(Q46906830)

English

Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults

scientific article published on 12 November 2007

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scholarly article

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults (English)

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

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1 reference

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inferred from title

4

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

Andrew N. Coogan

6

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

author name string

W Retz

1

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

M Rösler

2

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

C Kissling

3

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

R Hünnerkopf

5

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

J Thome

7

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

C Freitag

8

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

publication date

12 November 2007

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

Journal of Neural Transmission

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

115

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

2

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

323-329

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Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

https://scigraph.springernature.com/pub.10.1007/s00702-007-0822-5

0 references

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

1 reference

https://api.crossref.org/works/10.1007%2FS00702-007-0822-5

21 January 2018

Family-environment risk factors for attention-deficit hyperactivity disorder. A test of Rutter's indicators of adversity

1 reference

https://api.crossref.org/works/10.1007%2FS00702-007-0822-5

21 January 2018

Support for association between ADHD and two candidate genes: NET1 and DRD1.

1 reference

https://api.crossref.org/works/10.1007%2FS00702-007-0822-5

21 January 2018

Genotypic interaction between DRD4 and DAT1 loci is a high risk factor for attention-deficit/hyperactivity disorder in Chilean families

1 reference

https://api.crossref.org/works/10.1007%2FS00702-007-0822-5

21 January 2018

Development of diagnostic checklists for use in routine clinical care. A guideline designed to assess DSM-III-R diagnoses

1 reference

https://api.crossref.org/works/10.1007%2FS00702-007-0822-5

21 January 2018

Evaluation of potential gene-gene interactions for attention deficit hyperactivity disorder in the Han Chinese population.

1 reference

https://api.crossref.org/works/10.1007%2FS00702-007-0822-5

21 January 2018

Possible association of the alpha-2A adrenergic receptor gene (ADRA2A) with symptoms of attention-deficit/hyperactivity disorder.

1 reference

https://api.crossref.org/works/10.1007%2FS00702-007-0822-5

21 January 2018

DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: no evidence for association

1 reference

https://api.crossref.org/works/10.1007%2FS00702-007-0822-5

21 January 2018

Overview and neurobiology of attention-deficit/hyperactivity disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence of linkage or association between the norepinephrine transporter (NET) gene MnlI polymorphism and adult ADHD.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Attention-deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The epidemiology of attention-deficit/hyperactivity disorder (ADHD): a public health view

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

COMT Val108/158Met gene variant, birth weight, and conduct disorder in children with ADHD.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanism of action of agents used in attention-deficit/hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A functional serotonin transporter promoter gene polymorphism increases ADHD symptoms in delinquents: interaction with adverse childhood environment

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comparison of bayesian methods for haplotype reconstruction from population genotype data

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nature and nurture predispose to violent behavior: serotonergic genes and adverse childhood environment.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dopamine uptake through the norepinephrine transporter in brain regions with low levels of the dopamine transporter: evidence from knock-out mouse lines

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between alpha-2a-adrenergic receptor gene and ADHD inattentive type

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Reliability and validity of the Wender-Utah-Rating-Scale short form. Retrospective assessment of symptoms for attention deficit/hyperactivity disorder]

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of attention-deficit/hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism at the 3'-untranslated region of the CLOCK gene is associated with adult attention-deficit hyperactivity disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence of linkage or association between the norepinephrine transporter (NET) gene polymorphisms and ADHD in the Irish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal mapping of the human catechol-O-methyltransferase gene to 22q11.1----q11.2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of association between a catechol-O-methyltransferase gene polymorphism and attention deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of childhood disorders: XIX. ADHD, Part 3: Is ADHD a noradrenergic disorder?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal mapping of the human gene for the tricyclic antidepressant-sensitive noradrenaline transporter

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible involvement of alpha-2A adrenergic receptors in attention deficit hyperactivity disorder: radioligand binding and polymorphism studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage study of the alpha2A adrenergic receptor in attention-deficit hyperactivity disorder families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The norepinephrine transporter gene and attention-deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association and linkage of alpha-2A adrenergic receptor gene polymorphisms with childhood ADHD.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Tools for the diagnosis of attention-deficit/hyperactivity disorder in adults. Self-rating behaviour questionnaire and diagnostic checklist]

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primer3 on the WWW for general users and for biologist programmers

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catechol O-methyltransferase mRNA expression in human and rat brain: evidence for a role in cortical neuronal function

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Attention-deficit hyperactivity disorder and the adrenergic receptors alpha 1C and alpha 2C

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inferring candidate genes for attention deficit hyperactivity disorder (ADHD) assessed by the World Health Organization Adult ADHD Self-Report Scale (ASRS).

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism in the norepinephrine transporter gene alters promoter activity and is associated with attention-deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Wender Utah rating scale. The short-version for the assessment of the attention-deficit hyperactivity disorder in adults]

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is the alpha-2A adrenergic receptor gene (ADRA2A) associated with attention-deficit/hyperactivity disorder?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of attention deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meta-analysis of the association between the 7-repeat allele of the dopamine D(4) receptor gene and attention deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Faster haplotype frequency estimation using unrelated subjects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Additive effect of three noradrenergic genes (ADRA2a, ADRA2C, DBH) on attention-deficit hyperactivity disorder and learning disabilities in Tourette syndrome subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of attention deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Attention deficit hyperactivity disorder with reading disabilities: preliminary genetic findings on the involvement of the ADRA2A gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/17994190

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00702-007-0822-5

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

1 reference

Europe PubMed Central

26 December 2017

http://europepmc.org/abstract/MED/17994190

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