Yang X - Search Results

1

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: yang x. Front Genet. 2022 Dec 13;13:957915. doi: 10.3389/fgene.2022.957915. eCollection 2022. Front Genet. 2022. PMID: 36583017 Free PMC article.

2

Evaluation of a viral microarray based on simultaneous extraction and amplification of viral nucleotide acid for detecting human herpesviruses and enteroviruses.

Liu Y, Duan C, Zhang C, Yang X, Zhao Y, Dong R, Zhou J, Gai Z. Liu Y, et al. Among authors: yang x. PLoS One. 2015 Mar 16;10(3):e0117626. doi: 10.1371/journal.pone.0117626. eCollection 2015. PLoS One. 2015. PMID: 25774509 Free PMC article.

3

De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review.

Liu Y, Zhao D, Dong R, Yang X, Zhang Y, Tammimies K, Uddin M, Scherer SW, Gai Z. Liu Y, et al. Among authors: yang x. Am J Med Genet A. 2015 Jun;167(6):1381-5. doi: 10.1002/ajmg.a.37050. Epub 2015 Apr 6. Am J Med Genet A. 2015. PMID: 25851617

4

Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder.

Liu Y, Zhang Y, Zhao D, Dong R, Yang X, Tammimies K, Uddin M, Scherer SW, Gai Z. Liu Y, et al. Among authors: yang x. Am J Med Genet B Neuropsychiatr Genet. 2015 Jun;168B(4):258-64. doi: 10.1002/ajmg.b.32306. Epub 2015 Apr 29. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 25921429

5

Evaluation of High Resolution Melting for MTHFR C677T Genotyping in Congenital Heart Disease.

Wang Y, Zhang H, Yue S, Zhang K, Wang H, Dong R, Yang X, Liu Y, Ma Y. Wang Y, et al. Among authors: yang x. PLoS One. 2016 Mar 18;11(3):e0151140. doi: 10.1371/journal.pone.0151140. eCollection 2016. PLoS One. 2016. PMID: 26990189 Free PMC article. Clinical Trial.

6

Association of the ACE, GSTM1, IL-6, NOS3, and CYP1A1 polymorphisms with susceptibility of mycoplasma pneumoniae pneumonia in Chinese children.

Zhao J, Zhang W, Shen L, Yang X, Liu Y, Gai Z. Zhao J, et al. Among authors: yang x. Medicine (Baltimore). 2017 Apr;96(15):e6642. doi: 10.1097/MD.0000000000006642. Medicine (Baltimore). 2017. PMID: 28403117 Free PMC article.

7

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: yang x. 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

8

Generation of an induced pluripotent stem cell line (SDQLCHi003-a) from a patient with short rib-thoracic dysplasia syndrome type III carrying compound heterozygous mutations in DYNC2H1.

Zhang H, Ma Y, Song F, Yang X, Li Y, Guan J, Lv Y, Gao M, Ma J, Liu Y, Gai Z. Zhang H, et al. Among authors: yang x. Stem Cell Res. 2019 Aug;39:101505. doi: 10.1016/j.scr.2019.101505. Epub 2019 Jul 19. Stem Cell Res. 2019. PMID: 31415973 Free article.

9

Generation of two induced pluripotent stem cell lines from patients with unbalanced translocation (3;22).

Ma Y, Zhang H, Yang X, Li Y, Guan J, Zhang K, Huang Y, Pan G, Gai Z, Liu Y. Ma Y, et al. Among authors: yang x. Stem Cell Res. 2019 Oct;40:101545. doi: 10.1016/j.scr.2019.101545. Epub 2019 Aug 21. Stem Cell Res. 2019. PMID: 31472451 Free article.

10

Generation of an induced pluripotent stem cell line (SDQLCHi008-A) from a patient with ASD and DD carrying an 830 kb de novo deletion at chr7q11.22 including the exon 1 of AUTS2 gene.

Yang X, Zhou T, Zhang H, Li Y, Dong R, Liu N, Pan G, Liu Y, Gai Z. Yang X, et al. Stem Cell Res. 2019 Oct;40:101557. doi: 10.1016/j.scr.2019.101557. Epub 2019 Aug 31. Stem Cell Res. 2019. PMID: 31505389 Free article.

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