A common haplotype at the dopamine transporter gene 5' region is associated with attention-deficit/hyperactivity disorder.
about
Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese populationGenes, emotions and gut microbiota: The next frontier for the gastroenterologist.Genotype and ancestry modulate brain's DAT availability in healthy humans.Epigenetics in Developmental Disorder: ADHD and EndophenotypesButyrylcholinesterase genetic variants: association with cocaine dependence and related phenotypes.How animal models inform child and adolescent psychiatry.Bromocriptine does not alter speed-accuracy tradeoff.Attention deficit hyperactivity disorder: genetic association study in a cohort of Spanish childrenMAOA Influences the Trajectory of Attentional Development.Human dopamine transporter gene: differential regulation of 18-kb haplotypesMolecular genetics of attention-deficit/hyperactivity disorder: an overviewAttention-deficit/hyperactivity disorder and the dopaminergic hypotheses.Biochemical and genetic analyses of childhood attention deficit/hyperactivity disorder.Genetics of attention-deficit/hyperactivity disorder: current findings and future directions.ADHD pharmacogenetics across the life cycle: New findings and perspectives.The dopamine transporter role in psychiatric phenotypes.Separating the wheat from the chaff: systematic identification of functionally relevant noncoding variants in ADHD.The influence of genetic variants on striatal dopamine transporter and D2 receptor binding after TBI.Lack of influence of DAT1 and DRD2 gene variants on antidepressant response in generalized anxiety disorder.Pharmacogenetics of methylphenidate in childhood attention-deficit/hyperactivity disorder: long-term effects.Association between polymorphisms of the DBH and DAT1 genes and attention deficit hyperactivity disorder in children from Jordan.Association between a SLC6A3 intron 8 VNTR functional polymorphism and ADHD in a Brazilian sample of adult patients.The Brazilian contribution to Attention-Deficit/Hyperactivity Disorder molecular genetics in children and adolescents.Polymorphisms in the dopamine transporter gene are associated with visual hallucinations and levodopa equivalent dose in Brazilians with Parkinson's disease.
P2860
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P2860
A common haplotype at the dopamine transporter gene 5' region is associated with attention-deficit/hyperactivity disorder.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
A common haplotype at the dopa ...... eficit/hyperactivity disorder.
@en
A common haplotype at the dopa ...... eficit/hyperactivity disorder.
@nl
type
label
A common haplotype at the dopa ...... eficit/hyperactivity disorder.
@en
A common haplotype at the dopa ...... eficit/hyperactivity disorder.
@nl
prefLabel
A common haplotype at the dopa ...... eficit/hyperactivity disorder.
@en
A common haplotype at the dopa ...... eficit/hyperactivity disorder.
@nl
P2093
P2860
P921
P356
P1476
A common haplotype at the dopa ...... eficit/hyperactivity disorder.
@en
P2093
Angélica S Oliveira
Cristian Zeni
Guilherme V Polanczyk
Júlia P Genro
Tatiana Roman
P2860
P304
P356
10.1002/AJMG.B.30863
P577
2008-12-01T00:00:00Z