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Journal Abstract Search

303 related items for PubMed ID: 23468870

  • 1. Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
    Liu Y, Du Y, Liu W, Yang C, Liu Y, Wang H, Gong X.
    PLoS One; 2013; 8(2):e56639. PubMed ID: 23468870
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  • 3. Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients.
    Xu X, Xiong Z, Zhang L, Liu Y, Lu L, Peng Y, Guo H, Zhao J, Xia K, Hu Z.
    Mol Biol Rep; 2014 Jun; 41(6):4133-40. PubMed ID: 24570023
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  • 4. Neurexin gene family variants as risk factors for autism spectrum disorder.
    Wang J, Gong J, Li L, Chen Y, Liu L, Gu H, Luo X, Hou F, Zhang J, Song R.
    Autism Res; 2018 Jan; 11(1):37-43. PubMed ID: 29045040
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  • 5. Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism.
    Talebizadeh Z, Lam DY, Theodoro MF, Bittel DC, Lushington GH, Butler MG.
    J Med Genet; 2006 May; 43(5):e21. PubMed ID: 16648374
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  • 6. SHANK1 polymorphisms and SNP-SNP interactions among SHANK family: A possible cue for recognition to autism spectrum disorder in infant age.
    Qiu S, Li Y, Bai Y, Shi J, Cui H, Gu Y, Ren Y, Zhao Q, Zhang K, Lu M, Wang Y, Li Y, Zhong W, Zhu X, Liu Y, Cheng Y, Qiao Y, Liu Y.
    Autism Res; 2019 Mar; 12(3):375-383. PubMed ID: 30629339
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  • 8. Analysis of four neuroligin genes as candidates for autism.
    Ylisaukko-oja T, Rehnström K, Auranen M, Vanhala R, Alen R, Kempas E, Ellonen P, Turunen JA, Makkonen I, Riikonen R, Nieminen-von Wendt T, von Wendt L, Peltonen L, Järvelä I.
    Eur J Hum Genet; 2005 Dec; 13(12):1285-92. PubMed ID: 16077734
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  • 11. NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population.
    Gauthier J, Bonnel A, St-Onge J, Karemera L, Laurent S, Mottron L, Fombonne E, Joober R, Rouleau GA.
    Am J Med Genet B Neuropsychiatr Genet; 2005 Jan 05; 132B(1):74-5. PubMed ID: 15389766
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  • 13. Mutation analysis of the NRXN1 gene in a Chinese autism cohort.
    Liu Y, Hu Z, Xun G, Peng Y, Lu L, Xu X, Xiong Z, Xia L, Liu D, Li W, Zhao J, Xia K.
    J Psychiatr Res; 2012 May 05; 46(5):630-4. PubMed ID: 22405623
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  • 14. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
    Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL.
    Autism Res; 2009 Dec 05; 2(6):359-64. PubMed ID: 20029827
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  • 16. A commonly carried genetic variant, rs9616915, in SHANK3 gene is associated with a reduced risk of autism spectrum disorder: replication in a Chinese population.
    Shao S, Xu S, Yang J, Zhang T, He Z, Sun Z, Song R.
    Mol Biol Rep; 2014 Mar 05; 41(3):1591-5. PubMed ID: 24398551
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  • 17. Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.
    Qin J, Jia M, Wang L, Lu T, Ruan Y, Liu J, Guo Y, Zhang J, Yang X, Yue W, Zhang D.
    BMC Med Genet; 2009 Jun 30; 10():61. PubMed ID: 19566951
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  • 20. Identification of SHANK2 Pathogenic Variants in a Chinese Uygur Population with Schizophrenia.
    Zhang H, Wang D, Chen J, Li X, Yi Q, Shi Y.
    J Mol Neurosci; 2021 Jan 30; 71(1):1-8. PubMed ID: 32897530
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