Evidence map›Paper›PMID 26158416›Full record

ArticleeLife2015

Cerebellar associative sensory learning defects in five mouse autism models.

Alexander D Kloth, Aleksandra Badura, Amy Li, Adriana Cherskov, Sara G Connolly, Andrea Giovannucci, M Ali Bangash, Giorgio Grasselli, Olga Peñagarikano, Claire Piochon and 7 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

91 citing papers in PubMed, 158 citations in OpenAlex.

  1. PSD-95 drives binocular vision maturation critical for predation.bioRxiv : the preprint server for biology · 2026
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  4. A Novel Mouse Model for Developmental and Epileptic Encephalopathy by Purkinje Cell-Specific Deletion ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  7. Deletion of the Voltage-Gated Calcium Channel Gene, CaCerebellum (London, England) · 2025
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  11. Behavioral decline in Shank3Molecular autism · 2024
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  17. Behavioral regression in shank3Research square · 2024
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  18. Mice lackingProceedings of the National Academy of Sciences of the United States of America · 2024
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  19. Review
  20. Article

31 more citing papers are in PubMed but not listed here.

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

17 authors at 6 institutions in 2 countries.

Alexander D KlothDepartment of Molecular Biology and Princeton Neuroscience Institute, Princeton University, Princeton, United States.ORCID http://orcid.org/0000-0001-8119-1213
Aleksandra BaduraDepartment of Molecular Biology and Princeton Neuroscience Institute, Princeton University, Princeton, United States.
Amy LiDepartment of Molecular Biology and Princeton Neuroscience Institute, Princeton University, Princeton, United States.
Adriana CherskovDepartment of Molecular Biology and Princeton Neuroscience Institute, Princeton University, Princeton, United States.
Sara G ConnollyDepartment of Molecular Biology and Princeton Neuroscience Institute, Princeton University, Princeton, United States.
Andrea GiovannucciDepartment of Molecular Biology and Princeton Neuroscience Institute, Princeton University, Princeton, United States.
M Ali BangashDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, United States.
Giorgio GrasselliDepartment of Neurobiology, University of Chicago, Chicago, United States.ORCID http://orcid.org/0000-0002-2942-9615
Olga PeñagarikanoDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, United States.
Claire PiochonDepartment of Neurobiology, University of Chicago, Chicago, United States.
Peter T TsaiThe F.M. Kirby Neurobiology Center, Department of Neurology, Children's Hospital Boston, Harvard Medical School, Boston, United States.
Daniel H GeschwindDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, United States.
Christian HanselDepartment of Neurobiology, University of Chicago, Chicago, United States.
Mustafa SahinThe F.M. Kirby Neurobiology Center, Department of Neurology, Children's Hospital Boston, Harvard Medical School, Boston, United States.
Toru TakumiRIKEN Brain Science Institute, Wako, Japan.
Paul F WorleyDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, United States.
Samuel S-H WangDepartment of Molecular Biology and Princeton Neuroscience Institute, Princeton University, Princeton, United States.
Princeton University · USUniversity of Chicago · USBoston University · USJohns Hopkins University · USUniversity of California, Los Angeles · USRIKEN Center for Brain Science · JP

Funding

Imaging adaptive cerebellar processing at cellular resolution in awake miceR01NS045193 · NINDS · PRINCETON UNIVERSITY · PI WANG, SAMUEL SHENG-HUNG · 2003 to 2024
$7.5M
Dynamic regulation of Shank3 and ASDR01NS070301 · NINDS · JOHNS HOPKINS UNIVERSITY · PI SAVONENKO, ALENA, WORLEY, PAUL F · 2009 to 2016
$3.7M
Investigating readout of cerebellar synchrony in delay eyeblink conditioningF31MH098651 · NIMH · PRINCETON UNIVERSITY · PI KLOTH, ALEXANDER D · 2012 to 2013
$84k
NIMH NIH HHS F31 MH098651NINDS NIH HHS R01 NS045193NINDS NIH HHS R01 NS070301
6 · The paper itself

Abstract

Sensory integration difficulties have been reported in autism, but their underlying brain-circuit mechanisms are underexplored. Using five autism-related mouse models, Shank3+/ΔC, Mecp2(R308/Y), Cntnap2-/-, L7-Tsc1 (L7/Pcp2(Cre)::Tsc1(flox/+)), and patDp(15q11-13)/+, we report specific perturbations in delay eyeblink conditioning, a form of associative sensory learning requiring cerebellar plasticity. By distinguishing perturbations in the probability and characteristics of learned responses, we found that probability was reduced in Cntnap2-/-, patDp(15q11-13)/+, and L7/Pcp2(Cre)::Tsc1(flox/+), which are associated with Purkinje-cell/deep-nuclear gene expression, along with Shank3+/ΔC. Amplitudes were smaller in L7/Pcp2(Cre)::Tsc1(flox/+) as well as Shank3+/ΔC and Mecp2(R308/Y), which are associated with granule cell pathway expression. Shank3+/ΔC and Mecp2(R308/Y) also showed aberrant response timing and reduced Purkinje-cell dendritic spine density. Overall, our observations are potentially accounted for by defects in instructed learning in the olivocerebellar loop and response representation in the granule cell pathway. Our findings indicate that defects in associative temporal binding of sensory events are widespread in autism mouse models.

Indexed as

Association LearningAnimalsAutistic DisorderCerebellumConditioning, EyelidDisease Models, AnimalMicePurkinje Cellsassociative learningautism spectrum disordercerebellummouseneuroscience

Identifiers

PMID26158416
PMCPMC4512177
OpenAlexW1917392629

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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.