Evidence map›Paper›PMID 37371259›Full record

ArticleChildren (Basel, Switzerland)2023

Microcephaly, Short Stature, Intellectual Disability, Speech Absence and Cataract Are Associated with Novel Bi-Allelic Missense Variant in

Behjat Ul Mudassir, Zehra Agha

Open access · goldAbstract readCase Reports
In one paragraph

Article in Children (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Behjat Ul MudassirTranslational Genomics Laboratory, Department of Biosciences, COMSATS University, Islamabad 45550, Pakistan.ORCID 0000-0002-3957-9596
Zehra AghaTranslational Genomics Laboratory, Department of Biosciences, COMSATS University, Islamabad 45550, Pakistan.ORCID 0000-0003-3413-0578
COMSATS University Islamabad · PK

Funding

Pakistan Council of Scientific & Industrial Research ref. SW(HQ)DRS-2/2021/2065
6 · The paper itself

Abstract

The

Indexed as

MCPH and RTTN gene missense mutationmissense variant in RTTN geneRTTN gene related Seckel syndrome caseSeckel syndrome case in Islamabad

Identifiers

PMID37371259
PMCPMC10297240
OpenAlexW4380051011

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.