Evidence map›Paper›PMID 38052954›Full record

ArticleIndian journal of pediatrics2024

Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene.

Pradeep Kumar Gunasekaran, Ashna Kumar, Kandha Kumar Uk, Veena Laxmi, Sarbesh Tiwari, Lokesh Saini

Open access · bronzeAbstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Indian journal of pediatrics, 2024. 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
0.4field-weighted citation impact, top 34% 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, 2 citations in OpenAlex.

  1. Article
  2. NovelFrontiers in pediatrics · 2026
    Article
  3. Article
  4. Novel loss-of-function variants inFrontiers in pediatrics · 2024
    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

6 authors at 1 institution in 1 country.

Pradeep Kumar GunasekaranDepartment of Pediatrics, All India Institute of Medical Sciences, Jodhpur, 342005, Rajasthan, India.
Ashna KumarDepartment of Pediatrics, All India Institute of Medical Sciences, Jodhpur, 342005, Rajasthan, India.
Kandha Kumar UkDepartment of Pediatrics, All India Institute of Medical Sciences, Jodhpur, 342005, Rajasthan, India.
Veena LaxmiDepartment of Pediatrics, All India Institute of Medical Sciences, Jodhpur, 342005, Rajasthan, India.
Sarbesh TiwariDepartment of Diagnostic and Interventional Radiology, All India Institute of Medical Sciences, Jodhpur, 342005, Rajasthan, India.
Lokesh SainiDepartment of Pediatrics, All India Institute of Medical Sciences, Jodhpur, 342005, Rajasthan, India. drlokeshsaini@gmail.com.ORCID 0000-0003-3153-0736
All India Institute of Medical Sciences Jodhpur · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Adaptor Proteins, Signal TransducingSignal TransductionBase PairingChildChromosome DeletionHumansAdaptor Proteins, Signal TransducingWDR26 protein, human

Identifiers

PMID38052954
OpenAlexW4389396398

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.