These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

291 related articles for article (PubMed ID: 19890261)

  • 1. 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; 35(3):656-64. PubMed ID: 19890261
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 147B(8):1576-9. PubMed ID: 18802924
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 168B(2):89-96. PubMed ID: 25656223
    [TBL] [Abstract][Full Text] [Related]  

  • 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():21. PubMed ID: 26058807
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 264(5):401-8. PubMed ID: 24487615
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 144B(4):541-50. PubMed ID: 17440978
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 126(4):517-529. PubMed ID: 30923918
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 49(4):333-9. PubMed ID: 11239904
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence of an association between 10/10 genotype of DAT1 and endophenotypes of attention deficit/hyperactivity disorder.
    Agudelo JA; Gálvez JM; Fonseca DJ; Mateus HE; Talero-Gutiérrez C; Velez-Van-Meerbeke A
    Neurologia; 2015 Apr; 30(3):137-43. PubMed ID: 24461309
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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; 35(4):412-8. PubMed ID: 12947560
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 64(5):585-90. PubMed ID: 17485610
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Enlarged striatal volume in adults with ADHD carrying the 9-6 haplotype of the dopamine transporter gene DAT1.
    Onnink AM; Franke B; van Hulzen K; Zwiers MP; Mostert JC; Schene AH; Heslenfeld DJ; Oosterlaan J; Hoekstra PJ; Hartman CA; Vasquez AA; Kan CC; Buitelaar J; Hoogman M
    J Neural Transm (Vienna); 2016 Aug; 123(8):905-15. PubMed ID: 26935821
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A review and analysis of the relationship between neuropsychological measures and DAT1 in ADHD.
    Rommelse NN; Altink ME; Arias-Vásquez A; Buschgens CJ; Fliers E; Faraone SV; Buitelaar JK; Sergeant JA; Franke B; Oosterlaan J
    Am J Med Genet B Neuropsychiatr Genet; 2008 Dec; 147B(8):1536-46. PubMed ID: 18729135
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of dopamine gene variants, emotion dysregulation and ADHD in autism spectrum disorder.
    Gadow KD; Pinsonneault JK; Perlman G; Sadee W
    Res Dev Disabil; 2014 Jul; 35(7):1658-65. PubMed ID: 24780147
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 139B(1):1-6. PubMed ID: 16082693
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 33(10):2536-45. PubMed ID: 18046306
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.
    Bonvicini C; Faraone SV; Scassellati C
    Mol Psychiatry; 2016 Jul; 21(7):872-84. PubMed ID: 27217152
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lack of association between the dopamine transporter gene 3' VNTR polymorphism and attention deficit hyperactivity disorder in Chinese Han children: case-control and family-based studies.
    Wang Y; Wang Z; Yao K; Tanaka K; Yang Y; Shirakawa O; Maeda K
    Kobe J Med Sci; 2008 Feb; 53(6):327-33. PubMed ID: 18762727
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional genomics of attention-deficit/hyperactivity disorder (ADHD) risk alleles on dopamine transporter binding in ADHD and healthy control subjects.
    Spencer TJ; Biederman J; Faraone SV; Madras BK; Bonab AA; Dougherty DD; Batchelder H; Clarke A; Fischman AJ
    Biol Psychiatry; 2013 Jul; 74(2):84-9. PubMed ID: 23273726
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 156B(5):600-12. PubMed ID: 21595008
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.