Evidence map›Paper›PMID 34466237›Full record

ArticleClinical case reports2021

A novel biallelic

Saeed Farajzadeh Valilou, Javad Karimzad Hagh, Mohammad Salimi Asl, Isa Abdi Rad, Masoud Edizadeh, Arash Pooladi

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

Article in Clinical case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. A novel biallelicClinical case reports · 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

6 authors at 5 institutions in 1 country.

Saeed Farajzadeh ValilouDepartment of Medical Genetics and Sarem Cell Research Center (SCRC) Sarem Womens' Hospital Tehran Iran.ORCID https://orcid.org/0000-0001-7470-6485
Javad Karimzad HaghDepartment of Medical Genetics and Sarem Cell Research Center (SCRC) Sarem Womens' Hospital Tehran Iran.
Mohammad Salimi AslDepartment of Medical Genetics and Sarem Cell Research Center (SCRC) Sarem Womens' Hospital Tehran Iran.
Isa Abdi RadDepartament of Medical Genetics School of Medicine Urmia University of Medical Sciences Urmia Iran.
Masoud EdizadehBiotechnology Department School of Medicine Lorestan University of Medical Sciences Khorramabad Lorestan Iran.
Arash PooladiCancer and Immunology Research Center Research Institute for Health Development Kurdistan University of Medical Sciences Sanandaj Iran.ORCID https://orcid.org/0000-0001-5126-1006
Sarem Cell Research Center · IRKurdistan University of Medical Sciences · IRLorestan University of Medical Sciences · IRUniversal Scientific Education and Research Network · IRUrmia University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The report of LMNB2-related progressive myoclonus epilepsy and ataxia due to missense homozygous c.473G>T variant.

Indexed as

ataxialaminopathyLMNB2progressive myoclonus epilepsieswhole‐exome sequencing

Identifiers

PMID34466237
PMCPMC8381754
OpenAlexW3195855178

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.