Evidence map›Paper›PMID 36703628›Full record

ArticleFrontiers in neurology2022

Case report:

Svea Horn, Magdalena Danyel, Nina Erdmann, Felix Boschann, Cecilia Gunnarsson, Saskia Biskup, Jerome Juengling, Cornelia Potratz, Christine Prager, Angela M Kaindl

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

10 authors at 3 institutions in 2 countries.

Svea HornDepartment of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Magdalena DanyelInstitute of Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Nina ErdmannDepartment of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Felix BoschannInstitute of Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Cecilia GunnarssonDepartment of Clinical Genetics, Linköping University, Linköping, Sweden.
Saskia BiskupPraxis für Humangenetik Tübingen, Tübingen, Germany.
Jerome JuenglingPraxis für Humangenetik Tübingen, Tübingen, Germany.
Cornelia PotratzDepartment of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Christine PragerDepartment of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Angela M KaindlDepartment of Pediatric Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Charité - Universitätsmedizin Berlin · DEPraxis für Humangenetik Tübingen · DELinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biallelic variants in the kaptin gene

Indexed as

epilepsyKPTN genemacrocephalyneurodevelopment delaysplice site variant

Identifiers

PMID36703628
PMCPMC9871926
OpenAlexW4315433698

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.