Evidence map›Paper›PMID 36970538›Full record

ArticleFrontiers in neurology2023

Genetic variants and phenotype analysis in a five-generation Chinese pedigree with

Wenjuan Zhou, Yuzhen Ouyang, Yuqiao Ji, Qiong Xi, Lingling Zhao

Open access · goldFull text read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in neurology, 2023. 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
0.9field-weighted citation impact, top 28% 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, 4 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Wenjuan ZhouThird Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yuzhen OuyangThird Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yuqiao JiThird Xiangya Hospital, Central South University, Changsha, Hunan, China.
Qiong XiThird Xiangya Hospital, Central South University, Changsha, Hunan, China.
Lingling ZhaoThird Xiangya Hospital, Central South University, Changsha, Hunan, China.
Central South University · CNThird Xiangya Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Albeit the gene of Methods: We analyzed the clinical data and genetic variants of a Results: Based on a five-generation pedigree of Conclusion: A strong genotype-phenotype heterogeneity was observed among female patients with the same genotype in our

Indexed as

epilepsyPCDH19-FEPCDH19 variantspedigreephenotype heterogeneity

Identifiers

PMID36970538
PMCPMC10034091
OpenAlexW4323666728

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read3
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.