112 related articles for article (PubMed ID: 11121197)
21. 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]
22. No association between low- and high-activity catecholamine-methyl-transferase (COMT) and attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children.
Tahir E; Curran S; Yazgan Y; Ozbay F; Cirakoglu B; Asherson PJ
Am J Med Genet; 2000 Jun; 96(3):285-8. PubMed ID: 10898901
[TBL] [Abstract][Full Text] [Related]
23. Inferring candidate genes for attention deficit hyperactivity disorder (ADHD) assessed by the World Health Organization Adult ADHD Self-Report Scale (ASRS).
Reuter M; Kirsch P; Hennig J
J Neural Transm (Vienna); 2006 Jul; 113(7):929-38. PubMed ID: 16362639
[TBL] [Abstract][Full Text] [Related]
24. Meta-analysis of association between a catechol-O-methyltransferase gene polymorphism and attention deficit hyperactivity disorder.
Cheuk DK; Wong V
Behav Genet; 2006 Sep; 36(5):651-9. PubMed ID: 16676224
[TBL] [Abstract][Full Text] [Related]
25. Sleep and COMT polymorphism in ADHD children: preliminary actigraphic data.
Gruber R; Grizenko N; Schwartz G; Ben Amor L; Gauthier J; de Guzman R; Joober R
J Am Acad Child Adolesc Psychiatry; 2006 Aug; 45(8):982-989. PubMed ID: 16865041
[TBL] [Abstract][Full Text] [Related]
26. Association between homozygosity at the COMT gene locus and obsessive compulsive disorder.
Schindler KM; Richter MA; Kennedy JL; Pato MT; Pato CN
Am J Med Genet; 2000 Dec; 96(6):721-4. PubMed ID: 11121168
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. 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]
30. Family-based association study of the serotonin transporter promoter region polymorphism (5-HTTLPR) in attention deficit hyperactivity disorder.
Manor I; Eisenberg J; Tyano S; Sever Y; Cohen H; Ebstein RP; Kotler M
Am J Med Genet; 2001 Jan; 105(1):91-5. PubMed ID: 11425009
[TBL] [Abstract][Full Text] [Related]
31. Genotype link with extreme antisocial behavior: the contribution of cognitive pathways.
Langley K; Heron J; O'Donovan MC; Owen MJ; Thapar A
Arch Gen Psychiatry; 2010 Dec; 67(12):1317-23. PubMed ID: 21135332
[TBL] [Abstract][Full Text] [Related]
32. Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant.
Pálmason H; Moser D; Sigmund J; Vogler C; Hänig S; Schneider A; Seitz C; Marcus A; Meyer J; Freitag CM
J Neural Transm (Vienna); 2010 Feb; 117(2):259-67. PubMed ID: 19946713
[TBL] [Abstract][Full Text] [Related]
33. Gene-gene interaction between COMT and MAOA potentially predicts the intelligence of attention-deficit hyperactivity disorder boys in China.
Qian QJ; Yang L; Wang YF; Zhang HB; Guan LL; Chen Y; Ji N; Liu L; Faraone SV
Behav Genet; 2010 May; 40(3):357-65. PubMed ID: 19941049
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.
Michaelovsky E; Gothelf D; Korostishevsky M; Frisch A; Burg M; Carmel M; Steinberg T; Inbar D; Apter A; Weizman A
Int J Neuropsychopharmacol; 2008 May; 11(3):351-63. PubMed ID: 17949513
[TBL] [Abstract][Full Text] [Related]
36. Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study.
Payton A; Holmes J; Barrett JH; Hever T; Fitzpatrick H; Trumper AL; Harrington R; McGuffin P; O'Donovan M; Owen M; Ollier W; Worthington J; Thapar A
Am J Med Genet; 2001 Jul; 105(5):464-70. PubMed ID: 11449400
[TBL] [Abstract][Full Text] [Related]
37. [Study of genetic variants in the BDNF, COMT, DAT1 and SERT genes in Colombian children with attention deficit disorder].
Ortega-Rojas J; Arboleda-Bustos CE; Morales L; Benítez BA; Beltrán D; Izquierdo Á; Arboleda H; Vásquez R
Rev Colomb Psiquiatr; 2017; 46(4):222-228. PubMed ID: 29122229
[TBL] [Abstract][Full Text] [Related]
38. Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder.
Thapar A; Langley K; Fowler T; Rice F; Turic D; Whittinger N; Aggleton J; Van den Bree M; Owen M; O'Donovan M
Arch Gen Psychiatry; 2005 Nov; 62(11):1275-8. PubMed ID: 16275815
[TBL] [Abstract][Full Text] [Related]
39.
Akutagava-Martins GC; Salatino-Oliveira A; Kieling C; Genro JP; Polanczyk GV; Anselmi L; Menezes AM; Gonçalves H; Wehrmeister FC; Barros FC; Callegari-Jacques SM; Rohde LA; Hutz MH
J Psychiatry Neurosci; 2016 Oct; 41(6):405-412. PubMed ID: 27327562
[TBL] [Abstract][Full Text] [Related]
40. Structural correlates of COMT Val158Met polymorphism in childhood ADHD: a voxel-based morphometry study.
Villemonteix T; De Brito SA; Slama H; Kavec M; Balériaux D; Metens T; Baijot S; Mary A; Ramoz N; Septier M; Gorwood P; Peigneux P; Massat I
World J Biol Psychiatry; 2015 Apr; 16(3):190-9. PubMed ID: 25495556
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
