130 related articles for article (PubMed ID: 19371223)
1. Association between catechol-O-methyltransferase gene polymorphism and attention-deficit hyperactivity disorder in Korean population.
Song EY; Paik KC; Kim HW; Lim MH
Genet Test Mol Biomarkers; 2009 Apr; 13(2):233-6. PubMed ID: 19371223
[TBL] [Abstract][Full Text] [Related]
2. No association between attention-deficit hyperactivity disorder and catechol-O-methyltransferase gene in Chinese.
Jiang SD; Wu XD; Zhang Y; Tang GM; Qian YP; Wang DX
Yi Chuan Xue Bao; 2005 Aug; 32(8):784-8. PubMed ID: 16231731
[TBL] [Abstract][Full Text] [Related]
3. Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism.
Qian Q; Wang Y; Zhou R; Li J; Wang B; Glatt S; Faraone SV
Am J Med Genet B Neuropsychiatr Genet; 2003 Apr; 118B(1):103-9. PubMed ID: 12627475
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [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]
6. 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]
7. Association between TPH2 gene polymorphisms and attention deficit hyperactivity disorder in Korean children.
Park TW; Park YH; Kwon HJ; Lim MH
Genet Test Mol Biomarkers; 2013 Apr; 17(4):301-6. PubMed ID: 23461725
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Catechol-O-methyltransferase gene rs6267 polymorphism in children with attention deficit hyperactivity disorder].
Zhang YB; Luo XR; Liu X; Zhong Y; Zhu F; Chen LY
Zhongguo Dang Dai Er Ke Za Zhi; 2011 Feb; 13(2):127-30. PubMed ID: 21342622
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Clinical and genetic characteristics of Korean male alcoholics with and without attention deficit hyperactivity disorder.
Kim JW; Park CS; Hwang JW; Shin MS; Hong KE; Cho SC; Kim BN
Alcohol Alcohol; 2006; 41(4):407-11. PubMed ID: 16679343
[TBL] [Abstract][Full Text] [Related]
12. Evaluation of potential gene-gene interactions for attention deficit hyperactivity disorder in the Han Chinese population.
Qian Q; Wang Y; Li J; Yang L; Wang B; Zhou R; Glatt SJ; Faraone SV
Am J Med Genet B Neuropsychiatr Genet; 2007 Mar; 144B(2):200-6. PubMed ID: 17044099
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Association between dopamine Beta-hydroxylase gene polymorphisms and attention-deficit hyperactivity disorder in korean children.
Kwon HJ; Lim MH
Genet Test Mol Biomarkers; 2013 Jul; 17(7):529-34. PubMed ID: 23692268
[TBL] [Abstract][Full Text] [Related]
15. Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder.
Barr CL; Wigg K; Malone M; Schachar R; Tannock R; Roberts W; Kennedy JL
Am J Med Genet; 1999 Dec; 88(6):710-3. PubMed ID: 10581494
[TBL] [Abstract][Full Text] [Related]
16. Catechol-O-methyltransferase Val158Met polymorphism is associated with methylphenidate response in ADHD children.
Kereszturi E; Tarnok Z; Bognar E; Lakatos K; Farkas L; Gadoros J; Sasvari-Szekely M; Nemoda Z
Am J Med Genet B Neuropsychiatr Genet; 2008 Dec; 147B(8):1431-5. PubMed ID: 18214865
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Cathechol-O-methyltransferase Val(158)Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD.
Salatino-Oliveira A; Genro JP; Guimarães AP; Chazan R; Zeni C; Schmitz M; Polanczyk G; Roman T; Rohde LA; Hutz MH
J Neural Transm (Vienna); 2012 Jun; 119(6):729-33. PubMed ID: 22270685
[TBL] [Abstract][Full Text] [Related]
19. Catechol-O-methyltransferase valine158methionine polymorphism moderates methylphenidate effects on oppositional symptoms in boys with attention-deficit/hyperactivity disorder.
Salatino-Oliveira A; Genro JP; Zeni C; Polanczyk GV; Chazan R; Guimarães AP; Callegari-Jacques SM; Rohde LA; Hutz MH
Biol Psychiatry; 2011 Aug; 70(3):216-21. PubMed ID: 21550019
[TBL] [Abstract][Full Text] [Related]
20. Failure to replicate an association between the catechol-O-methyltransferase polymorphism and attention deficit hyperactivity disorder in a second, independently recruited Israeli cohort.
Manor I; Kotler M; Sever Y; Eisenberg J; Cohen H; Ebstein RP; Tyano S
Am J Med Genet; 2000 Dec; 96(6):858-60. PubMed ID: 11121197
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
