Evidence map›Paper›PMID 25360606›Full record

ArticlePsychiatric genetics2014

MACROD2 gene associated with autistic-like traits in a general population sample.

Rachel M Jones, Gemma Cadby, John Blangero, Lawrence J Abraham, Andrew J O Whitehouse, Eric K Moses

Abstract read
In one paragraph

Article in Psychiatric genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

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

  1. Pooled it
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  14. Peripheral Expression ofPsychiatry and clinical psychopharmacology · 2021
    Article
  15. Molecular Dysregulation in Autism Spectrum Disorder.Journal of personalized medicine · 2021
    Review
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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

6 authors.

Rachel M Jones *Centre for Genetic Origins of Health and Disease, Telethon Institute for Child Health Research, University of Western Australia, Perth, Australia.
Gemma Cadby *Centre for Genetic Origins of Health and Disease, Telethon Institute for Child Health Research, University of Western Australia, Perth, Australia.
John BlangeroDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, Texas, USA.
Lawrence J AbrahamCentre for Genetic Origins of Health and Disease, Telethon Institute for Child Health Research, University of Western Australia, Perth, Australia.
Andrew J O WhitehouseCentre for Child Health Research, Telethon Institute for Child Health Research, University of Western Australia, Perth, Australia.
Eric K MosesCentre for Genetic Origins of Health and Disease, Telethon Institute for Child Health Research, University of Western Australia, Perth, Australia.

Funding

SOLAR-Eclipse Computational Tools for Imaging GeneticsR01EB015611 · NIBIB · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KOCHUNOV, PETER V. · 2012 to 2024
$5.0M
NIBIB NIH HHS R01 EB015611
6 · The paper itself

Abstract

There is now substantial evidence that autistic-like traits in the general population lie on a continuum, with clinical autism spectrum disorders (ASD) representing the extreme end of this distribution. In this study, we sought to evaluate five independently identified genetic associations with ASD with autistic-like traits in the general population. In the study cohort, clinical phenotype and genomewide association genotype data were obtained from the Western Australian Pregnancy Cohort (Raine) Study. The outcome measure used was the Autism Spectrum Quotient (AQ), a quantitative measure of autistic-like traits of individuals in the cohort. Total AQ scores were calculated for each individual, as well as scores for three subscales. Five candidate single nucleotide polymorphism (SNP) associations with ASD, reported in previously published genomewide association studies, were selected using a nominal cutoff value of P less than 1.0×10. We tested whether these five SNPs were associated with total AQ and the subscales, after adjustment for possible confounders. SNP rs4141463 located in the macro domain containing 2 (MACROD2) gene was significantly associated with the Communication/Mindreading subscale. No other SNP was significantly associated with total AQ or the subscales. The MACROD2 gene is a strong positional candidate risk factor for autistic-like traits in the general population.

Indexed as

Autistic DisorderCohort StudiesDNA Repair EnzymesFemaleGenome-Wide Association StudyHumansHydrolasesMalePolymorphism, Single NucleotidePregnancyWestern AustraliaDNA Repair EnzymesHydrolasesMACROD2 protein, human

Identifiers

PMID25360606
PMCPMC4320645

What OpenQuestion holds

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Registered trials

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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.