Wang Y, Tang N, Zeng D. Huang J, et al. Among authors: zeng d. Cytogenet Genome Res. 2020;160(11-12):643-649. doi: 10.1159/000512605. Epub 2021 Mar 1. Cytogenet Genome Res. 2020. PMID: 33647914

4

Correction to: The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation.

Luo S, Chen X, Zeng D, Tang N, Yuan D, Zhong Q, Mao A, Xu R, Yan T. Luo S, et al. Among authors: zeng d. J Hum Genet. 2022 Apr;67(4):239-243. doi: 10.1038/s10038-021-00992-0. J Hum Genet. 2022. PMID: 34815527 Free PMC article. No abstract available.

5

Identification and Functional Characterization of a Novel Nonsense Variant in ARR3 in a Southern Chinese Family With High Myopia.

Yuan D, Yan T, Luo S, Huang J, Tan J, Zhang J, Zhang VW, Lan Y, Hu T, Guo J, Huang M, Zeng D. Yuan D, et al. Among authors: zeng d. Front Genet. 2021 Dec 13;12:765503. doi: 10.3389/fgene.2021.765503. eCollection 2021. Front Genet. 2021. PMID: 34966409 Free PMC article.

6

Detection of four rare thalassemia variants using Single-molecule realtime sequencing.

Luo S, Chen X, Zeng D, Tang N, Yuan D, Liu B, Chen L, Zhong Q, Li J, Liu Y, Chen J, Wang X, Yan T. Luo S, et al. Among authors: zeng d. Front Genet. 2022 Sep 2;13:974999. doi: 10.3389/fgene.2022.974999. eCollection 2022. Front Genet. 2022. PMID: 36159974 Free PMC article.

7

Prenatal diagnosis of paternal uniparental disomy for chromosome 2 in two fetuses with intrauterine growth restriction.

Tan X, Liu B, Yan T, Wei X, Qin Y, Zeng D, Yuan D. Tan X, et al. Among authors: zeng d. Mol Cytogenet. 2023 Aug 23;16(1):20. doi: 10.1186/s13039-023-00647-z. Mol Cytogenet. 2023. PMID: 37612666 Free PMC article.

8

Newborn screening with targeted sequencing: a multicenter investigation and a pilot clinical study in China.

Hao C, Guo R, Hu X, Qi Z, Guo Q, Liu X, Liu Y, Sun Y, Zhang X, Jin F, Wu X, Cai R, Zeng D, Hu X, Wang X, Ji X, Li W, Xing Q, Mu L, Jiang X, Yang X, Yang W, Zhang Y, Yin Q, Ni X, Li W. Hao C, et al. Among authors: zeng d. J Genet Genomics. 2022 Jan;49(1):13-19. doi: 10.1016/j.jgg.2021.08.008. Epub 2021 Aug 30. J Genet Genomics. 2022. PMID: 34474183 Free article.

9

Geographical and Ethnic Distributions of the MTHFR C677T, A1298C and MTRR A66G Gene Polymorphisms in Chinese Populations: A Meta-Analysis.

Wang X, Fu J, Li Q, Zeng D. Wang X, et al. Among authors: zeng d. PLoS One. 2016 Apr 18;11(4):e0152414. doi: 10.1371/journal.pone.0152414. eCollection 2016. PLoS One. 2016. PMID: 27089387 Free PMC article.

10

Interactions between genetic variants involved in the folate metabolic pathway and serum lipid, homocysteine levels on the risk of recurrent spontaneous abortion.

Lin Z, Li Q, Sun Y, Huang J, Wang W, Fu J, Xu J, Zeng D. Lin Z, et al. Among authors: zeng d. Lipids Health Dis. 2019 Jun 15;18(1):143. doi: 10.1186/s12944-019-1083-7. Lipids Health Dis. 2019. PMID: 31200713 Free PMC article.

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