Evidence map›Paper›PMID 36100669›Full record

ArticleMolecular psychiatry2022

Shank2/3 double knockout-based screening of cortical subregions links the retrosplenial area to the loss of social memory in autism spectrum disorders.

Débora Garrido, Stefania Beretta, Stefanie Grabrucker, Helen Friedericke Bauer, David Bayer, Carlo Sala, Chiara Verpelli, Francesco Roselli, Juergen Bockmann, Christian Proepper and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Altered Brain Structure in an ATRX-Deficient Mouse Model of Autism Spectrum Disorder.Autism research : official journal of the International Society for Autism Research · 2026
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  13. Review
  14. The Role of Zinc and NMDA Receptors in Autism Spectrum Disorders.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
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

12 authors at 3 institutions in 2 countries.

Débora Garrido *Institute of Anatomy and Cell Biology, Ulm University, 89081, Ulm, Germany.
Stefania Beretta *German Center for Neurodegenerative Diseases (DZNE), Ulm site, 89081, Ulm, Germany.
Stefanie GrabruckerInstitute of Anatomy and Cell Biology, Ulm University, 89081, Ulm, Germany.
Helen Friedericke BauerInstitute of Anatomy and Cell Biology, Ulm University, 89081, Ulm, Germany.
David BayerInternational Graduate School, Ulm University, 89081, Ulm, Germany.
Carlo SalaCNR, Institute for Neuroscience, Milano, Italy.ORCID http://orcid.org/0000-0003-0662-9523
Chiara VerpelliCNR, Institute for Neuroscience, Milano, Italy.ORCID http://orcid.org/0000-0003-2949-9725
Francesco RoselliGerman Center for Neurodegenerative Diseases (DZNE), Ulm site, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0001-9935-6899
Juergen BockmannInstitute of Anatomy and Cell Biology, Ulm University, 89081, Ulm, Germany.
Christian ProepperInstitute of Anatomy and Cell Biology, Ulm University, 89081, Ulm, Germany.
Alberto CataneseInstitute of Anatomy and Cell Biology, Ulm University, 89081, Ulm, Germany.ORCID http://orcid.org/0000-0002-8266-4913
Tobias M BoeckersInstitute of Anatomy and Cell Biology, Ulm University, 89081, Ulm, Germany. tobias.boeckers@uni-ulm.de.ORCID http://orcid.org/0000-0002-1486-8535
Universität Ulm · DENeuroscience Institute · ITGerman Center for Neurodegenerative Diseases · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Members of the Shank protein family are master scaffolds of the postsynaptic architecture and mutations within the SHANK genes are causally associated with autism spectrum disorders (ASDs). We generated a Shank2-Shank3 double knockout mouse that is showing severe autism related core symptoms, as well as a broad spectrum of comorbidities. We exploited this animal model to identify cortical brain areas linked to specific autistic traits by locally deleting Shank2 and Shank3 simultaneously. Our screening of 10 cortical subregions revealed that a Shank2/3 deletion within the retrosplenial area severely impairs social memory, a core symptom of ASD. Notably, DREADD-mediated neuronal activation could rescue the social impairment triggered by Shank2/3 depletion. Data indicate that the retrosplenial area has to be added to the list of defined brain regions that contribute to the spectrum of behavioural alterations seen in ASDs.

Indexed as

Autism Spectrum DisorderGyrus CinguliSocial InteractionAnimalsMiceMicrofilament ProteinsMutationNerve Tissue ProteinsNeuronsMicrofilament ProteinsNerve Tissue ProteinsShank2 protein, mouseShank3 protein, mouse

Identifiers

PMID36100669
PMCPMC9763120
OpenAlexW4295350461

What Socratic holds

Textmetadata
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 Socratic graph.