(Q34639456)

3 August 2017

title

Association and linkage of allelic variants of the dopamine transporter gene in ADHD. (English)

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11

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26

Hebebrand J

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22

Remschmidt H

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3 August 2017

Friedel S

1

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Saar K

2

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Sauer S

3

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Dempfle A

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Walitza S

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Renner T

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Romanos M

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Freitag C

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Seitz C

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Palmason H

10

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Windemuth-Kieselbach C

12

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Schimmelmann BG

13

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Wewetzer C

14

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Meyer J

15

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Warnke A

16

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Lesch KP

17

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Reinhardt R

18

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Herpertz-Dahlmann B

19

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3 August 2017

Linder M

20

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Hinney A

21

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Schäfer H

23

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Konrad K

24

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Hübner N

25

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language of work or name

English

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publication date

10 April 2007

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3 August 2017

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3 August 2017

volume

12

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3 August 2017

issue

10

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3 August 2017

page(s)

923-933

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001986

3 August 2017

exact match

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cites work

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A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11

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Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

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Recognition of psychostimulants, antidepressants, and other inhibitors of synaptic neurotransmitter uptake by the plasma membrane monoamine transporters

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Attention deficit hyperactivity disorder: binding of [99mTc]TRODAT-1 to the dopamine transporter before and after methylphenidate treatment.

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Dopamine transporter density in patients with attention deficit hyperactivity disorder.

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Dopamine transporter density in the basal ganglia assessed with [123I]IPT SPET in children with attention deficit hyperactivity disorder

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Unaltered dopamine transporter availability in adult attention deficit hyperactivity disorder

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The dopamine transporter and attention-deficit/hyperactivity disorder

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Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter

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Genetics of childhood disorders: XXIV. ADHD, part 8: hyperdopaminergic mice as an animal model of ADHD.

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Behavioural disturbances associated with hyperdopaminergia in dopamine-transporter knockout mice

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Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity

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Aberrant responses in social interaction of dopamine transporter knockout mice

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The human dopamine transporter gene: the 5'-flanking region reveals five diallelic polymorphic sites in a Caucasian population sample

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Nurr1 enhances transcription of the human dopamine transporter gene through a novel mechanism

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Sp1 and Sp3 activate transcription of the human dopamine transporter gene

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Promoter and intronic variants affect the transcriptional regulation of the human dopamine transporter gene

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Identification of additional variants within the human dopamine transporter gene provides further evidence for an association with bipolar disorder in two independent samples.

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Dopamine transporter (SLC6A3) 5' region haplotypes significantly affect transcriptional activity in vitro but are not associated with Parkinson's disease

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Common human 5' dopamine transporter (SLC6A3) haplotypes yield varying expression levels in vivo

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

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Human dopamine transporter gene: coding region conservation among normal, Tourette's disorder, alcohol dependence and attention-deficit hyperactivity disorder populations

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Sequence variation in the human dopamine transporter gene in children with attention deficit hyperactivity disorder

21 January 2018

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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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

DAT1, DRD4, and DRD5 polymorphisms are not associated with ADHD in Dutch families

21 January 2018

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No support for association between the dopamine transporter (DAT1) gene and ADHD.

21 January 2018

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Sequence variation in the 3'-untranslated region of the dopamine transporter gene and attention-deficit hyperactivity disorder (ADHD).

21 January 2018

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Meta-analysis of family-based association studies between the dopamine transporter gene and attention deficit hyperactivity disorder

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Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD).

21 January 2018

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Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these loci

21 January 2018

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Dopamine transporter: Basic science and human variation of a key molecule for dopaminergic function, locomotion, and parkinsonism

21 January 2018

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The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

A novel procedure for efficient genotyping of single nucleotide polymorphisms

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Extension of the GOOD assay for genotyping single nucleotide polymorphisms by matrix-assisted laser desorption/ionization mass spectrometry

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

MALDI mass spectrometry analysis of single nucleotide polymorphisms by photocleavage and charge-tagging

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Automated solid-phase extraction for purification of single nucleotide polymorphism genotyping products prior to matrix-assisted laser desorption/ionisation time-of-flight mass spectrometric analysis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Transmission/disequilibrium tests using multiple tightly linked markers

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

A powerful strategy to account for multiple testing in the context of haplotype analysis

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Confidence intervals for genotype relative risks and allele frequencies from the case parent trio design for candidate-gene studies

21 January 2018

1 reference

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A class of tests for linkage using affected pedigree members

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Allele-sharing models: LOD scores and accurate linkage tests

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Powerful regression-based quantitative-trait linkage analysis of general pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Assessing whether an allele can account in part for a linkage signal: the Genotype-IBD Sharing Test (GIST).

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Sample size requirements to control for stochastic variation in magnitude and location of allele-sharing linkage statistics in affected sibling pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Characterization and prediction of alternative splice sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

TRANSFAC: transcriptional regulation, from patterns to profiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Identification of probable genotyping errors by consideration of haplotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Family based association analysis of statistically derived quantitative traits for drug use in ADHD and the dopamine transporter gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

Increased striatal dopamine transporter in adult patients with attention deficit hyperactivity disorder: effects of methylphenidate as measured by single photon emission computed tomography

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

inferred from DOI database lookup

7 January 2021

based on heuristic

Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001986

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.MP.4001986

1 reference

3 August 2017

1 reference