Evidence map›Paper›PMID 31031587›Full record

ArticleFrontiers in neuroscience2019

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes.

Juan Xiong, Shimeng Chen, Nan Pang, Xiaolu Deng, Lifen Yang, Fang He, Liwen Wu, Chen Chen, Fei Yin, Jing Peng

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
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  3. Novel HUWE1-Related Neurodevelopmental Disorder: Genotypic and Phenotypic Expansion.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2026
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  15. Journal of clinical medicine · 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

10 authors at 2 institutions in 1 country.

Juan XiongDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Shimeng ChenDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Nan PangDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Xiaolu DengDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Lifen YangDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Fang HeDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Liwen WuDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Chen ChenDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Fei YinDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Jing PengDepartmen of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Central South University · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is frequently comorbid with other neurological disorders such as intellectual disability (ID) or global development delay (GDD) and epilepsy. The pathogenesis of ASD is complex. So far, studies have identified more than 1000 ASD risk genes. Most of them were also reported to relate with other neurological diseases, and only several of them have been confirmed as pathogenic genes for autism. Little is known about the roles of these risk genes in neurological diseases with ASD. In the present study, we recruited a cohort of 158 neurological disorder probands with 163 variants of 48 ASD risk genes. Of these, 50 individuals (31.6%) were diagnosed with ASD. In the ASD patient subset, we identified several rarely reported candidate genes including

Indexed as

autism risk geneautism spectrum disordergene functionneurological diseasesrisk factors

Identifiers

PMID31031587
PMCPMC6470315
OpenAlexW2937773561

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.