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189 related items for PubMed ID: 17579365

  • 1. Relationship between VNTR polymorphisms of the human dopamine transporter gene and expression in post-mortem midbrain tissue.
    Brookes KJ, Neale BM, Sugden K, Khan N, Asherson P, D'Souza UM.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Dec 05; 144B(8):1070-8. PubMed ID: 17579365
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  • 3. The VNTR polymorphism in the human dopamine transporter gene: improved detection and absence of association of VNTR alleles with attention-deficit hyperactivity disorder.
    Simsek M, Al-Sharbati M, Al-Adawi S, Lawatia K.
    Genet Test; 2006 Dec 05; 10(1):31-4. PubMed ID: 16545000
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  • 4. Association study and a systematic meta-analysis of the VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention-deficit hyperactivity disorder.
    Grünblatt E, Werling AM, Roth A, Romanos M, Walitza S.
    J Neural Transm (Vienna); 2019 Apr 05; 126(4):517-529. PubMed ID: 30923918
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  • 5. A 40-bp VNTR polymorphism in the 3'-untranslated region of DAT1/SLC6A3 is associated with ADHD but not with alcoholism.
    Šerý O, Paclt I, Drtílková I, Theiner P, Kopečková M, Zvolský P, Balcar VJ.
    Behav Brain Funct; 2015 Jun 11; 11():21. PubMed ID: 26058807
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  • 6. Dopamine transporter gene variation modulates activation of striatum in youth with ADHD.
    Bédard AC, Schulz KP, Cook EH, Fan J, Clerkin SM, Ivanov I, Halperin JM, Newcorn JH.
    Neuroimage; 2010 Nov 15; 53(3):935-42. PubMed ID: 20026227
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  • 9. The VNTR polymorphism of the human dopamine transporter (DAT1) gene affects gene expression.
    Fuke S, Suo S, Takahashi N, Koike H, Sasagawa N, Ishiura S.
    Pharmacogenomics J; 2001 Nov 15; 1(2):152-6. PubMed ID: 11911442
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  • 10. The variable number of tandem repeats element in DAT1 regulates in vitro dopamine transporter density.
    VanNess SH, Owens MJ, Kilts CD.
    BMC Genet; 2005 Nov 27; 6():55. PubMed ID: 16309561
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  • 11. No association between a common haplotype of the 6 and 10-repeat alleles in intron 8 and the 3'UTR of the DAT1 gene and adult attention deficit hyperactivity disorder.
    Brüggemann D, Sobanski E, Alm B, Schubert T, Schmalzried H, Philipsen A, Breen G, Becker T, Georgi A, Skowronek MH, Schulze TG, Treutlein J, Rietschel M.
    Psychiatr Genet; 2007 Apr 27; 17(2):121. PubMed ID: 17413453
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  • 14. Spatial attentional bias as a marker of genetic risk, symptom severity, and stimulant response in ADHD.
    Bellgrove MA, Barry E, Johnson KA, Cox M, Dáibhis A, Daly M, Hawi Z, Lambert D, Fitzgerald M, McNicholas F, Robertson IH, Gill M, Kirley A.
    Neuropsychopharmacology; 2008 Sep 27; 33(10):2536-45. PubMed ID: 18046306
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  • 15. An association between a dopamine transporter gene (SLC6A3) haplotype and ADHD symptom measures in nonclinical adults.
    Tong JH, Cummins TD, Johnson BP, McKinley LA, Pickering HE, Fanning P, Stefanac NR, Newman DP, Hawi Z, Bellgrove MA.
    Am J Med Genet B Neuropsychiatr Genet; 2015 Mar 27; 168B(2):89-96. PubMed ID: 25656223
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  • 16. A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample.
    Guindalini C, Howard M, Haddley K, Laranjeira R, Collier D, Ammar N, Craig I, O'Gara C, Bubb VJ, Greenwood T, Kelsoe J, Asherson P, Murray RM, Castelo A, Quinn JP, Vallada H, Breen G.
    Proc Natl Acad Sci U S A; 2006 Mar 21; 103(12):4552-7. PubMed ID: 16537431
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  • 17. Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants.
    Hill M, Anney RJ, Gill M, Hawi Z.
    Pharmacogenomics J; 2010 Oct 21; 10(5):442-7. PubMed ID: 20029387
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  • 19. Association between dopamine transporter genotypes and smoking cessation: a meta-analysis.
    Stapleton JA, Sutherland G, O'Gara C.
    Addict Biol; 2007 Jun 21; 12(2):221-6. PubMed ID: 17508996
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  • 20. Lack of association between a 3'UTR VNTR polymorphism of dopamine transporter gene (SLC6A3) and ADHD in a Brazilian sample of adult patients.
    Aparecida da Silva M, Cordeiro Q, Louzã M, Vallada H.
    J Atten Disord; 2011 May 21; 15(4):305-9. PubMed ID: 20332413
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