Evidence map›Paper›PMID 30988961›Full record

ArticleSultan Qaboos University medical journal2018

Individual Radiosensitivity Assessment of the Families of

Asghar Aghamohammadi, Seyed M Akrami, Marjan Yaghmaie, Nima Rezaei, Gholamreza Azizi, Mehdi Yaseri, Hassan Nosrati, Majid Zaki-Dizaji

Open access · diamondAbstract read
In one paragraph

Article in Sultan Qaboos University medical journal, 2018. 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
0.3field-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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  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

8 authors at 3 institutions in 1 country.

Asghar AghamohammadiResearch Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Seyed M AkramiDepartment of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Marjan YaghmaieResearch Center for Hematology, Oncology & Stem Cell Transplantation, Tehran University of Medical Sciences, Tehran, Iran.
Nima RezaeiResearch Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Gholamreza AziziNon-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran.
Mehdi YaseriDepartment of Epidemiology & Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Hassan NosratiResearch Center for Radiation Oncology, Cancer Institute, Tehran University of Medical Sciences, Tehran, Iran.
Majid Zaki-DizajiResearch Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Tehran University of Medical Sciences · IRChildren's Medical Center · IRJahrom University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectives

methodsThis study took place at the Tehran University of Medical Sciences, Tehran, Iran, between February and December 2017 and included 16 A-T patients, their parents (obligate heterozygotes) and 30 healthy controls. All of the subjects underwent individual radiosensitivity (IRS) assessment using a modified caffeine-treated G2-assay with G2-checkpoint abrogation.

resultsThe mean IRS of the obligate

conclusionThe modified G2-assay demonstrated adequate precision and relatively high sensitivity and specificity in detecting heterozygous

Indexed as

AdolescentAdultAtaxia TelangiectasiaAtaxia Telangiectasia Mutated ProteinsAtherosclerosisCaffeineChildChild, PreschoolDiabetes Mellitus, Type 2FemaleG2 Phase Cell Cycle CheckpointsHumansIranMaleMiddle AgedNeoplasmsAtaxia Telangiectasia Mutated ProteinsCaffeineAtaxia-TelangiectasiaChromosome BreakageGenetic Carrier ScreeningHeterozygoteRadiation SensitivitySensitivity and Specificity

Identifiers

PMID30988961
PMCPMC6443281
OpenAlexW2930043191

What OpenQuestion holds

Textmetadata
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.