(Q44736121)

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A high-density single-nucleotide polymorphism screen of 23 candidate genes in attention deficit hyperactivity disorder: suggesting multiple susceptibility genes among Chinese Han population

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scholarly article

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Europe PubMed Central

5 December 2017

A high-density single-nucleotide polymorphism screen of 23 candidate genes in attention deficit hyperactivity disorder: suggesting multiple susceptibility genes among Chinese Han population (English)

1 reference

Europe PubMed Central

5 December 2017

attention deficit hyperactivity disorder

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single-nucleotide polymorphism

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based on heuristic

inferred from title

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Stephen Faraone

8

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Europe PubMed Central

5 December 2017

author name string

L Guan

1

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Europe PubMed Central

5 December 2017

B Wang

2

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Europe PubMed Central

5 December 2017

Y Chen

3

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Europe PubMed Central

5 December 2017

L Yang

4

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Europe PubMed Central

5 December 2017

J Li

5

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Europe PubMed Central

5 December 2017

Q Qian

6

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Europe PubMed Central

5 December 2017

Z Wang

7

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Europe PubMed Central

5 December 2017

Y Wang

9

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Europe PubMed Central

5 December 2017

language of work or name

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publication date

8 January 2008

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Europe PubMed Central

5 December 2017

Molecular Psychiatry

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Europe PubMed Central

5 December 2017

14

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Europe PubMed Central

5 December 2017

5

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Europe PubMed Central

5 December 2017

546-554

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Europe PubMed Central

5 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.mp.4002139

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Attention-deficit hyperactivity disorder

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Molecular genetics of attention-deficit/hyperactivity disorder

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Animal models of attention-deficit hyperactivity disorder

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

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Functional hyperdopaminergia in dopamine transporter knock-out mice

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Neurobiology of executive functions: catecholamine influences on prefrontal cortical functions

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Neurobiology of attention-deficit hyperactivity disorder.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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The contribution of alpha 2-noradrenergic mechanisms of prefrontal cortical cognitive function. Potential significance for attention-deficit hyperactivity disorder

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7 January 2021

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Attention-deficit/hyperactivity disorder (ADHD) as a noradrenergic disorder

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7 January 2021

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Tryptophan depletion, executive functions, and disinhibition in aggressive, adolescent males.

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7 January 2021

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The spectrum of behaviors influenced by serotonin

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7 January 2021

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

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7 January 2021

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The IMAGE project: methodological issues for the molecular genetic analysis of ADHD.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Attention-deficit hyperactivity disorder

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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The persistence of attention-deficit/hyperactivity disorder into young adulthood as a function of reporting source and definition of disorder

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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A haplotype map of the human genome

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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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

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Decoding randomly ordered DNA arrays

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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High-throughput SNP genotyping on universal bead arrays

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Highly parallel SNP genotyping

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Haploview: analysis and visualization of LD and haplotype maps

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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The structure of haplotype blocks in the human genome

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Association study between the monoamine oxidase A gene and attention deficit hyperactivity disorder in Taiwanese samples

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Monoamine oxidase in neuropsychiatry and behavior

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Linkage studies between attention-deficit hyperactivity disorder and the monoamine oxidase genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Association analysis of monoamine oxidase a and attention deficit hyperactivity disorder

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Family-based and association studies of monoamine oxidase A and attention deficit hyperactivity disorder (ADHD): preferential transmission of the long promoter-region repeat and its association with impaired performance on a continuous [...]

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Association between attention deficit hyperactivity disorder and the DXS7 locus.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Dopa decarboxylase gene polymorphisms and attention deficit hyperactivity disorder (ADHD): no evidence for association in the Irish population

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Non-stimulant treatments for ADHD.

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Coloboma mouse mutant as an animal model of hyperkinesis and attention deficit hyperactivity disorder

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7 January 2021

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Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder

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7 January 2021

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Synaptosomal-associated protein 25 (SNAP-25) and attention deficit hyperactivity disorder (ADHD): evidence of linkage and association in the Irish population

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Biased paternal transmission of SNAP-25 risk alleles in attention-deficit hyperactivity disorder

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7 January 2021

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Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

based on heuristic

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Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

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based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

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based on heuristic

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Familial clustering of latent class and DSM-IV defined attention-deficit/hyperactivity disorder (ADHD) subtypes.

1 reference

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based on heuristic

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Familiality and heritability of subtypes of attention deficit hyperactivity disorder in a population sample of adolescent female twins

1 reference

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based on heuristic

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Genetic contributions to the development of ADHD subtypes from childhood to adolescence.

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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

1 reference

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7 January 2021

based on heuristic

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Mutational analysis of the nicotinic acetylcholine receptor alpha 4 subunit gene in attention deficit/hyperactivity disorder: evidence for association of an intronic polymorphism with attention problems

1 reference

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7 January 2021

based on heuristic

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Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism

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7 January 2021

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Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

based on heuristic

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Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

based on heuristic

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Family-based and case-control association studies of DRD4 and DAT1 polymorphisms in Chinese attention deficit hyperactivity disorder patients suggest long repeats contribute to genetic risk for the disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002139

7 January 2021

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Association study designs for complex diseases

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7 January 2021

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10.1038/SJ.MP.4002139

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Europe PubMed Central

5 December 2017

1 reference

Europe PubMed Central

5 December 2017

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