Gao Z - Search Results

1

Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities.

Wang Y, Liu M, Gao Z, Hua C, Jiang J, Zheng Y, Dong Z, Cao Y, Choy KW, Zhu X, Kong X. Wang Y, et al. Among authors: gao z. Ann Med. 2024 Dec;56(1):2399317. doi: 10.1080/07853890.2024.2399317. Epub 2024 Sep 6. Ann Med. 2024. PMID: 39239799 Free PMC article.

2

Whole-exome sequencing in deceased fetuses with ultrasound anomalies: a retrospective analysis.

Huang W, Zhu X, Sun G, Gao Z, Kong X. Huang W, et al. Among authors: gao z. BMC Med Genomics. 2023 Feb 16;16(1):25. doi: 10.1186/s12920-022-01427-1. BMC Med Genomics. 2023. PMID: 36797717 Free PMC article.

3

[Analysis of three families with recurrence of non-immune hydrops fetalis by trio whole exome sequencing].

Zhang T, Zhu X, Gao Z, Huang W, Kong X. Zhang T, et al. Among authors: gao z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Oct 10;38(10):937-941. doi: 10.3760/cma.j.cn511374-20200729-00564. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34625927 Chinese.

4

[Analysis of results of prenatal diagnosis for 67 pedigrees affected with Duchenne muscular dystrophy in the central plain region of China].

Gao Z, Liu L, Wang Y, Wang Y, Huang W, Kong X. Gao Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jul 10;39(7):669-673. doi: 10.3760/cma.j.cn511374-20210223-00153. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35810418 Chinese.

5

Prenatal exome sequencing for morphologically normal fetus: Should we be doing it?

Gao Z, Zhu X, Ren H, Wang Y, Hua C, Kong X. Gao Z, et al. Prenat Diagn. 2024 Jun 11. doi: 10.1002/pd.6624. Online ahead of print. Prenat Diagn. 2024. PMID: 38862389

6

Evaluation of optical genome mapping for detecting chromosomal translocation in clinical cytogenetics.

Dai P, Zhu X, Pei Y, Chen P, Li J, Gao Z, Liang Y, Kong X. Dai P, et al. Among authors: gao z. Mol Genet Genomic Med. 2022 Jun;10(6):e1936. doi: 10.1002/mgg3.1936. Epub 2022 Apr 6. Mol Genet Genomic Med. 2022. PMID: 35384386 Free PMC article.

7

[Application of CNV-seq and chromosomal karyotyping in the prenatal diagnosis for carriers of balanced translocations].

Qu S, Shi P, Zhang T, Gao Z, Guan H, Kong X. Qu S, et al. Among authors: gao z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Apr 10;39(4):366-369. doi: 10.3760/cma.j.cn511374-20200801-00572. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35446967 Chinese.

8

De novo KCNB1 missense variant causing developmental and epileptic encephalopathy: Two case reports.

Ren Y, Hu W, Gao Z, Shi J, Liu Y, Zhang H. Ren Y, et al. Among authors: gao z. Medicine (Baltimore). 2025 Jan 10;104(2):e41236. doi: 10.1097/MD.0000000000041236. Medicine (Baltimore). 2025. PMID: 39792727

9

A hybrid dual-branch model with recurrence plots and transposed transformer for stock trend prediction.

Su J, Li H, Wang R, Guo W, Hao Y, Kurths J, Gao Z. Su J, et al. Among authors: gao z. Chaos. 2025 Jan 1;35(1):013125. doi: 10.1063/5.0233275. Chaos. 2025. PMID: 39792696

10

Cell-Type Specific miRNA Regulatory Network Responses to ABA Stress Revealed by Time Series Transcriptional Atlases in Arabidopsis.

Gao Z, Su Y, Jiao G, Lou Z, Chang L, Yu R, Xu C, Han X, Wang Z, Li J, Deng XW, He H. Gao Z, et al. Adv Sci (Weinh). 2025 Jan 10:e2415083. doi: 10.1002/advs.202415083. Online ahead of print. Adv Sci (Weinh). 2025. PMID: 39792694

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