(Q43479612)

English

Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample

scientific article published in July 2005

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scholarly article

1 reference

Europe PubMed Central

23 November 2017

Association of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample (English)

1 reference

Europe PubMed Central

23 November 2017

1

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Europe PubMed Central

23 November 2017

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Europe PubMed Central

23 November 2017

author name string

Manly T

2

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Europe PubMed Central

23 November 2017

Savage R

3

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Europe PubMed Central

23 November 2017

Swanson J

4

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Europe PubMed Central

23 November 2017

Morisano D

5

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Europe PubMed Central

23 November 2017

Butler N

6

1 reference

Europe PubMed Central

23 November 2017

Grant C

7

1 reference

Europe PubMed Central

23 November 2017

Cross G

8

1 reference

Europe PubMed Central

23 November 2017

Bentley L

9

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Europe PubMed Central

23 November 2017

language of work or name

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publication date

1 July 2005

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Europe PubMed Central

23 November 2017

Molecular Psychiatry

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Europe PubMed Central

23 November 2017

10

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Europe PubMed Central

23 November 2017

686-698

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Europe PubMed Central

23 November 2017

7

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Europe PubMed Central

23 November 2017

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001641

0 references

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A genomewide scan for loci involved in attention-deficit/hyperactivity disorder

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High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder

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Human dopamine transporter gene (DAT1) maps to chromosome 5p15.3 and displays a VNTR.

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Global variation of a 40-bp VNTR in the 3'-untranslated region of the dopamine transporter gene (SLC6A3).

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The dopamine transporter gene is associated with attention deficit hyperactivity disorder in a Taiwanese sample.

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Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples

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Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder.

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Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity

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Attention-deficit hyperactivity disorder: a study of association with both the dopamine transporter gene and the dopamine D4 receptor gene

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No association of the dopamine transporter gene 3' VNTR polymorphism with ADHD subtypes in a population sample of twins

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Expression of the dopamine transporter gene is regulated by the 3' UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR.

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The VNTR polymorphism of the human dopamine transporter (DAT1) gene affects gene expression

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Functional effects of the DAT1 polymorphism on EEG measures in ADHD.

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Sex differences in school-aged children with pervasive attention deficit hyperactivity disorder.

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The differential assessment of children's attention: the Test of Everyday Attention for Children (TEA-Ch), normative sample and ADHD performance.

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Neuropsychological evaluation of deficits in executive functioning for ADHD children with or without learning disabilities.

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Neuropsychological analyses of impulsiveness in childhood hyperactivity.

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Psychological heterogeneity in AD/HD--a dual pathway model of behaviour and cognition

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The top and the bottom of ADHD: a neuropsychological perspective

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Etiology and pathogenesis of attention-deficit hyperactivity disorder (ADHD): significance of prematurity and perinatal hypoxic-haemodynamic encephalopathy

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Behavioral inhibition, sustained attention, and executive functions: constructing a unifying theory of ADHD

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Executive function and attention deficit hyperactivity disorder: stimulant medication and better executive function performance in children.

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Are planning, working memory, and inhibition associated with individual differences in preschool ADHD symptoms?

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Effects of methylphenidate on spatial working memory and planning in healthy young adults.

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The effects of dopamine and its antagonists on directional delay-period activity of prefrontal neurons in monkeys during an oculomotor delayed-response task

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Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

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Localization of a human system for sustained attention by positron emission tomography

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Frontal lesions and sustained attention.

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'Oops!': performance correlates of everyday attentional failures in traumatic brain injured and normal subjects.

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The Test of Everyday Attention for Children (TEA-Ch): patterns of performance in children with ADHD and clinical controls

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The relationship between cognition and action: performance of children 3 1/2-7 years old on a Stroop-like day-night test.

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A comprehensive review of genetic association studies

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Is ADHD a disinhibitory disorder?

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Deficient inhibition as a marker for familial ADHD.

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Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD.

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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

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Identifiers

10.1038/SJ.MP.4001641

1 reference

Europe PubMed Central

23 November 2017

1 reference

Europe PubMed Central

23 November 2017

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