Sun Y - Search Results

1

Risk of birth defects in children conceived with assisted reproductive technology: A meta-analysis.

Lu Y, Liu L, Zhang P, Sun Y, Ma C, Li Y. Lu Y, et al. Among authors: sun y. Medicine (Baltimore). 2022 Dec 30;101(52):e32405. doi: 10.1097/MD.0000000000032405. Medicine (Baltimore). 2022. PMID: 36596016 Free PMC article.

2

Polycystic Ovary Syndrome is Associated with Elevated Periostin Levels.

Chen X, Huo L, Ren L, Li Y, Sun Y, Li Y, Zhang P, Chen S, Song GY. Chen X, et al. Among authors: sun y. Exp Clin Endocrinol Diabetes. 2019 Oct;127(9):571-577. doi: 10.1055/a-0752-0061. Epub 2018 Oct 29. Exp Clin Endocrinol Diabetes. 2019. PMID: 30372763 Clinical Trial.

3

Cytogenetic analysis of 3387 umbilical cord blood in pregnant women at high risk for chromosomal abnormalities.

Sun Y, Zhang P, Zhang N, Rong L, Yu X, Huang X, Li Y. Sun Y, et al. Mol Cytogenet. 2020 Jan 23;13:2. doi: 10.1186/s13039-020-0469-6. eCollection 2020. Mol Cytogenet. 2020. PMID: 31998409 Free PMC article.

4

Prenatal diagnosis of a maternal 7.22-Mb deletion at chromosome 4q32.2q32.3 by SNP array.

Zhang P, Sun Y, Huo P, Tian H, Gao J, Li Y. Zhang P, et al. Among authors: sun y. Mol Cytogenet. 2020 Apr 10;13:12. doi: 10.1186/s13039-020-00480-8. eCollection 2020. Mol Cytogenet. 2020. PMID: 32308739 Free PMC article.

5

Prenatal diagnosis and neonatal phenotype of a de novo microdeletion of 17p11.2p12 associated with Smith-Magenis syndrome and external genital defects.

Zhang P, Sun Y, Tian H, Rong L, Wang F, Yu X, Li Y, Gao J. Zhang P, et al. Among authors: sun y. J Genet. 2020;99:50. J Genet. 2020. PMID: 32661203 Free article.

6

Prenatal diagnosis of the Dandy-Walker malformation associated with partial trisomy 12p and distal 15q deletion.

Sun Y, Zhang N, Tian H, Zhang P, Li Y. Sun Y, et al. J Genet. 2021;100:40. J Genet. 2021. PMID: 34238780 Free article.

7

[Clinical features and genetics analysis of a Chinese pedigree affected with developmental and epileptic encephalopathy 9].

Zhi Y, Wang T, Zhang P, Sun Y, Li J, Li Y. Zhi Y, et al. Among authors: sun y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Sep 10;39(9):969-973. doi: 10.3760/cma.j.cn511374-20210819-00680. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36082567 Chinese.

8

Clinical features and genetic analysis of Dandy-Walker syndrome.

Sun Y, Wang T, Zhang N, Zhang P, Li Y. Sun Y, et al. BMC Pregnancy Childbirth. 2023 Jan 18;23(1):40. doi: 10.1186/s12884-023-05367-1. BMC Pregnancy Childbirth. 2023. PMID: 36653756 Free PMC article.

9

A de novo homozygous missense mutation of the GUSB gene leads to mucopolysaccharidosis type VII identification in a family with twice adverse pregnancy outcomes due to non-immune hydrops fetalis.

Du R, Tian H, Zhao B, Shi X, Sun Y, Qiu B, Li Y. Du R, et al. Among authors: sun y. Mol Genet Metab Rep. 2023 Dec 6;38:101033. doi: 10.1016/j.ymgmr.2023.101033. eCollection 2024 Mar. Mol Genet Metab Rep. 2023. PMID: 38149215 Free PMC article.

10

CXC chemokine receptor type 5 may induce trophoblast dysfunction and participate in the processes of unexplained missed abortion, wherein p-ERK and interleukin-6 may be involved.

Zhi Y, Zhang P, Luo Y, Sun Y, Li J, Zhang M, Li Y. Zhi Y, et al. Among authors: sun y. Heliyon. 2024 May 17;10(11):e31465. doi: 10.1016/j.heliyon.2024.e31465. eCollection 2024 Jun 15. Heliyon. 2024. PMID: 38882363 Free PMC article.

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