These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


186 related items for PubMed ID: 18708184

  • 1. Neuregulin 3 genetic variations and susceptibility to schizophrenia in a Chinese population.
    Wang YC, Chen JY, Chen ML, Chen CH, Lai IC, Chen TT, Hong CJ, Tsai SJ, Liou YJ.
    Biol Psychiatry; 2008 Dec 15; 64(12):1093-6. PubMed ID: 18708184
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. No genetic evidence for Neuregulin 3 conferring risk of schizophrenia in the Chinese population.
    Zhang R, Du XY, Yu J, Xu N, Zheng YW, Zhao YL, Zhang H, Ma J.
    Psychiatry Res; 2013 Feb 28; 205(3):279-81. PubMed ID: 22981155
    [Abstract] [Full Text] [Related]

  • 4. Associations of histone deacetylase-2 and histone deacetylase-3 genes with schizophrenia in a Chinese population.
    Han H, Yu Y, Shi J, Yao Y, Li W, Kong N, Wu Y, Wang C, Wang S, Meng X, Kou C.
    Asia Pac Psychiatry; 2013 Mar 28; 5(1):11-6. PubMed ID: 23857786
    [Abstract] [Full Text] [Related]

  • 5. Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain.
    Kao WT, Wang Y, Kleinman JE, Lipska BK, Hyde TM, Weinberger DR, Law AJ.
    Proc Natl Acad Sci U S A; 2010 Aug 31; 107(35):15619-24. PubMed ID: 20713722
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Further evidence that the chromogranin B gene confers predisposition to schizophrenia: a family-based association study in Chinese.
    Wu S, Ma J, Xing Q, Xu Y, Meng J, Cao D, Feng G, He L.
    J Neural Transm (Vienna); 2007 Aug 31; 114(5):641-4. PubMed ID: 17143778
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population.
    Yue W, Yang Y, Zhang Y, Lu T, Hu X, Wang L, Ruan Y, Lv L, Zhang D.
    Behav Brain Funct; 2011 Apr 11; 7():7. PubMed ID: 21477380
    [Abstract] [Full Text] [Related]

  • 11. Association study on the DLG4 gene and schizophrenia in the Chinese Han population.
    Li XW, Liu BC, Wang Y, Zhao QZ, Shen Q, Yu T, Chen SQ, Yang FP, Li WD, Gao LH, Xu YF, Feng GY, He L, He G.
    Psychiatr Genet; 2013 Dec 11; 23(6):247-50. PubMed ID: 23921260
    [Abstract] [Full Text] [Related]

  • 12. Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia.
    Zhang F, St Clair D, Liu X, Sun X, Sham PC, Crombie C, Ma X, Wang Q, Meng H, Deng W, Yates P, Hu X, Walker N, Murray RM, Collier DA, Li T.
    Genes Brain Behav; 2005 Oct 11; 4(7):444-8. PubMed ID: 16176390
    [Abstract] [Full Text] [Related]

  • 13. The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.
    Fei Q, Wu Z, Wang H, Zhou X, Wang N, Ding Y, Wang Y, Qiu G.
    Spine (Phila Pa 1976); 2010 Apr 20; 35(9):983-8. PubMed ID: 20228709
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Family-based association studies of CAPON and schizophrenia in the Chinese Han population.
    Fang C, Tang W, Tang RQ, Wang L, Zhou GQ, Huang K, Li XW, Feng GY, He M, Du LZ, Zhu SM, Xing YL, Sang H, He L, Shi YY.
    Prog Neuropsychopharmacol Biol Psychiatry; 2008 Jul 01; 32(5):1210-3. PubMed ID: 18430503
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan.
    Glatt SJ, Faraone SV, Lasky-Su JA, Kanazawa T, Hwu HG, Tsuang MT.
    Mol Psychiatry; 2009 Sep 01; 14(9):885-93. PubMed ID: 18332877
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 10.