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Journal Abstract Search

560 related items for PubMed ID: 15158428

  • 1. Serotonin transporter promoter and intron 2 polymorphisms: relationship between allelic variants and gene expression.
    Hranilovic D, Stefulj J, Schwab S, Borrmann-Hassenbach M, Albus M, Jernej B, Wildenauer D.
    Biol Psychiatry; 2004 Jun 01; 55(11):1090-4. PubMed ID: 15158428
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  • 6. Serotonin transporter gene promoter (5-HTTLPR) and intron 2 (VNTR) polymorphisms: a study on Slovenian population of suicide victims.
    Pungercic G, Videtic A, Pestotnik A, Pajnic IZ, Zupanc T, Balazic J, Tomori M, Komel R.
    Psychiatr Genet; 2006 Oct 01; 16(5):187-91. PubMed ID: 16969272
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  • 10. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder.
    Kim SJ, Cox N, Courchesne R, Lord C, Corsello C, Akshoomoff N, Guter S, Leventhal BL, Courchesne E, Cook EH.
    Mol Psychiatry; 2002 Oct 01; 7(3):278-88. PubMed ID: 11920155
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  • 12. A polymorphism (5-HTTLPR) in the serotonin transporter promoter gene is associated with DSM-IV depression subtypes in seasonal affective disorder.
    Willeit M, Praschak-Rieder N, Neumeister A, Zill P, Leisch F, Stastny J, Hilger E, Thierry N, Konstantinidis A, Winkler D, Fuchs K, Sieghart W, Aschauer H, Ackenheil M, Bondy B, Kasper S.
    Mol Psychiatry; 2003 Nov 01; 8(11):942-6. PubMed ID: 14593433
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  • 13. Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy.
    Manna I, Labate A, Gambardella A, Forabosco P, La Russa A, Le Piane E, Aguglia U, Quattrone A.
    Neurosci Lett; 2007 Jun 21; 421(1):52-6. PubMed ID: 17548158
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  • 19. Socio-economic status covaries with central nervous system serotonergic responsivity as a function of allelic variation in the serotonin transporter gene-linked polymorphic region.
    Manuck SB, Flory JD, Ferrell RE, Muldoon MF.
    Psychoneuroendocrinology; 2004 Jun 21; 29(5):651-68. PubMed ID: 15041087
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  • 20. Analysis of the serotonin transporter gene linked polymorphism (5-HTTLPR) in anorexia nervosa.
    Sundaramurthy D, Pieri LF, Gape H, Markham AF, Campbell DA.
    Am J Med Genet; 2000 Feb 07; 96(1):53-5. PubMed ID: 10686552
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