Evidence map›Paper›PMID 31808517›Full record

ArticleBioscience reports2019

Integrative analysis of shared genetic pathogenesis by autism spectrum disorder and obsessive-compulsive disorder.

Dongbai Liu, Hongbao Cao, Kamil Can Kural, Qi Fang, Fuquan Zhang

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07400484 (A Study on the Differences in N-CAD Concentration and Brain Function Between Children With Autism Spectrum Disorder and Typically Developing Children), which is not on this map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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.

NCT07400484 recruitingnot on this mapstarted 2025, after this paper: background citation

A Study on the Differences in N-CAD Concentration and Brain Function Between Children With Autism Spectrum Disorder and Typically Developing Children

Typeobservational_patient_registrySponsorChen LiRan2025 to 2026Enrolled98ConditionsASD
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  10. Association betweenHeliyon · 2023
    Article
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  12. Genomic and proteomic biomarker landscape in clinical trials.Computational and structural biotechnology journal · 2023
    Article
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  16. CaFrontiers in pharmacology · 2022
    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

5 authors at 4 institutions in 3 countries.

Dongbai LiuDepartment of Neurology, The First People's Hospital Affiliated to Soochow University, Suzhou, Jiangsu Province, 215006, China.
Hongbao CaoDepartment of Psychiatry, First Hospital/First Clinical Medical College of Shanxi Medical University, Taiyuan, Shanxi Province, 030001, China.
Kamil Can KuralSchool of Systems Biology, George Mason University, Fairfax, VA 22030, U.S.A.
Qi FangDepartment of Neurology, The First People's Hospital Affiliated to Soochow University, Suzhou, Jiangsu Province, 215006, China.
Fuquan ZhangDepartment of Psychiatry, The Affiliated Brain Hospital of Nanjing Medical University, Nanjing, Jiansu Province, 210029, China.
Soochow University · CNGeorge Mason University · USNanjing Brain Hospital · CNRELX Group (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many common pathological features have been observed for both autism spectrum disorders (ASDs) and obsessive-compulsive disorder (OCD). However, no systematic analysis of the common gene markers associated with both ASD and OCD has been conducted so far. Here, two batches of large-scale literature-based disease-gene relation data (updated in 2017 and 2019, respectively) and gene expression data were integrated to study the possible association between OCD and ASD at the genetic level. Genes linked to OCD and ASD present significant overlap (P-value <2.64e-39). A genetic network of over 20 genes was constructed, through which OCD and ASD may exert influence on each other. The 2017-based analysis suggested six potential common risk genes for OCD and ASD (CDH2, ADCY8, APOE, TSPO, TOR1A, and OLIG2), and the 2019-based study identified two more genes (DISP1 and SETD1A). Notably, the gene APOE identified by the 2017-based analysis has been implicated to have an association with ASD in a recent study (2018) with DNA methylation analysis. Our results support the possible complex genetic associations between OCD and ASD. Genes linked to one disease are worth further investigation as potential risk factors for the other.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAdenylyl CyclasesAntigens, CDApolipoproteins EAutism Spectrum DisorderCadherinsFemaleGene Expression RegulationGene Regulatory NetworksHistone-Lysine N-MethyltransferaseHumansMaleMolecular ChaperonesObsessive-Compulsive DisorderOligodendrocyte Transcription Factor 2adenylyl cyclase 8Adenylyl CyclasesAntigens, CDApoE protein, humanApolipoproteins ECadherinsCDH2 protein, humanHistone-Lysine N-MethyltransferaseMolecular ChaperonesOLIG2 protein, humanOligodendrocyte Transcription Factor 2Receptors, GABASetd1A protein, humanTOR1A protein, humanTSPO protein, humanautism spectrum disordergene expression analysisNetwork connectivity analysisObsessive-compulsive disorder

Identifiers

PMID31808517
PMCPMC6928520
OpenAlexW2994566096

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.