Evidence map›Paper›PMID 35774559›Full record

ArticleFrontiers in neuroscience2022

Splicing Interruption by Intron Variants in

Wen Zhang, Fanghua Ye, Shimeng Chen, Jing Peng, Nan Pang, Fei Yin

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. CSNK2B Mutation: A Rare Cause of IGHD.Clinical endocrinology · 2025
    Article
  5. Review
  6. Article
  7. Article
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 1 country.

Wen ZhangDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Fanghua YeDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Shimeng ChenDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Jing PengDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Nan PangDepartment of Pediatrics, Xiangya Hospital, Central South University, Changsha, China.
Fei YinDepartment 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

PubMed holds no abstract for this paper.

Indexed as

CSNK2Bgenotypeintron variantsphenotypePoirier–Bienvenu neurodevelopmental syndrome

Identifiers

PMID35774559
PMCPMC9237577
OpenAlexW4282835917

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.