Liu Y - Search Results

1

Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.

Zhang Y, Liu Y, Zarrei M, Tong W, Dong R, Wang Y, Zhang H, Yang X, MacDonald JR, Uddin M, Scherer SW, Gai Z. Zhang Y, et al. Among authors: liu y. Am J Med Genet B Neuropsychiatr Genet. 2018 Jan;177(1):93-100. doi: 10.1002/ajmg.b.32608. Epub 2017 Nov 20. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29152845

2

Whole-genome sequencing of quartet families with autism spectrum disorder.

Yuen RK, Thiruvahindrapuram B, Merico D, Walker S, Tammimies K, Hoang N, Chrysler C, Nalpathamkalam T, Pellecchia G, Liu Y, Gazzellone MJ, D'Abate L, Deneault E, Howe JL, Liu RS, Thompson A, Zarrei M, Uddin M, Marshall CR, Ring RH, Zwaigenbaum L, Ray PN, Weksberg R, Carter MT, Fernandez BA, Roberts W, Szatmari P, Scherer SW. Yuen RK, et al. Among authors: liu rs, liu y. Nat Med. 2015 Feb;21(2):185-91. doi: 10.1038/nm.3792. Epub 2015 Jan 26. Nat Med. 2015. PMID: 25621899

3

Refining critical regions in 15q24 microdeletion syndrome pertaining to autism.

Liu Y, Zhang Y, Zarrei M, Dong R, Yang X, Zhao D, Scherer SW, Gai Z. Liu Y, et al. Am J Med Genet B Neuropsychiatr Genet. 2020 Jun;183(4):217-226. doi: 10.1002/ajmg.b.32778. Epub 2020 Jan 18. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 31953991

4

Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay.

Liu Y, Lv Y, Zarrei M, Dong R, Yang X, Higginbotham EJ, Li Y, Zhao D, Song F, Yang Y, Zhang H, Wang Y, Scherer SW, Gai Z. Liu Y, et al. NPJ Genom Med. 2022 Jan 12;7(1):1. doi: 10.1038/s41525-021-00271-z. NPJ Genom Med. 2022. PMID: 35022430 Free PMC article.

5

A synonymous mutation in PI4KA impacts the transcription and translation process of gene expression.

Zhang K, Kang L, Zhang H, Bai L, Pang H, Liu Q, Zhang X, Chen D, Yu H, Lv Y, Gao M, Liu Y, Gai Z, Wang D, Li X. Zhang K, et al. Among authors: liu y, liu q. Front Immunol. 2022 Oct 19;13:987666. doi: 10.3389/fimmu.2022.987666. eCollection 2022. Front Immunol. 2022. PMID: 36341355 Free PMC article.

6

[Genetic analysis of a child with combined oxidative phosphorylation deficiency 14 due to variant of FARS2 gene].

Ma J, Zhang H, Lyu Y, Gao M, Wang D, Gai Z, Liu Y. Ma J, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Dec 10;39(12):1393-1397. doi: 10.3760/cma.j.cn511374-20210731-00644. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 36453966 Chinese.

7

Establishment of an induced pluripotent stem cell (iPSC) line SDQLCHi045-A from peripheral blood mononuclear cells of a patient with Coffin-Siris syndrome 1 carrying a mutation in ARID1B gene.

Yang X, Liu C, Zhang H, Lv Y, Li Y, Li Z, Liu Y, Gai Z. Yang X, et al. Among authors: liu y, liu c. Stem Cell Res. 2023 Feb;66:102982. doi: 10.1016/j.scr.2022.102982. Epub 2022 Nov 24. Stem Cell Res. 2023. PMID: 36473251 Free article.

8

Establishment of a transgene-free iPS cell line (SDQLCHi046-A) from a young patient bearing a HDAC8 mutation and suffering from Cornelia de Lange Syndrome.

Li Z, Liu C, Xin H, Yang Y, Wang Y, Niu S, Gao C, Gai Z, Liu Y. Li Z, et al. Among authors: liu y, liu c. Stem Cell Res. 2023 Feb;66:102984. doi: 10.1016/j.scr.2022.102984. Epub 2022 Dec 5. Stem Cell Res. 2023. PMID: 36481505 Free article.

9

Phenotype and genotype analyses of Chinese patients with autosomal dominant mental retardation type 5 caused by SYNGAP1 gene mutations.

Wang Y, Lv Y, Li Z, Gao M, Yang X, Li Y, Shi J, Gao Z, Liu Y, Gai Z. Wang Y, et al. Among authors: liu y. Front Genet. 2022 Dec 13;13:957915. doi: 10.3389/fgene.2022.957915. eCollection 2022. Front Genet. 2022. PMID: 36583017 Free PMC article.

10

Diagnostic application of exome sequencing in Chinese children with suspected inherited kidney diseases.

Gao M, Yu F, Dong R, Zhang K, Lv Y, Ma J, Wang D, Zhang H, Gai Z, Liu Y. Gao M, et al. Among authors: liu y. Front Genet. 2023 Jan 6;13:933636. doi: 10.3389/fgene.2022.933636. eCollection 2022. Front Genet. 2023. PMID: 36685964 Free PMC article.

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