BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 22451510)

  • 1. Catechol-o-methyltransferase gene and executive function in children with ADHD.
    Choudhry Z; Sengupta S; Thakur G; Page V; Schmitz N; Grizenko N; Joober R
    J Atten Disord; 2014 Apr; 18(3):202-11. PubMed ID: 22451510
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.
    Halleland H; Lundervold AJ; Halmøy A; Haavik J; Johansson S
    Am J Med Genet B Neuropsychiatr Genet; 2009 Apr; 150B(3):403-10. PubMed ID: 18802928
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Catechol-O-methyltransferase (COMT) Val108/158 Met polymorphism does not modulate executive function in children with ADHD.
    Taerk E; Grizenko N; Ben Amor L; Lageix P; Mbekou V; Deguzman R; Torkaman-Zehi A; Ter Stepanian M; Baron C; Joober R
    BMC Med Genet; 2004 Dec; 5():30. PubMed ID: 15613245
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.
    Kocabas NA; Faghel C; Barreto M; Kasper S; Linotte S; Mendlewicz J; Noro M; Oswald P; Souery D; Zohar J; Massat I
    Int Clin Psychopharmacol; 2010 Jul; 25(4):218-27. PubMed ID: 20531207
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The divergent impact of COMT Val158Met on executive function in children with and without attention-deficit/hyperactivity disorder.
    Jin J; Liu L; Gao Q; Chan RC; Li H; Chen Y; Wang Y; Qian Q
    Genes Brain Behav; 2016 Feb; 15(2):271-9. PubMed ID: 26560848
    [TBL] [Abstract][Full Text] [Related]  

  • 6. COMT Val158Met variant and functional haplotypes associated with childhood ADHD history in women with bulimia nervosa.
    Yilmaz Z; Kaplan AS; Zai CC; Levitan RD; Kennedy JL
    Prog Neuropsychopharmacol Biol Psychiatry; 2011 Jun; 35(4):948-52. PubMed ID: 21300128
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype.
    Eisenberg J; Mei-Tal G; Steinberg A; Tartakovsky E; Zohar A; Gritsenko I; Nemanov L; Ebstein RP
    Am J Med Genet; 1999 Oct; 88(5):497-502. PubMed ID: 10490706
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Catechol-O-methyltransferase polymorphism is associated with the cortico-cerebellar functional connectivity of executive function in children with attention-deficit/hyperactivity disorder.
    Mizuno Y; Jung M; Fujisawa TX; Takiguchi S; Shimada K; Saito DN; Kosaka H; Tomoda A
    Sci Rep; 2017 Jul; 7(1):4850. PubMed ID: 28687733
    [TBL] [Abstract][Full Text] [Related]  

  • 9. No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study.
    Mills S; Langley K; Van den Bree M; Street E; Turic D; Owen MJ; O'Donovan MC; Thapar A
    BMC Psychiatry; 2004 Jun; 4():15. PubMed ID: 15182372
    [TBL] [Abstract][Full Text] [Related]  

  • 10. COMT gene haplotypes are closely associated with postoperative fentanyl dose in patients.
    Zhang F; Tong J; Hu J; Zhang H; Ouyang W; Huang D; Tang Q; Liao Q
    Anesth Analg; 2015 Apr; 120(4):933-40. PubMed ID: 25532715
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults.
    Retz W; Rösler M; Kissling C; Wiemann S; Hünnerkopf R; Coogan A; Thome J; Freitag C
    J Neural Transm (Vienna); 2008; 115(2):323-9. PubMed ID: 17994190
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association between COMT methylation and response to treatment in children with ADHD.
    Fageera W; Chaumette B; Fortier MÈ; Grizenko N; Labbe A; Sengupta SM; Joober R
    J Psychiatr Res; 2021 Mar; 135():86-93. PubMed ID: 33453563
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD).
    Turic D; Williams H; Langley K; Owen M; Thapar A; O'Donovan MC
    Am J Med Genet B Neuropsychiatr Genet; 2005 Feb; 133B(1):64-7. PubMed ID: 15635644
    [TBL] [Abstract][Full Text] [Related]  

  • 14. No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample.
    Hawi Z; Millar N; Daly G; Fitzgerald M; Gill M
    Am J Med Genet; 2000 Jun; 96(3):282-4. PubMed ID: 10898900
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association study of the functional Catechol-O-Methyltranferase (COMT) Val
    Khanthiyong B; Thanoi S; Reynolds GP; Nudmamud-Thanoi S
    Int J Med Sci; 2019; 16(11):1461-1465. PubMed ID: 31673237
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents.
    DeYoung CG; Getchell M; Koposov RA; Yrigollen CM; Haeffel GJ; af Klinteberg B; Oreland L; Ruchkin VV; Pakstis AJ; Grigorenko EL
    Psychiatr Genet; 2010 Feb; 20(1):20-4. PubMed ID: 19997043
    [TBL] [Abstract][Full Text] [Related]  

  • 17. No association between catechol-O-methyltransferase (COMT) genotype and attention deficit hyperactivity disorder (ADHD) in Japanese children.
    Yatsuga C; Toyohisa D; Fujisawa TX; Nishitani S; Shinohara K; Matsuura N; Ikeda S; Muramatsu M; Hamada A; Tomoda A
    Brain Dev; 2014 Aug; 36(7):620-5. PubMed ID: 24035255
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia.
    Vargas-Alarcón G; Fragoso JM; Cruz-Robles D; Vargas A; Vargas A; Lao-Villadóniga JI; García-Fructuoso F; Ramos-Kuri M; Hernández F; Springall R; Bojalil R; Vallejo M; Martínez-Lavín M
    Arthritis Res Ther; 2007; 9(5):R110. PubMed ID: 17961261
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene].
    Zhang XN; Ruan LM; Le YP; Zhang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):322-4. PubMed ID: 12903043
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Catechol-O-methyltransferase Val158-Met polymorphism and a response of hyperactive-impulsive symptoms to methylphenidate: A replication study from South Korea.
    Park S; Kim JW; Kim BN; Shin MS; Yoo HJ; Cho SC
    J Psychopharmacol; 2014 Jul; 28(7):671-6. PubMed ID: 24763183
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.