Evidence map›Paper›PMID 34354814›Full record

ArticleF1000Research2021

The diagnostic yield of whole exome sequencing as a first approach in consanguineous Omani renal ciliopathy syndrome patients.

Intisar Al Alawi, Mohammed Al Riyami, Miguel Barroso-Gil, Laura Powell, Eric Olinger, Issa Al Salmi, John A Sayer

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

Article in F1000Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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  5. Case Report: A Novel In-Frame Deletion ofFrontiers in genetics · 2021
    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 3 institutions in 2 countries.

Intisar Al AlawiTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, Tyne and Wear, NE13BZ, UK.
Mohammed Al RiyamiPediatric Nephrology Unit, Department of Child Health, Royal Hospital, Ministry of Health, Muscat, Oman.ORCID 0000-0003-3698-5609
Miguel Barroso-GilTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, Tyne and Wear, NE13BZ, UK.
Laura PowellTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, Tyne and Wear, NE13BZ, UK.
Eric OlingerTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, Tyne and Wear, NE13BZ, UK.ORCID 0000-0003-1178-7980
Issa Al SalmiRenal Medicine Department, Royal Hospital, Ministry of Health, Muscat, Oman.ORCID 0000-0002-3443-5972
John A SayerTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, Tyne and Wear, NE13BZ, UK.ORCID 0000-0003-1881-3782
Newcastle University · GBMinistry of Health · OMOman Medical College · OM

Funding

Medical Research Council
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CiliopathiesExomeChildConsanguinityExome SequencingHumansSyndromecystic kidney diseaseOmanrenal ciliopathywhole exomes sequencing

Identifiers

PMID34354814
PMCPMC8290205.2
OpenAlexW3138742260

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.