ReviewThe application of clinical genetics2015
The genetics of Ménière's disease.
Review in The application of clinical genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 4 of them syntheses that pooled 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.
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.
Who cites it
19 citing papers in PubMed, 4 syntheses or guidelines pooled it.
- Intratympanic gentamicin for Ménière's disease.The Cochrane database of systematic reviews · 2023Pooled it
- Intratympanic corticosteroids for Ménière's disease.The Cochrane database of systematic reviews · 2023Pooled it
- Surgical interventions for Ménière's disease.The Cochrane database of systematic reviews · 2023Pooled it
- Systemic pharmacological interventions for Ménière's disease.The Cochrane database of systematic reviews · 2023Pooled it
- ZDHHC5 may regulate the function of NKT cells and the immune response in Meniere's disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026Article
- Modern Perspectives on the Mechanisms and Non-Genetic Factors in Ménière's Disease-A Narrative Review.Biomedicines · 2026Review
- The Impact of Genetic Factors in Ménière's Disease.International journal of molecular sciences · 2026Review
- A national survey of the diagnosis and management of Ménière's disease among ENT consultants, UK.Annals of the Royal College of Surgeons of England · 2026Article
- Immunological mechanisms in Meniere's disease.Frontiers in immunology · 2025Review
- Lifestyle and dietary interventions for Ménière's disease.The Cochrane database of systematic reviews · 2023Review
- Positive pressure therapy for Ménière's disease.The Cochrane database of systematic reviews · 2023Review
- Nutraceuticals for Peripheral Vestibular Pathology: Properties, Usefulness, Future Perspectives and Medico-Legal Aspects.Nutrients · 2021Review
- The cardiovascular aspects of a Ménière's disease population - A pilot study.Journal of otology · 2019Article
- Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis.Frontiers in molecular neuroscience · 2019Article
- X-Linked Sensorineural Hearing Loss: A Literature Review.Current genomics · 2018Review
- Review
- Histopathology of Meniere's disease.Operative techniques in otolaryngology--head and neck surgery · 2016Article
- Motion Sickness: Current Knowledge and Recent Advance.CNS neuroscience & therapeutics · 2016Review
- An Exploratory Study to Detect Ménière's Disease in Conventional MRI Scans Using Radiomics.Frontiers in neurology · 2016Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Our understanding of the genetic basis of Ménière's disease (MD) is still limited. Although the familial clustering and the geographical and racial differences in incidence strongly suggest a certain role for genetic factors in the development of MD, no convincing evidence for an association with any gene exists, at present. In this review, starting from rational bases for a genetic approach to MD, we explored the numerous reports published in literature and summarize the recent advances in understanding of the genetic fundaments of the disease.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.