Evidence map›Paper›PMID 41822111›Full record

ArticleBrain communications2026

Christoph Jüschke, Kira Linsel, Marta Owczarek-Lipska, Nicola Brandt, Sarah Zunken, Janine Altmüller, Markus N Preising, Dennis Kastrati, Holger Thiele, Mervyn G Thomas and 7 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Brain communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Christoph JüschkeHuman Genetics, School VI-School of Medicine and Health Sciences, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.ORCID https://orcid.org/0000-0001-5842-4824
Kira LinselHuman Genetics, School VI-School of Medicine and Health Sciences, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.
Marta Owczarek-LipskaHuman Genetics, School VI-School of Medicine and Health Sciences, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.
Nicola BrandtDivision of Human Medicine, School VI-School of Medicine and Health Sciences, Research Group Anatomy, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.ORCID https://orcid.org/0000-0003-2483-9292
Sarah ZunkenHuman Genetics, School VI-School of Medicine and Health Sciences, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.
Janine AltmüllerCologne Center for Genomics (CCG) and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
Markus N PreisingDepartment of Ophthalmology, Justus-Liebig-University Giessen, Universitaetsklinikum Giessen and Marburg UKGM GmbH Giessen Campus, Giessen, Germany.ORCID https://orcid.org/0000-0002-1596-5978
Dennis KastratiHuman Genetics, School VI-School of Medicine and Health Sciences, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.
Holger ThieleCologne Center for Genomics (CCG) and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.
Mervyn G ThomasUlverscroft Eye Unit, School of Psychology and Vision Sciences, University of Leicester, Leicester LE2 7LX, UK.
Peter NürnbergCologne Center for Genomics (CCG) and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0002-7228-428X
Birgit LorenzDepartment of Ophthalmology, Justus-Liebig-University Giessen, Universitaetsklinikum Giessen and Marburg UKGM GmbH Giessen Campus, Giessen, Germany.
Ulrich KellnerRare Retinal Disease Center, MVZ Augenärztliches Diagnostik- und Therapiecentrum Siegburg GmbH, Siegburg, Germany.ORCID https://orcid.org/0000-0001-5221-4631
Anja U BräuerDivision of Human Medicine, School VI-School of Medicine and Health Sciences, Research Group Anatomy, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.ORCID https://orcid.org/0000-0003-3651-1470
G Christoph KorenkeDepartment of Neuropediatrics, University Children's Hospital, Klinikum Oldenburg, Oldenburg, Germany.
Irene GottlobUlverscroft Eye Unit, School of Psychology and Vision Sciences, University of Leicester, Leicester LE2 7LX, UK.
John NeidhardtHuman Genetics, School VI-School of Medicine and Health Sciences, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.ORCID https://orcid.org/0000-0002-9205-8394

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infantile nystagmus (IN) is a common neuro-ophthalmological disorder that presents as early-onset involuntary oscillations of the eyes. Here, we report a novel genotype-phenotype correlation that associates sequence alterations in the calcium voltage-gated channel auxiliary subunit beta 3 (

Indexed as

CaVβ subunithigh-voltage activated calcium channelidiopathic congenital nystagmusidiopathic infantile nystagmus (IIN)voltage-gated Ca2+ channel (VGCC)

Identifiers

PMID41822111
PMCPMC12977960

What OpenQuestion holds

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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.