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278 related items for PubMed ID: 16481140

  • 1. Serotonin transporter gene promoter polymorphism and autism: a family-based genetic association study in Japanese population.
    Koishi S, Yamamoto K, Matsumoto H, Koishi S, Enseki Y, Oya A, Asakura A, Aoki Y, Atsumi M, Iga T, Inomata J, Inoko H, Sasaki T, Nanba E, Kato N, Ishii T, Yamazaki K.
    Brain Dev; 2006 May; 28(4):257-60. PubMed ID: 16481140
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  • 3. Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples.
    Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Conciatori M, Damiani V, Baldi A, Keller F.
    Am J Med Genet; 2000 Feb 07; 96(1):123-7. PubMed ID: 10686565
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  • 4. Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura.
    Todt U, Freudenberg J, Goebel I, Heinze A, Heinze-Kuhn K, Rietschel M, Göbel H, Kubisch C.
    Neurology; 2006 Nov 14; 67(9):1707-9. PubMed ID: 17101915
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  • 5. Analysis of serotonin receptor 2A gene (HTR2A): association study with autism spectrum disorder in the Indian population and investigation of the gene expression in peripheral blood leukocytes.
    Guhathakurta S, Singh AS, Sinha S, Chatterjee A, Ahmed S, Ghosh S, Usha R.
    Neurochem Int; 2009 Dec 14; 55(8):754-9. PubMed ID: 19647026
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  • 11. Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder.
    Betancur C, Corbex M, Spielewoy C, Philippe A, Laplanche JL, Launay JM, Gillberg C, Mouren-Siméoni MC, Hamon M, Giros B, Nosten-Bertrand M, Leboyer M.
    Mol Psychiatry; 2002 Dec 14; 7(1):67-71. PubMed ID: 11803447
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  • 15. Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism.
    Coutinho AM, Oliveira G, Morgadinho T, Fesel C, Macedo TR, Bento C, Marques C, Ataíde A, Miguel T, Borges L, Vicente AM.
    Mol Psychiatry; 2004 Mar 14; 9(3):264-71. PubMed ID: 15094787
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  • 18. [Transmission disequilibrium test of polymorphisms of serotonin transporter gene and schizophrenia based on family trios].
    Sun WW, Fan JB, Qian XQ, Tang JX, Xing YL, Shi JG, Zhu SM, Liu HJ, Gu NF, Feng GY, He L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug 14; 20(4):342-4. PubMed ID: 12903048
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  • 19. Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.
    Wassink TH, Hazlett HC, Epping EA, Arndt S, Dager SR, Schellenberg GD, Dawson G, Piven J.
    Arch Gen Psychiatry; 2007 Jun 14; 64(6):709-17. PubMed ID: 17548752
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  • 20. The tryptophan hydroxylase 1 (TPH1) gene and risk of schizophrenia: a moderate-scale case-control study and meta-analysis.
    Watanabe Y, Nunokawa A, Kaneko N, Someya T.
    Neurosci Res; 2007 Nov 14; 59(3):322-6. PubMed ID: 17870198
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