Zhou Y - Search Results

1

IFNAR1 gene mutation may contribute to developmental stuttering in the Chinese population.

Sun Y, Gao Y, Zhou Y, Zhou Y, Zhang Y, Wang D, Tan LH. Sun Y, et al. Among authors: zhou y. Hereditas. 2021 Nov 18;158(1):46. doi: 10.1186/s41065-021-00211-y. Hereditas. 2021. PMID: 34794508 Free PMC article.

2

Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population.

Chen H, Wang G, Xia J, Zhou Y, Gao Y, Xu J, Huen MS, Siok WT, Jiang Y, Tan LH, Sun Y. Chen H, et al. Among authors: zhou y. Behav Brain Funct. 2014 Sep 1;10(1):29. doi: 10.1186/1744-9081-10-29. Behav Brain Funct. 2014. PMID: 25178928 Free PMC article.

3

Association study of stuttering candidate genes GNPTAB, GNPTG and NAGPA with dyslexia in Chinese population.

Chen H, Xu J, Zhou Y, Gao Y, Wang G, Xia J, Huen MS, Siok WT, Jiang Y, Tan LH, Sun Y. Chen H, et al. Among authors: zhou y. BMC Genet. 2015 Feb 3;16:7. doi: 10.1186/s12863-015-0172-5. BMC Genet. 2015. PMID: 25643770 Free PMC article.

4

Genetic polymorphism of nonsyndromic cleft lip with or without cleft palate is associated with developmental dyslexia in Chinese school-aged populations.

Wang B, Zhou Y, Leng S, Zheng L, Lv H, Wang F, Tan LH, Sun Y. Wang B, et al. Among authors: zhou y. J Hum Genet. 2017 Feb;62(2):265-268. doi: 10.1038/jhg.2016.121. Epub 2016 Oct 13. J Hum Genet. 2017. PMID: 27734840 Free PMC article.

5

Association study of FGF18 with developmental dyslexia in Chinese population.

Chen H, Zhou Y, Ge Z, Li Q, Sun Q, Zheng L, Lv H, Tan LH, Sun Y. Chen H, et al. Among authors: zhou y. Psychiatr Genet. 2018 Feb;28(1):8-11. doi: 10.1097/YPG.0000000000000187. Psychiatr Genet. 2018. PMID: 29240020

6

Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.

Sun Y, Gao Y, Zhou Y, Chen H, Wang G, Xu J, Xia J, Huen MS, Siok WT, Jiang Y, Tan LH. Sun Y, et al. Among authors: zhou y. Am J Med Genet B Neuropsychiatr Genet. 2014 Dec;165B(8):627-34. doi: 10.1002/ajmg.b.32267. Epub 2014 Sep 17. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 25230923

7

A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability.

Chen H, Gu XH, Zhou Y, Ge Z, Wang B, Siok WT, Wang G, Huen M, Jiang Y, Tan LH, Sun Y. Chen H, et al. Among authors: zhou y. Sci Rep. 2017 Feb 3;7:40365. doi: 10.1038/srep40365. Sci Rep. 2017. PMID: 28155865 Free PMC article.

8

The association study of nonsyndromic cleft lip with or without cleft palate identified risk variants of the GLI3 gene in a Chinese population.

Wang Y, Sun Y, Huang Y, Pan Y, Shi B, Ma J, Ma L, Lan F, Zhou Y, Shi J, Zhu J, Jiang H, Zhang L, Xiao X, Jiang M, Yin A, Yu L, Wang L, Cheng J, Yang Y. Wang Y, et al. Among authors: zhou y. J Genet. 2017 Sep;96(4):687-693. doi: 10.1007/s12041-017-0808-5. J Genet. 2017. PMID: 28947718

9

Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort.

Wang Y, Sun Y, Huang Y, Pan Y, Jia Z, Ma L, Ma L, Lan F, Zhou Y, Shi J, Yang X, Zhang L, Jiang H, Jiang M, Yin A, Cheng J, Wang L, Yang Y, Shi B. Wang Y, et al. Among authors: zhou y. Gene. 2016 Aug 15;588(1):69-73. doi: 10.1016/j.gene.2016.04.045. Epub 2016 Apr 26. Gene. 2016. PMID: 27129939

10

Erratum: A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability.

Chen H, Gu XH, Zhou Y, Ge Z, Wang B, Siok WT, Wang G, Huen M, Jiang Y, Tan LH, Sun Y. Chen H, et al. Among authors: zhou y. Sci Rep. 2017 Apr 11;7:44512. doi: 10.1038/srep44512. Sci Rep. 2017. PMID: 28398299 Free PMC article. No abstract available.

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