Li Y - Search Results

1

Detachable Dual-Targeting Nanoparticles for Improving the Antitumor Effect by Extracellular Matrix Depletion.

Duan S, Sun F, Qiao P, Zhu Z, Geng M, Gong X, Li Y, Yao H. Duan S, et al. Among authors: li y. ACS Biomater Sci Eng. 2023 Mar 13;9(3):1437-1449. doi: 10.1021/acsbiomaterials.2c01179. Epub 2023 Feb 16. ACS Biomater Sci Eng. 2023. PMID: 36795746

2

A novel missense variant in OTUD5 causes X-linked multiple congenital anomalies-neurodevelopmental syndrome.

Tian W, Li H, Li Y, Guo J, Wang H, Yang B, Li P, Cui X, Liu L. Tian W, et al. Among authors: li y, li h, li p. Mol Genet Genomic Med. 2024 Jan;12(1):e2325. doi: 10.1002/mgg3.2325. Epub 2023 Dec 1. Mol Genet Genomic Med. 2024. PMID: 38037881 Free PMC article.

3

Evaluation of the clinical utility of extended non-invasive prenatal testing in the detection of chromosomal aneuploidy and microdeletion/microduplication.

Tian W, Yuan Y, Yuan E, Zhang L, Liu L, Li Y, Guo J, Cui X, Li P, Cui S. Tian W, et al. Among authors: li y, li p. Eur J Med Res. 2023 Aug 30;28(1):304. doi: 10.1186/s40001-023-01285-2. Eur J Med Res. 2023. PMID: 37644576 Free PMC article.

4

[Genetic diagnosis and analysis of eight cases with central 22q11.2 deletion syndrome].

Guo J, Li P, Che J, Zhai S, Tian W, Li Y, Zhang H, Liu L. Guo J, et al. Among authors: li y, li p. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Feb 10;41(2):145-149. doi: 10.3760/cma.j.cn511374-20221125-00812. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38311551 Chinese.

5

[Prenatal ultrasonographic manifestations and genetic diagnosis of nine fetuses with 7q11.23 duplication syndrome].

Li P, Guo J, Che J, Cui F, Lyu Y, Zhang H, Li Y, Liu L. Li P, et al. Among authors: li y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Mar 10;41(3):266-270. doi: 10.3760/cma.j.cn511374-20221117-00795. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38448012 Chinese.

6

Genetic examination for fetuses with increased nuchal translucency by exome sequencing.

Sun Y, Liu L, Zhi Y, Li Y, Tian W, Yang B, Ye X, Cui S. Sun Y, et al. Among authors: li y. J Obstet Gynaecol Res. 2023 Feb;49(2):530-538. doi: 10.1111/jog.15482. Epub 2022 Oct 30. J Obstet Gynaecol Res. 2023. PMID: 36310088

7

Hyperglycemia in pregnancy did not worsen the short-term outcomes of very preterm infants: a propensity score matching study.

Li Y, Shen W, Zhang R, Mao J, Liu L, Chang YM, Ye XZ, Qiu YP, Ma L, Cheng R, Wu H, Chen DM, Chen L, Xu P, Mei H, Wang SN, Xu FL, Ju R, Tong XM, Lin XZ, Wu F. Li Y, et al. Front Pediatr. 2024 Mar 6;12:1341221. doi: 10.3389/fped.2024.1341221. eCollection 2024. Front Pediatr. 2024. PMID: 38510082 Free PMC article.

8

Genetic diagnosis of common fetal renal abnormalities detected on prenatal ultrasound.

Liu L, Li J, Li Y, Li H, Yang B, Fan H, Wang J, Gu Y, Yu H, Bai M, Yu T, Cui S, Cheng G, Ren C. Liu L, et al. Among authors: li y, li j, li h. Prenat Diagn. 2022 Jun;42(7):894-900. doi: 10.1002/pd.6154. Epub 2022 May 5. Prenat Diagn. 2022. PMID: 35478332

9

Variant analysis of PEX11B gene from a family with peroxisome biogenesis disorder 14B by whole exome sequencing.

Tian Y, Zhang L, Li Y, Gao J, Yu H, Guo Y, Jia L. Tian Y, et al. Among authors: li y. Mol Genet Genomic Med. 2020 Jan;8(1):10.1002/mgg3.1042. doi: 10.1002/mgg3.1042. Epub 2019 Nov 13. Mol Genet Genomic Med. 2020. PMID: 31724321 Free PMC article.

10

Pathogenic/likely pathogenic copy number variations and regions of homozygosity in fetal central nervous system malformations.

Zhi Y, Liu L, Cui S, Li Y, Chen X, Che J, Han X, Zhao L. Zhi Y, et al. Among authors: li y. Arch Gynecol Obstet. 2023 Dec;308(6):1723-1735. doi: 10.1007/s00404-022-06866-w. Epub 2022 Dec 5. Arch Gynecol Obstet. 2023. PMID: 36464758

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