Evidence map›Paper›PMID 29950161›Full record

ArticleJournal of neurodevelopmental disorders2018

Visual subcircuit-specific dysfunction and input-specific mispatterning in the superior colliculus of fragile X mice.

Rachel B Kay, Nicole A Gabreski, Jason W Triplett

Abstract read
In one paragraph

Article in Journal of neurodevelopmental disorders, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Connectivity, Computation, and Plasticity of the Early Visual System.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
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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

3 authors.

Rachel B KayCenter for Neuroscience Research, Children's National Medical Center, Washington, DC, USA.
Nicole A GabreskiCenter for Neuroscience Research, Children's National Medical Center, Washington, DC, USA.
Jason W TriplettCenter for Neuroscience Research, Children's National Medical Center, Washington, DC, USA. jtriplett@childrensnational.org.ORCID 0000-0002-8064-3617

Funding

Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2016 to 2020
$5.9M
Mechanisms of Synaptic Specificity in Visual CircuitsR01EY025627 · NEI · CHILDREN'S RESEARCH INSTITUTE · PI TRIPLETT, JASON · 2015 to 2025
$4.5M
NEI NIH HHS R01 EY025627NICHD NIH HHS U54 HD090257
6 · The paper itself

Abstract

backgroundSensory processing deficits are frequently co-morbid with neurodevelopmental disorders. For example, patients with fragile X syndrome (FXS), caused by a silencing of the FMR1 gene, exhibit impairments in visual function specific to the dorsal system, which processes motion information. However, the developmental and circuit mechanisms underlying this deficit remain unclear. Recently, the superior colliculus (SC), a midbrain structure regulating head and eye movements, has emerged as a model for dissecting visual circuit development and function. Previous studies have demonstrated a critical role for activity-dependent processes in the development of visual circuitry in the SC. Based on the known role of the FMR1 gene product in activity-dependent synaptic plasticity, we explored the function and organization of visual circuits in the SC of a mouse model of FXS (Fmr1

methodsWe utilized in vivo extracellular electrophysiology in combination with computer-controlled visual stimuli to determine the receptive field properties of visual neurons in the SC of control and Fmr1

resultsReceptive fields of visual neurons in the SC of Fmr1

conclusionsFmr1 is required for the proper development of visual circuit organization and function in the SC. We find that visual dysfunction is heterogeneously manifested in a subcircuit-specific manner in Fmr1

Indexed as

AnimalsDisease Models, AnimalFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeMaleMice, Inbred C57BLMice, KnockoutNeuronsPhotic StimulationSuperior ColliculiVisual FieldsVisual PathwaysVisual PerceptionFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Axis selectiveDirection selectiveReceptive field

Identifiers

PMID29950161
PMCPMC6022700

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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.