Evidence map›Paper›PMID 33623275›Full record

ArticleAnnals of Indian Academy of Neurology

Identification of a Novel Mutation in

Esra Sarigecili, Meltem Cobanogullari Direk, Mustafa Komur, Sevcan Tug Bozdogan, Cetin Okuyaz

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Annals of Indian Academy of Neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Esra SarigeciliDepartment of Pediatric Neurology, Faculty of Medicine, Mersin University, Mersin, Turkey.
Meltem Cobanogullari DirekDepartment of Pediatric Neurology, Faculty of Medicine, Mersin University, Mersin, Turkey.
Mustafa KomurDepartment of Pediatric Neurology, Faculty of Medicine, Mersin University, Mersin, Turkey.
Sevcan Tug BozdoganDepartment of Medical Genetics, Faculty of Medicine, Çukurova University, Adana, Turkey.
Cetin OkuyazDepartment of Pediatric Neurology, Faculty of Medicine, Mersin University, Mersin, Turkey.
Mersin Üniversitesi · TRCukurova University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a 2.5-year-old Turkish boy who first presented with nystagmus, lack of eye contact, and hypotonia at 2 months of age and developed refractory seizures when 6 months old. Extensive metabolic tests and imaging being noncontributory, whole-exome sequencing was carried out which revealed a heterozygote

Indexed as

EpilepsyGRIN2Aneurodevelopmental delaynystagmuswhole-exome sequencing

Identifiers

PMID33623275
PMCPMC7887506
OpenAlexW2913121021

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.