Zhao J - Search Results

1

Common and rare variants of the THBS1 gene associated with the risk for autism.

Lu L, Guo H, Peng Y, Xun G, Liu Y, Xiong Z, Tian D, Liu Y, Li W, Xu X, Zhao J, Hu Z, Xia K. Lu L, et al. Among authors: zhao j. Psychiatr Genet. 2014 Dec;24(6):235-40. doi: 10.1097/YPG.0000000000000054. Psychiatr Genet. 2014. PMID: 25304225

2

No association of neurotensin receptor 1 gene polymorphisms with verbal and visual learning in healthy Chinese-Han individuals.

Wang M, Ma H, Huang YL, Zhu G, Zhao JP. Wang M, et al. Psychiatr Genet. 2014 Jun;24(3):116-7. doi: 10.1097/YPG.0000000000000028. Psychiatr Genet. 2014. PMID: 24770449 No abstract available.

3

Disrupted white matter integrity in first-episode, drug-naive, late-onset depression.

Guo W, Liu F, Xun G, Hu M, Guo X, Xiao C, Chen H, Chen J, Zhao J. Guo W, et al. Among authors: zhao j. J Affect Disord. 2014 Jul;163:70-5. doi: 10.1016/j.jad.2014.03.044. Epub 2014 Apr 1. J Affect Disord. 2014. PMID: 24836090

4

AMPD1 functional variants associated with autism in Han Chinese population.

Zhang L, Ou J, Xu X, Peng Y, Guo H, Pan Y, Chen J, Wang T, Peng H, Liu Q, Tian D, Pan Q, Zou X, Zhao J, Hu Z, Xia K. Zhang L, et al. Among authors: zhao j. Eur Arch Psychiatry Clin Neurosci. 2015 Sep;265(6):511-7. doi: 10.1007/s00406-014-0524-6. Epub 2014 Aug 26. Eur Arch Psychiatry Clin Neurosci. 2015. PMID: 25155876

5

Association of genetic variants of GRIN2B with autism.

Pan Y, Chen J, Guo H, Ou J, Peng Y, Liu Q, Shen Y, Shi L, Liu Y, Xiong Z, Zhu T, Luo S, Hu Z, Zhao J, Xia K. Pan Y, et al. Among authors: zhao j. Sci Rep. 2015 Feb 6;5:8296. doi: 10.1038/srep08296. Sci Rep. 2015. PMID: 25656819 Free PMC article.

6

ZNF804A rs1344706 is associated with cortical thickness, surface area, and cortical volume of the unmedicated first episode schizophrenia and healthy controls.

Wei Q, Li M, Kang Z, Li L, Diao F, Zhang R, Wang J, Zheng L, Wen X, Zhang J, Zhao J, Huang R. Wei Q, et al. Among authors: zhao j. Am J Med Genet B Neuropsychiatr Genet. 2015 Jun;168B(4):265-73. doi: 10.1002/ajmg.b.32308. Epub 2015 Apr 29. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 25921517

7

Association and gene-gene interactions study of reelin signaling pathway related genes with autism in the Han Chinese population.

Shen Y, Xun G, Guo H, He Y, Ou J, Dong H, Xia K, Zhao J. Shen Y, et al. Among authors: zhao j. Autism Res. 2016 Apr;9(4):436-42. doi: 10.1002/aur.1540. Epub 2015 Aug 19. Autism Res. 2016. PMID: 26285919

8

Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia.

Zhou Z, Hu Z, Zhang L, Hu Z, Liu H, Liu Z, Du J, Zhao J, Zhou L, Xia K, Tang B, Shen L. Zhou Z, et al. Among authors: zhao j. Sci Rep. 2016 Apr 13;6:24327. doi: 10.1038/srep24327. Sci Rep. 2016. PMID: 27071546 Free PMC article.

9

Altered plasma levels of chemokines in autism and their association with social behaviors.

Shen Y, Ou J, Liu M, Shi L, Li Y, Xiao L, Dong H, Zhang F, Xia K, Zhao J. Shen Y, et al. Among authors: zhao j. Psychiatry Res. 2016 Oct 30;244:300-5. doi: 10.1016/j.psychres.2016.07.057. Epub 2016 Aug 2. Psychiatry Res. 2016. PMID: 27512919

10

Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression.

Pan Y, Zhang L, Liu Q, Li Y, Guo H, Peng Y, Peng H, Tang B, Hu Z, Zhao J, Xia K, Li JD. Pan Y, et al. Among authors: zhao j. Sci Rep. 2016 Oct 24;6:35970. doi: 10.1038/srep35970. Sci Rep. 2016. PMID: 27775065 Free PMC article.

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