Evidence map›Paper›PMID 29061647›Full record

ArticleGenetics2017

Pyridoxine-Dependent Epilepsy in Zebrafish Caused by Aldh7a1 Deficiency.

Izabella A Pena, Yann Roussel, Kate Daniel, Kevin Mongeon, Devon Johnstone, Hellen Weinschutz Mendes, Marjolein Bosma, Vishal Saxena, Nathalie Lepage, Pranesh Chakraborty and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

53 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Broad Vitamin BInternational journal of molecular sciences · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. LysineFrontiers in molecular neuroscience · 2025
    Review
  14. Vitamin BAnimals : an open access journal from MDPI · 2024
    Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

17 authors at 5 institutions in 2 countries.

Izabella A PenaChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada ipena2@uottawa.ca.ORCID 0000-0001-5242-3724
Yann RousselDepartment of Biology, University of Ottawa, Ontario K1N 6N5, Canada.
Kate DanielChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.
Kevin MongeonChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.
Devon JohnstoneChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.
Hellen Weinschutz MendesDepartment of Biology, University of Ottawa, Ontario K1N 6N5, Canada.
Marjolein BosmaDepartments of Pediatrics and Clinical Genetics, Academic Medical Centre, 1105 AZ Amsterdam, The Netherlands.
Vishal SaxenaDepartment of Biology, University of Ottawa, Ontario K1N 6N5, Canada.
Nathalie LepageChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.
Pranesh ChakrabortyChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.
David A DymentChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.
Clara D M van KarnebeekDepartments of Pediatrics and Clinical Genetics, Academic Medical Centre, 1105 AZ Amsterdam, The Netherlands.ORCID 0000-0003-3352-5631
Nanda Verhoeven-DuifDepartment of Genetics, Center for Molecular Medicine, University Medical Center (UMC), 3584 EA Utrecht, The Netherlands.
Tuan Vu BuiDepartment of Biology, University of Ottawa, Ontario K1N 6N5, Canada.ORCID 0000-0003-0024-1544
Kym M BoycottChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada ipena2@uottawa.ca.ORCID 0000-0003-4186-8052
Marc EkkerDepartment of Biology, University of Ottawa, Ontario K1N 6N5, Canada.
Alex MacKenzieChildren's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario K1H 8L1, Canada.
University of Ottawa · CAChildren's Hospital of Eastern Ontario · CAAmsterdam UMC Location University of Amsterdam · NLUniversity of British Columbia · CAUtrecht University · NL

Funding

CIHR
6 · The paper itself

Abstract

Pyridoxine-dependent epilepsy (PDE) is a rare disease characterized by mutations in the lysine degradation gene

Indexed as

Aldehyde DehydrogenaseAnimalsDisease Models, AnimalEpilepsygamma-Aminobutyric AcidGene Knockout TechniquesHumansLysineMutationPyridoxineSeizuresVitamin B 6ZebrafishAldehyde DehydrogenaseALDH7A1 protein, humangamma-Aminobutyric AcidLysinePyridoxineVitamin B 6aldh7a1lysine metabolismmetabolic epilepsypyridoxine-dependent epilepsyzebrafish model

Identifiers

PMID29061647
PMCPMC5714462
OpenAlexW2765501413

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.