Evidence map›Paper›PMID 16894395›Full record

ArticleMolecular psychiatry2006

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

K Brookes, X Xu, W Chen, K Zhou, B Neale, N Lowe, R Anney, R Aneey, B Franke, M Gill and 53 more

Erratum issuedOpen access · bronzeAbstract readComparative StudyMulticenter Study
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 221 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
221citing papers in PubMed, 10 pooled it
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

221 citing papers in PubMed, 10 syntheses or guidelines pooled it, 15 citations in OpenAlex.

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  8. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.Journal of the American Academy of Child and Adolescent Psychiatry · 2010
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  19. Serotonin dysfunction in ADHD.Journal of neurodevelopmental disorders · 2025
    Review
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161 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
    Aneey, R [corrected to Anney, R]
5 · Who and what money

Authors and funding

63 authors at 15 institutions in 9 countries.

K BrookesMRC Social Genetic Developmental and Psychiatry Centre, Institute of Psychiatry, London, UK.
X Xu
W Chen
K Zhou
B Neale
N Lowe
R Anney
R Aneey
B Franke
M Gill
R Ebstein
J Buitelaar
P Sham
D Campbell
J Knight
P Andreou
M Altink
R Arnold
F Boer
C Buschgens
L Butler
H Christiansen
L Feldman
K Fleischman
E Fliers
R Howe-Forbes
A Goldfarb
A Heise
I Gabriëls
I Korn-Lubetzki
L Johansson
R Marco
S Medad
R Minderaa
F Mulas
U Müller
A Mulligan
K Rabin
N Rommelse
V Sethna
J Sorohan
H Uebel
L Psychogiou
A Weeks
R Barrett
I Craig
T Banaschewski
E Sonuga-Barke
J Eisenberg
J Kuntsi
I Manor
P McGuffin
A Miranda
R D Oades
R Plomin
H Roeyers
A Rothenberger
J Sergeant
H-C Steinhausen
E Taylor
M Thompson
S V Faraone
P Asherson
Psychiatry Research Trust · GBGeha Mental Health Center · ILSt. James's Hospital · IERadboud University Nijmegen · NLUniversity of Southampton · GBUniversity of Göttingen · DEUniversitat de València · ESGhent University Hospital · BESocial Neuroscience Lab · DEUniversity of Zurich · CHVrije Universiteit Amsterdam · NLHerzog Hospital · ILShaare Zedek Medical Center · ILSUNY Upstate Medical University · USUniversity Medical Center Groningen · NL

Funding

International Multi-Center ADHD Genetics ProjectR01MH062873 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI FARAONE, STEPHEN V · 2002 to 2007
$7.2M
Medical Research Council G0300189Medical Research Council G0501329Medical Research Council G19/2NIMH NIH HHS R01MH62873
6 · The paper itself

Abstract

Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, starting in early childhood and persisting into adulthood in the majority of cases. Family and twin studies have demonstrated the importance of genetic factors and candidate gene association studies have identified several loci that exert small but significant effects on ADHD. To provide further clarification of reported associations and identify novel associated genes, we examined 1,038 single-nucleotide polymorphisms (SNPs) spanning 51 candidate genes involved in the regulation of neurotransmitter pathways, particularly dopamine, norepinephrine and serotonin pathways, in addition to circadian rhythm genes. Analysis used within family tests of association in a sample of 776 DSM-IV ADHD combined type cases ascertained for the International Multi-centre ADHD Gene project. We found nominal significance with one or more SNPs in 18 genes, including the two most replicated findings in the literature: DRD4 and DAT1. Gene-wide tests, adjusted for the number of SNPs analysed in each gene, identified associations with TPH2, ARRB2, SYP, DAT1, ADRB2, HES1, MAOA and PNMT. Further studies will be needed to confirm or refute the observed associations and their generalisability to other samples.

Indexed as

AdolescentAttention Deficit Disorder with HyperactivityChildChild, PreschoolDopamine Plasma Membrane Transport ProteinsGenetic MarkersGenetic Predisposition to DiseaseHaplotypesHumansLinkage DisequilibriumMonoamine OxidaseOncogene ProteinsPedigreePolymorphism, Single NucleotideReceptors, Dopamine D4Receptors, NicotinicDopamine Plasma Membrane Transport ProteinsDRD4 protein, humanGenetic MarkersMonoamine OxidaseNET1 protein, humanOncogene ProteinsReceptors, Dopamine D4Receptors, NicotinicSLC6A3 protein, humanSynaptosomal-Associated Protein 25TPH2 protein, humanTryptophan Hydroxylase

Identifiers

PMID16894395
OpenAlexW2149164700

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.