Evidence map›Paper›PMID 21302343›Full record

ArticleAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2011

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects.

Thais S Rizzi, Alejandro Arias-Vasquez, Nanda Rommelse, Jonna Kuntsi, Richard Anney, Philip Asherson, Jan Buitelaar, Tobias Banaschewski, Richard Ebstein, Dina Ruano and 33 more

Abstract readComparative Study
In one paragraph

Article in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

43 authors.

Thais S RizziDepartment of Functional Genomics, CNCR, Neuroscience Campus Amsterdam, VU University and VU Medical Center, Amsterdam, the Netherlands. t.rizzi@vumc.nl
Alejandro Arias-Vasquez
Nanda Rommelse
Jonna Kuntsi
Richard Anney
Philip Asherson
Jan Buitelaar
Tobias Banaschewski
Richard Ebstein
Dina Ruano
Sophie Van der Sluis
Christina A Markunas
Melanie E Garrett
Allison E Ashley-Koch
Scott H Kollins
Arthur D Anastopoulos
Narelle K Hansell
Margaret J Wright
Grant W Montgomery
Nicholas G Martin
Sarah E Harris
Gail Davies
Albert Tenesa
David J Porteous
John M Starr
Ian J Deary
Beate St Pourcain
George Davey Smith
Nicholas J Timpson
David M Evans
Michael Gill
Ana Miranda
Fernando Mulas
Robert D Oades
Herbert Roeyers
Aribert Rothenberger
Joseph Sergeant
Edmund Sonuga-Barke
Hans Christoph Steinhausen
Eric Taylor
Stephen V Faraone
Barbara Franke
Danielle Posthuma

Funding

International Multi-Center ADHD Genetics ProjectR01MH062873 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI FARAONE, STEPHEN V · 2002 to 2007
$7.2M
Candidate Gene Analysis of Persistent AD/HDR01NS049067 · NINDS · DUKE UNIVERSITY · PI ASHLEY-KOCH, ALLISON E · 2004 to 2008
$2.9M
Smoking/Nicotine Dependence in Attention Deficit Hyperactivity Disorder (ADHD)K24DA023464 · NIDA · DUKE UNIVERSITY · PI KOLLINS, SCOTT H · 2008 to 2018
$1.5M
Analysis of an ADHD Whole Genome Association ScanR01MH081803 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI FARAONE, STEPHEN V · 2007 to 2007
$157k
Biotechnology and Biological Sciences Research Council BB/F019394/1Medical Research Council G03001896Medical Research Council G0600705Medical Research Council G0700704Medical Research Council G0800582NIDA NIH HHS K24 DA023464NIMH NIH HHS R01 MH062873NIMH NIH HHS R01 MH081803NIMH NIH HHS R01MH081803NIMH NIH HHS R01MH62873NINDS NIH HHS NS049067NINDS NIH HHS R01 NS049067Wellcome TrustWellcome Trust 076467/Z05/z
6 · The paper itself

Abstract

Intelligence is a highly heritable trait for which it has proven difficult to identify the actual genes. In the past decade, five whole-genome linkage scans have suggested genomic regions important to human intelligence; however, so far none of the responsible genes or variants in those regions have been identified. Apart from these regions, a handful of candidate genes have been identified, although most of these are in need of replication. The recent growth in publicly available data sets that contain both whole genome association data and a wealth of phenotypic data, serves as an excellent resource for fine mapping and candidate gene replication. We used the publicly available data of 947 families participating in the International Multi-Centre ADHD Genetics (IMAGE) study to conduct an in silico fine mapping study of previously associated genomic locations, and to attempt replication of previously reported candidate genes for intelligence. Although this sample was ascertained for attention deficit/hyperactivity disorder (ADHD), intelligence quotient (IQ) scores were distributed normally. We tested 667 single nucleotide polymorphisms (SNPs) within 15 previously reported candidate genes for intelligence and 29451 SNPs in five genomic loci previously identified through whole genome linkage and association analyses. Significant SNPs were tested in four independent samples (4,357 subjects), one ascertained for ADHD, and three population-based samples. Associations between intelligence and SNPs in the ATXN1 and TRIM31 genes and in three genomic locations showed replicated association, but only in the samples ascertained for ADHD, suggesting that these genetic variants become particularly relevant to IQ on the background of a psychiatric disorder.

Indexed as

Ataxin-1AtaxinsAttention Deficit Disorder with HyperactivityCohort StudiesHumansIntelligenceMeta-Analysis as TopicNerve Tissue ProteinsNuclear FamilyNuclear ProteinsPhenotypePolymorphism, Single NucleotideTripartite Motif ProteinsUbiquitin-Protein LigasesWhite PeopleAtaxin-1AtaxinsATXN1 protein, humanNerve Tissue ProteinsNuclear ProteinsTRIM31 protein, humanTripartite Motif ProteinsUbiquitin-Protein Ligases

Identifiers

PMID21302343
PMCPMC3085124

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.