Evidence map›Paper›PMID 42653504›Full record

ArticleInternational journal of molecular sciences2026

Association of

Sara Romero-Vázquez, Cécile Méjécase, Ana Catalina Rodriguez-Martinez, Nicola Cronbach, Mariya Moosajee

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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

5 authors.

Sara Romero-VázquezUCL Institute of Ophthalmology, London EC1V 9EL, UK.
Cécile MéjécaseUCL Institute of Ophthalmology, London EC1V 9EL, UK.
Ana Catalina Rodriguez-MartinezUCL Institute of Ophthalmology, London EC1V 9EL, UK.
Nicola CronbachUCL Institute of Ophthalmology, London EC1V 9EL, UK.ORCID 0000-0001-8492-2608
Mariya MoosajeeUCL Institute of Ophthalmology, London EC1V 9EL, UK.ORCID 0000-0003-1688-5360

Funding

Wellcome TrustWellcome Trust 205174/Z/16/Z
6 · The paper itself

Abstract

PHARC (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa and cataracts) syndrome is a rare neurodegenerative inherited disorder characterized by a spectrum of these clinical phenotypes. Due to the considerable heterogeneity in the age of onset of the different clinical features and the similarities with other conditions, it is often misdiagnosed. Variants in the

Indexed as

AtaxiaCataractHearing Loss, SensorineuralMonoacylglycerol LipasesPolyneuropathiesRetinitis PigmentosaGenetic Association StudiesHumansMutationPhenotypeABHD12 protein, humanMonoacylglycerol LipasesABHD12ataxiacataractshearing lossPHARCpolyneuropathyretinitis pigmentosaVLC-lysophosphatidylserine

Identifiers

PMID42653504
PMCPMC13513054

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.