Evidence map›Paper›PMID 27131873›Full record

ArticleHuman genetics2016

Exploiting aberrant mRNA expression in autism for gene discovery and diagnosis.

Jinting Guan, Ence Yang, Jizhou Yang, Yong Zeng, Guoli Ji, James J Cai

Abstract read
PubMed Publisher
In one paragraph

Article in Human genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

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  10. Persistent homology analysis of brain transcriptome data in autism.Journal of the Royal Society, Interface · 2019
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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 at 2 institutions in 2 countries.

Jinting GuanDepartment of Automation, Xiamen University, Xiamen, Fujian, China.
Ence YangDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA.
Jizhou YangDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA.
Yong ZengDepartment of Automation, Xiamen University, Xiamen, Fujian, China.
Guoli JiDepartment of Automation, Xiamen University, Xiamen, Fujian, China. glji@xmu.edu.cn.
James J CaiDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA. jcai@tamu.edu.
Texas A&M University · USXiamen University · CN

Funding

MADS-box transcriptional regulation of dimorphic transition in Penicillium marneffeiR21AI126219 · NIAID · TEXAS A&M AGRILIFE RESEARCH · PI CAI, JAMES JING, LIN, XIAORONG · 2016 to 2017
$383k
NIAID NIH HHS R21 AI126219
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is characterized by substantial phenotypic and genetic heterogeneity, which greatly complicates the identification of genetic factors that contribute to the disease. Study designs have mainly focused on group differences between cases and controls. The problem is that, by their nature, group difference-based methods (e.g., differential expression analysis) blur or collapse the heterogeneity within groups. By ignoring genes with variable within-group expression, an important axis of genetic heterogeneity contributing to expression variability among affected individuals has been overlooked. To this end, we develop a new gene expression analysis method-aberrant gene expression analysis, based on the multivariate distance commonly used for outlier detection. Our method detects the discrepancies in gene expression dispersion between groups and identifies genes with significantly different expression variability. Using this new method, we re-visited RNA sequencing data generated from post-mortem brain tissues of 47 ASD and 57 control samples. We identified 54 functional gene sets whose expression dispersion in ASD samples is more pronounced than that in controls, as well as 76 co-expression modules present in controls but absent in ASD samples due to ASD-specific aberrant gene expression. We also exploited aberrantly expressed genes as biomarkers for ASD diagnosis. With a whole blood expression data set, we identified three aberrantly expressed gene sets whose expression levels serve as discriminating variables achieving >70 % classification accuracy. In summary, our method represents a novel discovery and diagnostic strategy for ASD. Our findings may help open an expression variability-centered research avenue for other genetically heterogeneous disorders.

Indexed as

Genetic Predisposition to DiseaseAutism Spectrum DisorderBrainFemaleGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksGenetic Association StudiesHumansMalePolymorphism, Single Nucleotide

Identifiers

PMID27131873
OpenAlexW2342665329

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.