Evidence map›Paper›PMID 31327966›Full record

ArticleIranian journal of child neurology2019

Genetic Analysis of

Jafar Nasiri, Mansoor Salehi, Majid Hosseinzadeh, Mahdi Zamani, Shirin Fattahpour, Omid Aryani, Esmat Fazel Najafabadi, Maryam Jabarzadeh, Sara Asadi, Tahereh Gholamrezapour and 2 more

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

Article in Iranian journal of child neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

12 authors at 4 institutions in 1 country.

Jafar NasiriDepartment of Paediatric Neurology, Faculty of Medicine, Child Growth and Development Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Mansoor SalehiMedical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Majid HosseinzadehDepartment of Medical Genetics, School of Medicine, International Campus, Tehran University of Medical Sciences, Tehran, Iran.
Mahdi ZamaniDepartment of Medical Genetics, School of Medicine, International Campus, Tehran University of Medical Sciences, Tehran, Iran.
Shirin FattahpourMedical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Omid AryaniDepartment of Neuroscience, Iran University of Medical Sciences, Tehran, Iran.
Esmat Fazel NajafabadiMedical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Maryam JabarzadehMedical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Sara AsadiMedical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Tahereh GholamrezapourMedical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Maryam SedghiMedical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Fatemeh GhorbaniMedical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Alzahra University · IRIsfahan University of Medical Sciences · IRTehran University of Medical Sciences · IRIran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesRett syndrome is an X linked dominant neurodevelopmental disorder which almost exclusively affects females. The syndrome is usually caused by mutations in MATERIALS &

methodsTo provide further insights into the distribution of mutations in

resultsDirect sequencing revealed

conclusionDefects in

Indexed as

Direct sequencingIranMECP2 mutationRett syndrome

Identifiers

PMID31327966
PMCPMC6586453
OpenAlexW2953637170

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.