Zhang Y - Search Results

1

CNV profiles of Chinese pediatric patients with developmental disorders.

Yuan H, Shangguan S, Li Z, Luo J, Su J, Yao R, Zhang S, Liang C, Chen Q, Gao Z, Zhu Y, Zhang S, Li W, Lu W, Zhang Y, Xie H, Liu F, Wang Q, Lin Y, Liu L, Wang X, Liang L, Zhong J, Li H, Qiu H, Zhang H, Yan M, Mireguli M, Liu Y, Zhang D, Wang H, Lv H, Xie B, Gui C, Cui X, Zou L, Wang J, Gusella JF, Shen Y, Chen X. Yuan H, et al. Among authors: zhang s, zhang d, zhang h, zhang y. Genet Med. 2021 Apr;23(4):669-678. doi: 10.1038/s41436-020-01048-y. Epub 2021 Jan 5. Genet Med. 2021. PMID: 33402738 Free article.

2

Confirming the contribution and genetic spectrum of de novo mutation in infantile spasms: Evidence from a Chinese cohort.

Liu L, Liu F, Wang Q, Xie H, Li Z, Lu Q, Wang Y, Zhang M, Zhang Y, Picker J, Cui X, Zou L, Chen X. Liu L, et al. Among authors: zhang m, zhang y. Mol Genet Genomic Med. 2021 Jun;9(6):e1689. doi: 10.1002/mgg3.1689. Epub 2021 May 5. Mol Genet Genomic Med. 2021. PMID: 33951346 Free PMC article.

3

Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study.

Sun Y, Peng J, Liang D, Ye X, Xu N, Chen L, Yan D, Zhang H, Xiao B, Qiu W, Shen Y, Pang N, Liu Y, Liang C, Qin Z, Luo J, Chen F, Wang J, Zhang Z, Wei H, Du J, Yan H, Duan R, Wang J, Zhang Y, Liao S, Sun K, Wu L, Yu Y. Sun Y, et al. Among authors: zhang z, zhang h, zhang y. Hum Mutat. 2022 May;43(5):568-581. doi: 10.1002/humu.24347. Epub 2022 Mar 1. Hum Mutat. 2022. PMID: 35143101

4

Possible Catch-Up Developmental Trajectories for Children with Mild Developmental Delay Caused by NAA15 Pathogenic Variants.

Tian Y, Xie H, Yang S, Shangguan S, Wang J, Jin C, Zhang Y, Cui X, Lyu Y, Chen X, Wang L. Tian Y, et al. Among authors: zhang y. Genes (Basel). 2022 Mar 18;13(3):536. doi: 10.3390/genes13030536. Genes (Basel). 2022. PMID: 35328089 Free PMC article. Review.

5

Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder.

Chen X, Wang J, Xie H, Zhou W, Wu Y, Wang J, Qin J, Guo J, Gu Q, Zhang X, Ji T, Zhang Y, Xiong Z, Wang L, Wu X, Latham GJ, Jiang Y. Chen X, et al. Among authors: zhang x, zhang y. BMC Pediatr. 2015 Jul 15;15:77. doi: 10.1186/s12887-015-0394-8. BMC Pediatr. 2015. PMID: 26174701 Free PMC article.

6

Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.

Liang D, Cram DS, Tan H, Linpeng S, Liu Y, Sun H, Zhang Y, Tian F, Zhu H, Xu M, Wang H, Yu F, Wu L. Liang D, et al. Among authors: zhang y. Genet Med. 2019 Sep;21(9):1998-2006. doi: 10.1038/s41436-019-0467-4. Epub 2019 Mar 4. Genet Med. 2019. PMID: 30828085 Free article.

7

Detection of Small CYP11B1 Deletions and One Founder Chimeric CYP11B2/CYP11B1 Gene in 11β-Hydroxylase Deficiency.

Xie H, Yin H, Ye X, Liu Y, Liu N, Zhang Y, Chen X, Chen X. Xie H, et al. Among authors: zhang y. Front Endocrinol (Lausanne). 2022 May 24;13:882863. doi: 10.3389/fendo.2022.882863. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35685215 Free PMC article.

8

Recurrent 8q13.2-13.3 microdeletions associated with branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks.

Chen X, Wang J, Mitchell E, Guo J, Wang L, Zhang Y, Hodge JC, Shen Y. Chen X, et al. Among authors: zhang y. BMC Med Genet. 2014 Aug 19;15:90. doi: 10.1186/s12881-014-0090-9. BMC Med Genet. 2014. PMID: 25135225 Free PMC article.

9

Non-bullous lesions as the first manifestation of bullous pemphigoid: A retrospective analysis of 181 cases.

Zhang Y, Luo Y, Han Y, Tian R, Li W, Yao X. Zhang Y, et al. J Dermatol. 2017 Jul;44(7):742-746. doi: 10.1111/1346-8138.13782. Epub 2017 Mar 3. J Dermatol. 2017. PMID: 28256743

10

Activation of aryl hydrocarbon receptor in Langerhans cells by a microbial metabolite of tryptophan negatively regulates skin inflammation.

Liu X, Zhang X, Zhang J, Luo Y, Xu B, Ling S, Zhang Y, Li W, Yao X. Liu X, et al. Among authors: zhang j, zhang x, zhang y. J Dermatol Sci. 2020 Dec;100(3):192-200. doi: 10.1016/j.jdermsci.2020.10.004. Epub 2020 Oct 9. J Dermatol Sci. 2020. PMID: 33082071

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