Evidence map›Paper›PMID 29550512›Full record

ReviewToxicology and applied pharmacology2018

C. elegans as a model in developmental neurotoxicology.

Joanna A Ruszkiewicz, Adi Pinkas, Mahfuzur R Miah, Rebecca L Weitz, Michael J A Lawes, Ayodele J Akinyemi, Omamuyovwi M Ijomone, Michael Aschner

Abstract readReview
In one paragraph

Review in Toxicology and applied pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

56 citing papers in PubMed, 139 citations in OpenAlex.

  1. Article
  2. High-Throughput Toxicity Screening withEnvironmental science & technology · 2026
    Review
  3. Review
  4. Dietary mycotoxin toxicity inAdvances in neurotoxicology · 2026
    Article
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  6. Article
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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 2 institutions in 2 countries.

Joanna A RuszkiewiczDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States. Electronic address: joanna.ruszkiewicz@einstein.yu.edu.
Adi PinkasDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States.
Mahfuzur R MiahDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States. Electronic address: mahfuzur.miah@phd.einstein.yu.edu.
Rebecca L WeitzDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States.
Michael J A LawesDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States.
Ayodele J AkinyemiDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States; Department of Biochemistry, Afe Babalola University, Ado-Ekiti, Ekiti State, Nigeria. Electronic address: ayodele.akinyemi@einstein.yu.edu.
Omamuyovwi M IjomoneDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States; Department of Anatomy, School of Health and Health Technology, Federal University of Technology Akure (FUTA), Nigeria. Electronic address: omamuyovwi.ijomone@einstein.edu.yu.
Michael AschnerDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York, United States. Electronic address: michael.aschner@einstein.yu.edu.
Albert Einstein College of Medicine · USAfe Babalola University · NG

Funding

Mechanisms of Manganese NeurotoxicityR01ES010563 · NIEHS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Michael Aschner, Aaron B Bowman · 2001 to 2026
$11.9M
Mechanisms of Methylmercury Induced Neuron ToxicityR01ES007331 · NIEHS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Michael Aschner, Aaron B Bowman · 1996 to 2026
$10.6M
Genetic Modulation of MeHg-Induced Oxidative Stress in the Developing BrainR01ES020852 · NIEHS · VANDERBILT UNIVERSITY · PI ASCHNER, MICHAEL · 2012 to 2016
$1.8M
NIEHS NIH HHS R01 ES007331NIEHS NIH HHS R01 ES010563NIEHS NIH HHS R01 ES020852
6 · The paper itself

Abstract

Due to many advantages Caenorhabditis elegans (C. elegans) has become a preferred model of choice in many fields, including neurodevelopmental toxicity studies. This review discusses the benefits of using C. elegans as an alternative to mammalian systems and gives examples of the uses of the nematode in evaluating the effects of major known neurodevelopmental toxins, including manganese, mercury, lead, fluoride, arsenic and organophosphorus pesticides. Reviewed data indicates numerous similarities with mammals in response to these toxins. Thus, C. elegans studies have the potential to predict possible effects of developmental neurotoxicants in higher animals, and may be used to identify new molecular pathways behind neurodevelopmental disruptions, as well as new toxicants.

Indexed as

AnimalsCaenorhabditis elegansHumansModels, AnimalNeuronsNeurotoxicity SyndromesRisk AssessmentSpecies SpecificityToxicity TestsC. elegansManganeseMercuryNeurodevelopmentNeurotoxicityPesticides

Identifiers

PMID29550512
PMCPMC6087488
OpenAlexW2790164716

What OpenQuestion holds

Textmetadata
LicenceTDM
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.