Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD. (Q34661589)

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English	Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.	scientific article

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scholarly article

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Europe PubMed Central

3 August 2017

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Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD. (English)

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Europe PubMed Central

3 August 2017

multicenter clinical trial

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attention deficit hyperactivity disorder

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1

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Stephen Faraone

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Martine Hoogman

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Martine Hoogman

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Noèlia Fernàndez-Castillo

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Noèlia Fernàndez-Castillo

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Josep Antoni Ramos-Quiroga

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Josep Antoni Ramos-Quiroga

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Bru Cormand

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Jan Haavik

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Philip Asherson

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Philip Asherson

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Klaus-Peter Lesch

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Klaus-Peter Lesch

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Lambertus Kiemeney

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Lambertus A Kiemeney

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Jan K Buitelaar

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Rosa Bosch

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Stefan Johansson

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Stefan Johansson

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Cristina Sànchez-Mora

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Sánchez-Mora C

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Marta Ribasés

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Alejandro Arias-Vásquez

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Alejandro Arias Vasquez

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Jasmin Romanos

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Andreas Reif

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Andrea Boreatti-Hümmer

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Andrea Boreatti-Hümmer

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Mònica Bayés

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Anne Halmøy

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Elisabeth T Landaas

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Elisabeth T Landaas

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Ole Bernt Fasmer

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Ole B Fasmer

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Per M Knappskog

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Per M Knappskog

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Angelien J G A M Heister

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Angelien J G A M Heister

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A Marije Boonstra

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A Marije Boonstra

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Cees C Kan

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author name string

Monika Heine

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Christian P Jacob

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Europe PubMed Central

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Miguel Casas

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Europe PubMed Central

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Núria Gómez-Barros

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Helene Halleland

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J J Sandra Kooij

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3 August 2017

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publication date

4 November 2009

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3 August 2017

Neuropsychopharmacology

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3 August 2017

35

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3 August 2017

656-664

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3

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Europe PubMed Central

3 August 2017

https://scigraph.springernature.com/pub.10.1038/npp.2009.170

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Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

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Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults

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Association of the dopamine transporter (SLC6A3/DAT1) gene 9-6 haplotype with adult ADHD.

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A meta-analysis of association studies between the 10-repeat allele of a VNTR polymorphism in the 3'-UTR of dopamine transporter gene and attention deficit hyperactivity disorder

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No association between a common haplotype of the 6 and 10-repeat alleles in intron 8 and the 3'UTR of the DAT1 gene and adult attention deficit hyperactivity disorder.

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An examination of the behavioral and neuropsychological correlates of three ADHD candidate gene polymorphisms (DRD4 7+, DBH TaqI A2, and DAT1 40 bp VNTR) in hyperactive and normal children followed to adulthood

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Attention-Deficit Hyperactivity Disorder in Girls

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The age-dependent decline of attention deficit hyperactivity disorder: a meta-analysis of follow-up studies

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Patterns and predictors of attention-deficit/hyperactivity disorder persistence into adulthood: results from the national comorbidity survey replication

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The dopamine transporter and attention-deficit/hyperactivity disorder

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In vivo neuroreceptor imaging in attention-deficit/hyperactivity disorder: a focus on the dopamine transporter

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Score tests for association between traits and haplotypes when linkage phase is ambiguous

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Attention-deficit/hyperactivity disorder in adults: an overview

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Association of paraoxonase 1 gene polymorphisms with risk of Parkinson's disease: a meta-analysis.

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Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity

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Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD.

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The Worldwide Prevalence of ADHD: A Systematic Review and Metaregression Analysis

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Age-dependent decline of symptoms of attention deficit hyperactivity disorder: impact of remission definition and symptom type.

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Young adult outcome of hyperactive children: adaptive functioning in major life activities

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GENEPOP (Version 1.2): Population Genetics Software for Exact Tests and Ecumenicism

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based on heuristic

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10.1038/NPP.2009.170

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Europe PubMed Central

3 August 2017

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Europe PubMed Central

3 August 2017

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Europe PubMed Central

3 August 2017

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