Evidence map›Paper›PMID 42792900›Full record

ArticleGenes2026

Configuration-Level Genetic Interpretation in Neurodevelopmental Disorders: A Single-Center Cohort of 2162 Children in China.

Lingxue Li, Dawei Cheng, Bing Wang, Fan Wu, Xinna Ji, Qian Chen

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lingxue LiDepartment of Neurology, Capital Institute of Pediatrics, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100020, China.ORCID 0000-0003-3705-5462
Dawei ChengDepartment of Neurology, Capital Center for Children's Health, Capital Medical University, Capital Institute of Pediatrics, Beijing 100020, China.
Bing WangDepartment of Neurology, Capital Institute of Pediatrics, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100020, China.
Fan WuDepartment of Neurology, Capital Institute of Pediatrics, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100020, China.
Xinna JiDepartment of Neurology, Capital Center for Children's Health, Capital Medical University, Capital Institute of Pediatrics, Beijing 100020, China.
Qian ChenDepartment of Neurology, Capital Center for Children's Health, Capital Medical University, Capital Institute of Pediatrics, Beijing 100020, China.ORCID 0000-0002-3296-7596

Funding

National Key Research and Development Program of China 2022YFC2703903
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Neurodevelopmental DisordersAdolescentChildChild, PreschoolChinaDNA, MitochondrialFemaleGenetic TestingHeteroplasmyHeterozygoteHumansInfantMaleMosaicismRetrospective StudiesUniparental DisomyDNA, Mitochondrialcompound heterozygosityexome sequencingmitochondrial DNA heteroplasmymosaicismmultilocus molecular diagnosisneurodevelopmental disordersuniparental disomy

Identifiers

PMID42792900
PMCPMC13606647

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.