Evidence map›Paper›PMID 24497871›Full record

ArticleJournal of research in medical sciences : the official journal of Isfahan University of Medical Sciences2013

Association of human mtDNA mutations with autism in Iranian patients.

Kazem Mousavizadeh, Mohammad Askari, Hajar Arian, Fazel Gourjipour, Amin R Nikpour, Maryam Tavafjadid, Omid Aryani, Behnam Kamalidehghan, Hamid R Maroof, Massoud Houshmand

Open access · greenAbstract read
In one paragraph

Article in Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, 2013. 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
0.2field-weighted citation impact, top 36% 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, 5 citations in OpenAlex.

  1. Review
  2. Autism spectrum disorder: A mitochondrial disorder.Iranian journal of child neurology · 2021
    Article
  3. Review
  4. Review
  5. 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

10 authors at 2 institutions in 2 countries.

Kazem MousavizadehDepartment of Molecular Biology, Cellular and Molecular Research Center, Tehran, Iran.
Mohammad AskariDepartment of Biotechnology, College of Allied Medicine, Tehran, Iran.
Hajar ArianDepartment of Medical Genetic, Special Medical Center, Tehran, Iran.
Fazel GourjipourDepartment of Molecular Biology, HIV Molecular Research Laboratory, School of Public Health and Health Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Amin R NikpourDepartment of Immunology, Kerman University of Medical Sciences, Kerman, Iran.
Maryam TavafjadidDepartment of Molecular Biology, Cellular and Molecular Research Center, Tehran, Iran.
Omid AryaniDepartment of Medical Genetic, Special Medical Center, Tehran, Iran.
Behnam KamalidehghanDepartment of Pharmacy, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Hamid R MaroofDepartment of Medical Genetic, Special Medical Center, Tehran, Iran.
Massoud HoushmandDepartment of Medical Genetic, Special Medical Center, Tehran, Iran ; Department of Medical Genetics, National Institute for Genetic Engineering and Biotechnology, Tehran, Iran.
Kerman University of Medical Sciences · IRUniversity of Malaya · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID24497871
PMCPMC3897084
OpenAlexW1710978703

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.