Evidence map›Paper›PMID 31680892›Full record

ArticleFrontiers in behavioral neuroscience2019

Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome.

Chloé Felgerolle, Betty Hébert, Maryvonne Ardourel, Géraldine Meyer-Dilhet, Arnaud Menuet, Kimberley Pinto-Morais, Jean-Charles Bizot, Jacques Pichon, Sylvain Briault, Olivier Perche

Open access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

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  7. Atypical Retinal Ganglion Cell Function in a Mouse Model of Fragile X Syndrome.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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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 3 institutions in 1 country.

Chloé FelgerolleUMR7355, CNRS, Orléans, France.
Betty HébertUMR7355, CNRS, Orléans, France.
Maryvonne ArdourelUMR7355, CNRS, Orléans, France.
Géraldine Meyer-DilhetUMR7355, CNRS, Orléans, France.
Arnaud MenuetUMR7355, CNRS, Orléans, France.
Kimberley Pinto-MoraisUMR7355, CNRS, Orléans, France.
Jean-Charles BizotKey-Obs, Orléans, France.
Jacques PichonUMR7355, CNRS, Orléans, France.
Sylvain BriaultUMR7355, CNRS, Orléans, France.
Olivier PercheUMR7355, CNRS, Orléans, France.
Université d'Orléans · FRImmunologie et Neurogénétique Expérimentales et Moléculaires · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fragile X Syndrome (FXS), the most common inherited form of human intellectual disability (ID) associated with autistic-like behaviors, is characterized by dys-sensitivity to sensory stimuli, especially vision. In the absence of Fragile Mental Retardation Protein (FMRP), both retinal and cerebral structures of the visual pathway are impaired, suggesting that perception and integration of visual stimuli are altered. However, behavioral consequences of these defects remain unknown. In this study, we used male

Indexed as

contrast sensitivitydepth perceptionFmr1−/y miceFMRPFragile X Syndromesensory sensitivityvisual abilities

Identifiers

PMID31680892
PMCPMC6797836
OpenAlexW2977355751

What OpenQuestion holds

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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.