Evidence map›Paper›PMID 36457583›Full record

ArticleIntractable & rare diseases research2022

KCNB1 frameshift variant caused inherited intellectual disability, developmental delay, and seizure.

Eyyup Uctepe, Fatma Nisa Esen, Sait Tümer, Hanifenur Mancılar, Ahmet Yeşilyurt

Open access · diamondAbstract read
In one paragraph

Article in Intractable & rare diseases research, 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
0.3field-weighted citation impact, top 44% 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, 4 citations in OpenAlex.

  1. Ion channels and actin: A tale of two friends.Histology and histopathology · 2025
    Review
  2. A novel autism-associatedFrontiers in cellular neuroscience · 2024
    Article
  3. 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.

Eyyup UctepeAcıbadem Ankara Tissue Typing Laboratory, Ankara, Turkey.
Fatma Nisa EsenAcibadem Labgen Genetic Diagnosis Center, İstanbul, Turkey.
Sait TümerAcibadem Labgen Genetic Diagnosis Center, İstanbul, Turkey.
Hanifenur MancılarAcibadem Labgen Genetic Diagnosis Center, İstanbul, Turkey.
Ahmet YeşilyurtAcibadem Labgen Genetic Diagnosis Center, İstanbul, Turkey.
Acıbadem University · TRAnkara University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Potassium voltage-gated channel subfamily B member 1 (

Indexed as

epilepsyintellectual disabilityintrafamilial phenotypic variabilityKCNB1

Identifiers

PMID36457583
PMCPMC9709620
OpenAlexW4310639025

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.