Evidence map›Paper›PMID 31239368›Full record

ArticleBioscience reports2019

Heterozygous

Yuan Wu, Yi Guo, Junhui Yi, Hongbo Xu, Lamei Yuan, Zhijian Yang, Hao Deng

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

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Genes · 2024
    Article
  4. Review
  5. Article
  6. 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

7 authors at 1 institution in 1 country.

Yuan WuCenter for Experimental Medicine and Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-9358-9146
Yi GuoCenter for Experimental Medicine and Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Junhui YiDepartment of Ophthalmology, The Third Xiangya Hospital, Central South University, Changsha, China.
Hongbo XuCenter for Experimental Medicine and Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Lamei YuanCenter for Experimental Medicine and Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0001-7558-0669
Zhijian YangCenter for Experimental Medicine and Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Hao DengCenter for Experimental Medicine and Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China hdeng008@yahoo.com.ORCID 0000-0003-3240-4352
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinitis pigmentosa (RP), the most common type of inherited retinal degeneration causing blindness, initially manifests as severely impaired rod function followed by deteriorating cone function. Mutations in the rhodopsin gene (

Indexed as

Genetic Predisposition to DiseaseAdultAsian PeopleExome SequencingFemaleGenetic Association StudiesHeterozygoteHumansMaleMiddle AgedMutation, MissensePedigreeRefractive ErrorsRetinitis PigmentosaRhodopsinRhodopsinmissense mutationretinitis pigmentosarhodopsinwhole exome sequencing

Identifiers

PMID31239368
PMCPMC6629948
OpenAlexW2954535098

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.