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 *

111 related articles for article (PubMed ID: 35130472)

  • 1. Driving risks of young drivers with symptoms of attention deficit hyperactivity disorder: association with the dopamine transporter gene VNTR polymorphism.
    Tokko T; Miškinyte G; Eensoo D; Harro J
    Nord J Psychiatry; 2022 Nov; 76(8):575-583. PubMed ID: 35130472
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

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

  • 6. 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]  

  • 7. Efficacy of intervention at traffic schools reducing impulsive action, and association with candidate gene variants.
    Luht K; Tokko T; Eensoo D; Vaht M; Harro J
    Acta Neuropsychiatr; 2019 Jun; 31(3):159-166. PubMed ID: 31182183
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 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. Association of the DAT1 polymorphism with attention deficit hyperactivity disorder (ADHD): a family-based approach.
    Lim MH; Kim HW; Paik KC; Cho SC; Yoon DY; Lee HJ
    Am J Med Genet B Neuropsychiatr Genet; 2006 Apr; 141B(3):309-11. PubMed ID: 16526026
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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; 10(1):31-4. PubMed ID: 16545000
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An examination of the behavioral and neuropsychological correlates of three ADHD candidate gene polymorphisms (DRD4 7+, DBH TaqI A2, and DAT1 40 bp VNTR) in hyperactive and normal children followed to adulthood.
    Barkley RA; Smith KM; Fischer M; Navia B
    Am J Med Genet B Neuropsychiatr Genet; 2006 Jul; 141B(5):487-98. PubMed ID: 16741944
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Dopamine transporter genotype modulates brain activity during a working memory task in children with ADHD.
    Pineau G; Villemonteix T; Slama H; Kavec M; Balériaux D; Metens T; Baijot S; Mary A; Ramoz N; Gorwood P; Peigneux P; Massat I
    Res Dev Disabil; 2019 Sep; 92():103430. PubMed ID: 31306870
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 4(2):83-92. PubMed ID: 15059031
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.