Evidence mapPaperPMID 39767643Full record

ArticleBiomedicines2024

Genetic Heterogeneity in Four Probands Reveals

Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B Williams, Zehra Agha

Abstract read
In one paragraph

Article in Biomedicines, 2024. 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
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

1 citing paper in PubMed.

  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

4 authors.

Behjat Ul MudassirTranslational Genomics Laboratory, Department of Biosciences, COMSATS University, Islamabad 45550, Pakistan.ORCID 0000-0002-3957-9596
Mujaddid MudassirRawalpindi Institute of Cardiology, Rawal Road, Rawalpindi 46000, Pakistan.
Jamal B WilliamsDepartment of Psychiatry, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA.ORCID 0000-0003-4597-7686
Zehra AghaTranslational Genomics Laboratory, Department of Biosciences, COMSATS University, Islamabad 45550, Pakistan.ORCID 0000-0003-3413-0578

Funding

HEC NRPU project awarded to Dr Zehra Agha 16281
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

cognitive diseases in four familiesharmful mutations in Pakistani familiesmono-allelic and bi-allelic variants causing NDDsneurodevelopmental syndromic probands

Identifiers

PMID39767643
PMCPMC11727043

What Socratic 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 Socratic graph.