Evidence map›Paper›PMID 37927744›Full record

ArticleCureus2023

Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moroccan Child.

Hinde El Mouhi, Meriame Abbassi, Hanane Sayel, Said Trhanint, Abdelhafid Natiq, Brahim El Hejjioui, Merym Jalte, Youssef Ahmadi, Sana Chaouki

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

9 authors at 4 institutions in 2 countries.

Hinde El MouhiLaboratory of Biomedical and Translational Research, Faculty of Medicine and Pharmacy and Dental Medicine, Sidi Mohamed Ben Abdellah University, Fez, MAR.
Meriame AbbassiLaboratory of Biomedical and Translational Research, Faculty of Medicine and Pharmacy and Dental Medicine, Sidi Mohamed Ben Abdellah University, Fez, MAR.
Hanane SayelLaboratory of Medical Genetics and Onco-genetics, Central Laboratory of Medical Analysis, Centre Hospitalier Universitaire (CHU) Hassan II, Fez, MAR.
Said TrhanintLaboratory of Medical Genetics and Onco-genetics, Central Laboratory of Medical Analysis, Centre Hospitalier Universitaire (CHU) Hassan II, Fez, MAR.
Abdelhafid NatiqDepartment of Genetics, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, MAR.
Brahim El HejjiouiLaboratory of Biomedical and Translational Research, Faculty of Medicine and Pharmacy and Dental Medicine, Sidi Mohamed Ben Abdellah University, Fez, MAR.
Merym JalteLaboratory of Biotechnology, Environment, Agri-food, and Health (LBEAH), Faculty of Sciences Dhar El Mahraz, Sidi Mohamed Ben Abdellah University, Fez, MAR.
Youssef AhmadiLaboratory of Medical Genetics and Onco-genetics, Central Laboratory of Medical Analysis, Centre Hospitalier Universitaire (CHU) Hassan II, Fez, MAR.
Sana ChaoukiLaboratory of Biomedical and Translational Research, Faculty of Medicine and Pharmacy and Dental Medicine, Sidi Mohamed Ben Abdellah University, Fez, MAR.
Centre Hospitalier Universitaire Hassan II · MAMohammed V University · MASidi Mohamed Ben Abdellah University · MACenter for Business Studies · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal dominant intellectual development disorder-6 (MRD6) arises from a

Indexed as

autosomal dominant intellectual development disorder-6de novo mutationexome sequencinggrin2bmoroccanmrd6

Identifiers

PMID37927744
PMCPMC10623208
OpenAlexW4387335883

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.