Evidence map›Paper›PMID 37766829›Full record

ArticleMolecular syndromology2023

X-Linked Hydrocephalus with New

Rania R Ahmed, Amina M Medhat, Germine M Hamdy, Laila K E Effat, Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam

Open access · greenAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular syndromology, 2023. 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
2.3field-weighted citation impact, top 12% 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, 4 citations in OpenAlex.

  1. Transcriptomic Analysis ofInternational journal of molecular sciences · 2026
    Article
  2. Transcriptomic Analysis ofbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Genetic and molecular mechanisms of hydrocephalus.Frontiers in molecular neuroscience · 2024
    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

6 authors at 2 institutions in 1 country.

Rania R AhmedMedical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Giza, Egypt.
Amina M MedhatDepartment of Biochemistry, Faculty of Science, Ain Shams University, Cairo, Egypt.
Germine M HamdyDepartment of Biochemistry, Faculty of Science, Ain Shams University, Cairo, Egypt.
Laila K E EffatMedical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Giza, Egypt.
Mohamed S Abdel-HamidMedical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Giza, Egypt.
Ghada M H Abdel-SalamClinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.
National Research Centre · EGAin Shams University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The underlying molecular defects of congenital hydrocephalus are heterogeneous and many isolated forms of hydrocephalus remain unsolved at the molecular level. Congenital hydrocephalus in males associated with agenesis of the corpus callosum is a notable characteristic of Methods and Results: Sequencing of the Conclusion: This report adds knowledge of novel pathogenic variants to the

Indexed as

Abnormal basal gangliaHirschsprung's diseaseHydrocephalusL1CAMRippled ventriclesX linked

Identifiers

PMID37766829
PMCPMC10521243
OpenAlexW4361208566

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.