Evidence map›Paper›PMID 42751493›Full record

ArticleNeurology. Genetics2026

Association of Bilateral Vestibulopathy With the

Felix L Heindl, Michael Strupp, Annette M Hartmann, Andreas Zwergal, Bettina Konte, Dan Rujescu, Ina Giegling

Abstract read
In one paragraph

Article in Neurology. Genetics, 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

7 authors.

Felix L HeindlDepartment of Neurology and German Center for Vertigo and Balance Disorders, LMU University Hospital, LMU Medizin, LMU Munich, Germany.ORCID https://orcid.org/0009-0000-6478-3313
Michael StruppDepartment of Neurology and German Center for Vertigo and Balance Disorders, LMU University Hospital, LMU Medizin, LMU Munich, Germany.ORCID https://orcid.org/0000-0002-9544-2279
Annette M HartmannDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Austria; and.ORCID https://orcid.org/0000-0003-0689-4335
Andreas ZwergalDepartment of Neurology and German Center for Vertigo and Balance Disorders, LMU University Hospital, LMU Medizin, LMU Munich, Germany.ORCID https://orcid.org/0000-0002-3839-8398
Bettina KonteDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Austria; and.
Dan RujescuDepartment of Psychiatry and Psychotherapy, Medical University of Vienna, Austria; and.ORCID https://orcid.org/0000-0002-1432-313X
Ina GieglingDepartment of Psychiatry and Psychotherapy, Comprehensive Center for Clinical Neurosciences and Mental Health, Medical University of Vienna, Austria.ORCID https://orcid.org/0000-0001-8407-7512

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Bilateral vestibulopathy (BVP) is a chronic disorder resulting from bilateral loss of peripheral vestibular function. Although several etiologies have been identified, such as ototoxic exposure, bilateral Menière disease, and, more recently, monogenic causes including Methods: We performed a genome-wide association study (GWAS) in a European cohort of 132 individuals with idiopathic BVP and 3,410 unaffected controls. Clinical and demographic data were collected from affected individuals. Patients were diagnosed according to the Bárány Society criteria using video head-impulse testing and/or caloric irrigation. After stringent quality control and outlier removal, genome-wide association testing was conducted on approximately 7.3 million imputed variants, followed by gene-based and functional post-GWAS analyses, including functional variant annotation, expression quantitative trait locus (eQTL) mapping, chromatin interaction analysis, gene-set enrichment, and regulatory motif annotation. Results: Three variants at 2 loci reached genome-wide significance. The strongest association was observed at the chromosome 19p12 Discussion: This study identifies the

Identifiers

PMID42751493
PMCPMC13579776

What OpenQuestion holds

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Registered trials

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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.