Evidence map›Paper›PMID 35991577›Full record

ArticleFrontiers in genetics2022

Case report: FOXP1 syndrome caused by a

Min Chen, Yixi Sun, Yeqing Qian, Na Chen, Hongge Li, Liya Wang, Minyue Dong

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
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

7 authors at 1 institution in 1 country.

Min ChenWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yixi SunWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Yeqing QianWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Na ChenWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Hongge LiWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Liya WangWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Minyue DongWomen's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
Women's Hospital, School of Medicine, Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FOXP1 syndrome is a rare neurodevelopmental disorder characterized by global developmental delay, intellectual disability, and language delay, with or without autistic features. Several splicing variants have been reported for this condition, but most of them lack functional evidence, and the actual effects of the sequence changes are still unknown. In this study, a

Indexed as

FOXP1 syndromeglobal developmental delayintellectual disabilityRNA analysissplicing variantWES

Identifiers

PMID35991577
PMCPMC9388729
OpenAlexW4289890750

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.