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Journal Abstract Search

289 related items for PubMed ID: 18802919

  • 1. A common haplotype at the dopamine transporter gene 5' region is associated with attention-deficit/hyperactivity disorder.
    Genro JP, Polanczyk GV, Zeni C, Oliveira AS, Roman T, Rohde LA, Hutz MH.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Dec 05; 147B(8):1568-75. PubMed ID: 18802919
    [Abstract] [Full Text] [Related]

  • 2. Association between the dopamine transporter gene and the inattentive subtype of attention deficit hyperactivity disorder in Taiwan.
    Shang CY, Gau SS, Liu CM, Hwu HG.
    Prog Neuropsychopharmacol Biol Psychiatry; 2011 Mar 30; 35(2):421-8. PubMed ID: 20800641
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  • 3. Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder.
    Barr CL, Xu C, Kroft J, Feng Y, Wigg K, Zai G, Tannock R, Schachar R, Malone M, Roberts W, Nöthen MM, Grünhage F, Vandenbergh DJ, Uhl G, Sunohara G, King N, Kennedy JL.
    Biol Psychiatry; 2001 Feb 15; 49(4):333-9. PubMed ID: 11239904
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  • 4. A promoter polymorphism (-839 C > T) at the dopamine transporter gene is associated with attention deficit/hyperactivity disorder in Brazilian children.
    Genro JP, Zeni C, Polanczyk GV, Roman T, Rohde LA, Hutz MH.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Mar 05; 144B(2):215-9. PubMed ID: 17044101
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  • 5. Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity.
    Brookes KJ, Xu X, Anney R, Franke B, Zhou K, Chen W, Banaschewski T, Buitelaar J, Ebstein R, Eisenberg J, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Faraone SV, Asherson P.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Dec 05; 147B(8):1519-23. PubMed ID: 18668530
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  • 6. Interacting effects of the dopamine transporter gene and psychosocial adversity on attention-deficit/hyperactivity disorder symptoms among 15-year-olds from a high-risk community sample.
    Laucht M, Skowronek MH, Becker K, Schmidt MH, Esser G, Schulze TG, Rietschel M.
    Arch Gen Psychiatry; 2007 May 05; 64(5):585-90. PubMed ID: 17485610
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  • 7. [Association studies of dopamine D4 receptor gene and dopamine transporter gene polymorphisms in Han Chinese patients with attention deficit hyperactivity disorder].
    Qian Q, Wang Y, Li J, Yang L, Wang B, Zhou R.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2003 Aug 05; 35(4):412-8. PubMed ID: 12947560
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  • 9. Further evidence for the association between a polymorphism in the promoter region of SLC6A3/DAT1 and ADHD: findings from a sample of adults.
    de Azeredo LA, Rovaris DL, Mota NR, Polina ER, Marques FZ, Contini V, Vitola ES, Belmonte-de-Abreu P, Rohde LA, Grevet EH, Bau CH.
    Eur Arch Psychiatry Clin Neurosci; 2014 Aug 05; 264(5):401-8. PubMed ID: 24487615
    [Abstract] [Full Text] [Related]

  • 10. Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD).
    Feng Y, Wigg KG, Makkar R, Ickowicz A, Pathare T, Tannock R, Roberts W, Malone M, Kennedy JL, Schachar R, Barr CL.
    Am J Med Genet B Neuropsychiatr Genet; 2005 Nov 05; 139B(1):1-6. PubMed ID: 16082693
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  • 11. Role of gene-gene/gene-environment interaction in the etiology of eastern Indian ADHD probands.
    Das M, Das Bhowmik A, Bhaduri N, Sarkar K, Ghosh P, Sinha S, Ray A, Chatterjee A, Mukhopadhyay K.
    Prog Neuropsychopharmacol Biol Psychiatry; 2011 Mar 30; 35(2):577-87. PubMed ID: 21216270
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  • 13. A meta-analysis of association studies between the 10-repeat allele of a VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention deficit hyperactivity disorder.
    Yang B, Chan RC, Jing J, Li T, Sham P, Chen RY.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jun 05; 144B(4):541-50. PubMed ID: 17440978
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  • 15. Association of the dopamine transporter (SLC6A3/DAT1) gene 9-6 haplotype with adult ADHD.
    Franke B, Hoogman M, Arias Vasquez A, Heister JG, Savelkoul PJ, Naber M, Scheffer H, Kiemeney LA, Kan CC, Kooij JJ, Buitelaar JK.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Dec 05; 147B(8):1576-9. PubMed ID: 18802924
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