Evidence map›Paper›PMID 35414199›Full record

ArticleASN neuro

KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures.

Sanja Dimitrijevic, Biljana Jekic, Suzana Cvjeticanin, Aleksandra Tucovic, Tamara Filipovic, Ivana Novaković, Bojana Ivić, Dimitrije Nikolic

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in ASN neuro. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Neuronal KActa pharmacologica Sinica · 2024
    Review
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

8 authors.

Sanja DimitrijevicSpecial Hospital for Cerebral Palsy and Developmental Neurology, School of Medicine, 54801University of Belgrade, Belgrade, Serbia.ORCID 0000-0002-6421-5786
Biljana JekicInstitute of Human Genetics, School of Medicine, 54801University of Belgrade, Belgrade, Serbia.
Suzana CvjeticaninInstitute of Human Genetics, School of Medicine, 54801University of Belgrade, Belgrade, Serbia.
Aleksandra TucovicInstitute of Oncology and Radiology, Belgrade, Serbia.
Tamara FilipovicInstitute for Rehabilitation, School of Medicine, 54801University of Belgrade, Belgrade, Serbia.
Ivana NovakovićInstitute of Human Genetics, School of Medicine, 54801University of Belgrade, Belgrade, Serbia.
Bojana IvićUniversity Clinic for Gynecology and Obstetrics "Narodni front", School of Medicine, 54801University of Belgrade, Belgrade, Serbia.
Dimitrije NikolicUniversity Children's Hospital Tiršova, School of Medicine, 54801University of Belgrade, Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Seizures, FebrileSymportersChildGenetic MarkersHumansK Cl- CotransportersPolymorphism, GeneticGenetic MarkersK Cl- CotransportersSLC12A5 protein, humanSymportersfebrile seizuregene polymorphismKCC2 geneTRPV1 gene

Identifiers

PMID35414199
PMCPMC9016559

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.