Evidence map›Paper›PMID 31334289›Full record

ArticleReports of biochemistry & molecular biology2019

Association Study of Sequence Variants in Voltage-gated Ca2+ Channel Subunit Alpha-1C and Autism Spectrum Disorders.

Arezou Sayad, Soudeh Ghafouri-Fard, Rezvan Noroozi, Mir Davood Omrani, Maziar Ganji, Romina Dastmalchi, Mark Glassy, Mohammad Taheri

Open access · greenAbstract read
In one paragraph

Article in Reports of biochemistry & molecular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 96% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. CACNA1C-Related Channelopathies.Handbook of experimental pharmacology · 2023
    Review
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 1 institution in 1 country.

Arezou SayadDepartment of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran.
Soudeh Ghafouri-FardDepartment of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran.
Rezvan NorooziPhytochemistry Research Center, Shahid Beheshti University of Medical sciences, Tehran, Iran.
Mir Davood OmraniDepartment of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran.
Maziar GanjiDepartment of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran.
Romina DastmalchiDepartment of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran.
Mark GlassyHagiwara Institute of Health Integrated Medical Sciences Association Foundation, Oceanside, CA, United States.
Mohammad TaheriDepartment of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran.
Shahid Beheshti University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutism spectrum disorders (ASDs) (MIM 209850) are a group of distinct neurodevelopmental disorders characterized by impaired social interactions and communication abilities and abnormal repetitive activities. Many genetic variants have been shown to be associated with ASD. Channelopathies are among putative culprits in the pathogenesis of many neurodevelopmental disorders, including autism. The calcium channel, voltage-dependent, L type, alpha 1C subunit gene (

methodsIn the present case-control study we investigated the associations of rs1006737, rs4765905, and rs4765913 polymorphisms within

resultsNone of these SNPs were associated with ASD risk in the assessed population. Although previous studies have shown an association between these polymorphisms and psychiatric disorders and an association between rs4765905 and ASD, we did not replicate those results in our study.

conclusionOur data indicate that these

Indexed as

Autism Spectrum DisorderCACNA1CChannelopathypolymorphism

Identifiers

PMID31334289
PMCPMC6590947
OpenAlexW2942774191

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.