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Journal Abstract Search

226 related items for PubMed ID: 18802924

  • 1. 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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  • 2. Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.
    Franke B, Vasquez AA, Johansson S, Hoogman M, Romanos J, Boreatti-Hümmer A, Heine M, Jacob CP, Lesch KP, Casas M, Ribasés M, Bosch R, Sánchez-Mora C, Gómez-Barros N, Fernàndez-Castillo N, Bayés M, Halmøy A, Halleland H, Landaas ET, Fasmer OB, Knappskog PM, Heister AJ, Kiemeney LA, Kooij JJ, Boonstra AM, Kan CC, Asherson P, Faraone SV, Buitelaar JK, Haavik J, Cormand B, Ramos-Quiroga JA, Reif A.
    Neuropsychopharmacology; 2010 Feb 05; 35(3):656-64. PubMed ID: 19890261
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  • 3. 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 05; 168B(2):89-96. PubMed ID: 25656223
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  • 4. 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. 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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  • 9. Polymorphisms of the dopamine transporter gene: influence on response to methylphenidate in attention deficit-hyperactivity disorder.
    Roman T, Rohde LA, Hutz MH.
    Am J Pharmacogenomics; 2004 Jun 05; 4(2):83-92. PubMed ID: 15059031
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  • 10. Genetic analyses of dopamine related genes in adult ADHD patients suggest an association with the DRD5-microsatellite repeat, but not with DRD4 or SLC6A3 VNTRs.
    Johansson S, Halleland H, Halmøy A, Jacobsen KK, Landaas ET, Dramsdahl M, Fasmer OB, Bergsholm P, Lundervold AJ, Gillberg C, Hugdahl K, Knappskog PM, Haavik J.
    Am J Med Genet B Neuropsychiatr Genet; 2008 Dec 05; 147B(8):1470-5. PubMed ID: 18081165
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  • 12. 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 05; 15(4):305-9. PubMed ID: 20332413
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  • 14. The dopamine transporter haplotype and reward-related striatal responses in adult ADHD.
    Hoogman M, Onnink M, Cools R, Aarts E, Kan C, Arias Vasquez A, Buitelaar J, Franke B.
    Eur Neuropsychopharmacol; 2013 Jun 05; 23(6):469-78. PubMed ID: 22749356
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  • 16. 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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  • 18. 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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  • 20. Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four European populations.
    Sánchez-Mora C, Ribasés M, Casas M, Bayés M, Bosch R, Fernàndez-Castillo N, Brunso L, Jacobsen KK, Landaas ET, Lundervold AJ, Gross-Lesch S, Kreiker S, Jacob CP, Lesch KP, Buitelaar JK, Hoogman M, Kiemeney LA, Kooij JJ, Mick E, Asherson P, Faraone SV, Franke B, Reif A, Johansson S, Haavik J, Ramos-Quiroga JA, Cormand B.
    Am J Med Genet B Neuropsychiatr Genet; 2011 Jul 15; 156B(5):600-12. PubMed ID: 21595008
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