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Journal Abstract Search


404 related items for PubMed ID: 18404133

  • 1. Some ADHD polymorphisms (in genes DAT1, DRD2, DRD3, DBH, 5-HTT) in case-control study of 100 subjects 6-10 age.
    Kopecková M, Paclt I, Petrásek J, Pacltová D, Malíková M, Zagatová V.
    Neuro Endocrinol Lett; 2008 Apr; 29(2):246-51. PubMed ID: 18404133
    [Abstract] [Full Text] [Related]

  • 2. Transmission disequilibrium testing of dopamine-related candidate gene polymorphisms in ADHD: confirmation of association of ADHD with DRD4 and DRD5.
    Kustanovich V, Ishii J, Crawford L, Yang M, McGough JJ, McCracken JT, Smalley SL, Nelson SF.
    Mol Psychiatry; 2004 Jul; 9(7):711-7. PubMed ID: 14699430
    [Abstract] [Full Text] [Related]

  • 3. Genetic interaction analysis for DRD4 and DAT1 genes in a group of Mexican ADHD patients.
    Gabriela ML, John DG, Magdalena BV, Ariadna GS, Francisco de LP, Liz SM, Lino PC, Josefina RG, Ernesto RZ, Carlos CF.
    Neurosci Lett; 2009 Feb 27; 451(3):257-60. PubMed ID: 19146920
    [Abstract] [Full Text] [Related]

  • 4. Family-based and case-control study of DRD2, DAT, 5HTT, COMT genes polymorphisms in alcohol dependence.
    Samochowiec J, Kucharska-Mazur J, Grzywacz A, Jabłoński M, Rommelspacher H, Samochowiec A, Sznabowicz M, Horodnicki J, Sagan L, Pełka-Wysiecka J.
    Neurosci Lett; 2006 Dec 13; 410(1):1-5. PubMed ID: 17079080
    [Abstract] [Full Text] [Related]

  • 5. Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci.
    Hawi Z, Lowe N, Kirley A, Gruenhage F, Nöthen M, Greenwood T, Kelsoe J, Fitzgerald M, Gill M.
    Mol Psychiatry; 2003 Mar 13; 8(3):299-308. PubMed ID: 12660802
    [Abstract] [Full Text] [Related]

  • 6. Candidate system analysis in ADHD: evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1.
    Ribasés M, Ramos-Quiroga JA, Hervás A, Sánchez-Mora C, Bosch R, Bielsa A, Gastaminza X, Lesch KP, Reif A, Renner TJ, Romanos M, Warnke A, Walitza S, Freitag C, Meyer J, Palmason H, Casas M, Bayés M, Cormand B.
    World J Biol Psychiatry; 2012 Apr 13; 13(4):281-92. PubMed ID: 22404661
    [Abstract] [Full Text] [Related]

  • 7. Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.
    Bhaduri N, Sinha S, Chattopadhyay A, Gangopadhyay PK, Singh M, Mukhopadhyay KK.
    Indian Pediatr; 2005 Feb 13; 42(2):123-9. PubMed ID: 15767706
    [Abstract] [Full Text] [Related]

  • 8. ADHD candidate gene study in a population-based birth cohort: association with DBH and DRD2.
    Nyman ES, Ogdie MN, Loukola A, Varilo T, Taanila A, Hurtig T, Moilanen IK, Loo SK, McGough JJ, Järvelin MR, Smalley SL, Nelson SF, Peltonen L.
    J Am Acad Child Adolesc Psychiatry; 2007 Dec 13; 46(12):1614-21. PubMed ID: 18030083
    [Abstract] [Full Text] [Related]

  • 9. No association between lithium full responders and the DRD1, DRD2, DRD3, DAT1, 5-HTTLPR and HTR2A genes in a Sardinian sample.
    Manchia M, Congiu D, Squassina A, Lampus S, Ardau R, Chillotti C, Severino G, Del Zompo M.
    Psychiatry Res; 2009 Sep 30; 169(2):164-6. PubMed ID: 19647327
    [Abstract] [Full Text] [Related]

  • 10. Lack of significant association between -1021C-->T polymorphism in the dopamine beta hydroxylase gene and attention deficit hyperactivity disorder.
    Bhaduri N, Mukhopadhyay K.
    Neurosci Lett; 2006 Jul 10; 402(1-2):12-6. PubMed ID: 16616989
    [Abstract] [Full Text] [Related]

  • 11. Association study between the DAT1, DBH and DRD2 genes and cocaine dependence in a Spanish sample.
    Fernàndez-Castillo N, Ribasés M, Roncero C, Casas M, Gonzalvo B, Cormand B.
    Psychiatr Genet; 2010 Dec 10; 20(6):317-20. PubMed ID: 20505554
    [Abstract] [Full Text] [Related]

  • 12. Candidate gene studies of attention-deficit/hyperactivity disorder.
    Faraone SV, Khan SA.
    J Clin Psychiatry; 2006 Dec 10; 67 Suppl 8():13-20. PubMed ID: 16961425
    [Abstract] [Full Text] [Related]

  • 13. Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: the additive and subtractive effect of the three dopaminergic genes--DRD2, D beta H, and DAT1.
    Comings DE, Wu S, Chiu C, Ring RH, Gade R, Ahn C, MacMurray JP, Dietz G, Muhleman D.
    Am J Med Genet; 1996 May 31; 67(3):264-88. PubMed ID: 8725745
    [Abstract] [Full Text] [Related]

  • 14. Dissecting the attention deficit hyperactivity disorder (ADHD) phenotype: sustained attention, response variability and spatial attentional asymmetries in relation to dopamine transporter (DAT1) genotype.
    Bellgrove MA, Hawi Z, Kirley A, Gill M, Robertson IH.
    Neuropsychologia; 2005 May 31; 43(13):1847-57. PubMed ID: 16168728
    [Abstract] [Full Text] [Related]

  • 15. Genetic polymorphisms in the dopamine-2 receptor (DRD2), dopamine-3 receptor (DRD3), and dopamine transporter (SLC6A3) genes in schizophrenia: Data from an association study.
    Sáiz PA, García-Portilla MP, Arango C, Morales B, Arias B, Corcoran P, Fernández JM, Alvarez V, Coto E, Bascarán MT, Bousoño M, Fañanas L, Bobes J.
    Prog Neuropsychopharmacol Biol Psychiatry; 2010 Feb 01; 34(1):26-31. PubMed ID: 19766158
    [Abstract] [Full Text] [Related]

  • 16. [Combination of DRD4 and DAT1 genotypes is an important risk factor for attention deficit disorder with hyperactivity families living in Santiago, Chile].
    Henríquez B H, Henríquez H M, Carrasco Ch X, Rothhammer A P, Llop R E, Aboitiz F, Rothhammer E F.
    Rev Med Chil; 2008 Jun 01; 136(6):719-24. PubMed ID: 18769827
    [Abstract] [Full Text] [Related]

  • 17. [Family based association study of DRD1, DRD2, DRD3, DRD4, DAT, COMT gene polymorphism in schizophrenia].
    Paweł K, Hauser J, Skibińska M, Szczepankiewicz A, Dmitrzak-Weglarz M, Gorzkowska K, Pawlak J, Czerski PM.
    Psychiatr Pol; 2010 Jun 01; 44(3):405-13. PubMed ID: 20672519
    [Abstract] [Full Text] [Related]

  • 18. The dopamine transporter gene and the impulsivity phenotype in attention deficit hyperactivity disorder: a case-control association study in a Korean sample.
    Kim JW, Kim BN, Cho SC.
    J Psychiatr Res; 2006 Dec 01; 40(8):730-7. PubMed ID: 16368111
    [Abstract] [Full Text] [Related]

  • 19. No causal role for the G482T and G689T polymorphisms in translation regulation of serotonin transporter (SLC6A4) or association with attention-deficit-hyperactivity disorder (ADHD).
    Banerjee E, Sinha S, Chatterjee A, Nandagopal K.
    Neurosci Lett; 2009 May 01; 454(3):244-8. PubMed ID: 19429092
    [Abstract] [Full Text] [Related]

  • 20. Dopaminergic haplotype as a predictor of spatial inattention in children with attention-deficit/hyperactivity disorder.
    Bellgrove MA, Johnson KA, Barry E, Mulligan A, Hawi Z, Gill M, Robertson I, Chambers CD.
    Arch Gen Psychiatry; 2009 Oct 01; 66(10):1135-42. PubMed ID: 19805704
    [Abstract] [Full Text] [Related]


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