Shi W - Search Results

1

The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis.

Shu Y, Wang L, Cheng X, Tangshewinsirikul C, Shi W, Yuan Y, Yan Z, Li H, Shen J, Chen B, Zou W. Shu Y, et al. Among authors: shi w. J Genet Genomics. 2019 Sep 20;46(9):445-449. doi: 10.1016/j.jgg.2019.09.003. Epub 2019 Sep 27. J Genet Genomics. 2019. PMID: 31628072 No abstract available.

2

[Principles and practices of post testing genetic counseling in the United States].

Chen JY, Xiang B, Sun H, Shi W, Zhao YC, Shen J, Qi M. Chen JY, et al. Among authors: shi w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jan 10;36(1):92-98. doi: 10.3760/cma.j.issn.1003-9406.2019.01.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30722096 Chinese. No abstract available.

3

[Prenatal diagnosis and genetic analysis of a fetus with 6q27 microdeletion].

Wu D, Shi W, Wang H, Hou Q, Zhang H, Li T, Zhang C, Yang Y, Liao S. Wu D, et al. Among authors: shi w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):718-721. doi: 10.3760/cma.j.issn.1003-9406.2017.05.022. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981941 Chinese.

4

[Clinical and genetic analysis of a boy with 9q34.3 microdeletion syndrome].

Wu D, Li T, Wang H, Shi W, Hou Q, Zhang H, Wang T, Yang Y, Liao S. Wu D, et al. Among authors: shi w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):849-852. doi: 10.3760/cma.j.issn.1003-9406.2017.06.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188614 Chinese.

5

[Analysis of PRRT2 gene mutations in a Chinese family affected with paroxysmal kinesigenic dyskinesia].

Zhang H, Shi W, Xiao H, Wu D, Qin L, Liao S. Zhang H, et al. Among authors: shi w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Feb;33(1):61-3. doi: 10.3760/cma.j.issn.1003-9406.2016.01.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 26829736 Chinese.

6

[Analysis of WAS gene mutation in a Chinese family affected with Wiskott-Aldrich syndrome].

Shi W, Hou Q, Zhang H, Lou G, Zhang Y, Liao S. Shi W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):207-209. doi: 10.3760/cma.j.issn.1003-9406.2018.02.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652993 Chinese.

7

[Research progress on the cognitive deficit of Down syndrome patients].

Shi W, Liao S. Shi W, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Dec 10;41(12):1503-1507. doi: 10.3760/cma.j.cn511374-20240624-00350. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 39653359 Review. Chinese.

8

Integrative Analysis Extracts a Core ceRNA Network of the Fetal Hippocampus With Down Syndrome.

Wang S, Tang X, Qin L, Shi W, Bian S, Wang Z, Wang Q, Wang X, Gu J, Hao B, Ding K, Liao S. Wang S, et al. Among authors: shi w. Front Genet. 2020 Nov 30;11:565955. doi: 10.3389/fgene.2020.565955. eCollection 2020. Front Genet. 2020. PMID: 33329702 Free PMC article.

9

Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis.

Wang H, Gao Y, Qin L, Zhang M, Shi W, Feng Z, Guo L, Zhu B, Liao S. Wang H, et al. Among authors: shi w. Orphanet J Rare Dis. 2023 May 7;18(1):107. doi: 10.1186/s13023-023-02705-6. Orphanet J Rare Dis. 2023. PMID: 37150818 Free PMC article.

10

Online application for the diagnosis of atherosclerosis by six genes.

Zhao Z, Chen S, Wei H, Ma W, Shi W, Si Y, Wang J, Wang L, Li X. Zhao Z, et al. Among authors: shi w. PLoS One. 2024 Apr 10;19(4):e0301912. doi: 10.1371/journal.pone.0301912. eCollection 2024. PLoS One. 2024. PMID: 38598492 Free PMC article.

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