Evidence map›Paper›PMID 29142762›Full record

ReviewJournal of pediatric genetics2017

Analysis of

Leila Chouiter, Sellama Nadifi

Abstract readReview
In one paragraph

Review in Journal of pediatric genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Genetic Analysis ofBiomedicines · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Novel compound heterozygous mutations inMolecular medicine reports · 2021
    Article
  11. Article
  12. Review
  13. Exome Sequencing in a Swiss Childhood Glaucoma Cohort RevealsTranslational vision science & technology · 2020
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Compound heterozygous mutations inInternational journal of ophthalmology · 2019
    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

2 authors.

Leila ChouiterDepartment of Medicine and Pharmacy, Hassan II University of Casablanca, Casablanca, Morocco.
Sellama NadifiLaboratory of Medical Genetics and Molecular Pathology, Department of Medicine and Pharmacy, Hassan II University of Casablanca, Casablanca, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary congenital glaucoma (PCG) is the most common type of infantile glaucoma, yet it remains a relatively rare disease, because the disease is often transmitted in an autosomal recessive pattern. However, PCG occurs up to 10 times more frequently in certain ethnic and geographical groups where consanguineous relationships are common. The aim of this study was to investigate the distribution of mutations in the cytochrome P450 1B1 gene (

Indexed as

CYP1B1cytochrome P450GLC3Aprimary congenital glaucoma

Identifiers

PMID29142762
PMCPMC5683959

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.