Zhou Q - Search Results

1

A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings.

Chai H, DiAdamo A, Grommisch B, Xu F, Zhou Q, Wen J, Mahoney M, Bale A, McGrath J, Spencer-Manzon M, Li P, Zhang H. Chai H, et al. Among authors: zhou q. Front Genet. 2019 Nov 20;10:1162. doi: 10.3389/fgene.2019.01162. eCollection 2019. Front Genet. 2019. PMID: 31850057 Free PMC article.

2

Copy number changes and methylation patterns in an isodicentric and a ring chromosome of 15q11-q13: report of two cases and review of literature.

Wang Q, Wu W, Xu Z, Luo F, Zhou Q, Li P, Xie J. Wang Q, et al. Among authors: zhou q. Mol Cytogenet. 2015 Dec 21;8:97. doi: 10.1186/s13039-015-0198-4. eCollection 2015. Mol Cytogenet. 2015. PMID: 26697114 Free PMC article.

3

Spectrum of Cytogenomic Abnormalities Revealed by Array Comparative Genomic Hybridization on Products of Conception Culture Failure and Normal Karyotype Samples.

Zhou Q, Wu SY, Amato K, DiAdamo A, Li P. Zhou Q, et al. J Genet Genomics. 2016 Mar 20;43(3):121-31. doi: 10.1016/j.jgg.2016.02.002. Epub 2016 Feb 13. J Genet Genomics. 2016. PMID: 27020032

4

Novel homozygous FANCL mutation and somatic heterozygous SETBP1 mutation in a Chinese girl with Fanconi Anemia.

Wu W, Liu Y, Zhou Q, Wang Q, Luo F, Xu Z, Geng Q, Li P, Zhang HZ, Xie J. Wu W, et al. Among authors: zhou q. Eur J Med Genet. 2017 Jul;60(7):369-373. doi: 10.1016/j.ejmg.2017.04.008. Epub 2017 Apr 15. Eur J Med Genet. 2017. PMID: 28419882

5

De novo paternal origin duplication of chromosome 11p15.5: report of two Chinese cases with Beckwith-Wiedemann syndrome.

Wang Q, Geng Q, Zhou Q, Luo F, Li P, Xie J. Wang Q, et al. Among authors: zhou q. Mol Cytogenet. 2017 Dec 19;10:46. doi: 10.1186/s13039-017-0347-z. eCollection 2017. Mol Cytogenet. 2017. PMID: 29270226 Free PMC article.

6

A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-Thalassemia.

Yang X, Zhou Q, Zhou W, Zhong M, Guo X, Wang X, Fan X, Yan S, Li L, Lai Y, Wang Y, Huang J, Ye Y, Zeng H, Chuan J, Du Y, Ma C, Li P, Song Z, Xu X. Yang X, et al. Among authors: zhou w, zhou q. Adv Sci (Weinh). 2019 Apr 1;6(11):1802332. doi: 10.1002/advs.201802332. eCollection 2019 Jun 5. Adv Sci (Weinh). 2019. PMID: 31179213 Free PMC article.

7

ERas Enhances Resistance to Cisplatin-Induced Apoptosis by Suppressing Autophagy in Gastric Cancer Cell.

Tian H, Wang W, Meng X, Wang M, Tan J, Jia W, Li P, Li J, Zhou Q. Tian H, et al. Among authors: zhou q. Front Cell Dev Biol. 2020 Jan 21;7:375. doi: 10.3389/fcell.2019.00375. eCollection 2019. Front Cell Dev Biol. 2020. PMID: 32083074 Free PMC article.

8

Exome sequencing analysis on products of conception: a cohort study to evaluate clinical utility and genetic etiology for pregnancy loss.

Zhao C, Chai H, Zhou Q, Wen J, Reddy UM, Kastury R, Jiang Y, Mak W, Bale AE, Zhang H, Li P. Zhao C, et al. Among authors: zhou q. Genet Med. 2021 Mar;23(3):435-442. doi: 10.1038/s41436-020-01008-6. Epub 2020 Oct 26. Genet Med. 2021. PMID: 33100332 Free article.

9

Estimation on risk of spontaneous abortions by genomic disorders from a meta-analysis of microarray results on large case series of pregnancy losses.

Peng G, Zhou Q, Chai H, Wen J, Zhao H, Taylor HS, Jiang YH, Li P. Peng G, et al. Among authors: zhou q. Mol Genet Genomic Med. 2023 Aug;11(8):e2181. doi: 10.1002/mgg3.2181. Epub 2023 Apr 4. Mol Genet Genomic Med. 2023. PMID: 37013615 Free PMC article.

10

Serum Anti-BRAT1 is a Common Molecular Biomarker for Gastrointestinal Cancers and Atherosclerosis.

Hu L, Liu J, Shimada H, Ito M, Sugimoto K, Hiwasa T, Zhou Q, Li J, Shen S, Wang H. Hu L, et al. Among authors: zhou q. Front Oncol. 2022 May 17;12:870086. doi: 10.3389/fonc.2022.870086. eCollection 2022. Front Oncol. 2022. PMID: 35656505 Free PMC article.

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