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Pubmed for Handhelds

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Journal Abstract Search

195 related items for PubMed ID: 29216786

  • 21.
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  • 22. A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.
    Zhang L, Qin Y, Gong X, Peng R, Cai C, Zheng Y, Du Y, Wang H.
    Transl Psychiatry; 2019 Jan 22; 9(1):31. PubMed ID: 30670685
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  • 23. Association study between inwardly rectifying potassium channels 2.1 and 4.1 and autism spectrum disorders.
    Sun C, Zou M, Li L, Li D, Ma Y, Xia W, Wu L, Ren H.
    Life Sci; 2018 Nov 15; 213():183-189. PubMed ID: 30304693
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  • 27. Genetic Evidence for Possible Involvement of the Calcium Channel Gene CACNA1A in Autism Pathogenesis in Chinese Han Population.
    Li J, You Y, Yue W, Jia M, Yu H, Lu T, Wu Z, Ruan Y, Wang L, Zhang D.
    PLoS One; 2015 Nov 15; 10(11):e0142887. PubMed ID: 26566276
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  • 31. Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan.
    Chien WH, Wu YY, Gau SS, Huang YS, Soong WT, Chiu YN, Chen CH.
    Prog Neuropsychopharmacol Biol Psychiatry; 2010 Feb 01; 34(1):189-92. PubMed ID: 19913066
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  • 35. Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism.
    Li J, Zhao L, You Y, Lu T, Jia M, Yu H, Ruan Y, Yue W, Liu J, Lu L, Zhang D, Wang L.
    PLoS One; 2015 Feb 01; 10(7):e0133247. PubMed ID: 26204268
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  • 37. LAMB1 polymorphism is associated with autism symptom severity in Korean autism spectrum disorder patients.
    Kim YJ, Park JK, Kang WS, Kim SK, Park HJ, Nam M, Kim JW.
    Nord J Psychiatry; 2015 Feb 01; 69(8):594-8. PubMed ID: 25774865
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  • 40. Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population.
    Yang P, Shu BC, Hallmayer JF, Lung FW.
    Neuropsychobiology; 2010 Feb 01; 62(2):104-15. PubMed ID: 20523082
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