Evidence map›Paper›PMID 33494179›Full record

ArticleGenes2021

Novel

Randi von Wrede, Monika Jeub, Idil Ariöz, Christian E Elger, Hubertus von Voss, Hanns-Georg Klein, Albert J Becker, Susanne Schoch, Rainer Surges, Wolfram S Kunz

Open access · goldAbstract read
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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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 2 institutions in 1 country.

Randi von WredeDepartment of Epileptology, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0002-9430-5037
Monika JeubBeta Neurologie GmbH, 53227 Bonn, Germany.
Idil AriözSection for Translational Epilepsy Research, Department of Neuropathology, University Hospital Bonn, 53127 Bonn, Germany.
Christian E ElgerBeta Neurologie GmbH, 53227 Bonn, Germany.
Hubertus von VossCenter for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues, 82152 Martinsried, Germany.
Hanns-Georg KleinCenter for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues, 82152 Martinsried, Germany.
Albert J BeckerSection for Translational Epilepsy Research, Department of Neuropathology, University Hospital Bonn, 53127 Bonn, Germany.
Susanne SchochDepartment of Epileptology, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0002-2046-2670
Rainer SurgesDepartment of Epileptology, University Hospital Bonn, 53127 Bonn, Germany.
Wolfram S KunzDepartment of Epileptology, University Hospital Bonn, 53127 Bonn, Germany.ORCID 0000-0003-1113-3493
University Hospital Bonn · DECS Diagnostics · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we describe four patients suffering from a rather broad spectrum of epilepsy-related disorders, ranging from developmental and epileptic encephalopathy with intellectual disability (DEE) to genetic generalized epilepsy (GGE), which all harbor novel

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseMutationPhenotypeAdultAmino Acid SequenceBase SequenceChildComputational BiologyElectroencephalographyEpilepsyEther-A-Go-Go Potassium ChannelsExome SequencingFemaleGerm-Line MutationHigh-Throughput Nucleotide SequencingEther-A-Go-Go Potassium ChannelsKCNH1 protein, humanepilepsyKCNH1 mutationsKv10.1 potassium channel

Identifiers

PMID33494179
PMCPMC7909785
OpenAlexW3122222023

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.