Evidence map›Paper›PMID 38674394›Full record

ArticleGenes2024

Allele-Specific Regulation of the Candidate Autism Liability Gene

Xi Yuan, Li Chen, David Saffen

Open access · goldAbstract read
In one paragraph

Article in Genes, 2024. 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
0.3field-weighted citation impact, top 46% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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

3 authors at 1 institution in 1 country.

Xi YuanInstitutes of Brain Science, Fudan University, Shanghai 200032, China.
Li ChenDepartment of Cellular and Genetic Medicine, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China.
David SaffenInstitutes of Brain Science, Fudan University, Shanghai 200032, China.
Fudan University · CN

Funding

National Natural Science Foundation of China 81571090
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AllelesPolymorphism, Single NucleotideAutism Spectrum DisorderAutistic DisorderCase-Control StudiesCell Line, TumorEnhancer Elements, GeneticFemaleGene Expression RegulationGenetic Predisposition to DiseaseGenotypeHumansMaleTrans-ActivatorsRAI1 protein, humanTrans-Activatorsautismautism spectrum disordersRARα/RXRαregulatory variantretinoic acid-induced 1 (RAI1)rs4925102

Identifiers

PMID38674394
PMCPMC11049881
OpenAlexW4394566910

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.