Evidence map›Paper›PMID 23677056›Full record

ReviewJournal of human genetics2013

Epigenomic strategies at the interface of genetic and environmental risk factors for autism.

Janine M LaSalle

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of human genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 94 citations in OpenAlex.

  1. Pooled it
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  14. X Chromosome Inactivation Timing is Not eFrontiers in genetics · 2022
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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

1 author at 1 institution in 1 country.

Janine M LaSalleMedical Microbiology and Immunology, Genome Center, MIND Institute, University of California, Davis, CA, USA. jmlasalle@ucdavis.edu
University of California Davis Medical Center · US

Funding

UC Davis Center for Children's Environmental Health (CCEH)P01ES011269 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI VAN DE WATER, JUDY A. · 2001 to 2018
$12.5M
The Role of MeCP2 in Rett SyndromeR01NS081913 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LASALLE, JANINE M · 2012 to 2016
$1.9M
Methylomic and genomic impacts of organic pollutants in Dup15q syndromeR01ES021707 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LASALLE, JANINE M · 2012 to 2016
$1.8M
Noncoding RNAs at the heart of the Prader-Willi locusR01NS076263 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LASALLE, JANINE M · 2011 to 2015
$1.6M
Exploring Interactions between Folate and Environmental Risk Factors for AutismR21ES021330 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SCHMIDT, REBECCA JEAN · 2012 to 2014
$481k
NIEHS NIH HHS P01 ES011269NIEHS NIH HHS R01 ES021707NIEHS NIH HHS R01ES021707NIEHS NIH HHS R21 ES021330NIEHS NIH HHS R21ES021330NINDS NIH HHS R01 NS076263NINDS NIH HHS R01NS076263NINDS NIH HHS R01 NS081913NINDS NIH HHS R01NS081913
6 · The paper itself

Abstract

Autism spectrum disorders (ASD) have been increasing in prevalence over the last two decades, primarily because of increased awareness and diagnosis. However, autism is clearly a complex human genetic disorder that involves interactions between genes and environment. Epigenetic mechanisms, such as DNA methylation, act at the interface of genetic and environmental risk and protective factors. Advancements in genome-wide sequencing has broadened the view of the human methylome and revealed the organization of the human genome into large-scale methylation domains that footprint over neurologically important genes involved in embryonic development. Future integrative epigenomic analyses of genetic risk factors with environmental exposures and methylome analyses are expected to be important for understanding the complex etiology of ASD.

Indexed as

Epigenesis, GeneticGene-Environment InteractionAutistic DisorderDNA MethylationEpigenomicsFemaleGenetic Predisposition to DiseaseGenome, HumanGenome-Wide Association StudyHumansInfant, NewbornPerinatal CarePregnancyRisk Factors

Identifiers

PMID23677056
PMCPMC3955092
OpenAlexW2021976298

What OpenQuestion holds

Textmetadata
LicenceTDM
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.