-
2
-
-
0033573227
-
Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder
-
Barr CL, Wigg K, Malone M et al (1999) Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder. Am J Med Genet 88:710-713
-
(1999)
Am J Med Genet
, vol.88
, pp. 710-713
-
-
Barr, C.L.1
Wigg, K.2
Malone, M.3
-
3
-
-
23844466593
-
The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD
-
Bellgrove MA, Domschke K, Hawi Z et al (2005) The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD. Exp Brain Res 163:352-360
-
(2005)
Exp Brain Res
, vol.163
, pp. 352-360
-
-
Bellgrove, M.A.1
Domschke, K.2
Hawi, Z.3
-
4
-
-
0002239040
-
Association between tridimensional personality questionnaire (TPQ) traits and three functional polymorphisms: Dopamine receptor D4 (DRD4), serotonin transporter promoter region (5-HTTLPR) and catechol-O-methyltransferase (COMT)
-
Benjamin J, Osher Y, Kotler M et al (2000) Association between tridimensional personality questionnaire (TPQ) traits and three functional polymorphisms: dopamine receptor D4 (DRD4), serotonin transporter promoter region (5-HTTLPR) and catechol-O-methyltransferase (COMT). Mol Psychiat 5:96-100
-
(2000)
Mol Psychiat
, vol.5
, pp. 96-100
-
-
Benjamin, J.1
Osher, Y.2
Kotler, M.3
-
5
-
-
0026034792
-
Human catechol-O-methyltransferase: Cloning and expression of the membraneassociated form
-
USA
-
Bertocci B, Miggiano V, Da Prada M et al (1991) Human catechol-O-methyltransferase: cloning and expression of the membraneassociated form. Proc Natl Acad Sci USA 88:1416-1420
-
(1991)
Proc Natl Acad Sci
, vol.88
, pp. 1416-1420
-
-
Bertocci, B.1
Miggiano, V.2
Da Prada, M.3
-
6
-
-
22144455050
-
Attention-deficit hyperactivity disorder
-
Biederman J, Faraone SV (2005) Attention-deficit hyperactivity disorder. Lancet 366:237-248
-
(2005)
Lancet
, vol.366
, pp. 237-248
-
-
Biederman, J.1
Faraone, S.V.2
-
7
-
-
0030922816
-
Bias in meta-analysis detected by a simple, graphical test
-
Egger M, Davey Smith G, Schneider M et al (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315:629-634
-
(1997)
BMJ
, vol.315
, pp. 629-634
-
-
Egger, M.1
Davey Smith, G.2
Schneider, M.3
-
8
-
-
84948761756
-
Principles of and procedures for systematic reviews
-
Egger M, Smith GD, Altman DG (eds) BMJ Publishing Group, London
-
Egger M, Smith GD (2001) Principles of and procedures for systematic reviews. In: Egger M, Smith GD, Altman DG (eds) Systematic reviews in health care: meta-analysis in context. BMJ Publishing Group, London, pp 23-42
-
(2001)
Systematic Reviews in Health Care: Meta-analysis in Context
, pp. 23-42
-
-
Egger, M.1
Smith, G.D.2
-
9
-
-
0033570041
-
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 et al (1999). 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. Am J Med Genet 88:497-502
-
(1999)
Am J Med Genet
, vol.88
, pp. 497-502
-
-
Eisenberg, J.1
Mei-Tal, G.2
Steinberg, A.3
-
11
-
-
0034941789
-
Meta-analysis of the association between the 7-repeat allele of the dopamine D(4) receptor gene and attention deficit hyperactivity disorder
-
Faraone SV, Doyle AE, Mick E et al (2001) Meta-analysis of the association between the 7-repeat allele of the dopamine D(4) receptor gene and attention deficit hyperactivity disorder. Am J Psychiat 158:1052-1057
-
(2001)
Am J Psychiat
, vol.158
, pp. 1052-1057
-
-
Faraone, S.V.1
Doyle, A.E.2
Mick, E.3
-
12
-
-
20444412281
-
Molecular genetics of attention-deficit/hyperactivity disorder
-
Faraone SV, Perlis RH, Doyle AE et al (2005) Molecular genetics of attention-deficit/hyperactivity disorder. Biol Psychiat 57:1313-1323
-
(2005)
Biol Psychiat
, vol.57
, pp. 1313-1323
-
-
Faraone, S.V.1
Perlis, R.H.2
Doyle, A.E.3
-
13
-
-
1642514265
-
The worldwide prevalence of ADHD: Is it an American condition?
-
Faraone SV, Sergeant J, Gillberg C et al (2003) The worldwide prevalence of ADHD: is it an American condition? World Psychiat 2:104-113
-
(2003)
World Psychiat
, vol.2
, pp. 104-113
-
-
Faraone, S.V.1
Sergeant, J.2
Gillberg, C.3
-
14
-
-
0032544012
-
Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior
-
USA
-
Gogos JA, Morgan M, Luine V et al (1998) Catechol-O-methyltransferase- deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior. Proc Natl Acad Sci USA 95:9991-9996
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 9991-9996
-
-
Gogos, J.A.1
Morgan, M.2
Luine, V.3
-
15
-
-
77956751404
-
The cortical dopamine system: Role in memory and cognition
-
Goldman-Rakic PS (1998) The cortical dopamine system: role in memory and cognition. Adv Pharmacol 42:707-711
-
(1998)
Adv Pharmacol
, vol.42
, pp. 707-711
-
-
Goldman-Rakic, P.S.1
-
16
-
-
0026518652
-
Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1-q11.2
-
Grossman MH, Emanuel BS, Budarf ML (1992) Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1-q11.2. Genomics 12:822-825
-
(1992)
Genomics
, vol.12
, pp. 822-825
-
-
Grossman, M.H.1
Emanuel, B.S.2
Budarf, M.L.3
-
17
-
-
0034640682
-
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 et al (2000) No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample. Am J Med Genet 96:282-284
-
(2000)
Am J Med Genet
, vol.96
, pp. 282-284
-
-
Hawi, Z.1
Millar, N.2
Daly, G.3
-
18
-
-
23944477067
-
No association between attention-deficit hyperactivity disorder and catechol-O-methyltransferase gene in Chinese
-
Jiang SD, Wu XD, Zhang Y et al (2005) No association between attention-deficit hyperactivity disorder and catechol-O-methyltransferase gene in Chinese. Yi Chuan Xue Bao 32:784-788
-
(2005)
Yi Chuan Xue Bao
, vol.32
, pp. 784-788
-
-
Jiang, S.D.1
Wu, X.D.2
Zhang, Y.3
-
19
-
-
0029745410
-
Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome
-
Lachman HM, Morrow B, Shprintzen R et al (1996) Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome. Am J Med Genet 67:468-472
-
(1996)
Am J Med Genet
, vol.67
, pp. 468-472
-
-
Lachman, H.M.1
Morrow, B.2
Shprintzen, R.3
-
20
-
-
0036915441
-
Dopamine system genes and attention deficit hyperactivity disorder: A meta-analysis
-
Maher BS, Marazita ML, Ferrell RE et al (2002) Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis. Psychiat Genet 12:207-215
-
(2002)
Psychiat Genet
, vol.12
, pp. 207-215
-
-
Maher, B.S.1
Marazita, M.L.2
Ferrell, R.E.3
-
21
-
-
0034606270
-
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 et al (2000) Failure to replicate an association between the catechol-O-methyltransferase polymorphism and attention deficit hyperactivity disorder in a second, independently recruited Israeli cohort. Am J Med Genet 96:858-860
-
(2000)
Am J Med Genet
, vol.96
, pp. 858-860
-
-
Manor, I.1
Kotler, M.2
Sever, Y.3
-
22
-
-
0031777394
-
Ethnic differences in catechol-O-methyltransferase pharmacogenetics: Frequency of the codon 108/158 low activity allele is lower in Kenyan than Caucasian or south-west Asian individuals
-
McLeod HL, Syvanen AC, Githang'a J et al (1998) Ethnic differences in catechol-O-methyltransferase pharmacogenetics: frequency of the codon 108/158 low activity allele is lower in Kenyan than Caucasian or south-west Asian individuals. Pharmacogenetics 8:195-199
-
(1998)
Pharmacogenetics
, vol.8
, pp. 195-199
-
-
McLeod, H.L.1
Syvanen, A.C.2
Githang'a, J.3
-
23
-
-
0026793049
-
Sex differences in densities of dopaminergic fibers and GABAergic neurons in the prenatal rat striatum
-
Ovtscharoff W, Eusterschulte B, Zienecker R et al (1992) Sex differences in densities of dopaminergic fibers and GABAergic neurons in the prenatal rat striatum. J Comp Neurol 323:299-304
-
(1992)
J Comp Neurol
, vol.323
, pp. 299-304
-
-
Ovtscharoff, W.1
Eusterschulte, B.2
Zienecker, R.3
-
24
-
-
0032777995
-
Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles
-
Palmatier MA, Kang AM, Kidd KK (1999) Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles. Biol Psychiat 46:557-567
-
(1999)
Biol Psychiat
, vol.46
, pp. 557-567
-
-
Palmatier, M.A.1
Kang, A.M.2
Kidd, K.K.3
-
25
-
-
0035827829
-
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 et al (2001) Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study. Am J Med Genet 105:464-470
-
(2001)
Am J Med Genet
, vol.105
, pp. 464-470
-
-
Payton, A.1
Holmes, J.2
Barrett, J.H.3
-
26
-
-
15744386142
-
Meta-analysis of family-based association studies between the dopamine transporter gene and attention deficit hyperactivity disorder
-
Purper-Ouakil D, Wohl M, Mouren MC et al (2005) Meta-analysis of family-based association studies between the dopamine transporter gene and attention deficit hyperactivity disorder. Psychiat Genet 15:53-59
-
(2005)
Psychiat Genet
, vol.15
, pp. 53-59
-
-
Purper-Ouakil, D.1
Wohl, M.2
Mouren, M.C.3
-
27
-
-
0038755196
-
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 et al (2003) Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism. Am J Med Genet B Neuropsychiat Genet 118:103-109
-
(2003)
Am J Med Genet B Neuropsychiat Genet
, vol.118
, pp. 103-109
-
-
Qian, Q.1
Wang, Y.2
Zhou, R.3
-
28
-
-
0037051153
-
How specific is a deficit of executive functioning for attention-deficit/hyperactivity disorder?
-
Sergeant JA, Geurts H, Oosterlaan J (2002) How specific is a deficit of executive functioning for attention-deficit/hyperactivity disorder? Behav Brain Res 130:3-28
-
(2002)
Behav Brain Res
, vol.130
, pp. 3-28
-
-
Sergeant, J.A.1
Geurts, H.2
Oosterlaan, J.3
-
29
-
-
26444510882
-
Catechol-O-methyltransferase (COMT) Val108/158 Met polymorphism does not modulate executive function in children with ADHD
-
Taerk E, Grizenko N, Ben Amor L et al (2004) Catechol-O-methyltransferase (COMT) Val108/158 Met polymorphism does not modulate executive function in children with ADHD. BMC Med Genet 5:30
-
(2004)
BMC Med Genet
, vol.5
, pp. 30
-
-
Taerk, E.1
Grizenko, N.2
Ben Amor, L.3
-
30
-
-
0034640691
-
No association between low- And high-activity catecholamine-O- methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children
-
Tahir E, Curran S, Yazgan Y et al (2000) No association between low- and high-activity catecholamine-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children. Am J Med Genet 96:285-288
-
(2000)
Am J Med Genet
, vol.96
, pp. 285-288
-
-
Tahir, E.1
Curran, S.2
Yazgan, Y.3
-
31
-
-
0027964721
-
Genomic organization of the human catechol-O-methyltransferase gene and its expression from two distinct promoters
-
Tenhunen J, Salminen M, Lundstrom K et al (1994) Genomic organization of the human catechol-O-methyltransferase gene and its expression from two distinct promoters. Eur J Biochem 223:1049-1059
-
(1994)
Eur J Biochem
, vol.223
, pp. 1049-1059
-
-
Tenhunen, J.1
Salminen, M.2
Lundstrom, K.3
-
32
-
-
12944312690
-
A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD)
-
Turic D, Williams H, Langley K et al (2005) A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD). Am J Med Genet B Neuropsychiat Genet 133:64-67ff
-
(2005)
Am J Med Genet B Neuropsychiat Genet
, vol.133
, pp. 64-67
-
-
Turic, D.1
Williams, H.2
Langley, K.3
-
33
-
-
0030836682
-
High-activity catechol-O-methyltransferase allele is more prevalent in polysubstance abusers
-
Vandenbergh DJ, Rodriguez LA, Miller IT et al (1997) High-activity catechol-O-methyltransferase allele is more prevalent in polysubstance abusers. Am J Med Genet 74:439-442
-
(1997)
Am J Med Genet
, vol.74
, pp. 439-442
-
-
Vandenbergh, D.J.1
Rodriguez, L.A.2
Miller, I.T.3
-
34
-
-
0041467783
-
Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene
-
Zhang XN, Ruan LM, Le YP et al (2003) Association analysis between attention-deficit hyperactivity disorder and Val158Met polymorphism of catechol-O-methyltransferase gene. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 20:322-324
-
(2003)
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
, vol.20
, pp. 322-324
-
-
Zhang, X.N.1
Ruan, L.M.2
Le, Y.P.3
|